CRITICAL CONSTANTS

The parameters of the liquid–gas critical point are important 15. VonNiederhausern, D. M., Wilson, G. M., and Giles, N. F., J. Chem. constants in determining the behavior of fluids. This table lists the Eng. Data , 45, 157, 2000. critical temperature, pressure, and molar volume, as well as the 16. Nikitin, E. D., Popov, A. P., Bogatishcheva, N. S., and Yatluk, Y. G., J. normal boiling point, for approximately 850 inorganic and organic Chem. Eng. Data, 47, 1012, 2002. 17. Wilson, G. M., VonNiederhausern, D. M., and Giles, N. F., J. Chem. substances. The properties and their units are: Eng. Data, 47, 761, 2002. 18. Wang, B. H., Adcock, J. L., Mathur, S. B., and Van Hook, W. A., J. T : Normal boiling point in kelvins at a pressure of 101.325 b Chem. Thermodynamics, 23, 699, 1991. kPa (1 atmosphere); an “s” following the value indicates 19. Chae, H. B., Schmidt, J. W., and Moldover, M. R., J. Phys. Chem ., 94, a sublimation point (temperature at which the solid is in 8840, 1990. equilibrium with the gas at a pressure of 101.325 kPa) 20. Dillon, I. G., Nelson, P. A., and Swanson, B. S., J. Chem. Phys ., 44, 4229, 1966. Tc: Critical temperature in kelvins 21. Physical Constants of Hydrocarbon and Non-Hydrocarbon Pc: Critical pressure in megapascals V : Critical molar volume in cm 3/mol Compounds , ASTM Data Series DS 4B, ASTM, Philadelphia, 1988. c 22. Nowak, P., Tielkes, T., Kleinraum, R., and Wagner, W., J. Chem. Thermodynamics, 29, 885, 1997. The number of digits given for Tb, Tc, and Pc indicates the esti- mated accuracy of these quantities; however, values of T greater 23. Steele, W. V., Chirico, R. D., Nguyen, A., and Knipmeyer, S. E., J. c Chem. Thermodynamics, than 750 K may be in error by 10 K or more. Although most V 27, 311, 1995 c 24. Duan, Y. Y., Shi, L., Zhu, M. S., and Han, L. Z., J. Chem. Eng. Data, 44, values are given to three figures, they cannot be assumed accurate 501, 1999. to better than a few percent. All values are experimentally deter- 25. Weber, L. A., and Defibaugh, D. R., J. Chem. Eng. Data, 41, 382, 1996. mined except for a few values, indicated by an asterisk*, which are 26. Duarte-Garza, H. A., Hwang, C. A., Kellerman, S. A., Miller, R. C., based on extrapolations. Methods of measurement are described Hall, K. R., and Holste, J. C., J. Chem. Eng. Data, 42, 497, 1997. and critiqued in Reference 1. 27. Weber, L. A., and Defibaugh, D. R., J. Chem. Eng. Data, 41, 1477, 1996. Many of the critical constants in this table are taken from re- 28. Fujiwara, K., Nakamura, S., and Noguchi, M., J. Chem. Eng. Data, 43, views produced by the IUPAC Commission on Thermodynamics 55, 1998. J. Chem. Eng. Data, (References 1– 8). Compounds are listed by molecular formula in 29. Widiatmo, J. V., Morimoto, Y., and Watanabe, K., 47, 1246, 2002. modified Hill order, with compounds not containing carbon pre- 30. Duarte-Garza, H. A., Stouffer, C. E., Hall, K. R., Holste, J. C., Marsh, K. ceding those that do contain carbon. N., and Gammon, B. E., J. Chem. Eng. Data, 42, 745, 1997. The assistance of Douglas Ambrose is gratefully acknowledged. 31. Nikitin, E. D., Pavlov, P. A., Popov, A. P., and Nikitina, H. E., J. Chem. Thermodynamics, 27, 945, 1995. References 32. Sako, T., Sato, M., Nakazawa, N., Oowa, M., Yasumoto, M., Ito, H., and Yamashita, S., J. Chem. Eng. Data, 41, 802, 1996. 33. Zhang, H-L, Sato, H., and Watanabe, K., J. Chem. Eng. Data, 40, 1281, 1. Ambrose, D., and Young, C. L., J. Chem. Eng. Data, 40, 345, 1995. 1995. [IUPAC Part 1] 34. Sifner, O., and Klomfar, J., J. Phys. Chem. Ref. Data, 23, 63, 1994. 2. Ambrose, D., and Tsonopoulos, C., J. Chem. Eng. Data, 40, 531, 1995. 35. Younglove, B. A., and McLinden, M. O., J. Phys. Chem. Ref. Data, 23, [IUPAC Part 2] 731, 1994. 3. Tsonopoulos, C., and Ambrose, D., J. Chem. Eng. Data , 40, 547, 1995. 36. Tillner-Roth, R., and Baehr, H. D., J. Phys. Chem. Ref. Data, 23, 657, [IUPAC Part 3] 1994. 4. Gude, M., and Teja, A. S., J. Chem. Eng. Data , 40, 1025, 1995. [IUPAC 37. Xiang, H. W., J. Phys. Chem. Ref. Data, 30, 1161, 2001. Part 4] 38. Goodwin, A. H. R., Defibaugh, D. R., and Weber, L. A., J. Chem. Eng. 5. Daubert, T. E., J. Chem. Eng. Data , 41, 365, 1996. [IUPAC Part 5] Data, 43, 846, 1998. 6. Tsonopoulos, C., and Ambrose, D., J. Chem. Eng. Data , 41, 645, 1996. 39. Lim, J. S., Park, K. H., Lee, B. G., and Kim, J-D., J. Chem. Eng. Data, 46, [IUPAC Part 6] 1580, 2001. 7. Kudcharker, A. P., Ambrose, D., and Tsonopoulos, C., J. Chem. Eng. 40. Linstrom, P. J., and Mallard, W. G., Eds., NIST Chemistry WebBook , Data , 46, 457, 2001. [IUPAC Part 7] NIST Standard Reference Database No. 69, July 2001, National 8. Tsonopoulos, C., and Ambrose, D., J. Chem. Eng. Data, 46, 480, 2001. Institute of Standards and Technology, Gaithersburg, MD 20899, [IUPAC Part 8] http://webbook.nist.gov. 9. Ambrose, D., “Vapor-Liquid Constants of Fluids”, in Stevenson, R. 41. ASHRAE Fundamentals Handbook 2001 , Chapter 19. Refrigerants, M., and Malanowski, S., Eds., Handbook of the Thermodynamics of American Society of Heating, Refrigerating, and Air-Conditioning Organic Compounds , Elsevier, New York, 1987. Engineers, Atlanta, GA, 2001. 10. Das, A., Frenkel, M., Gadalla, N. A. M., Kudchadker, S., Marsh, K. N., 42. Fialho, P. S., and Nieto de Castro, C. A., Int. J. Thermophys., 21, 385, Rodgers, A. S., and Wilhoit, R. C., J. Phys. Chem. Ref. Data , 22, 659, 2000. 1993. 43. Vargaftik, N. B., Int. J. Thermophys ., 11, 467, 1990 11. Wilson, L. C., Wilson, H. L., Wilding, W. V., and Wilson, G. M., J. 44. Vargaftik, N.B., Vinogradov, Y. K., and Yargin, V. S., Handbook of Chem. Eng. Data, 41, 1252, 1996. Physical Properties of Liquids and Gases, Third Edition , Begell House, 12. Daubert, T. E., Danner, R. P., Sibul, H. M., and Stebbins, C. C., New York, 1996. Physical and Thermodynamic Properties of Pure Compounds: Data 45. Schmidt, J. W., Carrillo-Nava, E., and Moldover, M. R., Fluid Phase Compilation , extant 2002 (core with supplements), Taylor & Francis, Equilibria , 122, 187, 1996. Bristol, PA. 46. Defibaugh, D. R., Gillis, K. A., Moldover, M. R., Morrison, G., and 13. Morton, D. W., Lui, M. P. W., Tran, C. A., and Young, C. L., J. Chem. Schmidt, J. W., Fluid Phase Equilibria, 81, 285, 1992. Eng. Data, 45, 437, 2000. 47. Salvi-Narkhede, M., Wang, B-H., Adcock, J. L., and Van Hook, W. A., 14. VonNiederhausern, D. M., Wilson, L. C., Giles, N. F., and Wilson, G. J. Chem. Thermodynamics, 24, 1065, 1992. M., J. Chem. Eng. Data , 45, 154, 2000. 48. Nikitin, E. D., Pavlov, P. A., and Pavlov, A. P., Fluid Phase Equilib ., 189, 151–161, 2001.

6-37 6-38 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

AlBr 3 Aluminum bromide 528 763 2.89 310 9

AlCl 3 Aluminum chloride 453 s 620 2.63 257 9

AlI 3 Aluminum iodide 655 983 408 9 Ar Argon 87.30 150.87 4.898 75 9 As Arsenic 876 1673 35 9

AsCl 3 Arsenic(III) chloride 403 654 252 9

AsH 3 Arsine 210.7 373.1 9

BBr 3 Boron tribromide 364 581 272 9

BCl 3 Boron trichloride 285.80 455 3.87 239 9

BF 3 Boron trifluoride 172 260.8 4.98 115 9

BI 3 Boron triiodide 482.7 773 356 9

B2H6 Diborane 180.8 289.8 4.05 9

BiBr 3 Bismuth tribromide 726 1220 301 9

BiCl 3 Bismuth trichloride 720 1179 12.0 261 9 BrH Hydrogen bromide 206.77 363.2 8.55 9 BrI Iodine bromide 389 719 139 9

Br 2 Bromine 332.0 588 10.34 127 9

Br 2Hg Mercury(II) bromide 595 1012 9

Br 3Ga Gallium(III) bromide 552 806.7 303 9

Br 3HSi Tribromosilane 382 610.0 305 9

Br 3P Phosphorus(III) bromide 446.4 711 300 9

Br 3Sb Antimony(III) bromide 553 904 300 9

Br 4Ge Germanium(IV) bromide 459.50 718 392 9

Br 4Hf Hafnium(IV) bromide 596 s 746 415 9

Br 4Si Tetrabromosilane 427 663 382 9

Br 4Sn Tin(IV) bromide 478 744 417 9

Br 4Ti Titanium(IV) bromide 503 795.7 391 9

Br 4Zr Zirconium(IV) bromide 633 s 805 424 9

Br 5Ta Tantalum(V) bromide 622 974 461 9

ClFO 3 Perchloryl fluoride 226.40 368.4 5.37 161 9

ClF 2N Nitrogen chloride difluoride 206 337.5 5.15 9

ClF 2P Phosphorus(III) chloride difluoride 225.9 362.4 4.52 9

ClF 2PS Phosphorothioc chloride difluoride 279.5 439.2 4.14 9

ClF 3Si Chlorotrifluorosilane 203.2 307.7 3.46 9

ClF 5 Chlorine pentafluoride 260.1 416 5.27 233 9

ClF 5S Sulfur chloride pentafluoride 254.10 390.9 9 ClH Hydrogen chloride 188 324.7 8.31 81 9

ClH 4N Ammonium chloride 611 s 1155 163.5 9

ClH 4P Phosphonium chloride 246 s 322.3 7.37 9 ClNO Nitrosyl chloride 267.7 440 9 ClOV Vanadyl chloride 400 636 171 9

Cl 2 Chlorine 239.11 416.9 7.991 123 9

Cl 2FP Phosphorus(III) dichloride fluoride 287.00 463.0 4.96 9

Cl 2F2Si Dichlorodifluorosilane 241 369.0 3.5 9

Cl 2Hg Mercury(II) chloride 577 973 174 9

Cl 2OSe Selenium oxychloride 450 730 7.09 235 9

Cl 3FSi Trichlorofluorosilane 285.40 438.6 3.58 9

Cl 3Ga Gallium(III) chloride 474 694 263 9

Cl 3HSi Trichlorosilane 306 479 268 9

Cl 3P Phosphorus(III) chloride 349.3 563 264 9

Cl 3Sb Antimony(III) chloride 493.5 794 272 9

Cl 4Ge Germanium(IV) chloride 359.70 553.2 3.861 330 9

Cl 4Hf Hafnium(IV) chloride 590 s 725.7 5.42 314 9

Cl 4ORe Rhenium(VI) oxytetrachloride 496 781 362 9

Cl 4OW Tungsten(VI) oxytetrachloride 500.70 782 338 9

Cl 4Si Tetrachlorosilane 330.80 508.1 3.593 326 9

Cl 4Sn Tin(IV) chloride 387.30 591.9 3.75 351 9

Cl 4Te Tellurium tetrachloride 660 1002 8.56 310 9

Cl 4Ti Titanium(IV) chloride 409.60 638 4.66 339 9

Cl 4Zr Zirconium(IV) chloride 604 s 778 5.77 319 9 Critical Constants 6-39

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

Cl 5Mo Molybdenum(V) chloride 541 850 369 9

Cl 5Nb Niobium(V) chloride 527.2 803.5 4.88 397 9

Cl 5P Phosphorus(V) chloride 433 s 646 9

Cl 5Ta Tantalum(V) chloride 512.50 767 402 9

Cl 6W Tungsten(VI) chloride 619.90 923 422 9 Cs Cesium 944 1938 9.4 341 43 FH Hydrogen fluoride 293 461 6.48 69 9

FNO 2 Nitryl fluoride 200.8 349.5 9

F2 Fluorine 85.03 144.13 5.172 66 9

F2HN Difluoramine 250 403 9

F2N2 cis -Difluorodiazine 167.40 272 7.09 9

F2N2 trans -Difluorodiazine 161.70 260 5.57 9

F2O Fluorine monoxide 128.40 215 9

F2Xe Xenon difluoride 387.50 631 9.32 148 9

F3N Nitrogen trifluoride 144.40 234.0 4.46 126 9

F3NO Trifluoramine oxide 185.7 303 6.43 147 9

F3P Phosphorus(III) fluoride 171.4 271.2 4.33 9

F3PS Phosphorothioc trifluoride 220.90 346.0 3.82 9

F4N2 Tetrafluorohydrazine 199 309 3.75 9

F4S Sulfur tetrafluoride 232.70 364 9

F4Si Tetrafluorosilane 187 259.0 3.72 9

F4Xe Xenon tetrafluoride 388.90 612 7.04 188 9

F5Nb Niobium(V) fluoride 502 737 6.28 155 9

F6Mo Molybdenum(VI) fluoride 307.2 473 4.75 226 9

F6S Sulfur hexafluoride 209.35 318.69 3.77 199 9

F6Se Selenium hexafluoride 226.55 345.5 9

F6Te Tellurium hexafluoride 234.25 356 9

F6U Uranium(VI) fluoride 329.65 505.8 4.66 250 9

F6W Tungsten(VI) fluoride 290.3 444 4.34 233 9

GaI 3 Gallium(III) iodide 613 951 395 9

GeH 4 Germane 185.1 312.2 4.95 147 9

GeI 4 Germanium(IV) iodide 650 973 500 9 HI Hydrogen iodide 237.60 424.0 8.31 9

H2 Hydrogen 20.28 32.97 1.293 65 9

H2O Water 373.2 647.14 22.06 56 9

H2O2 Hydrogen peroxide 423.4 728* 22* 31

H2S Hydrogen sulfide 213.60 373.2 8.94 99 9

H2Se Hydrogen selenide 231.90 411 8.92 9

H3N Ammonia 239.82 405.5 11.35 72 9

H3P Phosphine 185.40 324.5 6.54 9

H4N2 Hydrazine 386.70 653 14.7 9 He Helium 4.22 5.19 0.227 57 9

HfI 4 Hafnium iodide 667 s 916 528 9 Hg Mercury 629.88 1750 172.00 43 9

HgI 2 Mercury(II) iodide 627 1072 9

I2 Iodine 457.6 819 155 9

I3Sb Antimony(III) iodide 674 1102 9

I4Si Tetraiodosilane 560.50 944 558 9

I4Sn Tin(IV) iodide 637.50 968 531 9

I4Ti Titanium(IV) iodide 650 1040 505 9

I4Zr Zirconium(IV) iodide 704 s 960 530 9 K Potassium 1032 2223* 16* 209* 20 Kr Krypton 119.93 209.41 5.50 91 9 Li Lithium 1615 3223* 67* 66* 20 NO Nitric oxide 121.41 180 6.48 58 9

N2 Nitrogen 77.36 126.21 3.39 90 9

N2O Nitrous oxide 184.67 309.57 7.255 97 9

N2O4 Nitrogen tetroxide 294.30 431 10.1 167 9 Na Sodium 1156 2573* 35* 116* 20 Ne Neon 27.07 44.4 2.76 42 9 6-40 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

O2 Oxygen 90.20 154.59 5.043 73 9

O2S Sulfur dioxide 263.10 430.8 7.884 122 9

O3 Ozone 161.80 261.1 5.57 89 9

O3S Sulfur trioxide 318 491.0 8.2 127 9

O4Os Osmium(VIII) oxide 408 678 9

O7Re 2 Rhenium(VII) oxide 633 942 334 9 P Phosphorus 553.7 994 9 Rb Rubidium 961 2093* 16* 247* 20 Rn Radon 211.5 377 6.28 9 S Sulfur 717.75 1314 20.7 9 Se Selenium 958 1766 27.2 9 Xe Xenon 165.03 289.77 5.841 118 34

CBrClF 2 Bromochlorodifluoromethane 269.5 426.88 4.254 246 9

CBrF 3 Bromotrifluoromethane 215.4 340.2 3.97 196 9

CBr 2F2 Dibromodifluoromethane 295.91 471.3 4.45 9

CClF 3 Chlorotrifluoromethane 191.8 302 3.870 180 9

CCl 2F2 Dichlorodifluoromethane 243.4 384.95 4.136 217 9

CCl 2O Carbonyl chloride [Phosgene] 281 455 5.67 190 9

CCl 3F Trichlorofluoromethane 296.9 471.1 4.47 247 18

CCl 4 Tetrachloromethane 350.0 556.6 4.516 276 9

CF 3I Trifluoroiodomethane 250.7 396.44 3.953 226 24

CF 4 Tetrafluoromethane 145.2 227.6 3.74 140 9

CHBrF 2 Bromodifluoromethane 258.6 411.98 5.132 275 47

CHClF 2 Chlorodifluoromethane 232.5 369.5 5.035 164 18

CHCl 2F Dichlorofluoromethane 282.1 451.58 5.18 196 9

CHCl 3 Trichloromethane 334.32 536.4 5.47 239 9

CHF 3 Trifluoromethane 191.1 298.98 4.82 133 42 CHN Hydrogen cyanide 299 456.7 5.39 139 9

CH 2ClF Chlorofluoromethane 264.1 427 5.70 37

CH 2Cl 2 Dichloromethane 313 510 6.10 9

CH 2F2 Difluoromethane 221.6 351.56 5.83 123 42

CH 2O2 Formic acid 374 588 7

CH 3Cl Chloromethane 249.06 416.25 6.679 139 9

CH 3Cl 3Si Methyltrichlorosilane 338.8 517 3.28 348 9

CH 3F Fluoromethane 194.8 317.8 5.88 113 9

CH 3I Iodomethane 315.58 528 9

CH 3NO 2 Nitromethane 374.34 588 5.87 173 9

CH 4 Methane 111.67 190.56 4.599 98.60 2

CH 4O Methanol 337.8 512.5 8.084 117 4

CH 4S Methanethiol 279.1 470 7.23 147 8

CH 5ClSi Chloromethylsilane 280 517.8 9

CH 5N Methylamine 266.83 430.7 7.614 9

CH 6N2 Methylhydrazine 360.7 567 8.24 271 9

CH 6Si Methylsilane 215.7 352.4 8 CO Carbon monoxide 81.7 132.91 3.499 93 9 COS Carbon oxysulfide 223 375 5.88 137 9

CO 2 Carbon dioxide 194.6 s 304.13 7.375 94 22

CS 2 Carbon disulfide 319 552 7.90 173 9

C2Br 2ClF 3 1,2-Dibromo-1-chloro-1,2,2-trifluoroethane 366 560.7 3.61 368 9

C2Br 2F4 1,2-Dibromotetrafluoroethane 320.50 487.8 3.393 341 9

C2ClF 3 Chlorotrifluoroethene 245.4 379 4.05 212 9

C2ClF 5 Chloropentafluoroethane 234.1 353.2 3.229 252 9

C2Cl 2F4 1,1-Dichloro-1,2,2,2-tetrafluoroethane 276.6 418.6 3.30 294 9

C2Cl 2F4 1,2-Dichloro-1,1,2,2-tetrafluoroethane 276.7 418.78 3.252 297 42

C2Cl 3F3 1,1,1-Trichloro-2,2,2-trifluoroethane 318.7 482.9 40

C2Cl 3F3 1,1,2-Trichloro-1,2,2-trifluoroethane 320.9 487.3 3.42 325 9

C2Cl 4 Tetrachloroethene 394.5 620.2 9

C2Cl 4F2 1,1,2,2-Tetrachloro-1,2-difluoroethane 366.0 551 9

C2Cl 6 Hexachloroethane 457.85 695 3.34* 412* 12

C2F3N Trifluoroacetonitrile 204.4 311.11 3.618 202 9 Critical Constants 6-41

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C2F4 Tetrafluoroethene 197.3 306.5 3.94 172 9

C2F6 Hexafluoroethane 195.1 293 222 9

C2HClF 2 1-Chloro-2,2-difluoroethene 254.7 400.6 4.46 197 9

C2HClF 4 1-Chloro-1,1,2,2-tetrafluoroethane 261.5 399.9 3.72 244 9

C2HClF 4 1-Chloro-1,2,2,2-tetrafluoroethane 261 395.65 3.643 244 42

C2HCl 2F3 1,2-Dichloro-1,1,2-trifluoroethane 302.7 461.6 278 19

C2HCl 2F3 2,2-Dichloro-1,1,1-trifluoroethane 300.97 456.83 3.661 278 35

C2HCl 3 Trichloroethene 360.36 544.2 5.02 9

C2HF 3O2 Trifluoroacetic acid 346 491.3 3.258 204 9

C2HF 5 Pentafluoroethane 225.1 339.17 3.620 208.0 29,30

C2HF 5O Trifluoromethyl difluoromethyl ether 235 354.0 3.33 192 25,45,46

C2H2 Acetylene 188.45 308.3 6.138 112.2 6

C2H2ClF 3 2-Chloro-1,1,1-trifluoroethane 279.3 425.01 228 40

C2H2Cl 2 cis -1,2-Dichloroethene 333.3 544.2 9

C2H2Cl 2 trans -1,2-Dichloroethene 321.9 516.5 5.51 9

C2H2Cl 4 1,1,2,2-Tetrachloroethane 418.4 661.15 9

C2H2F2 1,1-Difluoroethene 187.5 302.9 4.46 154 9

C2H2F4 1,1,1,2-Tetrafluoroethane 247.07 374.18 4.065 198 36

C2H2F4 1,1,2,2-Tetrafluoroethane 253.3 391.74 4.615 191 19,42

C2H2F4O Bis(difluoromethyl) ether 275 420.25 4.228 223 46

C2H3Cl Chloroethene [Vinyl chloride] 259.4 432 5.67 179 12

C2H3ClF 2 1-Chloro-1,1-difluoroethane 264.1 410.34 4.048 225 19,32

C2H3Cl 2F 1,1-Dichloro-1-fluoroethane 305.2 477.5 4.194 255 26,42

C2H3Cl 3 1,1,1-Trichloroethane 347.24 545 4.30 9

C2H3Cl 3 1,1,2-Trichloroethane 387.0 602* 4.48* 281* 12

C2H3F Fluoroethene 201 327.9 5.24 144 9

C2H3F3 1,1,1-Trifluoroethane 225.90 345.86 3.764 194 27,28

C2H3F3 1,1,2-Trifluoroethane 276.9 429.8 5.241 207 40

C2H3F3O Methyl trifluoromethyl ether 249.49 378.02 3.588 228 47

C2H3N Acetonitrile 354.80 545.6 4.884 173 14

C2H4 Ethylene [Ethene] 169.38 282.34 5.041 131 6

C2H4Br 2 1,2-Dibromoethane 404.8 583.0 7.2 9

C2H4Cl 2 1,1-Dichloroethane 330.5 523 5.07 236 9

C2H4Cl 2 1,2-Dichloroethane 356.7 561 5.4 225 9

C2H4F2 1,1-Difluoroethane 249.10 386.7 4.50 181 9,19

C2H4O Acetaldehyde 293.3 466 154 7

C2H4O Oxirane [Ethylene oxide] 283.8 469 7.2 142 7

C2H4O2 Acetic acid 391.1 590.7 5.78 171 7

C2H4O2 Methyl formate 304.9 487.2 6.00 172 7

C2H5Br Bromoethane 311.7 503.9 6.23 215 9

C2H5Cl Chloroethane 285.5 460.4 5.3 9

C2H5F Fluoroethane 235.5 375.31 5.028 9

C2H6 Ethane 184.6 305.32 4.872 145.5 2

C2H6Cl 2Si Dichlorodimethylsilane 343.5 520.4 3.49 350 9

C2H6O Ethanol 351.44 514.0 6.137 168 4

C2H6O Dimethyl ether 248.4 400.2 5.34 168 7

C2H6O2 1,2-Ethanediol 470.5 720 8 7,14

C2H6S Ethanethiol 308.2 499 5.49 207 8

C2H6S Dimethyl sulfide 310.48 503 5.53 203.7 8

C2H6S2 Dimethyl disulfide 382.89 615 8

C2H7N Ethylamine 289.7 456 5.62 182 9

C2H7N Dimethylamine 280.03 437.22 5.340 9

C2H8N2 1,2-Ethanediamine 390 613.1 6.707 11,12

C2N2 Cyanogen 252.1 400 5.98 9

C3ClF 5O Chloropentafluoroacetone 281 410.6 2.878 9

C3Cl 2F6 1,3-Dichloro-1,1,2,2,3,3-hexafluoropropane 308.9 453 2.753 41

C3F6O Perfluoroacetone 245.8 357.14 2.84 329 9

C3F6O Perfluorooxetane 244.8 361.8 3.03 272 18,47

C3F8 Perfluoropropane 236.6 345.1 2.680 299 9

C3F8O2 Perfluorodimethoxymethane 263 372.3 2.333 363 18 6-42 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C3HF 7 1,1,1,2,3,3,3-Heptafluoropropane 256.8 374.89 2.929 274 39,47

C3HF 7O Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether 270 387.78 2.293 337 18,47

C3H2F6 1,1,1,2,3,3-Hexafluoropropane 279.3 412.38 3.412 269 33

C3H2F6 1,1,1,3,3,3-Hexafluoropropane 272.2 398.07 45

C3H2F6O 1,2,2,2-Tetrafluoroethyl difluoromethyl ether 296.50 428.95 3.050 315 32

C3H3F3 3,3,3-Trifluoropropene 256 376.2 3.80 211 9

C3H3F5 1,1,1,3,3-Pentafluoropropane 288.5 427.20 45

C3H3F5 1,1,1,2,2-Pentafluoropropane 255.8 380.11 3.137 273 9

C3H3F5 1,1,2,2,3-Pentafluoropropane 298.2 447.57 45

C3H3F5O Methyl pentafluoroethyl ether 278.74 406.80 2.887 301 32

C3H3F5O Difluoromethyl 2,2,2-trifluoroethyl ether 302.39 443.99 38

C3H3N Acrylonitrile 350.5 540 4.660 11,12

C3H3NO Isoxazole 368 552.0 9

C3H4 Allene 238.8 394 5.25 6

C3H4 Propyne 250.0 402.4 5.63 163.5 6

C3H5Cl 3-Chloropropene 318.3 514 9

C3H5F3O 2,2,2-Trifluoroethyl methyl ether 304.77 448.98 3.513 277 32

C3H5N Propanenitrile 370.29 561.3 4.26 229 9

C3H6 Propene 225.46 364.9 4.60 185 6

C3H6 Cyclopropane 240.34 398.0 5.54 162 5

C3H6Cl 2 1,2-Dichloropropane 369.6 578.5 13

C3H6Cl 2 1,3-Dichloropropane 394.1 614.6 13

C3H6O Allyl alcohol 370.2 545.1 4

C3H6O Propanal 321 505 5.26 204 7

C3H6O Acetone 329.20 508.1 4.700 213 7

C3H6O Methyloxirane [1,2-Propylene oxide] 308 485 5.2 190 7

C3H6O2 Propanoic acid 414.30 598.5 4.67 233 7

C3H6O2 Ethyl formate 327.6 508.54 4.74 229 7

C3H6O2 Methyl acetate 330.02 506.5 4.750 228 7

C3H6O3 Dimethyl carbonate 363.7 557 4.80 252 7

C3H7Cl 1-Chloropropane 319.7 503 4.58 9

C3H7Cl 2-Chloropropane 308.9 484 13

C3H7NO N,N -Dimethylformamide 426 649.6 262 9

C3H8 Propane 231.1 369.83 4.248 200 2

C3H8O 1-Propanol 370.4 536.8 5.169 218 4

C3H8O 2-Propanol 355.5 508.3 4.764 222 4

C3H8O Ethyl methyl ether 280.6 437.9 4.38 222 7

C3H8O2 1,2-Propylene glycol 460.8 676.4 5.941 7,14

C3H8O2 1,3-Propylene glycol [Trimethylene glycol] 487.6 718.2 6.55 14,17

C3H8O2 2-Methoxyethanol [Ethylene glycol monomethyl ether] 397.3 597.6 5.285 263 7,11,12

C3H8O2 Dimethoxymethane [Methylal] 315 491 3.96 213 7

C3H8O3 Glycerol 563 850 7.5 7

C3H8S 1-Propanethiol 341.0 537 4.6 286 8

C3H8S Ethyl methyl sulfide 339.9 533 4.25 8

C3H9BO 3 Trimethyl borate 340.7 501.7 3.59 9

C3H9ClSi Trimethylchlorosilane 333 497.8 3.20 366 9

C3H9N Propylamine 320.37 497.0 4.72 9

C3H9N Isopropylamine 304.91 471.8 4.54 221 9

C3H9N Trimethylamine 276.02 432.79 4.087 254 9

C4Br 2F8 1,4-Dibromooctafluorobutane 370 532.5 2.39 9

C4Cl 2F6 1,2-Dichloro-1,2,3,3,4,4-hexafluorocyclobutane 332.7 497* 2.73* 386* 12

C4F8 Perfluorocyclobutane 267.3 388.46 2.784 324 9

C4F10 Perfluorobutane 271.3 386.4 2.323 378 9

C4F10 Perfluoroisobutane 273 395.4 9

C4H2F8O Perfluoroethyl 2,2,2-trifluoroethyl ether 301.04 421.68 2.330 409 32

C4H3F7O Perfluoropropyl methyl ether 307.38 437.70 2.481 377 32

C4H3F7O Perfluoroisopropyl methyl ether 302.49 433.30 2.553 369 32

C4H4O Furan 304.7 490.2 5.3 218 7

C4H4O4 Maleic acid 620 7

C4H4S Thiophene 357.2 580 5.70 219 8 Critical Constants 6-43

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C4H5F5O Perfluoroethyl ethyl ether 301.26 431.23 2.533 366 32

C4H5N Pyrrole 402.94 639.7 6.34 200 10

C4H6 1,3-Butadiene 268.74 425 4.32 221 6

C4H6 1-Butyne 281.23 440 4.60 208 6

C4H6 2-Butyne 300.1 488.7 9

C4H6O2 Vinyl acetate 346.0 519.2 4.185 7

C4H6O2 γ-Butyrolactone 477 731 5.13 7,11

C4H6O3 Acetic anhydride 412.7 606 4.0 7

C4H6O3 Propylene carbonate 515 762.7 4.14 17

C4H7N Butanenitrile 390.8 585.4 3.88 9

C4H8 1-Butene 266.89 419.5 4.02 240.8 6

C4H8 cis -2-Butene 276.86 435.5 4.21 233.8 6

C4H8 trans -2-Butene 274.03 428.6 4.10 237.7 6

C4H8 Isobutene 266.3 417.9 4.000 238.8 6

C4H8 Cyclobutane 285.8 460.0 4.98 210 9

C4H8O Ethyl vinyl ether 308.7 475 4.07 7

C4H8O Butanal 348.0 537 4.32 258 7

C4H8O Isobutanal 337.7 544 5.1 7

C4H8O 2-Butanone [Methyl ethyl ketone] 352.74 536.7 4.207 267 7

C4H8O Tetrahydrofuran 338 540.5 5.19 224 7

C4H8OS S-Ethyl thioacetate 389.6 590.55 4.075 319 11,12

C4H8O2 Butanoic acid 436.90 615.2 4.06 292 7

C4H8O2 2-Methylpropanoic acid 427.60 605.0 3.70 290 7

C4H8O2 Propyl formate 354.1 538.0 4.06 285 7

C4H8O2 Isopropyl formate 341.4 535 3.95 7

C4H8O2 Ethyl acetate 350.26 523.3 3.87 286 7

C4H8O2 Methyl propanoate 353.0 530.7 4.00 282 7

C4H8O2 1,4-Dioxane 374.7 588 5.21 238 7

C4H8S Tetrahydrothiophene 394.3 632 5.4 8

C4H9Cl 1-Chlorobutane 351.6 539.2 13

C4H9Cl 2-Chlorobutane 341.4 518.6 13

C4H9Cl 2-Chloro-2-methylpropane 324.1 500 13

C4H9N Pyrrolidine 359.71 568 6.00 238 10

C4H10 Butane 272.7 425.12 3.796 255 2

C4H10 Isobutane 261.42 407.8 3.640 259 5

C4H10 O 1-Butanol 390.88 563.0 4.414 274 4

C4H10 O 2-Butanol [sec-Butyl alcohol] 372.66 536.2 4.202 269 4

C4H10 O 2-Methyl-1-propanol [Isobutyl alcohol] 381.04 547.8 4.295 274 4

C4H10 O 2-Methyl-2-propanol [tert-Butyl alcohol] 355.6 506.2 3.972 275 4

C4H10 O Diethyl ether 307.7 466.7 3.644 281 7

C4H10 O Methyl propyl ether 312.3 476.2 3.801 7

C4H10 O Isopropyl methyl ether 303.92 464.4 3.762 7

C4H10 O2 2-Methyl-1,3-propanediol 484.8 708.0 5.35 17

C4H10 O2 1,2-Butanediol 463.7 680 5.21 303 7,23

C4H10 O2 1,3-Butanediol 480.7 676 4.02 305 7,23

C4H10 O2 1,4-Butanediol [Tetramethylene glycol] 508 723.8 5.52 17

C4H10 O2 1,2-Dimethoxyethane [Ethylene glycol dimethyl ether] 357.7 540 3.90 308 7

C4H10 O2 1,2-Propylene glycol monomethyl ether 392 579.8 4.113 11,12

C4H10 O3 Diethylene glycol 519.0 750 4.7 7

C4H10 S 1-Butanethiol 371.7 570 4.0 324 8

C4H10 S Diethyl sulfide 365.3 557.8 3.90 317.6 8,15

C4H10 S2 Diethyl disulfide 427.2 642 8

C4H11 N Butylamine 350.15 531.9 4.25 277 10

C4H11 N sec -Butylamine 335.88 514.3 4.20 278 10

C4H11 N tert -Butylamine 317.19 483.9 3.84 292 10

C4H11 N Isobutylamine 340.90 519 4.07 278 10

C4H11 N Diethylamine 328.7 499.99 3.758 9

C4H12 N2O N-(2-Aminoethyl)ethanolamine 512 739.2 4.65 17

C4H12 Si Tetramethylsilane 299.8 448.6 2.821 361.6 8

C4H12 Sn Tetramethylstannane 351 521.8 2.981 8 6-44 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C4H13 N3 Bis(2-aminoethyl)amine 480 709.8 4.38 14,17

C5F12 Perfluoropentane 302.4 420.59 2.045 473 9

C5H2F6O2 Hexafluoroacetylacetone 327.30 485.1 2.767 9

C5H4O2 Furfural 434.9 670* 5.89* 7

C5H5N Pyridine 388.38 620.0 5.67 243 10

C5H6N2 2-Methylpyrazine 410 634.3 5.01 283 9

C5H6O 2-Methylfuran 337.9 528 4.7 247 7

C5H7N 1-Methylpyrrole 385.96 596.0 4.86 271 10

C5H7N 2-Methylpyrrole 420.8 654 5.08 266 10

C5H7N 3-Methylpyrrole 416.1 647 5.08 266 10

C5H8 1-Pentyne 313.3 493.5 9

C5H8 Cyclopentene 317.4 506.5 4.80 245 6

C5H8O Cyclopentanone 403.72 624 4.60 7

C5H8O 3,4-Dihydro-2 H-pyran 359 562 4.56 268 7

C5H9N Pentanenitrile 414.5 610.3 3.58 9

C5H9NO N-Methyl-2-pyrrolidone 475 721.8 311 9

C5H10 1-Pentene 303.11 464.8 3.56 298.4 6

C5H10 cis -2-Pentene 310.08 475 3.69 6

C5H10 trans -2-Pentene 309.49 471 3.52 9

C5H10 2-Methyl-1-butene 304.4 470 3.8 9

C5H10 3-Methyl-1-butene 293.3 452.7 3.53 304.9 6

C5H10 2-Methyl-2-butene 311.71 470 3.42 6

C5H10 Cyclopentane 322.5 511.7 4.51 259 5

C5H10 O Cyclopentanol 413.57 619.5 4.9 4

C5H10 O Allyl ethyl ether 340.8 518 7

C5H10 O Pentanal 376 567 3.97 313 7

C5H10 O 2-Pentanone [Methyl propyl ketone] 375.41 561.1 3.683 321 7

C5H10 O 3-Pentanone [Diethyl ketone] 374.9 561.4 3.729 331 7

C5H10 O 3-Methyl-2-butanone 367.48 553.0 3.80 308 7

C5H10 O Tetrahydropyran 361 572 4.77 263 7

C5H10 O 2-Methyltetrahydrofuran 351 537 3.76 267 7

C5H10 O2 Pentanoic acid 459.3 637.2 3.63 346 7

C5H10 O2 3-Methylbutanoic acid 449.7 629 3.40 7

C5H10 O2 Isobutyl formate 371.4 551 3.88 355 7

C5H10 O2 Propyl acetate 374.69 549.7 3.36 345 7

C5H10 O2 Isopropyl acetate 361.8 531.0 3.31 344 7

C5H10 O2 Ethyl propanoate 372.3 546.7 3.45 342 7

C5H10 O2 Methyl butanoate 376.0 554.5 3.47 340 7

C5H10 O2 Methyl isobutanoate 365.7 540.7 3.43 339 7

C5H10 O3 2-Methoxyethyl acetate 416 630.0 7

C5H11 Cl 1-Chloropentane 381.6 571.2 13

C5H11 Cl 2-Chloro-2-methylbutane 358.8 509.1 13

C5H11 N Piperidine 379.37 594 4.94 288 10

C5H12 Pentane 309.21 469.7 3.370 311 2

C5H12 Isopentane 301.03 460.4 3.38 306 5

C5H12 Neopentane 282.63 433.8 3.196 307 5

C5H12 O 1-Pentanol 411.13 588.1 3.897 326 4

C5H12 O 2-Pentanol 392.5 560.3 3.675 329 4

C5H12 O 3-Pentanol 389.40 559.6 325 4

C5H12 O 2-Methyl-1-butanol 400.7 575.4 3.94 4

C5H12 O 3-Methyl-1-butanol 404.3 577.2 3.93 4

C5H12 O 2-Methyl-2-butanol 375.6 543.7 3.71 4

C5H12 O 3-Methyl-2-butanol 386.1 556.1 3.87 4

C5H12 O Butyl methyl ether 343.31 512.7 3.37 329 7

C5H12 O Methyl tert -butyl ether 328.2 497.1 3.430 7

C5H12 O Ethyl propyl ether 336.36 500.2 3.370 339 7

C5H12 O2 2-Propoxyethanol 423.0 615 3.65 364 7

C5H12 O2 Diethoxymethane 361 531.7 7

C5H12 O2 1,2-Dimethoxypropane 369 543.0 7

C5H12 O2 2,2-Dimethoxypropane 356 510 7 Critical Constants 6-45

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C5H12 O3 Diethylene glycol monomethyl ether 466 672 3.67 11,12

C5H12 S 3-Methyl-1-butanethiol 389 594 8

C6BrF 5 Bromopentafluorobenzene 410 601 3.0 9

C6ClF 5 Chloropentafluorobenzene 391.11 570.81 3.238 376 9

C6Cl 2F4 1,2-Dichloro-3,4,5,6-tetrafluorobenzene 430.9 626 5.32 9

C6Cl 3F3 1,3,5-Trichloro-2,4,6-trifluorobenzene 471.6 684.8 3.27 448 9

C6F6 Hexafluorobenzene 353.41 516.73 3.273 335 9

C6F10 Perfluorocyclohexene 325.2 461.8 9

C6F12 Perfluoro-1-hexene 330.2 454.4 9

C6F12 Perfluorocyclohexane 325.95 457.2 2.43 9

C6F14 Perfluorohexane 329.8 448.77 1.868 606 9

C6F14 Perfluoro-2-methylpentane 330.8 455.3 1.923 532 9

C6F14 Perfluoro-3-methylpentane 331.6 450 1.69 9

C6F14 Perfluoro-2,3-dimethylbutane 333.0 463 1.87 525 9

C6HF 5 Pentafluorobenzene 358.89 530.97 3.531 324 9

C6HF 5O Pentafluorophenol 418.8 609 4.0 348 9

C6HF 11 Undecafluorocyclohexane 335.2 477.7 9

C6H2F4 1,2,3,4-Tetrafluorobenzene 367.5 550.83 3.791 313 9

C6H2F4 1,2,3,5-Tetrafluorobenzene 357.6 535.25 3.747 9

C6H2F4 1,2,4,5-Tetrafluorobenzene 363.4 543.35 3.801 9

C6H3ClF 2 1-Chloro-2,4-difluorobenzene 400 609.6 13

C6H3ClF 2 1-Chloro-2,5-difluorobenzene 401 612.5 13

C6H3ClF 2 1-Chloro-3,4-difluorobenzene 400 609.2 13

C6H3ClF 2 1-Chloro-3,5-difluorobenzene 391.7 592.0 13

C6H3F3 1,2,3-Trifluorobenzene 368 560.3 13

C6H3F3 1,2,4-Trifluorobenzene 363 551.1 13

C6H3F3 1,3,5-Trifluorobenzene 348.7 530.9 13

C6H4BrF 1-Bromo-2-fluorobenzene 427 669.6 13

C6H4BrF 1-Bromo-3-fluorobenzene 423 652.0 13

C6H4BrF 1-Bromo-4-fluorobenzene 424.7 654.8 13

C6H4ClF 1-Chloro-2-fluorobenzene 410.8 633.8 13

C6H4ClF 1-Chloro-3-fluorobenzene 400.8 615.9 13

C6H4ClF 1-Chloro-4-fluorobenzene 403 620.1 13

C6H4Cl 2 m-Dichlorobenzene 446 685.7 13

C6H4F2 o-Difluorobenzene 367 566.0 13

C6H4F2 m-Difluorobenzene 355.8 548.4 13

C6H4F2 p-Difluorobenzene 362 556.9 4.40 9,13

C6H5Br Bromobenzene 429.21 670 4.52 324 9

C6H5Cl Chlorobenzene 404.87 633.4 4.52 308 9,13

C6H5F Fluorobenzene 357.88 560.09 4.551 269 9

C6H5I Iodobenzene 461.6 721 4.52 351 9

C6H6 Benzene 353.24 562.05 4.895 256 3

C6H6O Phenol 455.02 694.2 5.93 7

C6H7N Aniline 457.32 699 4.89 287 9

C6H7N 2-Methylpyridine [2-Picoline] 402.53 621.0 4.60 292 10

C6H7N 3-Methylpyridine [3-Picoline] 417.29 645.0 4.65 288 10

C6H7N 4-Methylpyridine [4-Picoline] 418.51 645.7 4.70 292 10

C6H10 1,5-Hexadiene 332.6 508 6

C6H10 Cyclohexene 356.13 560.4 6

C6H10 O Cyclohexanone 428.58 665 4.6 7

C6H10 O 2-Methylcyclopentanone 412.7 631 7

C6H10 O Mesityl oxide 403 605 4.00 353 7

C6H10 O2 Ethyl trans -2-butenoate 411 599 7

C6H10 S Diallyl sulfide 411.8 653 8

C6H11 Cl Chlorocyclohexane 415 586 13

C6H11 N Hexanenitrile 436.80 633.8 3.30 9

C6H12 1-Hexene 336.63 504.0 3.21 355.1 6

C6H12 Cyclohexane 353.88 553.8 4.08 308 5

C6H12 Methylcyclopentane 345.0 532.7 3.79 318 5

C6H12 O Butyl vinyl ether 367 540 3.20 384 7 6-46 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C6H12 O Hexanal 404 592 3.46 378 7

C6H12 O 2-Hexanone [Butyl methyl ketone] 400.8 587.1 3.30 377 7

C6H12 O 3-Hexanone [Ethyl propyl ketone] 396.7 583.0 3.320 378 7

C6H12 O 4-Methyl-2-pentanone [Isobutyl methyl ketone] 389.7 574.6 3.270 7

C6H12 O 3,3-Dimethyl-2-butanone 379.3 570.9 3.43 382 7

C6H12 O Cyclohexanol 433.99 647.1 4.401 11,12

C6H12 O2 Hexanoic acid 478.4 655 3.38 413 7

C6H12 O2 Pentyl formate 403.6 576 3.46 412 7

C6H12 O2 Isopentyl formate 396.7 578 7

C6H12 O2 Butyl acetate 399.3 575.6 3.14 7

C6H12 O2 sec -Butyl acetate 385 571 3.01 7

C6H12 O2 Isobutyl acetate 389.7 561 2.99 401 7

C6H12 O2 Propyl propanoate 395.7 570 3.06 7

C6H12 O2 Ethyl butanoate 394.5 568.8 3.1 415 7

C6H12 O2 Ethyl 2-methylpropanoate 383.3 554 3.1 415 7

C6H12 O2 Methyl pentanoate 400.6 590 3.20 422 7

C6H12 O3 1,2-Propylene glycol monomethyl ether acetate 420 597.8 3.01 432 7

C6H12 O3 2-Ethoxyethyl acetate 429.6 608.0 3.17 443 7,23

C6H12 O3 Paraldehyde 397.5 563 7

C6H12 S Cyclohexanethiol 432.0 684 401 8

C6H13 Cl 1-Chlorohexane 408.3 599 13

C6H13 Cl 3-Chloro-3-methylpentane 389 528 13

C6H14 Hexane 341.88 507.6 3.025 368 2

C6H14 2-Methylpentane 333.41 497.7 3.04 368 5

C6H14 3-Methylpentane 336.42 504.6 3.12 368 5

C6H14 2,2-Dimethylbutane 322.88 489.0 3.10 358 5

C6H14 2,3-Dimethylbutane 331.08 500.0 3.15 361 5

C6H14 O 2-Methoxy-2-methylbutane 359.3 535 3.20 374 7

C6H14 O 1-Hexanol 430.8 610.3 3.417 387 4

C6H14 O 2-Hexanol 413 585.9 3.31 384 4

C6H14 O 3-Hexanol 408 582.4 3.36 383 4

C6H14 O 2-Methyl-1-pentanol 422 604.4 3.45 4

C6H14 O 4-Methyl-1-pentanol 425.1 603.5 4

C6H14 O 2-Methyl-2-pentanol 394.3 559.5 4

C6H14 O 4-Methyl-2-pentanol 404.8 574.4 4

C6H14 O 2-Methyl-3-pentanol 399.7 576.0 3.46 4

C6H14 O 3-Methyl-3-pentanol 395.6 575.6 3.52 4

C6H14 O Dipropyl ether 363.23 530.6 3.028 7

C6H14 O Diisopropyl ether 341.6 500.3 2.832 386 7

C6H14 O tert -Butyl ethyl ether 345.8 509.4 2.934 395 7

C6H14 O Methyl pentyl ether 372 546.5 3.042 391 7

C6H14 O2 1-Propoxy-2-propanol 423 605.1 3.051 14

C6H14 O2 2-Butoxyethanol 441.6 634 3.27 424 7

C6H14 O2 1,1-Diethoxyethane [Acetal] 375.40 540 3.22 7

C6H14 O2 1,2-Diethoxyethane [Ethylene glycol diethyl ether] 394.4 542 7

C6H14 O3 Diethylene glycol monoethyl ether [Carbitol] 469 670 3.167 11,12

C6H14 O3 Diethylene glycol dimethyl ether 435 617 7

C6H14 O4 Triethylene glycol 558 780 3.3 7

C6H15 N Dipropylamine 382.5 555.8 3.63 9

C6H15 N Diisopropylamine 357.1 523.1 3.02 9

C6H15 N Triethylamine 362 535.6 3.032 389 9

C7F8 Perfluorotoluene 377.7 534.47 2.705 428 9

C7F14 Perfluoro-1-heptene 354.2 478.2 9

C7F14 Perfluoromethylcyclohexane 349.5 485.91 2.019 570 9

C7F16 Perfluoroheptane 355.7 474.8 1.62 664 9

C7HF 15 1H-Pentadecafluoroheptane 369.2 495.8 9

C7H3F5 2,3,4,5,6-Pentafluorotoluene 390.7 566.52 3.126 384 9

C7H4BrF 3 1-Bromo-2-(trifluoromethyl)benzene 440.7 656.5 13

C7H4BrF 3 1-Bromo-3-(trifluoromethyl)benzene 424.7 627.1 13

C7H4BrF 3 1-Bromo-4-(trifluoromethyl)benzene 433 629.8 13 Critical Constants 6-47

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C7H5N Benzonitrile 464.3 699.4 4.21 9

C7H6F2 2,4-Difluorotoluene 390 581.4 13

C7H6F2 2,5-Difluorotoluene 391 587.8 13

C7H6F2 2,6-Difluorotoluene 385 581.8 13

C7H6F2 3,4-Difluorotoluene 385 598.5 13

C7H6O Benzaldehyde 452.0 695 4.7 7

C7H7F 2-Fluorotoluene 388 591.2 13

C7H7F 3-Fluorotoluene 388 591.8 13

C7H7F 4-Fluorotoluene 389.8 592.1 13

C7H8 Toluene 383.78 591.80 4.110 316 3,15

C7H8O o-Cresol 464.19 697.6 4.17 7

C7H8O m-Cresol 475.42 705.8 4.36 7

C7H8O p-Cresol 475.13 704.6 4.07 7

C7H8O Benzyl alcohol 478.46 715 4.3 9

C7H8O Anisole [Methoxybenzene] 426.9 646.5 4.24 341 7,11,12

C7H9N 2-Methylaniline 473.5 707 4.37 9

C7H9N 3-Methylaniline 476.5 707 4.28 9

C7H9N 4-Methylaniline 473.6 706 4.58 9

C7H9N N-Methylaniline 469.4 701 5.20 9

C7H9N 2,3-Dimethylpyridine 434.27 655.4 4.10 356 23

C7H9N 2,4-Dimethylpyridine 431.53 647 3.95 361 23

C7H9N 2,5-Dimethylpyridine 430.13 645 3.85 361 23

C7H9N 2,6-Dimethylpyridine 417.16 624 3.85 361 23

C7H9N 3,4-Dimethylpyridine 452.25 684 4.20 355 23

C7H9N 3,5-Dimethylpyridine 444.99 668 4.05 361 23

C7H14 1-Heptene 366.79 537.3 2.92 409 6

C7H14 Cycloheptane 391.6 604.2 3.82 353 5

C7H14 Methylcyclohexane 374.08 572.1 3.48 369 5

C7H14 Ethylcyclopentane 376.7 569.5 3.40 375 5

C7H14 1,1-Dimethylcyclopentane 360.7 547 3.45 21

C7H14 cis -1,2-Dimethylcyclopentane 372.7 565 3.45 21

C7H14 trans -1,2-Dimethylcyclopentane 365.1 553 3.45 21

C7H14 cis -1,3-Dimethylcyclopentane 364.0 551 3.45 21

C7H14 trans -1,3-Dimethylcyclopentane 364.9 553 3.45 21

C7H14 O Heptanal 426.0 617 3.16 434 7

C7H14 O 2-Heptanone [Methyl pentyl ketone] 424.20 611.4 2.97 436 7

C7H14 O 3-Heptanone [Ethyl butyl ketone] 420 606.6 433 7

C7H14 O 4-Heptanone 417 602.0 434 7

C7H14 O 5-Methyl-2-hexanone [Methyl isopentyl ketone] 417 604.1 7

C7H14 O 2-Methyl-3-hexanone 408 593.3 7

C7H14 O2 Heptanoic acid 495.4 678 3.16 7

C7H14 O2 Pentyl acetate 422.4 599 2.73 470 7,23

C7H14 O2 Isopentyl acetate 415.7 586.1 2.76 7

C7H14 O2 Butyl propanoate 420.0 594.5 7

C7H14 O2 Isobutyl propanoate 410 584 7

C7H14 O2 Propyl butanoate 416.2 593.1 2.72 7

C7H14 O2 Propyl isobutanoate 408.6 579.4 7

C7H14 O2 Ethyl pentanoate 419.3 593.3 7

C7H14 O2 Ethyl 3-methylbutanoate 408.2 582.4 7

C7H14 O3 Ethyl 3-ethoxypropanoate 439 621.0 2.66 458 7

C7H15 Cl 1-Chloroheptane 433.6 614 13

C7H16 Heptane 371.6 540.2 2.74 428 2

C7H16 2-Methylhexane 363.19 530.4 2.74 421 5

C7H16 3-Methylhexane 365 535.2 2.81 404 5

C7H16 3-Ethylpentane 366.7 540.6 2.89 416 5

C7H16 2,2-Dimethylpentane 352.4 520.5 2.77 416 5

C7H16 2,3-Dimethylpentane 362.93 537.3 2.91 393 5

C7H16 2,4-Dimethylpentane 353.64 519.8 2.74 418 5

C7H16 3,3-Dimethylpentane 359.21 536.4 2.95 414 5

C7H16 2,2,3-Trimethylbutane 354.01 531.1 2.95 398 5 6-48 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C7H16 O 2-Ethoxy-2-methylbutane 375 546 2.935 463 7

C7H16 O 1-Heptanol 449.60 632.6 3.058 435 4

C7H16 O 2-Heptanol 432 608.3 3.021 442 4

C7H16 O 3-Heptanol, ( S) 430 605.4 434 4

C7H16 O 4-Heptanol 429 602.6 432 4

C7H16 O2 1-Butoxy-2-propanol 444.7 624.9 2.739 14

C7H16 O2 1- tert -Butoxy-2-methoxyethane 574 7

C7H16 O2 2,2-Diethoxypropane 387 510.7 7

C7H16 O3 Diethylene glycol monopropyl ether 486 680 3.00 489 7

C7H20 Si 2 Bis(trimethylsilyl)methane 406 573.9 1.99 8

C8F16 O Perfluoro-2-butyltetrahydrofuran 375.8 500.2 1.607 588 9

C8F18 Perfluorooctane 379.1 502 1.66 9

C8H6S Benzo[b]thiophene 494 764 4.76 379 8

C8H7N 4-Methylbenzonitrile 490.2 723 9

C8H7N 1H-Indole 526.8 794 4.8 356 10

C8H8 Styrene 418 635.2 3.87 15

C8H8O Acetophenone 475 709.6 4.01 388 7,23

C8H8O2 Phenyl acetate 469 685.7 3.59 17

C8H8O3 Methyl salicylate 496.1 709 7

C8H10 Ethylbenzene 409.34 617.15 3.609 374 3,15

C8H10 o-Xylene 417.7 630.3 3.732 370 3

C8H10 m-Xylene 412.27 617.0 3.541 375 3

C8H10 p-Xylene 411.52 616.2 3.511 378 3

C8H10 O 2-Ethylphenol 477.7 703.0 7

C8H10 O 3-Ethylphenol 491.6 716.4 7

C8H10 O 4-Ethylphenol 491.1 716.4 7

C8H10 O 2,3-Xylenol 490.1 722.8 7

C8H10 O 2,4-Xylenol 484.13 707.6 7

C8H10 O 2,5-Xylenol 484.3 706.9 7

C8H10 O 2,6-Xylenol 474.22 701.0 7

C8H10 O 3,4-Xylenol 500 729.8 7

C8H10 O 3,5-Xylenol 494.89 715.6 7

C8H10 O α-Methylbenzenemethanol 478 699 3.77 14

C8H10 O Ethoxybenzene 442.96 647 3.4 7

C8H10 O 2-Methylanisole 444 662.0 7

C8H10 O 3-Methylanisole 448.7 665.3 7

C8H10 O 4-Methylanisole 448.7 666 7

C8H11 N N-Ethylaniline 476.2 698 9

C8H11 N N,N -Dimethylaniline 467.30 687 3.63 9

C8H14 O4 Diethyl succinate 490.9 663 7

C8H15 N Octanenitrile 478.40 674.4 2.85 9

C8H16 1-Octene 394.44 567.0 2.68 468 6

C8H16 Cyclooctane 422 647.2 3.56 410 5

C8H16 Ethylcyclohexane 405.1 609 3.04 21

C8H16 cis -1,2-Dimethylcyclohexane 403.0 606 2.95 21

C8H16 trans -1,2-Dimethylcyclohexane 396.7 596 2.94 21

C8H16 cis -1,3-Dimethylcyclohexane 393.3 591 2.94 21

C8H16 trans -1,3-Dimethylcyclohexane 397.7 598 2.94 21

C8H16 trans -1,4-Dimethylcyclohexane 392.6 587.7 5

C8H16 O Octanal 444 639 2.96 488 7

C8H16 O 2-Octanone [Hexyl methyl ketone] 445.7 632.7 497 7

C8H16 O 3-Octanone [Ethyl amyl ketone] 440.7 627.7 497 7

C8H16 O 4-Octanone [Butyl propyl ketone] 436 623.8 497 7

C8H16 O 2-Methyl-3-heptanone [Butyl isopropyl ketone] 431 614.9 7

C8H16 O 5-Methyl-3-heptanone 434 619.0 7

C8H16 O2 Octanoic acid 512 693 2.87 519 7

C8H16 O2 2-Ethylhexanoic acid 501 674 2.78 528 7

C8H16 O2 Hexyl acetate 444.7 618.4 7

C8H16 O2 Isopentyl propanoate 433.4 611 7

C8H16 O2 Butyl butanoate 439 612.1 7 Critical Constants 6-49

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C8H16 O2 Isobutyl butanoate 430.1 611 7

C8H16 O2 Isobutyl isobutanoate 421.8 602 7

C8H16 O2 Propyl 3-methylbutanoate 429.1 609 7

C8H16 O2 Ethyl hexanoate 440 615.2 7

C8H16 O2 Methyl heptanoate 447 628 7

C8H16 O3 2-Butoxyethyl acetate 465 640.7 2.694 549 7

C8H16 O4 Diethylene glycol monoethyl ether acetate 491.7 673.5 2.59 17

C8H17 Cl 1-Chlorooctane 456.7 643 13

C8H18 Octane 398.82 568.7 2.49 492 2

C8H18 2-Methylheptane 390.81 559.7 2.50 488 5

C8H18 3-Methylheptane 392.1 563.6 2.55 464 5

C8H18 4-Methylheptane 390.87 561.7 2.54 476 5

C8H18 3-Ethylhexane 391.8 565.5 2.61 455 5

C8H18 2,2-Dimethylhexane 380.01 549.8 2.53 478 5

C8H18 2,3-Dimethylhexane 388.77 563.5 2.63 468 5

C8H18 2,4-Dimethylhexane 382.7 553.5 2.56 472 5

C8H18 2,5-Dimethylhexane 382.27 550.0 2.49 482 5

C8H18 3,3-Dimethylhexane 385.12 562.0 2.65 443 5

C8H18 3,4-Dimethylhexane 390.88 568.8 2.69 466 5

C8H18 3-Ethyl-2-methylpentane 388.81 567.1 2.70 442 5

C8H18 3-Ethyl-3-methylpentane 391.42 576.5 2.81 455 5

C8H18 2,2,3-Trimethylpentane 383 563.5 2.73 436 5

C8H18 2,2,4-Trimethylpentane [Isooctane] 372.37 543.8 2.57 468 5

C8H18 2,3,3-Trimethylpentane 388.0 573.5 2.82 455 5

C8H18 2,3,4-Trimethylpentane 386.7 566.4 2.73 460 5

C8H18 2,2,3,3-Tetramethylbutane 379.60 567.8 2.87 461 9

C8H18 O 1-Octanol 468.31 652.5 2.777 497 4

C8H18 O 2-Octanol 452.5 629.6 2.754 519 4

C8H18 O 3-Octanol 444 628.5 515 4

C8H18 O 4-Octanol 449.5 625.1 515 4

C8H18 O 4-Methyl-3-heptanol 443 623.5 4

C8H18 O 5-Methyl-3-heptanol 445 621.2 4

C8H18 O 2-Ethyl-1-hexanol 457.8 640.6 2.8 4

C8H18 O Dibutyl ether 413.43 584 3.0 7

C8H18 O Di- tert -butyl ether 380.38 550 9

C8H18 O2 1- tert -Butoxy-2-ethoxyethane 421.2 585 7

C8H18 O3 Diethylene glycol monobutyl ether 504 692 2.79 7

C8H18 O3 Diethylene glycol diethyl ether 461 612 7

C8H18 O5 Tetraethylene glycol 601 800 3.2 7

C8H18 S 1-Octanethiol 472.3 667 504 8

C8H18 S Dibutyl sulfide 458 650 2.48 8

C8H19 N Dibutylamine 432.8 607.5 3.11 9

C8H19 N Diisobutylamine 412.8 584.4 3.20 9

C8H20 Si Tetraethylsilane 427.9 605 2.50 587 8

C9F20 Perfluorononane 398.5 524 1.56 9

C9H7N Quinoline 510.31 782 4.86 371 10

C9H7N Isoquinoline 516.37 803 5.10 374 10

C9H10 Indan 451.12 684.9 3.95 3

C9H12 Propylbenzene 432.39 638.35 3.200 440 3

C9H12 Isopropylbenzene [Cumene] 425.56 631.0 3.209 3

C9H12 2-Ethyltoluene 438.4 651 3.38 21

C9H12 3-Ethyltoluene 434.5 637 3.25 21

C9H12 4-Ethyltoluene 435 640.2 3.23 3

C9H12 1,2,3-Trimethylbenzene 449.27 664.5 3.454 3

C9H12 1,2,4-Trimethylbenzene 442.53 649.1 3.232 3

C9H12 1,3,5-Trimethylbenzene [Mesitylene] 437.89 637.3 3.127 3

C9H12 O 2-Methoxy-1,4-dimethylbenzene 467 677.3 7

C9H12 O 1-Methoxy-2,4-dimethylbenzene 465 682 7

C9H13 N 2-Methyl- N,N -dimethylaniline 467.3 668 3.12 9

C9H18 1-Nonene 420.1 594.0 526 6 6-50 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C9H18 Cyclononane 451.6 682 3.34 21

C9H18 1α,3α,5β-1,3,5-Trimethylcyclohexane 413.7 602.2 5

C9H18 O Nonanal 464 659 2.68 543 7

C9H18 O 2-Nonanone [Heptyl methyl ketone] 468.5 652.2 2.48 560 7,11,12

C9H18 O 3-Nonanone [Ethyl hexyl ketone] 463 648.1 560 7

C9H18 O 4-Nonanone [Pentyl propyl ketone] 460.7 643.7 560 7

C9H18 O 5-Nonanone [Dibutyl ketone] 461.60 641.4 2.32 560 7

C9H18 O2 Nonanoic acid 527.7 712 2.35 7

C9H18 O2 Isopentyl butanoate 452 619 7

C9H18 O2 Isobutyl 3-methylbutanoate 441.7 621 7

C9H18 O2 Ethyl heptanoate 460 634 7

C9H20 Nonane 423.97 594.6 2.29 555 2

C9H20 2-Methyloctane 416.4 582.8 2.31 5

C9H20 2,2-Dimethylheptane 405.9 576.7 2.35 5

C9H20 2,2,5-Trimethylhexane 397.24 569.8 5

C9H20 2,2,3,3-Tetramethylpentane 413.4 607.5 2.74 5

C9H20 2,2,3,4-Tetramethylpentane 406.2 592.6 2.60 5

C9H20 2,2,4,4-Tetramethylpentane 395.44 574.6 2.49 5

C9H20 2,3,3,4-Tetramethylpentane 414.7 607.5 2.72 5

C9H20 O 1-Nonanol 486.52 670.7 2.528 572 4

C9H20 O 2-Nonanol 466.7 649.6 2.53 575 4

C9H20 O 3-Nonanol 468 648.0 577 4

C9H20 O 4-Nonanol 465.7 645.1 575 4

C10 F8 Perfluoronaphthalene 482 673.1 9

C10 F18 Perfluorodecalin 415 566 1.52 9

C10 F22 Perfluorodecane 417.4 542 1.45 9

C10 H8 Naphthalene 491.1 748.4 4.05 407 3

C10 H9N 1-Naphthylamine 573.9 850 5.0 438 10

C10 H9N 2-Naphthylamine 579.4 850 4.9 438 10

C10 H12 1,2,3,4-Tetrahydronaphthalene [Tetralin] 480.8 720 3.65 408 4

C10 H14 Butylbenzene 456.46 660.5 2.89 497 3

C10 H14 Isobutylbenzene 445.94 650 3.05 4

C10 H14 1-Isopropyl-4-methylbenzene [ p-Cymene] 450.3 652 2.8 3

C10 H14 p-Diethylbenzene 456.9 657.9 2.803 3

C10 H14 1,2,4,5-Tetramethylbenzene [Durene] 470.0 676 2.9 3

C10 H14 O Thymol 505.7 698 7

C10 H16 d-Limonene 451 653 470 6

C10 H16 α-Pinene 429.4 644 454 6

C10 H16 3-Carene, (+) 444 658 487 6

C10 H18 1,3-Decadiene 442 615 9

C10 H18 cis -Decahydronaphthalene 469.0 702.3 3.20 9

C10 H18 trans -Decahydronaphthalene 460.5 687.1 9

C10 H20 1-Decene 443.7 617 2.22 584 6

C10 H20 O Decanal 481.7 674 2.60 599 7

C10 H20 O 2-Decanone [Methyl octyl ketone] 483 671.8 625 7

C10 H20 O 3-Decanone [Ethyl heptyl ketone] 476 667.6 628 7

C10 H20 O 4-Decanone [Hexyl propyl ketone] 479.7 662.9 628 7

C10 H20 O 5-Decanone [Butyl pentyl ketone] 477 661.0 628 7

C10 H20 O 5-Methyl-2-isopropylcyclohexanol [Menthol] 489 694 9

C10 H20 O2 Decanoic acid [Capric acid] 541.9 722 2.10 638 7

C10 H20 O2 2-Ethylhexyl acetate 472 642 2.09 681 7

C10 H20 O2 Ethyl octanoate 481.7 649 7

C10 H20 O4 Diethylene glycol monobutyl ether acetate 518 693.9 2.15 17

C10 H22 Decane 447.30 617.7 2.11 624 2

C10 H22 3,3,5-Trimethylheptane 428.9 609.5 2.32 5

C10 H22 2,2,3,3-Tetramethylhexane 433.5 623.0 2.51 5

C10 H22 2,2,5,5-Tetramethylhexane 410.6 581.4 2.19 5

C10 H22 O 1-Decanol 504.3 687.3 2.315 649 4

C10 H22 O 2-Decanol 484 668.6 646 4

C10 H22 O 3-Decanol 486 666.1 643 4 Critical Constants 6-51

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C10 H22 O 4-Decanol 483.7 663.7 643 4

C10 H22 O 5-Decanol 474 663.2 646 4

C10 H22 S Diisopentyl sulfide 484 664 8

C11 H10 1-Methylnaphthalene 517.9 772 3.60 3

C11 H10 2-Methylnaphthalene 514.3 761 3

C11 H16 Pentylbenzene 478.6 675 2.58 16

C11 H22 O 2-Undecanone 504.7 688 692 7

C11 H22 O 3-Undecanone 500 685 692 7

C11 H22 O 4-Undecanone 681 692 7

C11 H22 O 5-Undecanone 500 679 692 7

C11 H22 O 6-Undecanone 501 678 692 7

C11 H22 O2 Undecanoic acid 728 2.13 48

C11 H22 O2 Ethyl nonanoate 500.2 664 7

C11 H24 Undecane 469.1 639 1.98 689 2

C11 H24 O 1-Undecanol 518 703.6 2.147 718 4

C12 H8 Acenaphthylene 553 792 3.20 21

C12 H8O Dibenzofuran 560 824 3.64 495 7

C12 H8S Dibenzothiophene 605.7 897 3.86 512 8

C12 H9N Carbazole 627.84 901.8 3.13 454 10

C12 H10 Biphenyl 529.3 773 3.38 497 3

C12 H10 O Diphenyl ether 531.2 767 7

C12 H12 2,7-Dimethylnaphthalene 538 775 3.23 601 3

C12 H18 Hexylbenzene 499.3 695 2.35 16

C12 H18 Hexamethylbenzene 536.6 758 3

C12 H20 O [1,1’-Bicyclohexyl]-2-one 537 787 7

C12 H24 1-Dodecene 487.0 658 1.93 6

C12 H24 O 2-Dodecanone 519.7 702 752 7

C12 H24 O 3-Dodecanone 701 752 7

C12 H24 O 4-Dodecanone 697 759 7

C12 H24 O 5-Dodecanone 695 759 7

C12 H24 O 6-Dodecanone 694 762 7

C12 H24 O2 Dodecanoic acid 743 1.93 48

C12 H26 Dodecane 489.47 658 1.82 754 2

C12 H26 O 1-Dodecanol 533 719.4 1.994 4

C13 H9N Acridine 618.01 891.1 3.21 548 10

C13 H9N Phenanthridine 622.1 895 3.6 548 10

C13 H10 O Benzophenone 578.6 830 3.35 568 7

C13 H11 N 9-Methyl-9 H-carbazole 616.79 890 3.38 572 10

C13 H12 Diphenylmethane 538.2 760 2.71 563 3

C13 H20 Heptylbenzene 513 708 2.14 16

C13 H26 O 2-Tridecanone 536 717 820 7

C13 H26 O 3-Tridecanone 716 823 7

C13 H26 O 4-Tridecanone 712 823 7

C13 H26 O 5-Tridecanone 710 826 7

C13 H26 O 6-Tridecanone 709 826 7

C13 H26 O 7-Tridecanone 534 708 830 7

C14 H28 O2 Tridecanoic acid 763 1.64 48

C13 H26 O2 Methyl dodecanoate 540 712 7

C13 H28 Tridecane 508.62 675 1.68 823 2

C13 H28 O 1-Tridecanol 547 734 1.935 9

C14 H10 Anthracene 613.1 869.3 554 9

C14 H10 Phenanthrene 613 869 4

C14 H22 Octylbenzene 537 725 1.98 16

C14 H28 O 2-Tetradecanone 728 896 7

C14 H28 O 3-Tetradecanone 727 896 7

C14 H28 O 4-Tetradecanone 725 900 7

C14 H28 O 7-Tetradecanone 723 904 7

C14 H28 O2 Tetradecanoic acid 763 1.64 48

C14 H30 Tetradecane 526.73 693 1.57 894 2

C14 H30 O 1-Tetradecanol 560 747 1.81 9 6-52 Critical Constants

Molecular formula Name T /K T /KP /MPa V /cm 3 mol -1 Ref. b c c c

C15 H30 O2 Pentadecanoic acid 777 1.57 48

C15 H32 Pentadecane 543.8 708 1.48 966 2

C16 H26 Decylbenzene 566 752 1.72 16

C16 H32 O2 Hexadecanoic acid 785 1.49 48

C16 H34 Hexadecane 560.01 723 1.40 1034 2

C16 H34 2,2,4,4,6,8,8-Heptamethylnonane 519.5 692 5

C16 H34 O 1-Hexadecanol 585 770 1.61 9

C17 H28 Undecylbenzene 589 763 1.64 16

C17 H34 O2 Heptadecanoic acid 792 1.37 48

C17 H36 Heptadecane 575.2 736 1.34 1103 2

C17 H36 O 1-Heptadecanol 597 780 1.50 9

C18 H14 o-Terphenyl 605 857 2.99 731 3

C18 H14 m-Terphenyl 636 883 2.48 724 3

C18 H14 p-Terphenyl 649 908 2.99 729 3

C18 H36 O2 Octadecanoic acid 803 1.33 48

C18 H38 Octadecane 589.5 747 1.29 1189 2

C18 H38 O 1-Octadecanol 608 790 1.44 9

C19 H32 Tridecylbenzene 619 790 1.54 16

C19 H40 Nonadecane 603.1 755 1.16 3

C20 H40 O2 Eicosanoic acid 820 1.20 48

C20 H42 Eicosane 616 768 1.07 3

C20 H42 O 1-Eicosanol [Arachic alcohol] 629 809 1.30 9

C21 H44 Heneicosane 629.7 778 1.03 2

C22 H44 O2 Docosanoic acid 837 1.11 48

C22 H46 Docosane 641.8 786 0.98 2

C23 H48 Tricosane 653 790 0.92 2

C24 H50 Tetracosane 664.5 800 0.87 2

C30 H50 Squalene 694.5 795.9 0.59 15 46#-*."5*0/
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These precise vapor pressure values are recommended as sec- References ondary standards. Values are given in kPa (1 kPa = 0.0098692 atm = 7.5006 Torr). Reprinted by permission of IUPAC. 1. Marsh, K.N., Ed., Recommended Reference Materials for the Realization of Physicochemical Properties , Blackwell Scientific Publications, Oxford, 1987. 2. Ruzicka, K., Fulem, M., and Ruzicka, V., “Recommended Vapor Pressure of Solid Naphthalene”, J. Chem. Eng. Data , 50, 1956–1970, 2005. T n /K CO 2(s) H2O(s) C10 H8(s) –C 5H12 C6H6 C6F6 H2O Hg 180 27.62 3.04·10 -11 190 68.44 4.33·10 -10 200 155.11 0.0002 4.69·10 -9 210 327.17 0.0007 4.02·10 -8 220 0.0026 2.82·10 -7 230 0.0089 1.66·10 -6 240 0.0273 8.37·10 -6 250 0.0760 3.69·10 -5 7.60 260 0.1958 1.446·10 -4 12.98 270 0.4701 5.09·10 -4 21.15 0.485 280 0.00163 33.11 5.148 4.322 0.991 290 0.004798 50.01 8.606 7.463 1.919 300 0.01308 73.17 13.816 12.328 3.535 310 0.03328 104.07 21.389 19.576 6.228 320 0.07956 144.3 32.054 30.009 10.540 330 0.1797 195.7 46.656 44.578 17.202 340 0.3854 260.1 66.152 64.380 27.167 350 0.7884 339.4 91.609 90.664 41.647 360 435.9 124.192 124.816 62.139 370 551.5 165.2 168.4 90.453 380 688.8 215.9 223.0 128.74 390 850.2 277.7 290.4 179.48 400 1038 353.2 372.6 245.54 0.138 410 1256 441.0 471.5 330.15 0.215 420 1507 545.5 589.3 436.89 0.329 430 1793 667.6 728.3 569.73 0.493 440 2120 808.8 890.9 732.99 0.724 450 2490 971.1 1080 931.36 1.045 460 2910 1156 1297 1169.9 1.485 470 1366 1547 1453.9 2.078 480 1602 1833 1789.0 2.866 490 1868 2159 2181.4 3.899 500 2164 2530 2637.3 5.239 510 2494 2954 3163.3 6.955 520 2861 3766.4 9.131 530 3267 4453.9 11.861 540 3717 5233.5 15.256 550 4216 6113.4 19.438 560 4770 7102.0 25.547 570 8208.6 30.74 580 9443.0 38.19 590 10816 47.09 600 12339 57.64

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$ ) &JDPTBOF    ENTHALPY OF FUSION

4. Dinsdale, A. T., “SGTE Data for Pure Elements”, CALPHAD , 15, 317- This table lists the molar enthalpy (heat) of fusion, Δ fus H, of over 1100 inorganic and organic compounds. All values refer to the 425, 1991. enthalpy change at equilibrium between the liquid phase and the 5. Landolt-Börnstein, Numerical Data and Functional Relationships most stable solid phase at the phase transition temperature. Most in Science and Technology, New Series , IV/8A, “Enthalpies of Fusion and Transition of Organic Compounds”, Springer-Verlag, Heidelberg, values of Δ H are given at the normal melting point t . However, fus m 1995. a “t” following the entry in the melting point column indicate a 6. Landolt-Börnstein, Numerical Data and Functional Relationships triple-point temperature, where the solid, liquid, and gas phases in Science and Technology, New Series , IV/19A, “Thermodynamic are in equilibrium. Temperatures are given on the ITS-90 scale. Properties of Inorganic Materials compiled by SGTE”, Springer- A * following an entry indicates that the value includes the en- Verlag, Heidelberg; Part 1, 1999; Part 2; 1999; Part 3, 2000; Part 4, thalpy of transition between crystalline phases whose transforma- 2001. tion occurs within 1°C of the melting point. 7. Janz, G. J., et al., Physical Properties Data Compilations Relevant to Substances are listed by name, either an IUPAC systematic Energy Storage. II. Molten Salts , Nat. Stand. Ref. Data Sys.- Nat. Bur. Standards (U.S.), No. 61, Part 2, 1979. name or, in the case of drugs and other complex compounds, a 8. Dirand, M., Bouroukba, M., Chevallier, V., Petitjean, D., Behar, E., and common synonym. Inorganic compounds, including metal salts of Ruffier-Meray, V., “Normal Alkanes, Multialkane Synthetic Model organic acids, are listed first, followed by organic compounds. The Mixtures, and Real Petroleum Waxes: Crystallographic Structures, molecular formula in the Hill convention is included. Thermodynamic Properties, and Crystallization”, J. Chem. Eng. Data , 47, 115-143, 2002. References 9. Linstrom, P. J., and Mallard, W. G., Editors, NIST Chemistry WebBook , NIST Standard Reference Database No. 69, June 2005, National Institute of Standards and Technology, Gaithersburg, MD 20899, 1. Chase, M. W., Davies, C. A., Downey, J. R., Frurip, D. J., McDonald, R. . A., and Syverud, A. N., JANAF Thermochemical Tables, Third Edition, 10. Thermodynamic Research Center, National Institute of Standards J. Phys. Chem. Ref. Data , Vol. 14, Suppl. 1, 1985. and Technology, TRC Thermodynamic Tables , . 2. Chase, M. W., NIST-JANAF Thermochemical Tables, Fourth Edition, J. 11. Sangster, J., “Phase Diagrams and Thermodynamic Properties of Phys. Chem. Ref. Data, Monograph No. 9, 1998. Binary Systems of Drugs”, J. Phys. Chem. Ref. Data 28, 889, 1999. 3. Gurvich, L. V., Veyts, I. V., and Alcock, C. B., Thermodynamic Properties of Individual Substances, Fourth Edition; Vol. 2, Hemisphere Publishing Corp., New York, 1991; Vol. 3, CRC Press, Boca Raton, FL, 1994.

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Inorganic compounds (including salts of organic acids) Arsenic(III) oxide (claudetite) As 2O3 314 18

Actinium Ac 1050 12.0 Arsenic(V) oxide As 2O5 730 60

Aluminum Al 660.32 10.71 Arsenic(III) selenide As 2Se 3 377 40.8

Aluminum bromide AlBr 3 97.5 11.25 Arsenic(III) sulfide As 2S3 312 28.7

Aluminum chloride AlCl 3 192.6 35.35 Arsenic sulfide As 4S4 307 25.4

Aluminum fluoride AlF 3 2250 t 0.56 Arsenic(III) telluride As 2Te 3 375 46.0

Aluminum iodide AlI 3 188.28 15.90 Barium Ba 727 7.12

Aluminum oxide ( α) Al 2O3 2054 111.1 Barium bromide BaBr 2 857 32.2

Aluminum sulfide Al 2S3 1100 66 Barium carbonate CBaO 3 1555 40 Americium Am 1176 14.39 (high pres.) Barium chloride BaCl 961 15.85 Ammonia H3N -77.73 5.66 2 Barium fluoride BaF 1368 23.36 Ammonium chloride ClH 4N 520.1 10.6 2 Barium hydride BaH 1200 25 Ammonium fluoride FH 4N 238 12.6 2 Barium hydroxide BaH O 408 16 Ammonium iodide H4IN 551 21 2 2 Barium iodide BaI 711 26.5 Ammonium nitrate H4N2O3 169.7 5.86 2 Antimony (gray) Sb 630.628 19.79 Barium oxide BaO 1973 46 Barium sulfate BaO S 1580 40 Antimony(III) bromide Br 3Sb 97 14.6 4 Barium sulfide BaS 2227 63 Antimony(III) chloride Cl 3Sb 73.4 12.97 Beryllium Be 1287 7.895 Antimony(III) fluoride F3Sb 287 22.8 Beryllium bromide BeBr 508 18 Antimony(III) iodide I3Sb 171 22.8 2 Beryllium carbide CBe 2127 75.3 Antimony(III) oxide O3Sb 2 655 54 2

(valentinite) Beryllium chloride BeCl 2 415 8.66

Antimony(III) sulfide S3Sb 2 550 47.9 Beryllium fluoride BeF 2 552 4.77

Argon Ar -189.36 1.18 Beryllium iodide BeI 2 480 20.92

Arsenic (gray) As 817 24.44 Beryllium nitride Be 3N2 2200 111

Arsenic(III) bromide AsBr 3 31.1 11.7 Beryllium oxide BeO 2578 86

Arsenic(III) chloride AsCl 3 -16 10.1 Beryllium sulfate BeO 4S 1127 6

Arsenic(III) fluoride AsF 3 -5.9 10.4 Bismuth Bi 271.406 11.106

Arsenic(III) iodide AsI 3 141 21.8 Bismuth oxide Bi 2O3 825 14.7

6-110 Enthalpy of Fusion 6-111

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Bismuth sulfide Bi 2S3 777 78.2 Chromium(II) fluoride CrF 2 894 34

Bismuth tribromide BiBr 3 219 21.7 Chromium(III) fluoride CrF 3 1425 66

Bismuth trichloride BiCl 3 234 23.6 Chromium(II) iodide CrI 2 867 46

Bismuth trifluoride BiF 3 649 21.6 Chromium(III) iodide CrI 3 857 61

Bismuth triiodide BiI 3 408.6 39.1 Chromium(III) oxide Cr 2O3 2432 125

Boric acid BH 3O3 170.9 22.3 Chromium(VI) oxide CrO 3 197 14.2 Boron B 2075 50.2 Chromium(II) sulfide CrS 1567 25.5 Boron nitride BN 2967 81 Cobalt Co 1495 16.20

Boron oxide B2O3 450 24.56 Cobalt(II) bromide Br 2Co 678 43

Boron sulfide B2S3 563 48.12 Cobalt(II) chloride Cl 2Co 737 46.0

Boron trichloride BCl 3 -107.3 2.10 Cobalt(II) fluoride CoF 2 1127 58.1

Boron trifluoride BF 3 -126.8 4.20 Cobalt(II) iodide CoI 2 520 35

Bromine Br 2 -7.2 10.57 Cobalt(II) selenite CoO 3Se 659 16.3

Bromine pentafluoride BrF 5 -60.5 5.67 Cobalt(II) sulfide CoS 1117 30 Cadmium Cd 321.069 6.21 Copper Cu 1084.62 13.26

Cadmium bromide Br 2Cd 568 33.35 Copper(I) bromide BrCu 483 5.1

Cadmium chloride CdCl 2 568 48.58 Copper(I) chloride ClCu 423 7.08

Cadmium fluoride CdF 2 1075 22.6 Copper(II) chloride Cl 2Cu 598 15.0

Cadmium iodide CdI 2 388 15.3 Copper(II) fluoride CuF 2 836 55

Cadmium nitrate CdN 2O6 360 18.3 Copper(I) iodide CuI 591 7.93

Calcium Ca 842 8.54 Copper(I) oxide Cu 2O 1244 65.6

Calcium bromide Br 2Ca 742 29.1 Copper(II) oxide CuO 1227 49

Calcium carbonate (calcite) CCaO 3 1330 36 Copper(I) sulfide Cu 2S 1129 9.62

Calcium chloride CaCl 2 775 28.05 Curium Cm 1345 14.64

Calcium fluoride CaF 2 1418 30 Decaborane(14) B10 H14 98.78 21.97

Calcium hydride CaH 2 1000 6.7 Dysprosium Dy 1412 11.35

Calcium iodide CaI 2 783 41.8 Dysprosium(III) fluoride DyF 3 1157 58.6

Calcium nitrate CaN 2O6 561 23.4 Dysprosium(III) oxide Dy 2O3 2408 120 Calcium oxide CaO 2613 80 Einsteinium Es 860 9.41

Calcium sulfate CaO 4S 1460 28 Erbium Er 1529 19.90

Calcium sulfide CaS 2524 70 Erbium chloride Cl 3Er 776 32.6

Carbon (graphite) C 4489 117.4 Erbium fluoride ErF 3 1146 28.2

Cerium Ce 799 5.460 Erbium oxide Er 2O3 2418 130

Cerium(III) bromide Br 3Ce 732 51.9 Europium Eu 822 9.21

Cerium(III) chloride CeCl 3 807 53.1 Europium(II) bromide Br 2Eu 683 25.1

Cerium(III) fluoride CeF 3 1430 55.6 Europium(III) chloride Cl 3Eu 623 33.1

Cerium(III) iodide CeI 3 760 51.0 Europium(III) fluoride EuF 3 647 6.40

Cerium(III) oxide Ce 2O3 2250 120 Europium (II) oxide EuO 1967 40

Cerium(IV) oxide CeO 2 2480 80 Europium(III) oxide Eu 2O3 2350 117

Cesium Cs 28.5 2.09 Fluorine F2 -219.67 0.51

Cesium carbonate CCs 2O3 793 31 Gadolinium Gd 1313 9.67

Cesium chloride ClCs 646 20.4 Gadolinium(III) bromide Br 3Gd 785 38.1

Cesium chromate CrCs 2O4 963 35.3 Gadolinium(III) chloride Cl 3Gd 602 40.6

Cesium fluoride CsF 703 21.7 Gadolinium(III) fluoride F3Gd 1232 52.4

Cesium hydride CsH 528 15 Gadolinium(III) iodide GdI 3 930 54.0

Cesium hydroxide CsHO 342.3 7.78 Gadolinium(III) oxide Gd 2O3 2425 60 Cesium iodide CsI 632 25.7 Gallium Ga 29.7666 5.585

Cesium metaborate BCsO 2 732 27 Gallium antimonide GaSb 712 25.1

Cesium molybdate Cs 2MoO 4 956.3 31.8 Gallium arsenide AsGa 1238 87.64

Cesium nitrate CsNO 3 409 13.8 Gallium(III) bromide Br 3Ga 123 11.7

Cesium nitrite CsNO 2 406 10.9 Gallium(III) chloride Cl 3Ga 77.9 11.51

Cesium oxide Cs 2O 495 20 Gallium(III) iodide GaI 3 212 12.9

Cesium peroxide Cs 2O2 594 22 Gallium(III) oxide Ga 2O3 1807 100

Cesium sulfate Cs 2O4S 1005 35.7 Germanium Ge 938.25 36.94

Chlorine Cl 2 -101.5 6.40 Germanium(IV) bromide Br 4Ge 26.1 12

Chromium Cr 1907 21.00 Germanium(II) iodide GeI 2 428 33.3

Chromium(II) bromide Br 2Cr 842 45 Germanium(IV) iodide GeI 4 146 19.1

Chromium(III) bromide Br 3Cr 812 60 Germanium(IV) oxide GeO 2 1116 12.6

Chromium(II) chloride Cl 2Cr 824 45.0 Germanium(II) selenide GeSe 675 24.7

Chromium(III) chloride Cl 3Cr 827 60 Germanium(II) sulfide GeS 658 21.3 6-112 Enthalpy of Fusion

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Germanium(IV) sulfide GeS 2 840 16.3 Lead(II) oxide (massicot) OPb 887 25.6

Germanium(II) telluride GeTe 724 47.3 Lead(II) sulfate O4PbS 1087 40.2 Gold Au 1064.18 12.55 Lead(II) sulfide PbS 1113 49.4 Hafnium Hf 2233 27.20 Lithium Li 180.50 3.00

Hafnium nitride HfN 3310 62.8 Lithium aluminate AlLiO 2 1610 87.9

Hafnium(IV) oxide HfO 2 2800 96 Lithium bromide BrLi 550 17.66

Holmium Ho 1472 11.76 Lithium carbonate CLi 2O3 732 44.8

Holmium bromide Br 3Ho 919 50.1 Lithium chloride ClLi 610 19.8

Holmium chloride Cl 3Ho 720 30.5 Lithium chromate CrLi 2O4 482 30.5

Holmium fluoride F3Ho 1143 56.3 Lithium fluoride FLi 848.2 27.09

Holmium oxide Ho 2O3 2415 130 Lithium hexafluoroaluminate AlF 6Li 3 785 86.19

Hydrazine H4N2 1.54 12.66 Lithium hydride HLi 692 21.8

Hydrogen H2 -259.198 t 0.12 Lithium hydride- d DLi 694 22 Hydrogen bromide BrH -86.80 2.41 Lithium hydroxide HLiO 473 20.9 Hydrogen chloride ClH -114.17 2.00 Lithium iodide ILi 469 14.6

Hydrogen fluoride FH -83.36 4.58 Lithium metasilicate Li 2O3Si 1201 28

Hydrogen iodide HI -50.76 2.87 Lithium nitrate LiNO 3 253 26.7

Hydrogen peroxide H2O2 -0.43 12.50 Lithium nitrite LiNO 2 222 9.2

Hydrogen sulfide H2S -85.5 2.38 Lithium oxide Li 2O 1437 35.6

Indium In 156.60 3.291 Lithium perchlorate ClLiO 4 236 29.3

Indium antimonide InSb 524 47.7 Lithium sulfate Li 2O4S 860 9.00 Indium arsenide AsIn 942 77.0 Lutetium Lu 1663 18.65

Indium(I) bromide BrIn 285 24.3 Lutetium oxide Lu 2O3 2490 133

Indium(III) bromide Br 3In 420 26 Magnesium Mg 650 8.48

Indium(I) chloride ClIn 225 9.20 Magnesium bromide Br 2Mg 711 39.3

Indium(III) chloride Cl 3In 583 27 Magnesium carbonate CMgO 3 990 59

Indium(III) fluoride F3In 1172 64 Magnesium chloride Cl 2Mg 714 43.1

Indium(I) iodide IIn 364.4 17.26 Magnesium fluoride F2Mg 1263 58.7

Indium(II) iodide I2In 155 1.29 Magnesium hydride H2Mg 327 14

Indium(III) iodide I3In 207 18.48 Magnesium iodide I2Mg 634 26

Indium(III) oxide In 2O3 1912 105 Magnesium orthosilicate Mg 2O4Si 1897 71 Indium(II) sulfide InS 692 36.0 Magnesium oxide MgO 2825 77

Iodine I2 113.7 15.52 Magnesium phosphate Mg 3O8P2 1348 121

Iodine chloride ClI 27.38 11.6 Magnesium sulfate MgO 4S 1137 14.6 Iridium Ir 2446 41.12 Magnesium sulfide MgS 2226 63

Iridium(VI) fluoride F6Ir 44 8.40 Magnesium tetraboride B4Mg 727 0.0 Iron Fe 1538 13.81 Manganese Mn 1246 12.91

Iron boride (FeB) BFe 1658 62.66 Manganese(II) bromide Br 2Mn 698 33.5

Iron(II) bromide Br 2Fe 691 43.0 Manganese(II) chloride Cl 2Mn 650 30.7

Iron(II) chloride Cl 2Fe 677 42.83 Manganese(II) fluoride F2Mn 900 30

Iron(III) chloride Cl 3Fe 307.6 40 Manganese(II) iodide I2Mn 638 41.8

Iron(II) fluoride F2Fe 1100 50 Manganese(II) oxide MnO 1842 43.9

Iron(III) fluoride F3Fe 367 0.58 Manganese(II) sulfide ( α form) MnS 1530 26.1

Iron(II) iodide FeI 2 594 39 Mercury Hg -38.829 2.295

Iron(II) oxide FeO 1377 24.1 Mercury(II) bromide Br 2Hg 241 17.9

Iron(II,III) oxide Fe 3O4 1597 138 Mercury(II) chloride Cl 2Hg 277 19.41

Iron(III) oxide Fe 2O3 1539 87 Mercury(II) fluoride F2Hg 645 23.0

Iron sodium oxide FeNaO 2 1347 49.4 Mercury(I) iodide Hg 2I2 290 31.4

Iron(II) sulfide FeS 1188 31.5 Mercury(II) iodide (yellow) HgI 2 256 15.6 Krypton Kr -157.38 1.64 Mercury(II) sulfide (black) HgS 820 40

Lanthanum La 920 6.20 Metaboric acid ( γ form) BHO 2 236 14.3

Lanthanum bromide Br 3La 788 54.0 Molybdenum Mo 2623 37.48

Lanthanum chloride Cl 3La 858 54.4 Molybdenum boride (Mo 2B5)B5Mo 2 2210 226

Lanthanum fluoride F3La 1493 50.2 Molybdenum(IV) chloride Cl 4Mo 317 16.7

Lanthanum iodide I3La 778 56.1 Molybdenum(V) chloride Cl 5Mo 194 19

Lead Pb 327.462 4.774 Molybdenum(VI) Cl 2MoO 2 176 17.0 dioxydichloride Lead(II) bromide Br 2Pb 371 16.44 Molybdenum(V) fluoride F Mo 45.67 6.1 Lead(II) chloride Cl 2Pb 501 21.88 5 Molybdenum(VI) fluoride F Mo 17.5 4.33 Lead(II) fluoride F2Pb 830 14.7 6 Molybdenum monoboride BMo 2600 55.23 Lead(II) iodide I2Pb 410 23.4

Molybdenum(VI) oxide MoO 3 802 48.7 Enthalpy of Fusion 6-113

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Molybdenum(VI) Cl 4MoO 105 14.3 Plutonium(III) iodide I3Pu 777 50.2 oxytetrachloride Plutonium(III) oxide O3Pu 2 2085 113 Molybdenum(VI) F MoO 97.2 4 4 Plutonium(IV) oxide O2Pu 2390 67 oxytetrafluoride Polonium Po 254 10.0

Molybdenum(V) Cl 3MoO 310 22 Potassium K 63.5 2.335 oxytrichloride Potassium aluminate AlKO 1713 82 Molybdenum(III) sulfide Mo S 1807 0.13 2 2 3 Potassium bromide BrK 734 25.52 Neodymium Nd 1016 7.14 Potassium carbonate CK O 899 27.6 Neodymium(III) bromide Br Nd 682 45.3 2 3 3 Potassium chloride ClK 771 26.28 Neodymium(III) chloride Cl Nd 759 48.5 3 Potassium chromate CrK O 974 33.0 Neodymium(III) fluoride F Nd 1377 54.8 2 4 3 Potassium cyanide CKN 622 14.6 Neodymium(III) iodide I Nd 787 41.5 3 Potassium fluoride FK 858 27.2 Neon Ne -248.609 0.328 Potassium fluoroborate BF 4K 570 17.66 Neptunium Np 644 3.20 Potassium hydride HK 619 21 Nickel Ni 1455 17.48 Potassium hydrogen fluoride F HK 238.8 6.62 Nickel boride (Ni B) BNi 1125 42.15 2 2 2 Potassium hydroxide HKO 406 7.90 Nickel boride (Ni B) BNi 1166 72.28 3 3 Potassium iodide IK 681 24.0 Nickel(II) bromide Br 2Ni 963 56 Potassium metaborate BKO 2 947 31.38 Nickel(II) chloride Cl 2Ni 1031 77.9 Potassium nitrate KNO 3 334 9.6 Nickel(II) fluoride F2Ni 1380 69 Potassium nitrite KNO 2 438 16.7 Nickel(II) iodide I2Ni 800 48 Potassium oxide K2O 740 27 Nickel(II) oxide NiO 1957 50.7 Potassium peroxide K O 545 20.5 Nickel(II) sulfide NiS 976 30.1 2 2 Potassium sulfate K2O4S 1069 36.6 Nickel disulfide NiS 2 1007 65.7 Potassium sulfide K2S 948 16.15 Nickel subsulfide Ni 3S2 789 19.7 Potassium superoxide KO 2 535 20.6 Niobium Nb 2477 30 Praseodymium Pr 931 6.89 Niobium(V) bromide Br 5Nb 254 24.0 Praseodymium(III) bromide Br 3Pr 693 47.3 Niobium(V) chloride Cl 5Nb 205.8 33.9 Praseodymium(III) chloride Cl 3Pr 786 50.6 Niobium(V) fluoride F5Nb 80 12.2 Praseodymium(III) fluoride F3Pr 1399 57.3 Niobium(V) iodide I5Nb 327 37.7 Praseodymium(III) iodide I3Pr 738 53.1 Niobium nitride NNb 2050 46.0 Protactinium Pa 1572 12.34 Niobium(II) oxide NbO 1937 85.4 Radium Ra 696 7.7 Niobium(IV) oxide NbO 1901 92 2 Rhenium Re 3185 34.08 Niobium(V) oxide Nb O 1512 104.3 2 5 Rhenium(VII) oxide O Re 327 65.7 Nitric acid HNO -41.6 10.5 7 2 3 Rhodium Rh 1964 26.59 Nitric oxide NO -163.6 2.30 Rubidium Rb 39.30 2.19 Nitrogen N -210.0 0.71 2 Rubidium bromide BrRb 692 23.3 Nitrogen tetroxide N O -9.3 14.65 2 4 Rubidium carbonate CO Rb 873 30 Nitrous oxide N O -90.8 6.54 3 2 2 Rubidium chloride ClRb 724 24.4 Osmium Os 3033 57.85 Rubidium fluoride FRb 795 25.8 Osmium(VIII) oxide O Os 40.6 14.3 4 Rubidium hydride HRb 585 22 Oxygen O -218.79 0.44 2 Rubidium hydroxide HORb 385 8.0 Palladium Pd 1554.8 16.74 Rubidium iodide IRb 656 22.1 Palladium(II) chloride Cl Pd 679 18.41 2 Rubidium metaborate BO Rb 860 31 Phosphinic acid H O P 26.5 9.7 2 3 2 Rubidium nitrate NO Rb 310 4.6 Phosphonic acid H O P 74.4 12.8 3 3 3 Rubidium nitrite NO Rb 422 12.1 Phosphoric acid H O P 42.4 13.4 2 3 4 Rubidium oxide ORb 505 20 Phosphorus (white) P 44.15 0.659 2 Rubidium peroxide O2Rb 2 570 21 Phosphorus (red) P 579.2 18.54 Rubidium sulfate O Rb S 1066 37.3 Phosphorus(III) chloride Cl P -93 7.10 4 2 3 Rubidium superoxide O Rb 540 21 Phosphorus heptasulfide P S 308 36.6 2 4 7 Ruthenium Ru 2334 38.59 Phosphorus(V) oxide O P 562 27.2 5 2 Ruthenium(V) fluoride F Ru 101 74.5 Phosphorus sesquisulfide P S 173 20.1 5 4 3 Samarium Sm 1072 8.62 Phosphoryl chloride Cl 3OP 1.18 13.1 Samarium(III) oxide O3Sm 2 2335 119 Platinum Pt 1768.2 22.175 Scandium Sc 1541 14.10 Plutonium Pu 640 2.824 Scandium chloride Cl Sc 967 67.4 Plutonium(III) bromide Br Pu 681 58.6 3 3 Scandium fluoride F Sc 1552 62.6 Plutonium(III) chloride Cl Pu 760 63.6 3 3 Scandium oxide O Sc 2489 127 Plutonium(III) fluoride F Pu 1396 59.8 3 2 3 Selenium (gray) Se 220.8 6.69 Plutonium(IV) fluoride F4Pu 1037 42.7 Selenium dioxide O2Se 360 17.6 Plutonium(VI) fluoride F6Pu 51.6 18.6 6-114 Enthalpy of Fusion

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Silicon Si 1414 50.21 Tantalum(V) oxide O5Ta 2 1875 120

Silicon dioxide (cristobalite) O2Si 1722 9.6 Technetium Tc 2157 33.29 Silicon monosulfide SSi 1090 31 Tellurium Te 449.51 17.38

Silver Ag 961.78 11.30 Tellurium dioxide O2Te 733 28.9

Silver(I) bromide AgBr 430 9.163 Tellurium tetrabromide Br 4Te 380 24.7

Silver(I) chloride AgCl 455 13.054 Tellurium tetrachloride Cl 4Te 224 18.9 Silver(I) iodide AgI 558 9.414 Terbium Tb 1359 10.15

Silver(I) nitrate AgNO 3 210 11.72 Terbium(III) bromide Br 3Tb 830 31.5

Silver(I) oxide Ag 2O 827 15 Terbium(III) chloride Cl 3Tb 582 19.5

Silver(I) sulfate Ag 2O4S 660 17.99 Tetrachlorosilane Cl 4Si -68.74 7.60

Silver(I) sulfide Ag 2S 836 7.9 Tetraiodosilane I4Si 120.5 19.7 Sodium Na 97.794 2.60 Thallium Tl 304 4.142

Sodium bromate BrNaO 3 381 28.11 Thallium(I) bromide BrTl 460 16.4

Sodium bromide BrNa 747 26.23 Thallium(I) carbonate CO 3Tl 2 273 18

Sodium carbonate CNa 2O3 856 29.7 Thallium(I) chloride ClTl 431 15.56

Sodium chlorate ClNaO 3 248 22.6 Thallium(I) fluoride FTl 326 13.87

Sodium chloride ClNa 800.7 28.16 Thallium(I) formate CHO 2Tl 101 10.9

Sodium chromate CrNa 2O4 794 24.7 Thallium(I) iodide ITl 441.7 14.7

Sodium cyanide CNNa 562 8.79 Thallium(I) nitrate NO 3Tl 206 9.6

Sodium fluoride FNa 996 33.35 Thallium(I) oxide OTl 2 579 30.3

Sodium formate CHNaO 2 257.3 17.7 Thallium(III) oxide O3Tl 2 834 53

Sodium hexafluoroaluminate AlF 6Na 3 1013 114.4 Thallium(I) sulfate O4STl 2 632 23.8

Sodium hexafluorosilicate F6Na 2Si 847 99.6 Thallium(I) sulfide STl 2 457 23.0 Sodium hydride HNa 638 26 Thorium Th 1750 13.81

Sodium hydroxide HNaO 323 6.60 Thorium(IV) bromide Br 4Th 679 54.4

Sodium iodate INaO 3 422 35.1 Thorium(IV) chloride Cl 4Th 770 43.9

Sodium iodide INa 661 23.7 Thorium(IV) fluoride F4Th 1110 41.8

Sodium metaborate BNaO 2 966 36.2 Thorium(IV) iodide I4Th 566 48.1

Sodium metasilicate Na 2O3Si 1089 51.8 Thorium(IV) oxide O2Th 3350 90

Sodium nitrate NNaO 3 306.5 15.5 Thulium Tm 1545 16.84

Sodium nitrite NNaO 2 284 14.9 Thulium(III) chloride Cl 3Tm 845 34.9

Sodium oxide Na 2O 1134 47.7 Thulium(III) fluoride F3Tm 1158 28.9

Sodium peroxide Na 2O2 675 24.5 Tin (white) Sn 231.93 7.148

Sodium sulfate Na 2O4S 884 23.85 Tin(II) bromide Br 2Sn 232 18.0

Sodium sulfide Na 2S 1172 19 Tin(IV) bromide Br 4Sn 29.1 12.2

Sodium sulfite Na 2O3S 911 25.9 Tin(II) chloride Cl 2Sn 247.0 14.52

Strontium Sr 777 7.43 Tin(IV) chloride Cl 4Sn -34.07 9.20

Strontium bromide Br 2Sr 657 10.5 Tin(II) fluoride F2Sn 215 10.5

Strontium carbonate CO 3Sr 1494 40 Tin(IV) fluoride F4Sn 442 27.6

Strontium chloride Cl 2Sr 874 16.22 Tin(II) iodide I2Sn 320 18.0

Strontium fluoride F2Sr 1477 29.7 Tin(IV) iodide I4Sn 402 0.16

Strontium hydride H2Sr 1050 23 Tin(II) oxide OSn 977 27.7

Strontium hydroxide H2O2Sr 535 23 Tin(IV) oxide O2Sn 1630 23.4

Strontium iodide I2Sr 538 19.7 Tin(II) sulfide SSn 881 31.6

Strontium nitrate N2O6Sr 570 44.6 Tin(II) telluride SnTe 806 45.2 Strontium oxide OSr 2531 81 Titanium Ti 1668 14.15

Strontium sulfate O4SSr 1606 36 Titanium boride B2Ti 2920 100.4

Strontium sulfide SSr 2226 63 Titanium(IV) bromide Br 4Ti 38.3 12.9

Sulfur (monoclinic) S 115.21 1.721 Titanium(II) chloride Cl 2Ti 1035 34.3

Sulfur hexafluoride F6S -49.596 5.02 Titanium(IV) chloride Cl 4Ti -24.12 9.97

Sulfuric acid H2O4S 10.31 10.71 Titanium(IV) fluoride F4Ti 377 41

Sulfur trioxide ( γ-form) O3S 16.8 8.60 Titanium(IV) iodide I4Ti 155 19.8 Tantalum Ta 3017 36.57 Titanium nitride NTi 2947 66.9

Tantalum boride (TaB 2)B2Ta 3100 83.68 Titanium(III) oxide O3Ti 2 1842 104.6

Tantalum(V) bromide Br 5Ta 240 37.7 Titanium(IV) oxide (rutile) O2Ti 1912 68

Tantalum(V) chloride Cl 5Ta 216.6 35.1 Titanium(II) sulfide STi 1927 32

Tantalum(V) fluoride F5Ta 96.9 12 Tungsten W 3422 52.31

Tantalum(V) iodide I5Ta 496 7.74 Tungsten boride (WB) BW 2800 80

Tantalum nitride (TaN) NTa 3090 6.7 Tungsten boride (W2B) BW2 2740 117

Tantalum nitride (Ta 2N) NTa 2 2727 92.0 Tungsten boride (W2B5)B5W2 2370 240 Enthalpy of Fusion 6-115

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Tungsten(V) bromide Br 5W 286 17.2 Zirconium(II) iodide I2Zr 827 28

Tungsten(V) chloride Cl 5W 253 20.6 Zirconium(III) iodide I3Zr 727 33

Tungsten(VI) chloride Cl 6W 282 6.69 Zirconium(IV) iodide I4Zr 500 32

Tungsten(VI) fluoride F6W 1.9 4.10 Zirconium nitride NZr 2952 67.4

Tungsten(VI) oxide O3W 1473 73 Zirconium(IV) oxide O2Zr 2710 90

Tungsten(VI) oxytetrachloride Cl 4OW 210 18.8 Zirconium(IV) sulfide S2Zr 1550 45

Tungsten(VI) oxytetrafluoride F4OW 105 6 Uranium U 1135 9.14 Organic compounds

Uranium(III) bromide Br 3U 727 43.9 Acenaphthene C12 H10 93.4 21.49

Uranium(IV) bromide Br 4U 519 55.2 Acenaphthylene C12 H8 91.8 6.9

Uranium(IV) chloride Cl 4U 590 44.8 Acetaldehyde C2H4O -123.37 2.31

Uranium(III) fluoride F3U 1495 36.8 Acetamide C2H5NO 80.16 15.59

Uranium(IV) fluoride F4U 1036 47 Acetaminophen C8H9NO 2 169.3 30.5

Uranium(V) fluoride F5U 348 35 Acetanilide C8H9NO 114.3 21.3

Uranium(VI) fluoride F6U 64.06 19.2 Acetic acid C2H4O2 16.64 11.73

Uranium(IV) iodide I4U 506 42.1 Acetic anhydride C4H6O3 -74.1 10.5

Uranium(IV) oxide O2U 2847 74.2 Acetone C3H6O -94.7 5.77

Uranyl chloride Cl 2O2U 577 44.06 Acetonitrile C2H3N -43.82 8.16

Vanadium V 1910 21.5 Acrylic acid C3H4O2 12.5 9.51

Vanadium(II) chloride Cl 2V 1350 35.0 Acrylonitrile C3H3N -83.48 6.23

Vanadium(IV) chloride Cl 4V -28 2.30 Allene C3H4 -136.6 4.40

Vanadium(II) fluoride F2V 1490 44 Allobarbital C10 H12 N2O3 172 32.3

Vanadium(III) fluoride F3V 1395 57 2-Aminobenzoic acid C7H7NO 2 146 20.5

Vanadium(V) fluoride F5V 19.5 49.96 4-Aminobenzoic acid C7H7NO 2 188.2 22.5

Vanadium(II) oxide OV 1790 50 3-Amino-1-propanol C3H9NO 12.4 19.7

Vanadium(III) oxide O3V2 1957 140 Aminopyrine C13 H17 N3O 107.5 27.6

Vanadium(IV) oxide O2V 1545 56.0 Ampyrone C11 H13 N3O 109 24.9

Vanadium(V) oxide O5V2 681 64 Aniline C6H7N -6.02 10.54

Water H2O 0.00 6.01 Anisole C7H8O -37.13 12.9

Xenon Xe -111.745 t 2.27 Anthracene C14 H10 215.76 29.4

Xenon difluoride F2Xe 129.03 16.8 Antipyrine C11 H12 N2O 112 27.3

Xenon tetrafluoride F4Xe 117.1 16.3 trans -Azobenzene C12 H10 N2 67.88 22.52

Xenon hexafluoride F6Xe 49.48 5.74 trans -Azoxybenzene C12 H10 N2O 34.6 17.9

Ytterbium Yb 824 7.66 Barbital C8H12 N2O3 190 24.7

Ytterbium(III) chloride Cl 3Yb 854 35.4 Benzaldehyde C7H6O -57.1 9.32

Yttrium Y 1522 11.39 Benzamide C7H7NO 127.3 19.5

Yttrium chloride Cl 3Y 721 31.5 Benz[a]anthracene C18 H12 160.5 21.4

Yttrium fluoride F3Y 1155 27.9 Benzene C6H6 5.49 9.87

Yttrium oxide O3Y2 2439 81 Benzeneacetic acid C8H8O2 76.5 16.3

Zinc Zn 419.53 7.068 1,2-Benzenediamine C6H8N2 102.1 23.1

Zinc bromide Br 2Zn 402 15.7 1,3-Benzenediamine C6H8N2 66.0 15.57

Zinc chloride Cl 2Zn 325 10.30 1,4-Benzenediamine C6H8N2 141.1 23.8

Zinc fluoride F2Zn 872 40 Benzenethiol C6H6S -14.93 11.48

Zinc iodide I2Zn 450 17 p-Benzidine C12 H12 N2 127 19.1

Zinc oxide OZn 1974 70 Benzil C14 H10 O2 94.87 23.5

Zinc phosphide (ZnP 2)P2Zn 980 92.9 Benzocaine C9H11 NO 2 89.7 22.3

Zinc selenite O3SeZn 621 46.4 Benzoic acid C7H6O2 122.35 18.02

Zinc sulfide (wurtzite) SZn 1827 30 Benzonitrile C7H5N -13.99 9.1

Zinc telluride TeZn 1295 63 Benzo[c]phenanthrene C18 H12 68 16.3

Zirconium Zr 1854.7 21.00 Benzophenone C13 H10 O 47.9 18.19

Zirconium boride B2Zr 3050 104.6 Benzo[a]pyrene C20 H12 181.1 17.3

Zirconium(II) bromide Br 2Zr 827 28 Benzo[e]pyrene C20 H12 181.4 16.6

Zirconium(III) bromide Br 3Zr 727 33 p-Benzoquinone C6H4O2 115 18.5

Zirconium(IV) bromide Br 4Zr 450 Benzoyl chloride C7H5ClO -0.4 19.2

Zirconium(II) chloride Cl 2Zr 722 27.0 Benzyl alcohol C7H8O -15.4 8.97

Zirconium(III) chloride Cl 3Zr 627 30 2,2’-Binaphthalene C20 H14 187.9 38.9

Zirconium(IV) chloride Cl 4Zr 437 29 Biphenyl C12 H10 68.93 18.57

Zirconium(II) fluoride F2Zr 902 37.7 Bromobenzene C6H5Br -30.72 10.70

Zirconium(III) fluoride F3Zr 927 50 1-Bromobutane C4H9Br -112.6 9.23

Zirconium(IV) fluoride F4Zr 910 61 2-Bromobutane C4H9Br -112.65 6.89 6-116 Enthalpy of Fusion

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Bromoethane C2H5Br -118.6 7.47 2-Chlorophenol C6H5ClO 9.4 13.0

Bromoethene C2H3Br -139.54 5.12 3-Chlorophenol C6H5ClO 32.6 14.9

1-Bromoheptane C7H15 Br -56.1 21.8 4-Chlorophenol C6H5ClO 42.8 14.1

1-Bromohexane C6H13 Br -83.7 18.1 1-Chloropropane C3H7Cl -122.9 5.54

Bromomethane CH 3Br -93.68 5.98 2-Chloropropane C3H7Cl -117.18 7.39

1-Bromonaphthalene C10 H7Br 6.1 15.2 2-Chlorotoluene C7H7Cl -35.8 9.6

2-Bromonaphthalene C10 H7Br 55.9 14.4 Chlorotrifluoroethene C2ClF 3 -158.2 5.55

1-Bromooctane C8H17 Br -55.0 24.7 Chrysene C18 H12 255.5 26.2

1-Bromopentane C5H11 Br -88.0 14.37 Coronene C24 H12 437.4 19.2

1-Bromopropane C3H7Br -110.3 6.44 o-Cresol C7H8O 31.03 15.82

2-Bromopropane C3H7Br -89.0 6.53 m-Cresol C7H8O 12.24 10.71

Bromotrichloromethane CBrCl 3 -5.65 2.53 p-Cresol C7H8O 34.77 12.71

1,2-Butadiene C4H6 -136.2 6.96 Cyanamide CH 2N2 45.56 7.27

1,3-Butadiene C4H6 -108.91 7.98 Cyanogen C2N2 -27.83 8.11

Butanal C4H8O -96.86 10.77 Cyclobutane C4H8 -90.7 1.09

Butane C4H10 -138.3 4.66 Cycloheptane C7H14 -8.46 1.88

1,4-Butanediol C4H10 O2 20.4 18.70 Cycloheptanol C7H14 O 7.2 1.60

1-Butanethiol C4H10 S -115.7 10.46 Cyclohexane C6H12 6.59 2.68

Butanoic acid C4H8O2 -5.1 11.59 Cyclohexanol C6H12 O 25.93 1.78

1-Butanol C4H10 O -88.6 9.37 Cyclohexanone C6H10 O -27.9 1.328

2-Butanol C4H10 O -88.5 5.97 Cyclohexene C6H10 -103.5 3.29

2-Butanone C4H8O -86.64 8.39 Cyclohexylamine C6H13 N -17.8 17.5

1-Butene C4H8 -185.34 3.96 Cyclohexylbenzene C12 H16 7.07 15.6 cis -2-Butene C4H8 -138.88 7.31 Cyclooctane C8H16 14.59 2.41 trans -2-Butene C4H8 -105.52 9.76 Cyclopentane C5H10 -93.4 0.61 cis -2-Butenoic acid C4H6O2 15 12.6 Cyclopentanol C5H10 O -17.5 1.535 trans -2-Butenoic acid C4H6O2 71.5 13.0 Cyclopentene C5H8 -135.0 3.36 tert -Butylamine C4H11 N -66.94 0.882 Cyclopentylamine C5H11 N -82.7 8.31

Butylbenzene C10 H14 -87.85 11.22 Cyclopropane C3H6 -127.58 5.44

Butylcyclohexane C10 H20 -74.73 14.16 Cyclopropylamine C3H7N -35.39 13.18

Butyl methyl ether C5H12 O -115.7 10.85 cis -Decahydronaphthalene C10 H18 -42.9 9.49

1-Butyne C4H6 -125.7 6.03 trans -Decahydronaphthalene C10 H18 -30.4 14.41

2-Butyne C4H6 -32.2 9.23 Decanal C10 H20 O -4.0 34.5

γ-Butyrolactone C4H6O2 -43.61 9.57 Decane C10 H22 -29.6 28.72

Caffeine C8H10 N4O2 236.3 22.0 Decanoic acid C10 H20 O2 31.4 27.8

Carbazole C12 H9N 246.3 24.1 1-Decanol C10 H22 O 6.9 43

Carbon dioxide CO 2 -56.558 9.02 1-Decene C10 H20 -66.3 13.81

Carbon diselenide CSe 2 -43.7 6.36 1,2-Dibromoethane C2H4Br 2 9.84 10.89

Carbon disulfide CS 2 -112.1 4.39 1,2-Dibromopropane C3H6Br 2 -55.49 8.94

Carbon monoxide CO -205.02 0.833 1,3-Dibromopropane C3H6Br 2 -34.5 14.6

Carbon oxysulfide COS -138.8 4.73 1,2-Dibromotetrafluoroethane C2Br 2F4 -110.32 7.04

Carbonyl chloride CCl 2O -127.78 5.74 o-Dichlorobenzene C6H4Cl 2 -17.0 12.4

Chloroacetic acid C2H3ClO 2 63 12.28 m-Dichlorobenzene C6H4Cl 2 -24.8 12.6

2-Chloroaniline C6H6ClN -1.9 11.9 p-Dichlorobenzene C6H4Cl 2 53.09 18.19

3-Chloroaniline C6H6ClN -10.28 10.15 1,1-Dichloroethane C2H4Cl 2 -96.9 7.87

4-Chloroaniline C6H6ClN 70.5 20.0 1,2-Dichloroethane C2H4Cl 2 -35.7 8.84

Chlorobenzene C6H5Cl -45.31 9.6 1,1-Dichloroethene C2H2Cl 2 -122.56 6.51

2-Chlorobenzoic acid C7H5ClO 2 140.2 25.6 cis -1,2-Dichloroethene C2H2Cl 2 -80.0 7.2

Chlorocyclohexane C6H11 Cl -43.81 2.043 Dichloromethane CH 2Cl 2 -97.2 4.60

Chlorodifluoromethane CHClF 2 -157.42 4.12 1,2-Dichloropropane C3H6Cl 2 -100.53 6.40

Chloroethane C2H5Cl -138.4 4.45 2,2-Dichloropropane C3H6Cl 2 -33.9 2.30

Chloroethene C2H3Cl -153.84 4.92 1,2-Dichloro-1,1,2,2- C2Cl 2F4 -92.53 1.51 tetrafluoroethane Chloromethane CH 3Cl -97.7 6.43 Diethyl ether C H O -116.2 7.19 2-Chloro-2-methylpropane C4H9Cl -25.60 2.07 4 10 3,3-Diethylpentane C H -33.1 10.09 1-Chloronaphthalene C10 H7Cl -2.5 12.9 9 20 Diethyl sulfide C H S -103.91 10.90 2-Chloronaphthalene C10 H7Cl 58.0 14.0 4 10 o-Difluorobenzene C H F -47.1 11.05 1-Chloro-2-nitrobenzene C6H4ClNO 2 32.1 17.9 6 4 2 m-Difluorobenzene C H F -69.12 8.58 1-Chloro-3-nitrobenzene C6H4ClNO 2 44.4 19.4 6 4 2 Diisopropyl ether C H O -85.4 12.04 1-Chloro-4-nitrobenzene C6H4ClNO 2 82 14.1 6 14 1,2-Dimethoxyethane C H O -69.20 12.6 Chloropentafluoroethane C2ClF 5 -99.4 1.86 4 10 2

Dimethoxymethane C3H8O2 -105.1 8.33 Enthalpy of Fusion 6-117

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Dimethylamine C2H7N -92.18 5.94 Formamide CH 3NO 2.49 8.44

2,2-Dimethylbutane C6H14 -98.8 0.58 Formic acid CH 2O2 8.3 12.68

2,3-Dimethylbutane C6H14 -128.10 0.79 Furan C4H4O -85.61 3.80

2,3-Dimethyl-2-butene C6H12 -74.19 6.45 Furfural C5H4O2 -38.1 14.37

1,1-Dimethylcyclohexane C8H16 -33.3 2.07 Furfuryl alcohol C5H6O2 -14.6 13.13 cis -1,2-Dimethylcyclohexane C8H16 -49.8 1.64 Glycerol C3H8O3 18.1 18.3 trans -1,2-Dimethylcyclohexane C8H16 -88.15 10.49 Heneicosane C21 H44 40.01 45.21 cis -1,3-Dimethylcyclohexane C8H16 -75.53 10.82 Heptacosane C27 H56 59.23 61.9 trans -1,3-Dimethylcyclohexane C8H16 -90.07 9.87 Heptadecane C17 H36 22.0 40.16 cis -1,4-Dimethylcyclohexane C8H16 -87.39 9.31 Heptanal C7H14 O -43.4 23.2 trans -1,4-Dimethylcyclohexane C8H16 -36.93 12.33 Heptane C7H16 -90.55 14.03

Dimethyl disulfide C2H6S2 -84.67 9.19 Heptanoic acid C7H14 O2 -7.17 15.13

Dimethyl ether C2H6O -141.5 4.94 1-Heptanol C7H16 O -33.2 18.17

N,N -Dimethylformamide C3H7NO -60.48 7.90 1-Heptene C7H14 -118.9 12.41

1,1-Dimethylhydrazine C2H8N2 -57.20 10.07 Hexachlorobenzene C6Cl 6 228.83 25.2

1,2-Dimethylhydrazine C2H8N2 -8.9 13.64 Hexachloroethane C2Cl 6 186.8t 9.75

Dimethyl oxalate C4H6O4 54.8 21.1 Hexacontane C60 H122 99.3 193.2

2,2-Dimethylpentane C7H16 -123.7 5.82 Hexacosane C26 H54 56.1 60.0

2,4-Dimethylpentane C7H16 -119.2 6.85 Hexadecane C16 H34 18.12 53.36

3,3-Dimethylpentane C7H16 -134.4 6.85 Hexadecanoic acid C16 H32 O2 62.5 53.7

Dimethyl sulfide C2H6S -98.24 7.99 1-Hexadecanol C16 H34 O 49.2 33.6

Dimethyl sulfone C2H6O2S 108.9 18.30 Hexafluorobenzene C6F6 5.03 11.59

Dimethyl sulfoxide C2H6OS 17.89 14.37 Hexafluoroethane C2F6 -100.05 2.69

N,N-Dimethylurea C3H8N2O 182.1 23.0 Hexamethylbenzene C12 H18 165.5 20.6

N,N’ -Dimethylurea C3H8N2O 106.6 13.0 Hexanal C6H12 O -56 13.3

Dimethyl zinc C2H6Zn -43.0 6.83 Hexane C6H14 -95.35 13.08

1,4-Dioxane C4H8O2 11.85 12.84 1,6-Hexanedioic acid C6H10 O4 152.5 36.3

1,3-Dioxolane C3H6O2 -97.22 6.57 1,6-Hexanediol C6H14 O2 41.5 22.2

Diphenylamine C12 H11 N 53.2 18.5 1-Hexanol C6H14 O -47.4 15.38

Diphenyl ether C12 H10 O 26.864 17.22 2-Hexanone C6H12 O -55.5 14.9

Diphenylmethane C13 H12 25.4 18.6 3-Hexanone C6H12 O -55.4 13.49

Dipropyl ether C6H14 O -114.8 10.8 Hexatetracontane C46 H94 87.6 176.0

Divinyl ether C4H6O -100.6 7.9 Hexatriacontane C36 H74 75.8 87.7

Docosane C22 H46 43.6 48.8 1-Hexene C6H12 -139.76 9.35

Dodecane C12 H26 -9.57 36.8 cis -2-Hexene C6H12 -141.11 8.88

Dodecanoic acid C12 H24 O2 43.8 36.3 Hydrogen cyanide CHN -13.29 8.41

1-Dodecanol C12 H26 O 23.9 40.2 p-Hydroquinone C6H6O2 172.4 26.8

1-Dodecene C12 H24 -35.2 19.9 2-Hydroxybenzoic acid C7H6O3 159.0 14.2

Dotriacontane C32 H66 69.4 75.8 Imidazole C3H4N2 89.5 12.82

Eicosane C20 H42 36.6 69.9 Indan C9H10 -51.38 8.60

1-Eicosanol C20 H42 O 65.4 42 Indene C9H8 -1.5 10.20

Estradiol benzoate C25 H28 O3 193 41.8 Indomethacin C19 H16 ClNO 4 160 36.9

Ethane C2H6 -182.79 2.72* Iodobenzene C6H5I -31.3 9.75

1,2-Ethanediamine C2H8N2 11.14 22.58 Isobutane C4H10 -159.4 4.54

1,2-Ethanediol C2H6O2 -12.69 9.96 Isobutene C4H8 -140.7 5.92

Ethanethiol C2H6S -147.88 4.98 Isopentane C5H12 -159.77 5.15

Ethanol C2H6O -114.14 4.931 Isopropylamine C3H9N -95.13 7.33

Ethinylestradiol C20 H24 O2 183.5 27.9 Isopropylbenzene C9H12 -96.02 7.33

Ethyl acetate C4H8O2 -83.8 10.48 1-Isopropyl-4-methylbenzene C10 H14 -67.94 9.66

Ethylbenzene C8H10 -94.96 9.18 Isoquinoline C9H7N 26.47 13.54

Ethylcyclohexane C8H16 -111.3 8.33 Khellin C14 H12 O5 154 32.3

Ethylene C2H4 -169.15 3.35 Maleic anhydride C4H2O3 52.56 13.60

Ethyl methyl sulfide C3H8S -105.93 9.76 Methane CH 4 -182.47 0.94

3-Ethylpentane C7H16 -118.55 9.55 Methanethiol CH 4S -123 5.91

2-Ethyltoluene C9H12 -79.83 9.96 Methanol CH 4O -97.53 3.215

3-Ethyltoluene C9H12 -95.6 7.6 Methyl acetate C3H6O2 -98.25 7.49

4-Ethyltoluene C9H12 -62.35 12.7 Methylamine CH 5N -93.5 6.13

Fluoranthene C16 H10 110.19 18.69 2-Methylaniline C7H9N -14.41 11.66

9H-Fluorene C13 H10 114.77 19.58 3-Methylaniline C7H9N -31.3 7.9

Fluorobenzene C6H5F -42.18 11.31 4-Methylaniline C7H9N 43.6 18.9 6-118 Enthalpy of Fusion

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Methyl benzoate C8H8O2 -12.4 9.74 1-Octene C8H16 -101.7 15.31

2-Methyl-1,3-butadiene C5H8 -145.9 4.93 2-Oxepanone C6H10 O2 -1.0 13.83

2-Methyl-2-butanol C5H12 O -9.1 4.46 Oxetane C3H6O -97 6.5

3-Methyl-2-butanone C5H10 O -93.1 9.34 Oxirane C2H4O -112.5 5.17

2-Methyl-1-butene C5H10 -137.53 7.91 4-Oxopentanoic acid C5H8O3 33 9.22

3-Methyl-1-butene C5H10 -168.43 5.36 Paraldehyde C6H12 O3 12.6 13.5

2-Methyl-2-butene C5H10 -133.72 7.60 Pentachloroethane C2HCl 5 -28.78 11.3

Methyl tert -butyl ether C5H12 O -108.6 7.60 Pentacontane C50 H102 92.1 162.4

Methylcyclohexane C7H14 -126.6 6.75 Pentacosane C25 H52 53.93 56.9

Methylcyclopentane C6H12 -142.42 6.93 Pentadecane C15 H32 9.95 34.6

Methylcyclopropane C4H8 -177.6 2.8 cis -1,3-Pentadiene C5H8 -140.8 5.64

2-Methylfuran C5H6O -91.3 8.55 trans -1,3-Pentadiene C5H8 -87.4 7.14

2-Methylheptane C8H18 -109.02 11.92 1,4-Pentadiene C5H8 -148.2 6.12

3-Methylheptane C8H18 -120.48 11.69 Pentaerythritol C5H12 O4 258 4.8

4-Methylheptane C8H18 -121.0 10.8 Pentafluorobenzene C6HF 5 -47.4 10.87

2-Methylhexane C7H16 -118.2 9.19 Pentafluorophenol C6HF 5O 37.5 16.41

Methylhydrazine CH 6N2 -52.36 10.42 2,3,4,5,6-Pentafluorotoluene C7H3F5 -29.78 13.1

Methyl methacrylate C5H8O2 -47.55 14.4 Pentane C5H12 -129.67 8.40

1-Methylnaphthalene C11 H10 -30.43 6.95 Pentanedioic acid C5H8O4 97.8 20.3

2-Methylnaphthalene C11 H10 34.6 12.13 Pentanenitrile C5H9N -96.2 9

Methyl nitrate CH 3NO 3 -83.0 8.24 1-Pentanethiol C5H12 S -75.65 17.53

Methyloxirane C3H6O -111.9 6.53 Pentanoic acid C5H10 O2 -33.6 14.16

2-Methylpentane C6H14 -153.6 6.27 1-Pentanol C5H12 O -77.6 10.50

3-Methylpentane C6H14 -162.90 5.30 2-Pentanone C5H10 O -76.8 10.63

2-Methyl-1-propanol C4H10 O -101.9 6.32 3-Pentanone C5H10 O -39 11.59

2-Methyl-2-propanol C4H10 O 25.69 6.70 Pentatriacontane C35 H72 74.6 86.3

2-Methylpyridine C6H7N -66.68 9.72 1-Pentene C5H10 -165.12 5.94

3-Methylpyridine C6H7N -18.14 14.18 cis -2-Pentene C5H10 -151.36 7.11

4-Methylpyridine C6H7N 3.67 12.58 trans -2-Pentene C5H10 -140.21 8.35

N-Methylurea C2H6N2O 104.9 14.0 Perfluoroacetone C3F6O -125.45 8.38

Morpholine C4H9NO -4.8 14.5 Perfluorobutane C4F10 -129.1 7.66

Naphthalene C10 H8 80.26 19.01 Perfluorocyclobutane C4F8 -40.19 2.77

1-Naphthol C10 H8O 95.0 23.1 Perfluoroheptane C7F16 -51.2 6.95

2-Naphthol C10 H8O 121.5 18.1 Perfluorohexane C6F14 -88.2 6.84

Neopentane C5H12 -16.4 3.10 Perfluoropropane C3F8 -147.70 0.477

Niacinamide C6H6N2O 130 23.2 Perfluorotoluene C7F8 -65.49 11.54

2-Nitroaniline C6H6N2O2 71.0 16.1 Perylene C20 H12 277.76 31.9

3-Nitroaniline C6H6N2O2 113.4 23.6 Phenacetin C10 H13 NO 2 134 33.0

4-Nitroaniline C6H6N2O2 147.5 21.2 Phenanthrene C14 H10 99.24 16.46

Nitrobenzene C6H5NO 2 5.7 12.12 Phenobarbital C12 H12 N2O3 174.0 27.8

Nitroethane C2H5NO 2 -89.5 9.85 Phenol C6H6O 40.89 11.51

Nitromethane CH 3NO 2 -28.38 9.70 α-Phenylbenzeneacetic acid C14 H12 O2 147.29 31.3

2-Nitrophenol C6H5NO 3 44.8 17.7 Phenylbutazone C19 H20 N2O2 105 27.7

3-Nitrophenol C6H5NO 3 96.8 20.6 Phenylhydrazine C6H8N2 20.6 14.05

4-Nitrophenol C6H5NO 3 113.6 18.8 Piperidine C5H11 N -11.02 14.85

Nitrosobenzene C6H5NO 67 31.0 Potassium acetate C2H3KO 2 309 7.65

4-Nitrotoluene C7H7NO 2 51.63 16.81 Propane C3H8 -187.63 3.50

Nonacosane C29 H60 63.7 66.9 1,3-Propanediol C3H8O2 -27.7 7.1

Nonadecane C19 H40 32.0 45.8 Propanenitrile C3H5N -92.78 5.03

Nonanal C9H18 O -19.3 30.5 1-Propanethiol C3H8S -113.13 5.48

Nonane C9H20 -53.46 15.47 2-Propanethiol C3H8S -130.5 5.74

Nonanoic acid C9H18 O2 12.4 19.82 Propanoic acid C3H6O2 -20.5 10.66

5-Nonanone C9H18 O -3.8 24.93 1-Propanol C3H8O -124.39 5.37

Octacosane C28 H58 61.1 65.1 2-Propanol C3H8O -87.9 5.41

Octadecane C18 H38 28.2 61.7 Propene C3H6 -185.24 3.003

1-Octadecanol C18 H38 O 57.9 45 Propylamine C3H9N -84.75 10.97

Octane C8H18 -56.82 20.73 Propylbenzene C9H12 -99.6 9.27

Octanoic acid C8H16 O2 16.5 21.35 Propylcyclohexane C9H18 -94.9 10.37

1-Octanol C8H18 O -14.8 23.7 Pyrazine C4H4N2 51.0 12.9

Octatriacontane C38 H78 78.6 133.2 1H-Pyrazole C3H4N2 70.7 14.0 Enthalpy of Fusion 6-119

Molecular Δfus H/ kJ Molecular Δfus H/ kJ -1 -1 Name formula tm/°C mol Name formula tm/°C mol

Pyrene C16 H10 150.62 17.36 Thiazole C3H3NS -33.62 9.57

Pyridine C5H5N -41.70 8.28 Thietane C3H6S -73.24 8.25

Pyrocatechol C6H6O2 104.6 22.8 Thiophene C4H4S -38.21 5.07

Pyrrole C4H5N -23.39 7.91 Thiourea CH 4N2S 178 14.0

Pyrrolidine C4H9N -57.79 8.58 Thymol C10 H14 O 49.5 21.3

Quinoline C9H7N -14.78 10.66 Toluene C7H8 -94.95 6.64

Resorcinol C6H6O2 109.4 20.4 o-Toluic acid C8H8O2 103.5 19.5

Sebacic acid C10 H18 O4 130.9 40.8 m-Toluic acid C8H8O2 109.9 15.7

Sodium acetate C2H3NaO 2 328.2 17.9 p-Toluic acid C8H8O2 179.6 22.7

Sodium hydrogen carbonate CHNaO 3 527 25 Triacontane C30 H62 65.1 68.3

Spiro[2.2]pentane C5H8 -107.0 6.43 1,3,5-Triazine C3H3N3 80.3 14.56

Stearic acid C18 H36 O2 69.3 61.2 Tribromomethane CHBr 3 8.69 11.05 trans -Stilbene C14 H12 124.2 27.7 Trichloroacetic acid C2HCl 3O2 59.2 5.90

Styrene C8H8 -30.65 10.9 1,2,3-Trichlorobenzene C6H3Cl 3 51.3 17.9

Succinic acid C4H6O4 187.9 32.4 1,2,4-Trichlorobenzene C6H3Cl 3 16.92 16.4

Succinic anhydride C4H4O3 119 20.4 1,3,5-Trichlorobenzene C6H3Cl 3 62.8 18.1

Succinonitrile C4H4N2 58.06 3.70 1,1,1-Trichloroethane C2H3Cl 3 -30.01 2.35

Sulfacetamide C8H10 N2O3S 183 22.4 1,1,2-Trichloroethane C2H3Cl 3 -36.3 11.46

Sulfadiazine C10 H10 N4O2S 258 42.6 Trichloroethene C2HCl 3 -84.7 8.45

Sulfamerazine C11 H12 N4O2S 236 38.7 Trichlorofluoromethane CCl 3F -110.44 6.89

Sulfamethoxazole C10 H11 N3O3S 170 32.2 Trichloromethane CHCl 3 -63.41 9.5

Sulfamethoxypyridazine C11 H12 N4O3S 182.5 31.3 1,1,2-Trichloro-1,2,2- C2Cl 3F3 -36.22 2.47 trifluoroethane Sulfapyridine C11 H11 N3O2S 192 34.4 Tricosane C H 47.76 50.86 Sulfathiazole C9H9N3O2S2 202 26.4 23 48 Tridecane C H -5.4 28.50 Sulfisoxazole C11 H13 N3O3S 196 30.2 13 28 1-Tridecanol C H O 31.7 41.4 o-Terphenyl C18 H14 56.20 17.19 13 28 1,1,1-Trifluoroethane C H F -111.3 6.19 p-Terphenyl C18 H14 213.9 35.3 2 3 3 Trifluoromethane CHF -155.2 4.06 Tetrabromomethane CBr 4 92.3 3.76 3 Triiodomethane CHI 121.2 16.44 1,1,2,2-Tetrachloro-1,2- C2Cl 4F2 24.8 3.67 3

difluoroethane Trimethoprim C14 H18 N4O3 199 49.4

1,1,2,2-Tetrachloroethane C2H2Cl 4 -42.4 9.17 Trimethylamine C3H9N -117.1 7

Tetrachloroethene C2Cl 4 -22.3 10.88 1,2,3-Trimethylbenzene C9H12 -25.4 8.18

Tetrachloromethane CCl 4 -22.62 2.56 1,2,4-Trimethylbenzene C9H12 -43.77 13.19

Tetracontane C40 H82 81.5 135.5 1,3,5-Trimethylbenzene C9H12 -44.72 9.51

Tetracosane C24 H50 50.4 54.4 2,2,3-Trimethylbutane C7H16 -24.6 2.26

Tetradecane C14 H30 5.82 45.07 2,2,4-Trimethylpentane C8H18 -107.3 9.20

Tetradecanoic acid C14 H28 O2 54.2 45.1 1,3,5-Trinitrobenzene C6H3N3O6 122.9 15.4

1-Tetradecanol C14 H30 O 38.2 25.1* Trinitroglycerol C3H5N3O9 13.5 21.87

1,2,3,5-Tetrafluorobenzene C6H2F4 -46.25 6.36 2,4,6-Trinitrotoluene C7H5N3O6 80.5 22.9

1,2,4,5-Tetrafluorobenzene C6H2F4 3.88 15.05 1,3,5-Trioxane C3H6O3 60.29 15.11

Tetrafluoroethene C2F4 -131.15 7.72 Triphenylamine C18 H15 N 126.5 24.9

Tetrafluoromethane CF 4 -183.60 0.704 Triphenylene C18 H12 197.8 24.74

Tetrahydrofuran C4H8O -108.44 8.54 Tritriacontane C33 H68 71.2 79.5

Tetrahydropyran C5H10 O -49.1 1.8 Undecane C11 H24 -25.5 22.2

Tetrahydrothiophene C4H8S -96.2 7.35 Urea CH 4N2O 133.3 13.9

1,2,4,5-Tetramethylbenzene C10 H14 79.3 21 o-Xylene C8H10 -25.2 13.6

Tetramethyl lead C4H12 Pb -30.2 10.80 m-Xylene C8H10 -47.8 11.6

2,2,3,3-Tetramethylpentane C9H20 -9.75 2.33 p-Xylene C8H10 13.25 17.12

2,2,4,4-Tetramethylpentane C9H20 -66.54 9.74 2,3-Xylenol C8H10 O 72.5 21.0

Tetramethylsilane C4H12 Si -99.06 6.87 2,5-Xylenol C8H10 O 74.8 23.4

Tetramethylstannane C4H12 Sn -55.1 9.30 2,6-Xylenol C8H10 O 45.8 18.9

Tetratetracontane C44 H90 85.6 149.6 3,4-Xylenol C8H10 O 65.1 18.1

Tetratriacontane C34 H70 72.5 79.4 3,5-Xylenol C8H10 O 63.4 17.4

1H-Tetrazole CH 2N4 157.3 18.2 PRESSURE AND TEMPERATURE DEPENDENCE OF LIQUID DENSITY

This table gives data on the variation of the density of some References common liquids with pressure and temperature. The pressure de- pendence is described to first order by the isothermal compress- 1. Lide, D. R., and Kehiaian, H. V., CRC Handbook of Thermophysical ibility coefficient κ defined as and Thermochemical Data , CRC Press, Boca Raton, FL, 1994. 2. Le Neindre, B., Effets des Hautes et Très Hautes Pressions , in Techniques κ = -(1/ V) (∂ V/∂ P) de l’Ingénieur , Paris, 1991. T 3. Landolt-Börnstein, Numerical Data and Functional Relationships in where V is the volume, and the temperature dependence by the Science and Technology, New Series , IV/4, High-Pressure Properties of cubic expansion coefficient α, Matter , Springer–Verlag, Heidelberg, 1980. 4. Riddick, J.A., Bunger, W.B., and Sakano, T.K., Organic Solvents, Fourth α = (1/ V) (∂ V/∂ T) Edition , John Wiley & Sons, New York, 1986. P 5. Isaacs, N. S., Liquid Phase High Pressure Chemistry , John Wiley, New Substances are listed by molecular formula in the Hill order. More York, 1981. precise data on the variation of density with temperature over a wide temperature range can be found in Reference 1.

Molecular Isothermal compressibility Cubic thermal expansion formula Name t/°C κ × 10 4/MPa –1 t/°C α × 10 3/°C –1

Cl 3P Phosphorus trichloride 20 9.45 20 1.9

H2O Water 20 4.591 20 0.206 25 4.524 25 0.256 30 4.475 30 0.302 Hg Mercury 20 0.401 20 0.1811

CCl 4 Tetrachloromethane 20 10.50 20 1.14 40 12.20 40 1.21 70 15.6 70 1.33

CHBr 3 Tribromomethane 50 8.76 25 0.91

CHCl 3 Trichloromethane 20 9.96 20 1.21 50 12.9 50 1.33

CH 2Br 2 Dibromomethane 27 6.85

CH 2Cl 2 Dichloromethane 25 10.3 25 1.39

CH 3I Iodomethane 27 10.3 25 1.26

CH 4O Methanol 20 12.14 20 1.49 40 13.83 40 1.59

CS 2 Carbon disulfide 20 9.38 20 1.12 40 10.6 35 1.16

C2Cl 4 Tetrachloroethylene 25 7.56 25 1.02

C2HCl 3 Trichloroethylene 25 8.57 25 1.17

C2H2Cl 2 trans -1,2-Dichloroethylene 25 11.2 25 1.36

C2H4Cl 2 1,1-Dichloroethane 20 7.97 25 0.93

C2H4Cl 2 1,2-Dichloroethane 30 8.46 20 1.14

C2H4O2 Acetic acid 20 9.08 20 1.08 80 13.7 80 1.38

C2H5Br Bromoethane 20 11.53 20 1.31

C2H5I Iodoethane 20 9.82 25 1.17

C2H6O Ethanol 20 11.19 20 1.40 70 15.93 70 1.67

C2H6O2 Ethylene glycol 20 3.64 20 0.626

C3H6O Acetone 20 12.62 20 1.46 40 15.6 40 1.57

C3H7Br 1-Bromopropane 0 10.22 25 1.2

C3H7Cl 1-Chloropropane 0 12.09 20 1.4

C3H7I 1-Iodopropane 0 10.22 25 1.09

C3H8O 1-Propanol 0 8.43 0 1.22

C3H8O 2-Propanol 40 13.32 40 1.55

C3H8O2 1,2-Propanediol 0 4.45 20 0.695

C3H8O2 1,3-Propanediol 0 4.09 20 0.61

C3H8O3 Glycerol 0 2.54 20 0.520

C4H8O2 Ethyl acetate 20 11.32 20 1.35 60 16.2 60 1.54

6-120 Pressure and Temperature Dependence of Liquid Density 6-121

Molecular Isothermal compressibility Cubic thermal expansion formula Name t/°C κ × 10 4/MPa –1 t/°C α × 10 3/°C –1

C4H9Br 1-Bromobutane 25 10.26 20 1.13

C4H9I 1-Iodobutane 0 7.73 25 1.02

C4H10 O 1-Butanol 0 8.10 0 1.12

C4H10 O Diethyl ether 20 18.65 20 1.65 30 20.85 30 1.72

C4H10 O3 Diethylene glycol 0 3.34 20 0.635

C5H10 Cyclopentane 20 13.31 20 1.35

C5H11 Br 1-Bromopentane 0 8.42 25 1.04

C5H11 I 1-Iodopentane 0 7.56

C5H12 Pentane 25 21.80 25 1.64

C5H12 O 1-Pentanol 0 7.71 0 1.02

C6H5Br Bromobenzene 20 6.46 20 0.86

C6H5Cl Chlorobenzene 20 7.45 20 0.94

C6H5NO 2 Nitrobenzene 20 4.93 25 0.833

C6H6 Benzene 25 9.66 25 1.14 45 11.28 45 1.21

C6H6O Phenol 60 6.05 60 0.82

C6H7N Aniline 20 4.53 20 0.81 80 6.32 80 0.91

C6H12 Cyclohexane 20 11.30 20 1.15 60 15.2 60 1.29

C6H14 Hexane 25 16.69 25 1.41 45 20.27 45 1.52

C6H14 2-Methylpentane 0 13.97 25 1.43

C6H14 3-Methylpentane 0 14.57 25 1.40

C6H14 2,3-Dimethylbutane 20 17.97 25 1.39

C6H14 O 1-Hexanol 25 8.24 25 1.03

C6H15 NO 3 Triethanolamine 0 3.61 55 0.53

C7H8 Toluene 20 8.96 20 1.05 50 11.0 50 1.13

C7H8O Anisole 20 6.60 20 0.951

C7H14 Cycloheptane 20 9.22

C7H16 Heptane 25 14.38 25 1.26

C8H10 o-Xylene 25 8.10 25 0.96

C8H10 m-Xylene 20 8.46 20 0.99

C8H10 p-Xylene 25 8.59 25 1.00

C8H16 Cyclooctane 20 8.03

C8H18 Octane 25 12.82 25 1.16 45 15.06 45 1.23

C8H18 O 1-Octanol 25 7.64 25 0.827

C9H12 Mesitylene 25 8.14 25 0.94

C9H14 O6 Triacetin 0 4.49 25 0.94

C9H20 Nonane 25 11.75 25 1.08

C10 H22 Decane 25 10.94 25 1.02

C11 H24 Undecane 25 10.31 25 0.97

C12 H26 Dodecane 25 9.88 25 0.93

C13 H28 Tridecane 25 9.48 25 0.90

C14 H30 Tetradecane 25 9.10 25 0.87

C15 H32 Pentadecane 25 8.82

C16 H22 O4 Butyl phthalate 0 5.0 25 0.86

C16 H34 Hexadecane 25 8.57 45 9.78

C19 H36 O2 Methyl oleate 0 6.18 60 0.85 PROPERTIES OF CRYOGENIC FLUIDS

This table gives physical and thermodynamic properties of eight In the case of air, the value given for the triple point temperature cryogenic fluids. The properties are: is the incipient solidification temperature, and the normal boiling point value is the incipient boiling (bubble) point. See Reference 3 M Molar mass in grams per mole for more details. Tt Triple point temperature in kelvins P Triple point pressure in kilopascals t References ρt (l) Liquid density at the triple point in grams per milliliter 1. Younglove, B. A., J. Phys. Chem. Ref. Data , 11, Suppl. 1, 1982. ∆fus H @ Tt Enthalpy of fusion at the triple point in joules per 2. Daubert, T. E., Danner, R. P., Sibul, H. M., and Stebbins, C. C., gram Physical and Thermodynamic Properties of Pure Compounds: Data

Tb Normal boiling point in kelvins at a pressure of Compilation , extant 1994 (core with 4 supplements), Taylor & Francis, 101325 pascals (760 mmHg) Bristol, PA (also available as database). 3. Sytchev, V. V., et al., Thermodynamic Properties of Air , Hemisphere ∆vap H @ Tb Enthalpy of vaporization at the normal boiling point in joules per gram Publishing, New York, 1987. 4. Jacobsen, R. T., Stewart, R. B., and Jahangiri, M., J. Phys. Chem. Ref. ρ (l) @ T Liquid density at the normal boiling point in b Data , 15, 735, 1986. [Nitrogen] grams per milliliter 5. Stewart, R. B., Jacobsen, R. T., and Wagner, W., J. Phys. Chem. Ref. ρ (g) @ Tb Vapor density at the normal boiling point in Data , 20, 917, 1991. [Oxygen] grams per liter 6. McCarty, R. D., J. Phys. Chem. Ref. Data , 2, 923, 1973. [Helium] Also,

Cp (l) @ Tb Liquid heat capacity at constant pressure at the Donnelly, R. J., private communication. normal boiling point in joules per gram kelvin 7. Stewart, R. B. and Jacobsen, R. T., J. Phys. Chem. Ref. Data , 18, 639, 1989. [Argon] Cp (g) @ Tb Vapor heat capacity at constant pressure at the normal boiling point in joules per gram kelvin 8. Setzmann, U. and Wagner, W., J. Phys. Chem. Ref. Data , 20, 1061, 1991. [Methane] T Critical temperature in kelvins c 9. Vargaftik, N. B., Thermophysical Properties of Liquids and Gases , 2nd P Critical pressure in megapascals c ed., John Wiley, New York, 1975. ρc Critical density in grams per milliliter

Property Units Air N2 O2 H2 He Ne Ar Kr Xe CH 4 M g/mol 28.96 28.014 31.999 2.0159 4.0026 20.180 39.948 83.800 131.290 16.043

Tt K 59.75 63.15 54.3584 13.8 24.5561 83.8058 115.8 161.4 90.694

Pt kPa 12.463 0.14633 7.042 50 68.95 72.92 81.59 11.696

ρt (l) g/mL 0.959 0.870 1.306 0.0770 1.251 1.417 2.449 2.978 0.4515

∆fus H @ Tt J/g 25.3 13.7 59.5 16.8 28.0 16.3 13.8 58.41

Tb K 78.67 77.35 90.188 20.28 4.2221 27.07 87.293 119.92 165.10 111.668

∆vap H @ Tb J/g 198.7 198.8 213.1 445 20.7 84.8 161.0 108.4 96.1 510.83

ρ (l) @ Tb g/mL 0.8754 0.807 1.141 0.0708 0.124901 1.204 1.396 2.418 2.953 0.4224

ρ (g) @ Tb g/L 3.199 4.622 4.467 1.3390 16.89 9.51 5.79 8.94 1.816

Cp (l) @ Tb J/g K 1.865 2.042 1.699 9.668 4.545 1.877 1.078 0.533 0.340 3.481

Cp (g) @ Tb J/g K 1.341 0.980 12.24 9.78 0.570 0.248 0.158 2.218

Tc K 132.5 126.20 154.581 32.98 5.1953 44.40 150.663 209.40 289.73 190.56

Pc MPa 3.766 3.390 5.043 1.293 0.227460 2.760 4.860 5.500 5.840 4.592

ρc g/mL 0.316 0.313 0.436 0.031 0.06964 0.484 0.531 0.919 1.110 0.1627

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 THERMAL PROPERTIES OF MERCURY Lev R. Fokin

The first of these tables gives the molar heat capacity at constant Reference pressure of liquid and gaseous mercury as a function of tempera- ture. To convert to specific heat in units of J/g K, divide these val- Douglas, T. B., Ball, A. T., and Ginnings, D. C., J. Res. Natl. Bur. Stands ., ues by 200.59, the atomic weight of mercury. 46, 334, 1951.

Cp/(J/mol K) Cp/(J/mol K) Cp/(J/mol K) t/°C Liquid Gas t/°C Liquid Gas t/°C Liquid Gas –38.84 28.2746 20.786 140 27.3675 20.786 340 27.1500 20.836 –20 28.1466 20.786 160 27.3090 20.786 356.73 27.1677 20.849 0 28.0190 20.786 180 27.2588 20.790 360 27.1709 20.853 20 27.9002 20.786 200 27.2169 20.790 380 27.1981 20.870 25 27.8717 20.786 220 27.1834 20.794 400 27.2324 20.891 40 27.7897 20.786 240 27.1583 20.794 420 27.2738 20.916 60 27.6880 20.786 260 27.1412 20.799 440 27.3207 20.941 80 27.5952 20.786 280 27.1320 20.807 460 27.3742 20.974 100 27.5106 20.786 300 27.1303 20.815 480 27.4332 21.008 120 27.4349 20.786 320 27.1366 20.824 500 27.4985 21.046

The second table gives the molar heat capacity of solid mercury References in its rhombohedral (α–mercury) form. 1. Busey and Giaque, J. Am. Chem. Soc., 75, 806, 1953. 2. Amitin, Lebedeva, and Paukov, Rus. J. Phys. Chem., 2666, 1979.

t/°C Cp/(J/mol K) t/°C Cp/(J/mol K) t/°C Cp/(J/mol K) t/°C Cp/(J/mol K) –268.99 0.99* –248.15 12.74 –193.15 23.16 –93.15 26.69 –268.99 0.97** –243.15 14.78 –183.15 23.76 –73.15 27.28 –268.15 1.6 –233.15 17.90 –173.15 24.24 –53.15 27.96 –263.15 4.6 –223.15 19.94 –153.15 25.00 –38.87 28.5 –258.15 7.6 –213.15 21.40 –133.15 25.61 * Superconducting state –253.15 10.33 –203.15 22.42 –113.15 26.15 ** Normal state

The final table gives the cubic thermal expansion coefficient where v is the specific volume (given in the table on the preceding

α, the isothermal compressibility coefficient κT, and the speed of page). sound U for liquid mercury as a function of temperature. These properties are defined as follows: Reference

1¥ uv ´ 1 ¥ uv ´ 2 ¥ uP ´ 1 Vukalovich, M. P., et al., Thermophysical Properties of Mercury , Moscow AK ¦ µ T  ¦ µ U  R  v v § uT¶ v § uP ¶ §¦ uR¶¶µ Standard Press, 1971. p T s

6 –1 6 –1 κT × 10 /bar κT × 10 /bar t/°C α × 10 4/K –1 At 1 bar At 1000 bar U/m s –1 t/°C α × 10 4/K –1 At 1 bar At 1000 bar U/m s –1 –20 1.818 3.83 1470 120 1.8058 4.513 4.33 1404.7 0 1.8144 3.918 3.78 1460.8 140 1.8074 4.622 1395.4 20 1.8110 4.013 3.87 1451.4 160 1.8100 4.731 4.53 1386.1 40 1.8083 4.109 3.96 1442.0 180 1.8136 4.844 1376.7 60 1.8064 4.207 1432.7 200 1.818 4.96 1367 80 1.8053 4.308 4.14 1423.4 250 1.834 5.26 1344 100 1.8051 4.410 1414.1 300 1.856 5.59 1321

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$M 01 1IPTQIPSVT 7
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$M 07 7BOBEZM
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$M 14 1IPTQIPSVT 7
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$M '1 1IPTQIPSVT 7
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$M (F (FSNBOJVN *7
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$M 1C -FBE *7
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$M 4J 5FUSBDIMPSPTJMBOF   &  o& & 

$M 4O 5JO *7
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$M 5J 5JUBOJVN *7
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PYJEF   &  o&  /0 /JUSJD
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/ /JUSPHFO   &  & o& 

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0 0YZHFO   & 


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04 4VMGVS
EJPYJEF   &  o&  & 

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04 4VMGVS
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& o&  4 4VMGVS   &  o& &  4F 4FMFOJVN   &  o&  9F 9FOPO  

$#S$M'  #SPNPDIMPSPEJGMVPSPNFUIBOF   &  o& 

$#S$M  #SPNPUSJDIMPSPNFUIBOF   &  o& 

$#S'  #SPNPUSJGMVPSPNFUIBOF   &  o& 

$#S $M  %JCSPNPEJDIMPSPNFUIBOF   &  o& 

$#S ' %JCSPNPEJGMVPSPNFUIBOF   &  o& & 

$#S $M 5SJCSPNPDIMPSPNFUIBOF  

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$#S /0  5SJCSPNPOJUSPNFUIBOF   &  o& 

$$M'  $IMPSPUSJGMVPSPNFUIBOF   &  o& 

$$M ' %JDIMPSPEJGMVPSPNFUIBOF   &  o& 

$$M 0 $BSCPOZM
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$$M % 5SJDIMPSPNFUIBOF E  

$$M ' 5SJDIMPSPGMVPSPNFUIBOF   &  o& & 

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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

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$)$M  5SJDIMPSPNFUIBOF   &  o& & 

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$) $M0 4 .FUIBOFTVMGPOZM
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$) * *PEPNFUIBOF   &  o& & 

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$) /0  /JUSPNFUIBOF   &  o&  & 

$) /0  .FUIZM
OJUSJUF   &  o&  & 

$) /0  .FUIZM
OJUSBUF  

$)  .FUIBOF   &  & o& 

$) 0 .FUIBOPM   &  o&  & 

$) / .FUIZMBNJOF   &  o& o& 

$/ 0 5FUSBOJUSPNFUIBOF   $04 $BSCPO
PYZTVMGJEF   &  o&  $04F $BSCPO
PYZTFMFOJEF   &  o& 

$0  $BSCPO
EJPYJEF   &  & o& 

$4  $BSCPO
EJTVMGJEF   &  o& & 

$#S '  %JCSPNPUFUSBGMVPSPFUIBOF  

$$M '  %JDIMPSPUFUSBGMVPSPFUIBOF   &  o& o& 

$$M 0 0YBMZM
DIMPSJEF  

$$M / 5SJDIMPSPBDFUPOJUSJMF  

$$M  5FUSBDIMPSPFUIZMFOF  

$$M '    5FUSBDIMPSP EJGMVPSPFUIBOF  

$)#S 0 5SJCSPNPBDFUBMEFIZEF  

$)$M  5SJDIMPSPFUIZMFOF   &  o& 

$)$M '   5SJDIMPSP EJGMVPSPFUIBOF   &  o& 

$)$M 0 5SJDIMPSPBDFUBMEFIZEF  

$)$M 0 5SJDIMPSPBDFUJD
BDJE   &  & o& 

$)$M  1FOUBDIMPSPFUIBOF   &  o& 

$)' 0 5SJGMVPSPBDFUJD
BDJE   &  o& & 

$) "DFUZMFOF  

$)#S  DJT  %JCSPNPFUIZMFOF  

$)#S  USBOT  %JCSPNPFUIZMFOF  

$)#S     5FUSBCSPNPFUIBOF   &  o& 

$)$M   %JDIMPSPFUIZMFOF  

$)$M  DJT  %JDIMPSPFUIZMFOF  

$)$M  USBOT  %JDIMPSPFUIZMFOF  

$)$M 0 %JDIMPSPBDFUJD
BDJE   &  o& & 

$)$M     5FUSBDIMPSPFUIBOF   &  o& 

$)$M     5FUSBDIMPSPFUIBOF  

$)* DJT  %JJPEPFUIZMFOF  

$)$M0 "DFUZM
DIMPSJEF  

$)$M0  $IMPSPBDFUJD
BDJE   &  o& 

$)$M /0   %JDIMPSPOJUSPFUIBOF   &  o& 

$)$M    5SJDIMPSPFUIBOF   &  o&  & 

$)$M    5SJDIMPSPFUIBOF   &  o& 

$)'0   5SJGMVPSPFUIBOPM   &  o&  

$)/ "DFUPOJUSJMF   &  o&  & 

$)/0 .FUIZM
JTPDZBOBUF  

$) &UIZMFOF   &  & o& 

$)#S$M #SPNPDIMPSPFUIBOF   &  o& & 

$)#S   %JCSPNPFUIBOF   &  o& 

$)$M   %JDIMPSPFUIBOF   &  o&  1FSNJUUJWJUZ
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PG
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$)$M   %JDIMPSPFUIBOF   &  o& 

$)$M 0 #JT DIMPSPNFUIZM
FUIFS  

$)/0 &UIZMFOF
HMZDPM
EJOJUSBUF  

$)0 "DFUBMEFIZEF  

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PYJEF   &  o&  & 

$)04 5IJPBDFUJD
BDJE  

$)0 "DFUJD
BDJE   o&  &  o& 

$)0 .FUIZM
GPSNBUF   &  o& 

$)04 &UIZMFOF
HMZDPM
TVMGJUF   &  o&  

$)#S #SPNPFUIBOF   &  o& & 

$)$M $IMPSPFUIBOF   &  o&  & 

$)$M0 $IMPSPFUIBOPM   &  o&  

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$)/ &UIZMFOFJNJOF   &  o&  

$)/0 "DFUBNJEF   o&  &  o& 

$)/0 /.FUIZMGPSNBNJEF   &  o&  & 

$)/0 "DFUBMEPYJNF  

$)/0  /JUSPFUIBOF   &  o& 

$)/0  .FUIZM
DBSCBNBUF   &  o& 

$)/0  &UIZM
OJUSBUF  

$) &UIBOF   &  o& o& 

$)0 &UIBOPM   &  o&  & 

$)0 %JNFUIZM
FUIFS   &  o& & 

$)04 %JNFUIZM
TVMGPYJEF   &  &  o& 

$)0 &UIZMFOF
HMZDPM   &  o&  & 

$)04 %JNFUIZM
TVMGPOF   &  o&  

$)04 %JNFUIZM
TVMGBUF  

$)4 &UIBOFUIJPM  

$)4 %JNFUIZM
TVMGJEF  

$)4  &UIBOFEJUIJPM   &  o& 

$)4 %JNFUIZM
EJTVMGJEF   &  o& 

$)/ &UIZMBNJOF   &  o& 

$)/0 &UIBOPMBNJOF   &  o&  & 

$)/  &UIBOFEJBNJOF   &  o&  & 

$$M 0 )FYBDIMPSPBDFUPOF   &  o& & 

$'0 1FSGMVPSPBDFUPOF   &  o& & 

$)/ $ZBOPBDFUZMFOF   &  o&  & 

$)'0      )FYBGMVPSPQSPQBOPM  

$)$M0  $IMPSP EJPYPMBOPOF  

$)/ "DSZMPOJUSJMF   &  o&  & 

$)/0  $ZBOPBDFUJD
BDJE  

$) "MMFOF   &  o& o& 

$) 1SPQZOF   &  o& 

$)$M'  $IMPSP  USJGMVPSPQSPQBOF   &  o& & 

$)$M/0 $IMPSPFUIZM
JTPDZBOBUF   &  o&  

$)$M 0  %JDIMPSPBDFUPOF  

$)'0    5FUSBGMVPSPQSPQBOPM  

$)0 1SPQBSHZM
BMDPIPM   &  o&  & 

$)0 &UIZMFOF
DBSCPOBUF   &  o&  

$)#S #SPNPQSPQFOF  

$)#S0  #SPNPQSPQBOPJD
BDJE  

$)#S    5SJCSPNPQSPQBOF   &  o& 

$)$M $IMPSPQSPQFOF  

$)$M $IMPSPQSPQFOF  

$)$M/ 0 $IMPSP QSPQBOFEJPM
EJOJUSBUF  

$)$M0 &QJDIMPSPIZESJO  

$)$M0  &UIZM
DIMPSPGPSNBUF   &  o& 

$)$M0  .FUIZM
DIMPSPBDFUBUF  

$)$M    5SJDIMPSPQSPQBOF  

$)* *PEPQSPQFOF  

$)/ 1SPQBOFOJUSJMF   &  o&  & 

$)/0 &UIZM
JTPDZBOBUF  

$)/4 &UIZM
JTPUIJPDZBOBUF   
1FSNJUUJWJUZ
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PG
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$)/0 5SJOJUSPHMZDFSPM  

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$)#S   %JCSPNPQSPQBOF   &  o& 

$)#S   %JCSPNPQSPQBOF   &  o& & 

$)$M/0  $IMPSPOJUSPQSPQBOF  

$)$M   %JDIMPSPQSPQBOF   &  o& 

$)$M   %JDIMPSPQSPQBOF   &  o& 

$)$M   %JDIMPSPQSPQBOF   &  o& 

$)/0  %JOJUSPQSPQBOF  

$)0 "MMZM
BMDPIPM   &  o&  & 

$)0 1SPQBOBM  

$)0 "DFUPOF   &  o&  & 

$)0 1SPQBOPJD
BDJE   &  & & 

$)0 &UIZM
GPSNBUF   &  o& 

$)0 .FUIZM
BDFUBUF   &  o& 

$)0 )ZESPYZQSPQBOPJD
BDJE  

$)0 %JNFUIZM
DBSCPOBUF  

$)0   5SJPYBOF  

$)#S #SPNPQSPQBOF   &  o& 

$)#S #SPNPQSPQBOF   &  o& & 

$)$M $IMPSPQSPQBOF   &  o& 

$)$M0 $IMPSPQSPQBOPM   &  o&  & 

$)$M0 $IMPSPQSPQBOPM   o&  &  o& 

$)$M0  $IMPSP QSPQBOFEJPM  

$)* *PEPQSPQBOF   &  o& 

$)* *PEPQSPQBOF  

$)/0 /&UIZMGPSNBNJEF   &  o&  & 

$)/0 / /%JNFUIZMGPSNBNJEF   &  o&  & 

$)/0 /.FUIZMBDFUBNJEF   &  o&  & 

$)/0  /JUSPQSPQBOF   &  o&  & 

$)/0  /JUSPQSPQBOF   &  o&  

$)/0  1SPQZM
OJUSJUF   &  o&  & 

$)/0  *TPQSPQZM
OJUSJUF   &  o&  & 

$)/0  &UIZM
DBSCBNBUF   &  o& & 

$) 1SPQBOF   &  o& & 

$)0 1SPQBOPM   &  o&  & 

$)0 1SPQBOPM   &  o&  & 

$)0  1SPQZMFOF
HMZDPM   &  o&  & 

$)0  1SPQZMFOF
HMZDPM   &  o&  & 

$)0 &UIZMFOF
HMZDPM
NPOPNFUIZM
FUIFS   &  o&  & 

$)0 %JNFUIPYZNFUIBOF   &  o& & 

$)0 (MZDFSPM   &  o& o& 

$)4 1SPQBOFUIJPM   &  o& 

$)4 1SPQBOFUIJPM  

$)4  1SPQBOFEJUIJPM   &  o& & 

$)4  1SPQBOFEJUIJPM   &  & o& 

$)#0  5SJNFUIZM
CPSBUF  

$)$M4J 5SJNFUIZMDIMPSPTJMBOF   o&  &  o& 

$)/ 1SPQZMBNJOF   &  o& & 

$)/ *TPQSPQZMBNJOF   &  o&  & 

$)/ 5SJNFUIZMBNJOF   &  o& 

$)01 5SJNFUIZM
QIPTQIBUF  

$$M  )FYBDIMPSP CVUBEJFOF  

$$M 0 5SJDIMPSPBDFUJD
BOIZESJEF  

$'0 5SJGMVPSPBDFUJD
BDJE
BOIZESJEF  

$)$M 0 %JDIMPSPBDFUJD
BOIZESJEF  

$)0 .BMFJD
BOIZESJEF  

$)'0       )FQUBGMVPSPCVUBOPM  

$)/ 4VDDJOPOJUSJMF   &  o&  & 

$)/ 1ZSB[JOF  

$)0 'VSBO   &  & o& 

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$)$M $IMPSP CVUBEJFOF   1FSNJUUJWJUZ
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PG
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$)$M 0 &UIZM
USJDIMPSPBDFUBUF  

$)/ 1ZSSPMF   &  o& o& 

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JTPDZOBUF   &  o& 

$)  #VUBEJFOF   &  o& 

$)0 %JWJOZM
FUIFS  

$)0 &UIPYZBDFUZMFOF  

$)0 $ZDMPCVUBOPOF   &  o&  & 

$)0 .FUIZM
BDSZMBUF   &  o& 

$)0  #VUBOFEJPOF   &  o& 

$)0 Ȣ#VUZSPMBDUPOF  

$)0 "DFUJD
BOIZESJEF  

$)0 1SPQZMFOF
DBSCPOBUF   &  o&  & 

$)#S DJT #SPNPCVUFOF  

$)#S USBOT #SPNPCVUFOF  

$)#S0  #SPNPCVUBOPJD
BDJE  

$)#S0  &UIZM
CSPNPBDFUBUF   &  o& 

$)#S0  .FUIZM
CSPNPQSPQBOPBUF   &  & 

$)$M0  1SPQZM
DIMPSPDBSCPOBUF  

$)$M0  .FUIZM
DIMPSPQSPQBOPBUF   &  o& 

$)/ #VUBOFOJUSJMF   &  o& 

$)/ .FUIZMQSPQBOFOJUSJMF   &  o& 

$)/0 1ZSSPMJEPOF   &  o&  & 

$) #VUFOF   &  o& 

$) DJT #VUFOF   &  o& 

$) *TPCVUFOF   &  o& 

$)#S   %JCSPNPCVUBOF   &  o&  & 

$)#S   %JCSPNPCVUBOF   &  o&  & 

$)#S   %JCSPNPCVUBOF   &  o& & 

$)#S   %JCSPNPCVUBOF   &  o& & 

$)#S   %JCSPNPNFUIZMQSPQBOF  

$)$M   %JDIMPSPCVUBOF   &  o&  & 

$)$M   %JDIMPSPCVUBOF   &  & o& 

$)$M   %JDIMPSPNFUIZMQSPQBOF   &  o&  & 

$)$M 0 #JT DIMPSPFUIZM
FUIFS  

$)0 #VUBOBM  

$)0 #VUBOPOF   &  & o& 

$)0 5FUSBIZESPGVSBO   &  o&  & 

$)0 #VUBOPJD
BDJE   &  & 

$)0 .FUIZMQSPQBOPJD
BDJE  

$)0 1SPQZM
GPSNBUF  

$)0 &UIZM
BDFUBUF   &  o& & 

$)0 .FUIZM
QSPQBOPBUF   &  o& 

$)0  %JPYBOF   &  o& 

$)0 )ZESPYZCVUBOPJD
BDJE  

$)0 )ZESPYZCVUBOPJD
BDJE  

$)0 &UIZM
NFUIZM
DBSCPOBUF  

$)0 &UIZMFOF
HMZDPM
NPOPBDFUBUF  

$)#S #SPNPCVUBOF   &  o& & 

$)#S #SPNPCVUBOF   &  o& 

$)#S #SPNPNFUIZMQSPQBOF   &  o&  & 

$)#S #SPNPNFUIZMQSPQBOF   &  o&  & 

$)$M $IMPSPCVUBOF   &  o& o& 

$)$M $IMPSPCVUBOF   &  o&  & 

$)$M $IMPSPNFUIZMQSPQBOF   &  o& & 

$)$M $IMPSPNFUIZMQSPQBOF   &  o&  & 

$)* *PEPCVUBOF   &  o& & 

$)* *PEPCVUBOF   &  o& o& 

$)* *PEPNFUIZMQSPQBOF   &  & o& 

$)/ 1ZSSPMJEJOF   &  o&  & 

$)/0 /.FUIZMQSPQBOBNJEF  

$)/0 /&UIZMBDFUBNJEF   &  o&  & 

$)/0 / /%JNFUIZMBDFUBNJEF   &  o&  & 

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PYJNF   
1FSNJUUJWJUZ
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PG
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$)/0 .PSQIPMJOF  

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DBSCBNBUF   &  o& 

$)/0  &UIZM /NFUIZM
DBSCBNBUF   &  o&  & 

$)/0  /"DFUZMFUIBOPMBNJOF   &  o&  & 

$)/0  #VUZM
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$) #VUBOF   &  o& o& 

$) *TPCVUBOF   &  o& & 

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$) 0 #VUBOPM   &  o&  & 

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$) 0 %JFUIZM
FUIFS   &  o& 

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$) 0 &UIZMFOF
HMZDPM
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FUIFS  

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FUIFS   &  o&  & 

$) 04 #JT IZESPYZFUIZM
TVMGJEF   &  o&  & 

$) 0 %JFUIZMFOF
HMZDPM   &  o&  & 

$) 04 %JFUIZM
TVMGJUF  

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TVMGBUF  

$) 4 #VUBOFUIJPM   &  o& 

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$) 04J %JNFUIPYZEJNFUIZMTJMBOF  

$) 04J 5SJNFUIPYZNFUIZMTJMBOF  

$) 04J 5FUSBNFUIZM
TJMJDBUF  

$) 4J %JFUIZMTJMBOF  

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$) / %JFUIZMFOFUSJBNJOF   &  o&  & 

$'F0  *SPO
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$)$M/ $IMPSPQZSJEJOF   &  o&  & 

$)'0        0DUBGMVPSPQFOUBOPM  

$)0 'VSGVSBM  

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$)0 .FUIZMGVSBO  

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BMDPIPM  

$)$M 0 1SPQZM
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$)0 &UIZM
BDSZMBUF   &  o&  & 

$)0 .FUIZM
USBOT CVUFOPBUF  

$)0 .FUIZM
NFUIBDSZMBUF   &  o&  & 

$)0  1FOUBOFEJPOF  

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NBMPOBUF   &  o& & 

$)#S0  &UIZM
CSPNPQSPQBOPBUF  

$)$M0  *TPCVUZM
DIMPSPDBSCPOBUF  

$)$M0  &UIZM
DIMPSPQSPQBOPBUF   &  o& 

$)$M0  &UIZM
DIMPSPQSPQBOPBUF   &  o& 

$)$M0  .FUIZM
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PG
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GPSN /BNF 5, ȤS BCD 3BOHF,

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$)/0 /.FUIZMQZSSPMJEPOF  

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$) 0 1FOUBOPOF   &  o&  & 

$) 0 1FOUBOPOF   &  & o& 

$) 0 .FUIZMCVUBOPOF   &  o&  & 

$) 0 5FUSBIZESPQZSBO   &  o& & 

$) 0 .FUIZMUFUSBIZESPGVSBO  

$) 0 1FOUBOPJD
BDJE   &  o& & 

$) 0 #VUZM
GPSNBUF   &  o& & 

$) 0 *TPCVUZM
GPSNBUF  

$) 0 1SPQZM
BDFUBUF   &  o& & 

$) 0 &UIZM
QSPQBOPBUF  

$) 0 .FUIZM
CVUBOPBUF   &  o&  & 

$) 0 5FUSBIZESPGVSGVSZM
BMDPIPM  

$) 04 .FUIZM
TVMGPMBOF   &  o& & 

$) 0 %JFUIZM
DBSCPOBUF  

$) 0 &UIZM
MBDUBUF   &  o& o& 

$) 0   1SPQBOFUSJPMBDFUBUF   &  o&  o& 

$) #S #SPNPNFUIZMCVUBOF  

$) #S #SPNPQFOUBOF   &  o& & 

$) #S #SPNPQFOUBOF  

$) #S #SPNPNFUIZMCVUBOF   &  o&  & 

$) $M $IMPSPQFOUBOF   &  o& & 

$) $M $IMPSPNFUIZMCVUBOF   &  o& & 

$) $M $IMPSPNFUIZMCVUBOF   &  o&  & 

$) ' 'MVPSPQFOUBOF  

$) * *PEPQFOUBOF   &  o& & 

$) * *PEPQFOUBOF  

$) * *PEPNFUIZMCVUBOF  

$) * *PEPNFUIZMCVUBOF  

$) / 1JQFSJEJOF   &  o& o& 

$) / /.FUIZMQZSSPMJEJOF  

$) /0  %JNFUIZMQSPQBOBNJEF   &  o&  & 

$) /0 / /%JFUIZMGPSNBNJEF  

$) /0 1FOUBOPOF
PYJNF  

$) /0  1FOUZM
OJUSJUF  

$) 1FOUBOF  

$) *TPQFOUBOF   &  o& o& 

$) /FPQFOUBOF   &  o& & 

$) /0 5FUSBNFUIZMVSFB  

$) 0 1FOUBOPM   &  o&  & 

$) 0 1FOUBOPM   &  o&  & 

$) 0 1FOUBOPM   &  o&  & 

$) 0 .FUIZMCVUBOPM   &  &  o& 

$) 0 .FUIZMCVUBOPM   &  o&  & 

$) 0 .FUIZMCVUBOPM   &  o&  & 

$) 0 .FUIZMCVUBOPM  

$) 0  %JNFUIZMQSPQBOPM   &  o&  &  
1FSNJUUJWJUZ
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PG
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$) 0  1FOUBOFEJPM   &  o&  & 

$) 0  1FOUBOFEJPM   &  o&  & 

$) 0  1FOUBOFEJPM   &  o&  & 

$) 0  1FOUBOFEJPM   &  o&  & 

$) 0  1FOUBOFEJPM   &  o&  & 

$) 0 %JFUIPYZNFUIBOF   &  & o& 

$) 0 5FUSBNFUIPYZNFUIBOF  

$) 0 9ZMJUPM  

$) 4 1FOUBOFUIJPM   &  o& o& 

$) 4 .FUIZMCVUBOFUIJPM   &  o& & 

$) 4 5FUSBLJT NFUIZMUIJP NFUIBOF  

$) / 1FOUZMBNJOF   &  o& & 

$) /    5FUSBNFUIZMHVBOJEJOF  

$) 04J &UIPYZUSJNFUIZMTJMBOF  

$' )FYBGMVPSPCFO[FOF   &  o& o& 

$' 1FSGMVPSPIFYBOF  

$)/0   5SJOJUSPQIFOPM  

$)#S' #SPNPGMVPSPCFO[FOF  

$)#S' #SPNPGMVPSPCFO[FOF  

$)#S' #SPNPGMVPSPCFO[FOF  

$)#S/0  #SPNPOJUSPCFO[FOF   &  o&  & 

$)#S  P%JCSPNPCFO[FOF   o& & o& 

$)#S  N%JCSPNPCFO[FOF   &  o& & 

$)#S  Q%JCSPNPCFO[FOF  

$)$M' $IMPSPGMVPSPCFO[FOF  

$)$M' $IMPSPGMVPSPCFO[FOF  

$)$M' $IMPSPGMVPSPCFO[FOF  

$)$M/0  $IMPSPOJUSPCFO[FOF   &  o&  & 

$)$M/0  $IMPSPOJUSPCFO[FOF   &  o&  & 

$)$M/0  $IMPSPOJUSPCFO[FOF  

$)$M  P%JDIMPSPCFO[FOF   &  & o& 

$)$M  N%JDIMPSPCFO[FOF   &  o& o& 

$)$M  Q%JDIMPSPCFO[FOF   &  o& o& 

$)'* 'MVPSPJPEPCFO[FOF  

$)'* 'MVPSPJPEPCFO[FOF  

$)' P%JGMVPSPCFO[FOF   &  o&  & 

$)' N%JGMVPSPCFO[FOF   &  o& & 

$)* P%JJPEPCFO[FOF   &  o&  & 

$)* N%JJPEPCFO[FOF  

$)* Q%JJPEPCFO[FOF  

$)/ 1ZSJEJOFDBSCPOJUSJMF   &  o&  & 

$)/ 1ZSJEJOFDBSCPOJUSJMF   &  o&  & 

$)/ 1ZSJEJOFDBSCPOJUSJMF   &  o& & 

$)/0  %JOJUSPCFO[FOF   &  o&  & 

$)#S #SPNPCFO[FOF   &  o& o& 

$)$M $IMPSPCFO[FOF   &  o& & 

$)$M0 P$IMPSPQIFOPM   &  o&  & 

$)$M0 N$IMPSPQIFOPM  

$)$M0 Q$IMPSPQIFOPM   &  o& & 

$)$M0 4 #FO[FOFTVMGPOZM
DIMPSJEF   &  o&  & 

$)$M4 $IMPSPCFO[FOFUIJPM  

$)' 'MVPSPCFO[FOF  

$)* *PEPCFO[FOF   &  o& & 

$)/04 /4VMGJOZMBOJMJOF  

$)/0  /JUSPCFO[FOF   &  o&  & 

$)/0  P/JUSPQIFOPM   &  o& & 

$)/0  N/JUSPQIFOPM   &  o&  & 

$)/0  Q/JUSPQIFOPM   &  o&  & 

$) #FO[FOF   &  o& o& 

$)#S/ N#SPNPBOJMJOF  

$)$M/ P$IMPSPBOJMJOF  

$)$M/ N$IMPSPBOJMJOF  

$)/0 P/JUSPBOJMJOF   &  o&  &  1FSNJUUJWJUZ
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PG
-JRVJET


.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$)/0 N/JUSPBOJMJOF   &  o&  & 

$)/0 Q/JUSPBOJMJOF   &  o&  & 

$)0 1IFOPM   &  o&  & 

$)0 1ZSPDBUFDIPM   &  o&  & 

$)0 3FTPSDJOPM   &  o& & 

$)4 #FO[FOFUIJPM   &  o& & 

$)/ "OJMJOF   &  & o& 

$)/ .FUIZMQZSJEJOF   &  o&  & 

$)/ .FUIZMQZSJEJOF   &  o&  & 

$)/ .FUIZMQZSJEJOF   &  o&  & 

$)/0 .FUIZMQZSJEJOFPYJEF   &  o&  & 

$)/0 .FUIZMQZSJEJOFPYJEF   &  o&  & 

$)  $ZDMPIFYBEJFOF  

$)  $ZDMPIFYBEJFOF   &  o& o& 

$)/ 1IFOZMIZESB[JOF  

$)/  %JNFUIZMQZSB[JOF  

$)/  %JNFUIZMQZSB[JOF  

$)0  $ZDMPIFYBOFEJPOF  

$)$M 0 #VUZM
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$)$M 0 *TPCVUZM
USJDIMPSPBDFUBUF  

$)/ $ZDMPQFOUBOFDBSCPOJUSJMF   &  o&  & 

$)  )FYBEJFOF   &  o& o& 

$) DJT DJT  )FYBEJFOF   &  o& o& 

$) USBOT USBOT  )FYBEJFOF   &  o& o& 

$) .FUIZM QFOUBEJFOF  

$) .FUIZM QFOUBEJFOF  

$) .FUIZM QFOUBEJFOF   &  o& & 

$)  %JNFUIZM CVUBEJFOF   &  o& & 

$) )FYZOF   &  o& & 

$) $ZDMPIFYFOF   &  o& & 

$) 0 #VUPYZBDFUZMFOF  

$) 0 $ZDMPIFYBOPOF   &  o&  & 

$) 0 .FTJUZM
PYJEF  

$) 0 &UIZM
CVUFOPBUF  

$) 0 &UIZM
NFUIBDSZMBUF   &  o&  & 

$) 0 &UIZM
BDFUPBDFUBUF  

$) 0 1SPQBOPJD
BOIZESJEF  

$) 0 .POPNFUIZM
HMVUBSBUF   &  o& & 

$) 0 %JFUIZM
PYBMBUF   &  o& & 

$) 0 %JNFUIZM
TVDDJOBUF   &  o& & 

$) 0 &UIZMFOF
HMZDPM
EJBDFUBUF   &  o& & 

$) #S #SPNPDZDMPIFYBOF  

$) #S0  &UIZM
CSPNPCVUBOPBUF   &  o&  & 

$) #S0  &UIZM
CSPNPNFUIZMQSPQBOPBUF   &  o&  & 

$) $M $IMPSPDZDMPIFYBOF  

$) / )FYBOFOJUSJMF  

$) / .FUIZMQFOUBOFOJUSJMF  

$) /0 $ZDMPIFYBOPOF
PYJNF  

$) )FYFOF   &  o& & 

$) USBOT )FYFOF   &  o& o& 

$) DJT )FYFOF   &  o& & 

$) USBOT )FYFOF  

$) $ZDMPIFYBOF   &  o& o& 

$) .FUIZMDZDMPQFOUBOF   &  o& o& 

$) &UIZMDZDMPCVUBOF  

$) #S   %JCSPNPIFYBOF   o&  &  o& 

$) #S   %JCSPNPIFYBOF  

$) $M   %JDIMPSPIFYBOF   &  & o& 

$) 0 .FUIZMDZDMPQFOUBOPM   &  o&  & 

$) 0 *TPCVUZM
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FUIFS   &  o& o& 

$) 0 )FYBOPOF   &  o&  & 

$) 0 .FUIZMQFOUBOPOF   &  o& & 

$) 0  %JNFUIZMCVUBOPOF   &  o&  &  
1FSNJUUJWJUZ
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PG
-JRVJET

.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$) 0 $ZDMPIFYBOPM   &  o&  & 

$) 0 )FYBOPJD
BDJE   &  & o& 

$) 0 &UIZMCVUBOPJD
BDJE  

$) 0 UFSU #VUZMBDFUJD
BDJE  

$) 0 1FOUZM
GPSNBUF  

$) 0 *TPQFOUZM
GPSNBUF   &  o&  & 

$) 0 #VUZM
BDFUBUF   &  o& & 

$) 0 TFD #VUZM
BDFUBUF   &  o& & 

$) 0 UFSU #VUZM
BDFUBUF   &  o&  & 

$) 0 *TPCVUZM
BDFUBUF   &  o& & 

$) 0 1SPQZM
QSPQBOPBUF  

$) 0 &UIZM
CVUBOPBUF   &  o&  & 

$) 0 .FUIZM
QFOUBOPBUF  

$) 0 %JBDFUPOF
BMDPIPM  

$) 0 &UIZMFOF
HMZDPM
NPOPFUIZM

FUIFS
  &  o& &  BDFUBUF

$) 4 $ZDMPIFYBOFUIJPM  

$) #S #SPNPIFYBOF   &  o& & 

$) $M $IMPSPIFYBOF   &  o& & 

$) $M0 $IMPSPIFYBOPM   o&  &  o& 

$) * *PEPIFYBOF   &  o& & 

$) / $ZDMPIFYZMBNJOF  

$) /0 /1SPQZMQSPQBOBNJEF   &  o&  & 

$) /0 /#VUZMBDFUBNJEF   &  o&  & 

$) /0 / / %JFUIZMBDFUBNJEF  

$) )FYBOF   &  & o& 

$) .FUIZMQFOUBOF   &  & o& 

$) .FUIZMQFOUBOF   &  o& & 

$)  %JNFUIZMCVUBOF   &  o& o& 

$)  %JNFUIZMCVUBOF   &  o& & 

$) 0 )FYBOPM   &  o&  & 

$) 0 )FYBOPM  

$) 0 )FYBOPM  

$) 0 .FUIZMQFOUBOPM  

$) 0 .FUIZMQFOUBOPM  

$) 0 &UIZMCVUBOPM  

$) 0  %JNFUIZMCVUBOPM   &  o&  & 

$) 0 %JQSPQZM
FUIFS   &  o& & 

$) 0 %JJTPQSPQZM
FUIFS  

$) 04 %JQSPQZM
TVMGPYJEF   &  o&  & 

$) 0 .FUIZM QFOUBOFEJPM   &  o&  & 

$) 0 &UIZMFOF
HMZDPM
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FUIFS   &  o& & 

$) 04 %JQSPQZM
TVMGPOF   &  o&  & 

$) 0   )FYBOFUSJPM   &  o&  & 

$) 0 %JFUIZMFOF
HMZDPM
EJNFUIZM
FUIFS   &  o&  & 

$) 0 5SJFUIZMFOF
HMZDPM   &  o&  & 

$) 0 %(MVDJUPM  

$) 0 %.BOOJUPM  

$) 4 )FYBOFUIJPM   &  o& & 

$) # 5SJFUIZMCPSBOF  

$) / )FYZMBNJOF   &  o& & 

$) / %JQSPQZMBNJOF   &  o& & 

$) / 5SJFUIZMBNJOF   &  o& o& 

$) 01 5SJFUIZMQIPTQIJOF
PYJEF  

$) 01 5SJFUIZM
QIPTQIBUF   &  o&  & 

$) 14 5SJFUIZMQIPTQIJOF
TVMGJEF  

$) 04J %JFUIPYZEJNFUIZMTJMBOF  

$) 4J 5SJFUIZMTJMBOF  

$) /01 )FYBNFUIZMQIPTQIPSJD
USJBNJEF   &  o&  & 

$) / / /}#JT BNJOPFUIZM  



  &  o&  &  FUIBOFEJBNJOF

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$) 04J  )FYBNFUIZMDZDMPUSJTJMPYBOF   1FSNJUUJWJUZ
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PG
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$) /4J  )FYBNFUIZMEJTJMB[BOF   &  & o& 

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$' 1FSGMVPSPIFQUBOF  

$)$M      1FOUBDIMPSPUPMVFOF  

$)$M/0 $IMPSPQIFOZM
JTPDZBOBUF   &  o& 

$)#S0 #FO[PZM
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$)$M0 #FO[PZM
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$)'0 #FO[PZM
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$)' 5SJGMVPSPNFUIZM CFO[FOF  

$)/ #FO[POJUSJMF   &  o&  & 

$)/0 1IFOZM
JTPDZBOBUF   &  o& & 

$)$M/0  $IMPSPOJUSPUPMVFOF  

$)$M   %JDIMPSPUPMVFOF  

$)$M   %JDIMPSPUPMVFOF  

$)$M   %JDIMPSPUPMVFOF  

$)$M  %JDIMPSPNFUIZM CFO[FOF  

$)0 #FO[BMEFIZEF   &  o& & 

$)0 4BMJDZMBMEFIZEF   &  o&  & 

$)#S P #SPNPUPMVFOF   &  o& & 

$)#S N #SPNPUPMVFOF   &  o& & 

$)#S Q #SPNPUPMVFOF   &  o& o& 

$)#S #SPNPNFUIZM CFO[FOF   &  o& & 

$)#S0 P #SPNPBOJTPMF   &  o& o& 

$)#S0 Q #SPNPBOJTPMF   &  & o& 

$)$M P $IMPSPUPMVFOF   &  o& & 

$)$M N $IMPSPUPMVFOF   &  o& & 

$)$M Q $IMPSPUPMVFOF   &  & o& 

$)$M $IMPSPNFUIZM CFO[FOF   &  o& & 

$)$M0 Q $IMPSPBOJTPMF   &  & o& 

$)$M0 4 Q 5PMVFOFTVMGPOZM
DIMPSJEF  

$)$M0 4 .FUIPYZCFO[FOFTVMGPOZM
DIMPSJEF  

$)' P 'MVPSPUPMVFOF  

$)' N 'MVPSPUPMVFOF  

$)' Q 'MVPSPUPMVFOF  

$)* Q *PEPUPMVFOF  

$)/ 7JOZMQZSJEJOF  

$)/ 7JOZMQZSJEJOF  

$)/0  #FO[ZM
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$)/0  P /JUSPUPMVFOF   &  o&  & 

$)/0  N /JUSPUPMVFOF   &  o&  & 

$)/0  Q /JUSPUPMVFOF  

$)/0 4 /JUSPUIJPBOJTPMF  

$)/0  /JUSPBOJTPMF   &  o&  & 

$)/0  /JUSPBOJTPMF   &  o&  & 

$)/0  /JUSPBOJTPMF   &  o&  & 

$) 5PMVFOF   &  o& & 

$)0 P $SFTPM   &  o& & 

$)0 N $SFTPM   &  o&  & 

$)0 Q $SFTPM   &  o&  & 

$)0 #FO[ZM
BMDPIPM   &  o&  & 

$)0 "OJTPMF   &  o& & 

$)0 .FUIPYZQIFOPM   &  o& & 

$)0 .FUIPYZQIFOPM   &  o&  & 

$)0 .FUIPYZQIFOPM   &  o&  & 

$)04 &UIZM
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$)04 .FUIZM
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TVMGPOF  

$)4 #FO[FOFNFUIBOFUIJPM   &  o& & 

$)4 .FUIZMCFO[FOFUIJPM   &  o& & 

$)4 .FUIZMUIJP CFO[FOF   &  o& & 

$)/ #FO[ZMBNJOF  

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1FSNJUUJWJUZ
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$)/ /.FUIZMBOJMJOF  

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$)/0  %JNFUIZMQZSJEJOFPYJEF   &  o&  & 

$)/0 P .FUIPYZBOJMJOF   &  o& & 

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$)/0 Q .FUIPYZBOJMJOF   &  o&  & 

$) / .FUIZMQIFOZMIZESB[JOF  

$) $M 0 *TPQFOUZM
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$)  )FQUBEJFOF   &  o& & 

$) $ZDMPIFQUFOF   &  o& & 

$) 0 $ZDMPIFQUBOPOF   &  o&  & 

$) 0 .FUIZMDZDMPIFYBOPOF  

$) 0 .FUIZMDZDMPIFYBOPOF  

$) 0 .FUIZMDZDMPIFYBOPOF  

$) 0 $ZDMPIFYBOFDBSCPYZMJD
BDJE  

$) 0 $ZDMPIFYZM
GPSNBUF  

$) 0 #VUZM
BDSZMBUF   &  o&  & 

$) 0 .POPNFUIZM
BEJQBUF   &  o& & 

$) 0 %JFUIZM
NBMPOBUF   &  o& & 

$) 0 %JNFUIZM
HMVUBSBUF   &  o& & 

$) 0   1SPQBOFUSJPM EJBDFUBUF   &  o& & 

$) )FQUFOF   &  & o& 

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$) 0 )FQUBOPOF  

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$) 0 $ZDMPIFYBOFNFUIBOPM   &  o&  & 

$) 0 .FUIZMDZDMPIFYBOPM   &  o&  & 

$) 0 .FUIZMDZDMPIFYBOPM   &  o&  & 

$) 0 .FUIZMDZDMPIFYBOPM   &  o&  & 

$) 0 )FQUBOPJD
BDJE   &  o& & 

$) 0 1FOUZM
BDFUBUF   &  o& & 

$) 0 *TPQFOUZM
BDFUBUF  

$) 0 #VUZM
QSPQBOPBUF  

$) 0 1SPQZM
CVUBOPBUF  

$) 0 &UIZM
QFOUBOPBUF  

$) 0 &UIZM
NFUIZMCVUBOPBUF  

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$) #S #SPNPIFQUBOF   &  o& & 

$) #S #SPNPIFQUBOF  

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GPSN /BNF 5, ȤS BCD 3BOHF,

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$) 0 .FUIZMIFYBOPM  

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$) 0 &UIZM
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$)$M     5FUSBDIMPSP    EJNFUIZMCFO[FOF

$)$M     5FUSBDIMPSP    EJNFUIZMCFO[FOF

$)0 1IFOPYZBDFUZMFOF  

$)/ #FO[FOFBDFUPOJUSJMF   &  o&  & 

$)/0  .FUIPYZQIFOZM
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$) 4UZSFOF   &  o& & 

$)0 "DFUPQIFOPOF   &  & o& 

$)0 #FO[FOFBDFUJD
BDJE   &  & 

$)0 #FO[ZM
GPSNBUF   &  o&  & 

$)0 1IFOZM
BDFUBUF   &  o& & 

$)0 .FUIZM
CFO[PBUF   &  o& & 

$)0 )ZESPYZBDFUZM CFO[FOF   &  o& o& 

$)0 .FUIPYZCFO[BMEFIZEF  

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$)#S0 #SPNPFUIPYZCFO[FOF   &  o& & 

$)$M $IMPSPFUIZMCFO[FOF  

$)$M $IMPSPFUIZMCFO[FOF  

$)$M $IMPSPFUIZMCFO[FOF  

$)/0  &UIZMOJUSPCFO[FOF  

$)/0  .FUIZM
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$) &UIZMCFO[FOF   &  o& & 

$) P 9ZMFOF   &  o& & 

$) N 9ZMFOF   &  o& o& 

$) Q 9ZMFOF   &  & o& 

$) 0  9ZMFOPM   &  o& & 

$) 0  9ZMFOPM   &  o& & 

$) 0  9ZMFOPM   &  o& & 

$) 0  9ZMFOPM   &  o& & 

$) 0  9ZMFOPM   &  o&  & 

$) 0  9ZMFOPM   &  o&  & 

$) 0 #FO[FOFFUIBOPM   &  o&  & 

$) 0 1IFOZMFUIBOPM   &  o&  & 

$) 0 1IFOFUPMF   o&  &  o&  
1FSNJUUJWJUZ
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$) 0 .FUIZMBOJTPMF   &  o& & 

$) 0 .FUIZMBOJTPMF   &  o& & 

$) 0 .FUIZMBOJTPMF   &  o& & 

$) 0  %JNFUIPYZCFO[FOF   &  o& & 

$) 0  %JNFUIPYZCFO[FOF   &  o& & 

$) 0  %JNFUIPYZCFO[FOF   &  o& & 

$) 04 &UIZM
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$) 4 &UIZMUIJP CFO[FOF  

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$) / / / %JNFUIZMBOJMJOF   &  o& & 

$) /   5SJNFUIZMQZSJEJOF   &  o& & 

$) /0 &UIPYZBOJMJOF  

$) /0 )FYBNFUIZMFOF
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$) 0 %JFUIZM
NBMFBUF   &  o& & 

$) 0 %JFUIZM
GVNBSBUF  

$)  0DUBEJFOF   &  o& o& 

$) DJT $ZDMPPDUFOF   &  o& & 

$)  %JNFUIZMDZDMPIFYFOF   &  o& & 

$)  %JNFUIZMDZDMPIFYFOF   &  o& & 

$) 0 .FUIZM
DZDMPIFYBOFDBSCPYZMBUF  

$) 0 $ZDMPIFYZM
BDFUBUF  

$) 0 #VUBOPJD
BOIZESJEF  

$) 0 .FUIZMQSPQBOPJD
BOIZESJEF  

$) 0 %JJTPQSPQZM
PYBMBUF   &  o& & 

$) 0 %JFUIZM
TVDDJOBUF   &  & o& 

$) 0 %JNFUIZM
BEJQBUF   &  o& & 

$) / 0DUBOFOJUSJMF  

$) 0DUFOF   &  & o& 

$) DJT 0DUFOF  

$) USBOT 0DUFOF  

$) DJT 0DUFOF  

$) USBOT 0DUFOF  

$) .FUIZMIFQUFOF  

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$)   5SJNFUIZMQFOUFOF  

$) $ZDMPPDUBOF   &  o& o& 

$) #S   %JCSPNPPDUBOF   &  & o& 

$) $M   %JDIMPSPPDUBOF  

$) 0 0DUBOPOF   o&  &  o& 

$) 0 0DUBOPOF  

$) 0 0DUBOPJD
BDJE   &  o& 

$) 0 &UIZMIFYBOPJD
BDJE  

$) 0 )FYZM
BDFUBUF  

$) 0 1FOUZM
QSPQBOPBUF  

$) 0 *TPQFOUZM
QSPQBOPBUF   &  o& & 

$) 0 #VUZM
CVUBOPBUF   &  o& & 

$) 0 1SPQZM
QFOUBOPBUF  

$) 0 &UIZM
IFYBOPBUF   &  o& & 

$) 0 .FUIZM
IFQUBOPBUF  

$) 0 *TPQFOUZM
MBDUBUF   &  o&  & 

$) #S #SPNPPDUBOF   &  o& & 

$) #S #SPNPPDUBOF  

$) $M $IMPSPPDUBOF   &  o& & 

$) $M $IMPSPPDUBOF  

$) ' 'MVPSPPDUBOF  

$) * *PEPPDUBOF   &  o& & 

$) /0  /JUSPPDUBOF  

$) 0DUBOF   &  o& o& 

$) .FUIZMIFQUBOF  

$) &UIZMIFYBOF  

$)  %JNFUIZMIFYBOF  

$)  %JNFUIZMIFYBOF   &  o& &  1FSNJUUJWJUZ
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PG
-JRVJET


.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$)  %JNFUIZMIFYBOF  

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$) &UIZMNFUIZMQFOUBOF   &  o& & 

$)   5SJNFUIZMQFOUBOF  

$)   5SJNFUIZMQFOUBOF   &  o& & 

$)   5SJNFUIZMQFOUBOF  

$)   5SJNFUIZMQFOUBOF  

$) 0 0DUBOPM   &  o&  & 

$) 0 0DUBOPM   &  o&  & 

$) 0 0DUBOPM   &  o&  & 

$) 0 0DUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   &  o& & 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM  

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM   o&  & o& 

$) 0 .FUIZMIFQUBOPM   o&  & o& 

$) 0 .FUIZMIFQUBOPM   o&  & o& 

$) 0 .FUIZMIFQUBOPM   &  o& 

$) 0 .FUIZMIFQUBOPM   &  o& & 

$) 0 .FUIZMIFQUBOPM   &  & o& 

$) 0 .FUIZMIFQUBOPM   &  o&  & 

$) 0 .FUIZMIFQUBOPM  

$) 0 &UIZMIFYBOPM   &  o&  & 

$) 0  %JNFUIZMIFYBOPM   &  o& & 

$) 0 %JCVUZM
FUIFS   &  o& & 

$) 04 %JCVUZM
TVMGPYJEF   &  o&  & 

$) 0 &UIZM IFYBOFEJPM   &  o&  & 

$) 04 %JCVUZM
TVMGPOF   &  o&  & 

$) 0 5SJFUIZMFOF
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FUIFS  

$) 0 5FUSBFUIZMFOF
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$) 4 0DUBOFUIJPM   &  o& & 

$) 4 %JCVUZM
TVMGJEF  

$) / 0DUZMBNJOF   &  o& & 

$) / %JCVUZMBNJOF   &  o& & 

$) 04J &UIZM
TJMJDBUF  

$) 4J 5FUSBFUIZMTJMBOF  

$) 4O 5FUSBFUIZMTUBOOBOF  

$) / 5FUSBFUIZMFOFQFOUBNJOF   &  o&  & 

$) 04J  0DUBNFUIZMDZDMPUFUSBTJMPYBOF   &  o& & 

$)/0 5PMVFOF EJJTPDZBOBUF   &  o& & 

$)0 )#FO[PQZSBOPOF   &  o&  & 

$)/ 2VJOPMJOF   &  o&  & 

$)/ *TPRVJOPMJOF   &  o&  & 

$)0 $JOOBNBMEFIZEF   &  o&  & 

$)0  "DFUZMPYZ CFO[PJD
BDJE   &  o& 

$) 1SPQFOZMCFO[FOF  

$) "MMZMCFO[FOF  

$) *TPQSPQFOZMCFO[FOF  

$) 04 "DFUZMUIJPBOJTPMF  

$) 0 &UIZM
CFO[PBUF   &  o& & 

$) 0 .FUIZM
NFUIZMCFO[PBUF  

$) 0 #FO[ZM
BDFUBUF   &  o& & 

$) 0 1IFOZM
QSPQBOPBUF  

$) 0 "DFUZMBOJTPMF  

$) 0 &UIZM
TBMJDZMBUF   &  o& & 

$) 0 .FUIZM
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1FSNJUUJWJUZ
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GPSN /BNF 5, ȤS BCD 3BOHF,

$) #S #SPNPQSPQZM CFO[FOF   &  o& & 

$) /0 /&UIZMCFO[BNJEF   o&  &  o& 

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$) /0  &UIZM
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$) 1SPQZMCFO[FOF   &  & o& 

$) *TPQSPQZMCFO[FOF   &  o& & 

$) P &UIZMUPMVFOF  

$) N &UIZMUPMVFOF  

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$)   5SJNFUIZMCFO[FOF   &  o& & 

$)   5SJNFUIZMCFO[FOF   &  o& & 

$) 0 #FO[FOFQSPQBOPM   &  o&  & 

$) 0 Ƞ&UIZMCFO[FOFNFUIBOPM   &  o&  & 

$) 0 Ƞ Ƞ%JNFUIZMCFO[FOFNFUIBOPM   &  & o& 

$) 0 1IFOZMQSPQBOPM   &  o&  & 

$) 0 #FO[ZM
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FUIFS  

$) 0  %JNFUIZMBOJTPMF   &  o& & 

$) 0  %JNFUIZMBOJTPMF   &  o& o& 

$) 04 #VUZM
UIJPQIFOFDBSCPYZMBUF  

$) 4 #FO[FOFQSPQBOFUIJPM   &  o& & 

$) / #FO[ZMFUIZMBNJOF  

$) / /1SPQZMBOJMJOF  

$) / .FUIZM / / EJNFUIZMBOJMJOF  

$) / .FUIZM / / EJNFUIZMBOJMJOF  

$) 04J 5SJNFUIZMQIFOPYZTJMBOF  

$) 0 5SJBDFUJO   &  o& & 

$) 4J 5SJNFUIZMQIFOZMTJMBOF   &  & o& 

$) 0 /POFOPJD
BDJE  

$) 0 $ZDMPIFYZM
QSPQBOPBUF  

$) 0 &UIZM
DZDMPIFYBOFDBSCPYZMBUF  

$) 0 %JFUIZM
HMVUBSBUF  

$) / /POBOFOJUSJMF  

$) /POFOF   &  & o& 

$) #S   %JCSPNPOPOBOF   &  o& & 

$) 0 /POBOPOF  

$) 0 /POBOPOF  

$) 0 %J UFSU CVUZM
LFUPOF  

$) 0  %JNFUIZMIFQUBOPOF   &  o&  & 

$) 0 /POBOPJD
BDJE   &  & o& 

$) 0 .FUIZMPDUBOPJD
BDJE  

$) 0 &UIZMIFQUBOPJD
BDJE  

$) 0 )FQUZM
BDFUBUF  

$) 0 1FOUZM
CVUBOPBUF   &  o& o& 

$) 0 *TPQFOUZM
CVUBOPBUF  

$) 0 *TPCVUZM
QFOUBOPBUF  

$) 0 .FUIZM
PDUBOPBUF  

$) #S #SPNPOPOBOF   &  o& o& 

$) $M $IMPSPOPOBOF   &  o& o& 

$) /0 / /%JCVUZMGPSNBNJEF  

$) /POBOF   &  o& & 

$) .FUIZMPDUBOF  

$) .FUIZMPDUBOF  

$)  %JNFUIZMIFQUBOF  

$)  %JNFUIZMIFQUBOF  

$)  %JNFUIZMIFQUBOF  

$) /0 5FUSBFUIZMVSFB   &  o&  & 

$) 0 /POBOPM   &  o&  & 

$) 0 /POBOPM   &  o&  & 

$) 0 /POBOPM   &  o&  & 

$) 0 /POBOPM   &  & o& 

$) 0 /POBOPM   o&  & o& 

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GPSN /BNF 5, ȤS BCD 3BOHF,

$) / /POZMBNJOF   &  o& & 

$) / 5SJQSPQZMBNJOF   &  o& & 

$) 01 5SJQSPQZM
QIPTQIBUF   &  o&  & 

$ )#S #SPNPOBQIUIBMFOF   &  o& & 

$ )$M $IMPSPOBQIUIBMFOF   &  o& & 

$ )/0  /JUSPOBQIUIBMFOF   &  o& o& 

$ ) /BQIUIBMFOF  

$ )0 /BQIUIPM   &  o& & 

$ )0 /BQIUIPM   &  o& & 

$ )/ /BQIUIZMBNJOF   &  o& & 

$ )/ /BQIUIZMBNJOF   &  o& & 

$ )/ .FUIZMRVJOPMJOF   &  o& o& 

$ )/ .FUIZMRVJOPMJOF   &  o& & 

$ )/ .FUIZMRVJOPMJOF   &  o& & 

$ )/ .FUIZMRVJOPMJOF   &  o& & 

$ ) 0 .FUIZM
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$ ) 0 %JNFUIZM
QIUIBMBUF  

$ )    5FUSBIZESPOBQIUIBMFOF   &  & o& 

$ ) &UIZMTUZSFOF  

$ ) %JDZDMPQFOUBEJFOF   &  o& & 

$ ) 0 5FUSBIZESPOBQIUIPM   &  o&  & 

$ ) 0 *TPQSPQZMCFO[BMEFIZEF  

$ ) 0 "MMZMNFUIPYZQIFOPM   &  o&  & 

$ ) 0 1IFOZMFUIZM
BDFUBUF  

$ ) 0 #FO[ZM
QSPQBOPBUF   &  & o& 

$ ) 0 1IFOZM
CVUBOPBUF  

$ ) 0 1SPQZM
CFO[PBUF   &  o& & 

$ ) 0 &UIZM
QIFOZMBDFUBUF  

$ ) #VUZMCFO[FOF  

$ ) TFD #VUZMCFO[FOF   &  o& o& 

$ ) UFSU #VUZMCFO[FOF   &  o& o& 

$ ) *TPCVUZMCFO[FOF   &  o& o& 

$ ) *TPQSPQZMNFUIZMCFO[FOF   &  o& o& 

$ ) P %JFUIZMCFO[FOF  

$ ) N %JFUIZMCFO[FOF  

$ ) Q %JFUIZMCFO[FOF  

$ ) &UIZM EJNFUIZMCFO[FOF  

$ )    5FUSBNFUIZMCFO[FOF   &  o& & 

$ )    5FUSBNFUIZMCFO[FOF   &  o& o& 

$ ) / -/JDPUJOF   &  o& & 

$ ) 0 1IFOZMNFUIZMQSPQBOPM   &  o& & 

$ ) 0 #VUZM
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FUIFS  

$ ) 0 5IZNPM  

$ ) / / /%JFUIZMBOJMJOF   &  & o& 

$ ) Ȣ5FSQJOFOF  

$ ) E-JNPOFOF  

$ ) M-JNPOFOF  

$ ) 5FSQJOPMFOF  

$ ) Ƞ1JOFOF  

$ ) ȡ1JOFOF  

$ ) Ƞ5FSQJOFOF  

$ ) ȡ.ZSDFOF  

$ ) 0 $BSWFOPOF  

$ ) 0 E'FODIPOF  

$ ) $M $IMPSPCPSOBOF  

$ ) 1JOBOF  

$ ) DJT %FDBIZESPOBQIUIBMFOF   &  o& & 

$ ) USBOT %FDBIZESPOBQIUIBMFOF   &  o& & 

$ ) 0 &VDBMZQUPM  

$ ) 0 $ZDMPIFYZM
CVUBOPBUF  

$ ) 0 %JFUIZM
BEJQBUF   &  o& & 

$ ) %FDFOF   &  & o& 

$ ) DJT %FDFOF   
1FSNJUUJWJUZ
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GPSN /BNF 5, ȤS BCD 3BOHF,

$ ) USBOT %FDFOF  

$ ) .FUIZMOPOFOF  

$ )   5SJNFUIZMIFQUFOF  

$ ) #S   %JCSPNPEFDBOF   &  o& & 

$ ) $M   %JDIMPSPEFDBOF   o&  & o& 

$ ) 0 %FDBOPOF  

$ ) 0 .FOUIPM   &  o& & 

$ ) 0  %JNFUIZMPDUBOPJD
BDJE  

$ ) 0 0DUZM
BDFUBUF   o&  & o& 

$ ) 0 .FUIZMIFQUZM
BDFUBUF   &  o&  & 

$ ) 0 1FOUZM
QFOUBOPBUF   &  o& & 

$ ) 0 *TPQFOUZM
QFOUBOPBUF  

$ ) 0 *TPQFOUZM
JTPQFOUBOPBUF   &  o& & 

$ ) 0 .FUIZM
OPOBOPBUF  

$ ) #S #SPNPEFDBOF   &  o& & 

$ ) $M $IMPSPEFDBOF   &  o& o& 

$ ) /0 / /%JCVUZMBDFUBNJEF  

$ ) %FDBOF   &  o& & 

$ )  %JNFUIZMPDUBOF  

$ ) 1SPQZMIFQUBOF  

$ ) 0 %FDBOPM   &  o&  & 

$ ) 0 %FDBOPM   &  o&  & 

$ ) 0 %FDBOPM   &  o&  & 

$ ) 0 %FDBOPM   o&  & o& 

$ ) 0 %FDBOPM   o&  & o& 

$ ) 0  %JNFUIZMPDUBOPM   &  o&  & 

$ ) 0 %JQFOUZM
FUIFS  

$ ) 0 %JJTPQFOUZM
FUIFS   &  o& & 

$ ) 04 %JQFOUZM
TVMGPYJEF  

$ ) 0 5FUSBFUIZMFOF
HMZDPM
EJNFUIZM
FUIFS  

$ ) 4 %JQFOUZM
TVMGJEF  

$ ) / %FDZMBNJOF   &  o& & 

$ ) 04J  %FDBNFUIZMUFUSBTJMPYBOF  

$ ) 04J  %FDBNFUIZMDZDMPQFOUBTJMPYBOF  

$ ) .FUIZMOBQIUIBMFOF   &  o& & 

$ ) .FUIZMOBQIUIBMFOF  

$ ) 0 .FUIPYZOBQIUIBMFOF   &  o& & 

$ ) 0 .FUIPYZOBQIUIBMFOF   &  o& & 

$ ) 0 &UIZM
USBOT DJOOBNBUF  

$ ) 0 &UIZM
CFO[PZMBDFUBUF   &  & o& 

$ ) 0 #FO[ZM
CVUBOPBUF  

$ ) 0 1IFOZM
QFOUBOPBUF  

$ ) 0 #VUZM
CFO[PBUF   &  o& o& 

$ ) 0 *TPCVUZM
CFO[PBUF  

$ )  %JFUIZMNFUIZMCFO[FOF  

$ ) 1FOUBNFUIZMCFO[FOF   &  o& & 

$ ) 6OEFDFOF   &  & o& 

$ ) 0 6OEFDBOPOF  

$ ) 0 /POZM
BDFUBUF  

$ ) 0 1FOUZM
IFYBOPBUF   &  o& & 

$ ) #S #SPNPVOEFDBOF  

$ ) 6OEFDBOF   &  o& o& 

$ ) 0 6OEFDBOPM  

$ ) / 6OEFDZMBNJOF   &  o& & 

$ ' / 5SJT QFSGMVPSPCVUZM BNJOF  

$ )0 %JCFO[PGVSBO  

$ ) #JQIFOZM   &  & o& 

$ ) /0 USBOT "[PYZCFO[FOF  

$ ) 0 %JQIFOZM
FUIFS  

$ ) 0 "DFUPOBQIUIPOF   &  o&  & 

$ ) 04 %JQIFOZM
TVMGPYJEF  

$ ) 04 %JQIFOZM
TVMGPOF  

$ ) 4 %JQIFOZM
TVMGJEF   1FSNJUUJWJUZ
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GPSN /BNF 5, ȤS BCD 3BOHF,

$ ) / %JQIFOZMBNJOF  

$ ) /0 //BQIUIZMFOZMBDFUBNJEF   &  o&  o& 

$ )  %JNFUIZMOBQIUIBMFOF  

$ ) 0 &UIPYZOBQIUIBMFOF  

$ ) 0 1SPQZM
DJOOBNBUF  

$ ) 0 %JFUIZM
QIUIBMBUF  

$ ) 0 $ZDMPIFYZMQIFOPM  

$ ) 0 $ZDMPIFYZMQIFOPM  

$ ) 0 1FOUZM
CFO[PBUF  

$ ) 0 1FOUZM
TBMJDZMBUF  

$ ) 0 *TPQFOUZM
TBMJDZMBUF   &  o& o& 

$ ) /0 /#VUZM /QIFOZMBDFUBNJEF  

$ ) )FYZMCFO[FOF  

$ )   5SJFUIZMCFO[FOF  

$ ) )FYBNFUIZMCFO[FOF   &  o& & 

$ ) 0 M#PSOZM
BDFUBUF   &  & o& 

$ ) 0 %JDZDMPIFYZM
FUIFS   &  o& & 

$ ) 0 $ZDMPEPEFDBOPOF   &  o&  & 

$ ) 0 %JCVUZM
UBSUSBUF  

$ ) %PEFDFOF   &  & o& 

$ ) 0 %FDZM
BDFUBUF  

$ ) 0 &UIZM
EFDBOPBUF   &  o& & 

$ ) 0 .FUIZM
VOEFDBOPBUF  

$ ) #S #SPNPEPEFDBOF   &  o& & 

$ ) $M $IMPSPEPEFDBOF   &  o& & 

$ ) * *PEPEPEFDBOF   &  & o& 

$ ) %PEFDBOF   &  o& o& 

$ ) 0 %PEFDBOPM   &  o& & 

$ ) 0 #VUZMPDUBOPM  

$ ) #0  5SJCVUZM
CPSBUF  

$ ) / %PEFDZMBNJOF   &  & o& 

$ ) / 5SJCVUZMBNJOF   &  & o& 

$ ) 01 5SJCVUZM
QIPTQIBUF   &  o& & 

$ ) 04J 5FUSBQSPQPYZTJMBOF  

$ ) 4O 5FUSBQSPQZMTUBOOBOF  

$ ) 04J  )FYBFUIZMEJTJMPYBOF   &  o& & 

$ ) 0 #FO[PQIFOPOF   &  o&  & 

$ ) 0 1IFOZM
TBMJDZMBUF   &  o&  & 

$ ) %JQIFOZMNFUIBOF   &  o& 

$ ) 0 #FO[ZM
QIFOZM
FUIFS  

$ ) 0 )FYZM
CFO[PBUF  

$ ) )FQUZMCFO[FOF  

$ ) 0 Ƞ*POPOF  

$ ) 0 ȡ*POPOF  

$ ) 0 %JFUIZM
OPOBOFEJPBUF  

$ ) 5SJEFDFOF   &  & o& 

$ ) 0 5SJEFDBOPOF  

$ ) 0 &UIZM
VOEFDBOPBUF  

$ ) 0 .FUIZM
EPEFDBOPBUF  

$ ) #S #SPNPUSJEFDBOF  

$ ) 5SJEFDBOF   &  o& o& 

$ ) #VUZMOPOBOF  

$ ) 0 5SJEFDBOPM  

$ ) "OUISBDFOF   &  o& & 

$ ) 1IFOBOUISFOF  

$ ) 0 #FO[JM   o&  &  o& 

$ ) 0 #FO[ZM
CFO[PBUF   &  o& o& 

$ ) 0 #FO[ZM
TBMJDZMBUF  

$ )  %JQIFOZMFUIBOF   &  o& & 

$ ) 0 %JCFO[ZM
FUIFS   &  o& & 

$ ) / %JCFO[ZMBNJOF  

$ ) 04J %JNFUIZMEJQIFOPYZTJMBOF   &  o& & 

$ ) 0 1FOUZM
DJOOBNBUF   
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.PM
GPSN /BNF 5, ȤS BCD 3BOHF,

$ ) 0DUZMCFO[FOF  

$ ) 0 %JJTPCVUZM
BEJQBUF  

$ ) 0 %JFUIZM
TFCBDBUF   &  o&  & 

$ ) 0 %PEFDZM
BDFUBUF  

$ ) 0 &UIZM
MBVSBUF  

$ ) 0 .FUIZM
USJEFDBOPBUF  

$ ) #S #SPNPUFUSBEFDBOF   &  o& & 

$ ) 5FUSBEFDBOF   &  o& o& 

$ ) 0 5FUSBEFDBOPM   &  o& o& 

$ ) / 5FUSBEFDZMBNJOF  

$ ) 0 1IFOZM
 BDFUZMPYZ CFO[PBUF  

$ ) 0 5SJCVUZSJO   &  o& & 

$ ) 0 .FUIZM
UFUSBEFDBOPBUF  

$ ) #S #SPNPQFOUBEFDBOF  

$ ) 1FOUBEFDBOF   &  o& o& 

$ ) 0 1FOUBEFDBOPM  

$ ) / 1FOUBEFDZMBNJOF  

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