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Peroxy Compounds Human Health and Ecological Draft Risk Assessment DP 455445, 455446
Peroxy Compounds Human Health and Ecological Draft Risk Assessment DP 455445, 455446 UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, D.C. 20460 OFFICE OF CHEMICAL SAFETY AND POLLUTION PREVENTION MEMORANDUM Date: March 11, 2020 SUBJECT: Registration Review Draft Risk Assessment for the Peroxy Compounds PC Code: 000595, 063201, 063604, 063607, DP Barcode: 455445, 455446 063209, 128860 Decision No: 558073, 558074 Docket No: EPA-HQ-OPP-2009-0546 Regulatory Action: Registration Review Case No: 6059, 4072, 5081 Risk Assessment Type: DRA CAS No: 7722-84-1, 79-21-0, 33734-57-5, 15630-89-4, 10058-23-8, 70693-62-8 TO: Kendall Ziner, Chemical Review Manager Rick Fehir, Ph.D., Team Lead Rose Kyprianou, Branch Chief Regulatory Management Branch (RMB) II Antimicrobials Division (7510P) Office of Pesticide Programs FROM: Andrew Byro, Ph.D., Chemist Kathryn Korthauer, Biologist Timothy Dole, Industrial Hygienist Deborah Burgin, Ph.D., DABT, Toxicologist Risk Assessment and Science Support Branch Antimicrobials Division (7510P) Office of Pesticide Programs THROUGH: Judy Facey, Ph.D., Human Health Risk Assessment Process Leader MP for JF Diana Hsieh, Ecological Risk Assessment Process Leader MP for DH Timothy Leighton, Senior Science Advisor MP for TL Laura Parsons, Associate Branch Chief Melissa Panger, Ph.D., Branch Chief Risk Assessment and Science Support Branch Antimicrobials Division (7510P) This document provides the draft human health and ecological risk assessment conducted in support of the antimicrobial use sites of the following peroxy compounds: hydrogen peroxide, peracetic acid, peroxyoctanoic acid, and sodium percarbonate. Page 1 of 74 Peroxy Compounds Human Health and Ecological Draft Risk Assessment DP 455445, 455446 Although the peroxymonosulfate compounds were included in the peroxy compounds Final Work Plan (FWP), they will not be included in this risk assessment. -
The Radiochemistry of Beryllium
National Academy of Sciences National Research Council I NUCLEAR SCIENCE SERIES The Radiochemistry ·of Beryllium COMMITTEE ON NUCLEAR SCIENCE L. F. CURTISS, Chairman ROBLEY D. EVANS, Vice Chairman National Bureau of Standards MassaChusetts Institute of Technol0gy J. A. DeJUREN, Secretary ./Westinghouse Electric Corporation H.J. CURTIS G. G. MANOV Brookhaven National' LaboratOry Tracerlab, Inc. SAMUEL EPSTEIN W. WAYNE MEINKE CalUornia Institute of Technology University of Michigan HERBERT GOLDSTEIN A.H. SNELL Nuclear Development Corporation of , oak Ridge National Laboratory America E. A. UEHLING H.J. GOMBERG University of Washington University of Michigan D. M. VAN PATTER E.D.KLEMA Bartol Research Foundation Northwestern University ROBERT L. PLATZMAN Argonne National Laboratory LIAISON MEMBERS PAUL C .. AEBERSOLD W.D.URRY Atomic Energy Commission U. S. Air Force J. HOW ARD McMILLEN WILLIAM E. WRIGHT National Science Foundation Office of Naval Research SUBCOMMITTEE ON RADIOCHEMISTRY W. WAYNE MEINKE, Chairman HAROLD KIRBY University of Michigan Mound Laboratory GREGORY R. CHOPPIN GEORGE LEDDICOTTE Florida State University. Oak Ridge National Laboratory GEORGE A. COW AN JULIAN NIELSEN Los Alamos Scientific Laboratory Hanford Laboratories ARTHUR W. FAIRHALL ELLIS P. STEINBERG University of Washington Argonne National Laboratory JEROME HUDIS PETER C. STEVENSON Brookhaven National Laboratory University of California (Livermore) EARL HYDE LEO YAFFE University of CalUornia (Berkeley) McGill University CONSULTANTS NATHAN BALLOU WILLIAM MARLOW Naval Radiological Defense Laboratory N atlonal Bureau of Standards JAMESDeVOE University of Michigan CHF.MISTRY-RADIATION AND RADK>CHEMIST The Radiochemistry of Beryllium By A. W. FAIRHALL. Department of Chemistry University of Washington Seattle, Washington May 1960 ' Subcommittee on Radiochemistry National Academy of Sciences - National Research Council Printed in USA. -
Exposure Data
BERYLLIUM AND BERYLLIUM eOMPOUNDS Beryllium and beryllium compounds were considered by previous Working Groups, In 1971,1979 and 1987 (lARe, 1972, 1980, 1987a). New data have since become available, and these are included in the present monograph and have been taken into consideration In the evaluation. The agents considered herein Include (a) metallic beryllium, (b) beryllium- aluminium and -copper alloys and (c) some beryllum compounds. 1. Exposure Data 1.1 Chemical and physical data and analysis 1.1.1 Synonyms, trade names and molecular formulae Synonyms, trade names and molecular formulae for beryllium, beryllum-aluminium and -copper alloys and certain beryllium compounds are presented in Thble 1. The list is not exhaustive, nor does it comprise necessarily the most commercially important beryllum- containing substances; rather, it indicates the range of beryllum compounds available. 1. 1.2 Chemical and physical properties of the pure substances Selected chemical and physical properties of beryllium, beryllum-aluminium and -copper alloys and the beryllium compounds covered in this monograph are presented in Thble 2. The French chemist Vauquelin discovered beryllium in 1798 as the oxide, while analysing emerald to prove an analogous composition (Newland, 1984). The metallc element was first isolated in independent experiments by Wöhler (1828) and Bussy (1828), who called it 'glucinium' owing to the sweet taste of its salts; that name is stil used in the French chemical literature. Wöhler's name 'beryllum' was offcially recognized by IUPAe in 1957 (WHO, 1990). The atomic weight and corn mon valence of beryllum were originally the subject of much controversy but were correctly predicted by Mendeleev to be 9 and + 2, respectively (Everest, 1973). -
WO 2015/025175 Al 26 February 2015 (26.02.2015) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2015/025175 Al 26 February 2015 (26.02.2015) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C09K 5/06 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/GB2014/052580 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 22 August 2014 (22.08.2014) KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, (25) Filing Language: English OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, (26) Publication Language: English SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, (30) Priority Data: ZW. 13 15098.2 23 August 2013 (23.08.2013) GB (84) Designated States (unless otherwise indicated, for every (71) Applicant: SUNAMP LIMITED [GB/GB]; Unit 1, Satel kind of regional protection available): ARIPO (BW, GH, lite Place, Macmerry, Edinburgh EH33 1RY (GB). GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (72) Inventors: BISSELL, Andrew John; C/o SunAmp, Unit TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, 1, Satellite Place, Macmerry, Edinburgh EH33 1RY (GB). -
Crown Chemical Resistance Chart
Crown Polymers, Corp. 11111 Kiley Drive Huntley, IL. 60142 USA www.crownpolymers.com 847-659-0300 phone 847-659-0310 facisimile 888-732-1270 toll free Chemical Resistance Chart Crown Polymers Floor and Secondary Containment Systems Products: CrownShield covers the following five (4) formulas: CrownShield 50, Product No. 320 CrownCote, Product No. 401 CrownShield 40-2, Product No. 323 CrownShield 28, Product No. 322 CrownPro AcidShield, Product No. 350 CrownCote AcidShield, Product No. 430 CrownPro SolventShield, Product No. 351 CrownCote SolventShield, Product No. 440 This chart shows chemical resistance of Crown Polymers foundational floor and secondary containment product line that would be exposed to chemical spill or immersion conditions. The chart was designed to provide general product information. For specific applications, contact your local Crown Polymers Floor and Secondary Containment Representative or call direct to the factory. ; Resistant to chemical immersion up to 7 days followed by wash down with water 6 Spillage environments that will be cleaned up within 72 hours after initial exposure. 9 Not Recommended Chemical CrownShield SolventShield AcidShield Chemical CrownShield SolventShield AcidShield 1, 4-Dichloro-2-butene 9 6 6 Aluminum Bromate ; ; ; 1, 4-Dioxane 9 6 6 Aluminum Bromide ; ; ; 1-1-1 Trichloroethane 9 ; ; Aluminum Chloride ; ; ; 2, 4-Pentanedione 6 ; 6 Aluminum Fluoride (25%) ; ; ; 3, 4-Dichloro-1-butene 6 6 6 Aluminum Hydroxide ; ; ; 4-Picoline (0-50%) 9 6 6 Aluminum Iodine ; ; ; Acetic Acid (0-15%) 9 6 6 -
Sodium-Bismuthate
He a lt h 2 0 Fire 0 2 0 Re a c t iv it y 0 Pe rs o n a l Pro t e c t io n J Material Safety Data Sheet Sodium bismuthate MSDS Section 1: Chemical Product and Company Identification Product Name: Sodium bismuthate Contact Information: Catalog Codes: SLS3700, SLS1480 Sciencelab.com, Inc. 14025 Smith Rd. CAS#: 12232-99-4 Houston, Texas 77396 RTECS: VZ1750000 US Sales: 1-800-901-7247 International Sales: 1-281-441-4400 TSCA: TSCA 8(b) inventory: Sodium bismuthate Order Online: ScienceLab.com CI#: Not available. CHEMTREC (24HR Emergency Telephone), call: Synonym: 1-800-424-9300 Chemical Name: Not available. International CHEMTREC, call: 1-703-527-3887 Chemical Formula: NaBiO3 For non-emergency assistance, call: 1-281-441-4400 Section 2: Composition and Information on Ingredients Composition: Name CAS # % by Weight Sodium bismuthate 12232-99-4 100 Toxicological Data on Ingredients: Sodium bismuthate LD50: Not available. LC50: Not available. Section 3: Hazards Identification Potential Acute Health Effects: Hazardous in case of eye contact (irritant), of inhalation. Potential Chronic Health Effects: Hazardous in case of eye contact (irritant), of inhalation. CARCINOGENIC EFFECTS: Not available. MUTAGENIC EFFECTS: Not available. TERATOGENIC EFFECTS: Not available. DEVELOPMENTAL TOXICITY: Not available. The substance is toxic to lungs, mucous membranes. Repeated or prolonged exposure to the substance can produce target organs damage. Section 4: First Aid Measures Eye Contact: Check for and remove any contact lenses. Do not use an eye ointment. Seek medical attention. Skin Contact: No known effect on skin contact, rinse with water for a few minutes. -
Using Sodium Bismuthate As an Oxidant and Sym-Diphenylcarbazide As a Complexing Agent
Chem. Anal. (Warsaw), 49, 405 (2004) Flow-Injection System for the Spectrophotometric Determination of Mn (II) Using Sodium Bismuthate as an Oxidant and Sym-diphenylcarbazide as a Complexing Agent by M. Noroozifar* and M. Khorasani-Motlagh Department of Chemistry, Sistan and Baluchestan University, Zahedan P.O. Box 98165-181, Iran Key words: flow-injection, manganese determination, sodium bismuthate reactor, sym-diphenylcarbazide Flow-injection spectrophotometric determination of manganese in aqueous solution, using a solid sodium bismuthate reactor has been presented. Manganese (Mn2+) can be determi- ned spectrophotometrically at 308 nm after its on-line oxidation to MnO at the room 4 temperature. In acidic media permanganate immediately reacts with sym-diphenylcarbazide to form a complex, the absorbance of which is measured. The linear range of the method was 5 × 10-71 × 10-4 mol L-1 with a detection limit (3σ) of 6 × 10-8 mol L-1. The proposed procedure was applied to the determination of Mn2+ in effluents and food, with a relative standard deviation better than 1.85%. The sampling frequency as high as 110 h-1 could be achieved. Zaproponowano spektrofotometryczn¹ metodê oznaczania manganu w wodnych roztworach w uk³adzie przep³ywowo-wstrzykowym z zastosowaniem reaktora z bizmutanem sodu. Mangan (Mn2+) oznaczano spektrofotometrycznie po uprzednim utlenieniu on-line, w temperaturze pokojowej, do MnO. W rodowisku kwanym nadmanganian natychmiast 4 reaguje z sym-difenylokarbazydem tworz¹c kompleks, którego absorbancja by³a mierzona. Zakres liniowoci metody wynosi³ 5 × 10-71 × 10-4 mol L-1, a granica wykrywalnoci (3σ) 6 × 10-8 mol L-1. Proponowan¹ metodê zastosowano do oznaczania Mn2+ w ciekach i ¿ywnoci uzyskuj¹c wzglêdne odchylenie standardowe lepsze ni¿ 1,85%. -
Optical Absorption in Gel Grown Barium Oxalate Single Crystals
OPTOELECTRONICS AND ADVANCED MATERIALS – RAPID COMMUNICATIONS Vol. 4, No. 11, November 2010, p. 1713 - 1716 Optical absorption in gel grown barium oxalate single crystals P. V. DALAL*, K. B. SARAF, M. P. DESHPANDEa P. G. Department of Physics, Pratap College, Amalner -425 401 aDepartment of Physics, Sardar Patel University, Vallabh Vidyanagar -388 120, Gujarat, India Single crystals of barium oxalate have been grown by simple gel technique using agar gel as the growth medium at ambient temperature. The slow and controlled reaction between barium chloride and oxalic acid in agar gel has formed barium oxalate. Optical absorption spectra of this grown crystal is recorded in the wavelength region from 200 to 800 nm. The absorption spectra reveal transitions involving absorption and emission of phonons and also show that the crystal is transparent in the region 500 to 800 nm. The detail study supports the existence of forbidden indirect transition in the material. Different segment of α1/3 vs hν graph were used to distinguish individual contribution of phonons and scattering of charge carriers in the lattice is found due to acoustic phonons. (Received October 27, 2010; accepted November 10, 2010) Keywords: Barium oxalate single crystal, Agar-agar gel, X-ray diffraction, Photo-absorption, Photon energy 1. Introduction The reaction, which leads to the growth of crystals can be, expressed as Barium oxalate is a pyro-nature material that shows great promise in pyrotechnic and high temperature BaCl2 + H2C2O4 = BaC2O4 +2HCl electronic applications. The high dielectric constant and melting point of barium oxalate is an advantage to The optimum conditions for the growth of barium improve hardness of barium titanate in capacitor industries oxalate single crystals were: concentration of gel 1.5%, [1]. -
Chemistry Inventory; Fall
CHEMISTRY FALL 2005 MSDS Mfg.'s Name Chemical Name Quantity Stored Storage Conditions (on file = 9) Aluminum 9 1.5 kg Aluminum chloride, anhydrous, 98.5% 9 0.2 kg Aluminum chloride · 6H2O 9 0.5 kg Aluminum hydroxide 9 0.5 kg Aluminum nitrate 9 0.5 kg Aluminum sulfate 9 0.5 kg Ammonia, concentrated 9 4.0 L Ammonium acetate 9 0.2 kg Ammonium chloride 9 Ammonium dihydrogen phosphate (monobasic) 9 0.4 kg J.T. Baker Ammonium hydrogen phosphate (dibasic) No 0.5 kg Ammonium nitrate 9 2.5 kg Ammonium oxalate 9 0.7 kg Ammonium peroxydisulfate 9 0.5 kg Ammonium sulfate 9 0.2 kg Antimony 9 0.4 kg Barium chloride, anhydrous 9 2.5 kg Barium chloride · 2H2O 9 2.5 kg Barium nitrate 9 0.8 kg Bismuth 9 2.0 kg Boric Acid 9 0.4 kg Brass 9 Bromine 9 2.5 kg Cadmium 9 0.1 kg Cadmium nitrate 9 0.3 kg Calcium acetate · xH2O 9 0.5 kg Calcium carbide 9 1.0 kg Calcium carbonate 9 2.2 kg Calcium chloride 9 1.0 kg Calcium hydroxide 9 0.3 kg Calcium nitrate · 4H2O 9 1.0 kg Calcium oxide 9 0.3 kg Calcium sulfate · 2H2O 9 1.0 kg Carbon 9 0.1 kg Ceric ammonium nitrate 9 0.5 kg Cesium chloride 9 0.01 kg Chromium 9 0.01 kg Chromium chloride 9 0.5 kg Chromium nitrate 9 0.5 kg Cobalt 9 0.025 kg Cobalt chloride 9 0.7 kg Cobalt nitrate 9 0.6 kg Copper (assorted) 9 4.0 kg Copper acetate 9 0.05 kg Copper chloride 9 0.1 kg Copper nitrate 9 3.5 kg Copper oxide 9 0.4 kg Cupric sulfate, anhydrous 9 0.5 kg Cupric sulfate · 5H2O 9 2.75 kg EDTA 9 0.6 kg Iodine 9 2.0 kg Iron (assorted) 9 5.0 kg MSDS Mfg.'s Name Chemical Name Quantity Stored Storage Conditions (on file = 9) Ferric ammonium -
WO 2016/074683 Al 19 May 2016 (19.05.2016) W P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2016/074683 Al 19 May 2016 (19.05.2016) W P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C12N 15/10 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/DK20 15/050343 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 11 November 2015 ( 11. 1 1.2015) KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, (25) Filing Language: English PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (26) Publication Language: English SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: PA 2014 00655 11 November 2014 ( 11. 1 1.2014) DK (84) Designated States (unless otherwise indicated, for every 62/077,933 11 November 2014 ( 11. 11.2014) US kind of regional protection available): ARIPO (BW, GH, 62/202,3 18 7 August 2015 (07.08.2015) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (71) Applicant: LUNDORF PEDERSEN MATERIALS APS TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, [DK/DK]; Nordvej 16 B, Himmelev, DK-4000 Roskilde DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (DK). -
Severe Corrosion of Steel and Copper by Strontium Bromide In
Corrosion Science 138 (2018) 275–283 Contents lists available at ScienceDirect Corrosion Science journal homepage: www.elsevier.com/locate/corsci Severe corrosion of steel and copper by strontium bromide in T thermochemical heat storage reactors ⁎ Pierre D’Ansa, , Emilie Courbonb, Marc Frèreb, Gilbert Descyc, Tiriana Segatoa, Marc Degreza a Université Libre de Bruxelles (ULB), 4MAT Department, 50, Avenue F.D. Roosevelt, CP194/03, 1050, Brussels, Belgium b UMONS, Institut de Recherche en Energie – Laboratoire de Thermodynamique, 31 Boulevard Dolez, 7000, Mons, Belgium c BE-SOL R&D, 2 rue de la Griotte, 5580, Rochefort, Belgium ARTICLE INFO ABSTRACT Keywords: Thermochemical heat storage exploits thermal solar energy to produce sustainable residential heating, obtained A. Copper by exothermal reaction between bromides and water vapour. A protocol to test the corrosion of surrounding A. Carbon steel −1 materials is discussed in the case of SrBr2 contacting copper or steel. Corrosion depth > 1 mm y is found for B. Weight loss steel in conditions where the salt remains mostly solid, due to a reaction between SrBr2 and atmospheric CO2 B. XRD that produces HBr. Temperature and the dissolution of the salt (deliquescence) also play a key role. B. Cyclic voltammetry Potentiodynamic tests, the limitations of which are discussed, corroborate the salt degradation in the case of C. Reactor conditions steel. 1. Introduction Since the late eighties, several papers have been dedicated to the corrosion problem in the case of PCMs, with tests focused on the While electrical power storage is becoming widespread through melting process or the liquid phase [21–34], and quite often in organic applications like electrical vehicles, thermal energy storage still needs compounds [30,35,36]. -
Flexaust Chemical Resistance Guide
Chemical Resistance Guide Rating Code: A=Excellent B=Good C=Fair D=Not Recommended ND=No Data HOSE MATERIAL Santoprene Polyethelene Buna-N Neoprene Hypalon Teflon Acrylic Silicone Polyurethane PVC Aluminum SS 304 SS 316 Polypropylene Chemical (TPR) (LLPE) Acetaldehyde D C D A ND A D ND C B B A A B Acetamide A C B A ND B D ND ND ND ND ND A A Acetate Solvents D D D A D ND ND ND C ND ND ND A D Acetic Acid, glacial C D C A D B D A ND B ND ND A B Acetic Acid, 5% B A A A A A D A A A ND A A A Acetic Acid, 10% B A B A B A D A A A A A A A Acetic Acid, 20% B A B A B A D A A A ND A A A Acetic Acid, 30% B C B A ND A D A A A ND A A A Acetic Acid, 50% B C C A ND B D A A A ND A A A Acetic Acid, 80% B C ND A ND ND ND A A A ND A A B Acetic Anhydride D C A A ND C D A C ND C A A A Acetone D C C A D B D A C B A A A B Acetone Cyanhydrin D B C A ND A D ND ND ND ND ND ND ND Acetonitrile C C B A ND ND ND ND ND ND A A A ND Acetophenone D D D A ND D D ND ND ND ND A A A Acetyl Acetone D D D A ND D C ND ND ND ND ND ND ND Acetyl Chloride D D D A ND C D ND C ND ND A A ND Acetylene B C C A ND B A A A ND A A A D Acetylene Dichloride D D D A ND ND ND ND ND ND ND ND ND ND Acrolein B ND B A ND ND ND ND ND ND ND ND ND ND Acrylonitrile D D C A ND D ND A C B ND ND ND B Adipic Acid B D ND A ND ND ND ND A ND ND ND ND ND Alcohol, Allyl A A A A ND ND ND ND ND ND ND ND ND ND Alcohol, Amyl B A B A ND D D B C A ND ND A B Alcohol, Benzyl D C B A D ND D ND ND ND ND ND A A Alcohol, Butyl C A A A ND B D ND A A ND ND ND B Alcohol, Diacetone D C B A ND B C ND ND ND ND ND ND D Alcohol,