Hazardous Chemicals Vapor Phase Library
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
The Asymmetric Synthesis of Styrene-Oxide and Its Reactions with Dialkylmagnesium Reagents and Boron Hydrides
University of New Hampshire University of New Hampshire Scholars' Repository Doctoral Dissertations Student Scholarship Summer 1971 THE ASYMMETRIC SYNTHESIS OF STYRENE-OXIDE AND ITS REACTIONS WITH DIALKYLMAGNESIUM REAGENTS AND BORON HYDRIDES RONALD LEROY ATKINS Follow this and additional works at: https://scholars.unh.edu/dissertation Recommended Citation ATKINS, RONALD LEROY, "THE ASYMMETRIC SYNTHESIS OF STYRENE-OXIDE AND ITS REACTIONS WITH DIALKYLMAGNESIUM REAGENTS AND BORON HYDRIDES" (1971). Doctoral Dissertations. 964. https://scholars.unh.edu/dissertation/964 This Dissertation is brought to you for free and open access by the Student Scholarship at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. 72-3736 ATKINS, Ronald Leroy, 1939- THE ASYMMETRIC SYNTHESIS OF STYRENE OXIDE AND ITS REACTIONS WITH DIALKYLMAGNESIUM REAGENTS AND BORON HYDRIDES. University of New Hampshire, Ph.D., 1971 Chemistry, organic University Microfilms, A XEROX Company, Ann Arbor, Michigan © 1971 Ronald LeRoy Atkina ALL RIGHTS RESERVED THE ASYMMETRIC SYNTHESIS OF STYRENE OXIDE AND ITS REACTIONS WITH DIALKYLMAGNESIUM REAGENTS AND BORON HYDRIDES by RONALD L. ATKINS B. S., The University of Wyoming, 1966 M. S., The University of Wyoming, 1968 A THESIS Submitted to the University of New Hampshire In Partial Fulfillment of The Requirements for the Degree of DOCTOR OF PHILOSOPHY Graduate School Department of Chemistry August, 1971 This thesis has been examined and approved. f b w < M & > YUffvyido— The^js Director, James D. Morrison Asspaiate Professor of Chemistry & L DJitdsh-iU. _____ Colin D. -
EWG VERIFIED™ Products Cannot Contain Any of the Ingredients Outlined in This Document
EWG’S UNACCEPTABLE LIST: Baby Diapers EWG VERIFIED™ products cannot contain any of the ingredients outlined in this document. Appendix A. Substances prohibited inEWG VERIFIED diapers based on GHS hazard classifications. A = aquatic toxicity, C = carcinogenicity, D = reproductive toxicity (development), F = reproductive toxicity (fertility), L = reproductive toxicity (lactation [breast-feeding children]), M = mutagenic, Sr = sensitization (respiratory), Ss =sensitization (skin) Chemical name(s) EC Number(s) CAS Number(s) Hazards ((4-phenylbutyl)hydroxyphosphoryl)acetic acid 412-170-7 83623-61-4 Ss (-)(3S,4R)-4-(4-fluorophenyl)-3-(3,4-methylenedioxy-phenoxymethyl)-N-benzylpiperidine hydrochloride 432-360-3 105813-13-6 SsA (+)-(1S,2S,3S,5R)-2,6,6-trimethylbicyclo[3.1.1]heptane-3-spiro-1'-(cyclohex-2'-en-4'-one) 430-460-1 133636-82-5 SsA (+/-)-(R*,R*)-6-fluoro-3,4-dihydro-2-oxiranyl-2H-1-benzopyran; 6-fluoro-2-(2-oxiranyl)chromane 419-620-1 - Ss (±) trans-3,3-dimethyl-5-(2,2,3-trimethyl-cyclopent-3-en-1-yl)-pent-4-en-2-ol 411-580-3 107898-54-4 A (±)-[(R*,R*) and (R*,S*)]-6-fluoro-3,4-dihydro-2-oxiranyl-2H-1-benzopyran 419-600-2 99199-90-3 Ss (±)-4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(1-methyl-1H-imidazol-5-yl)methyl]-1-methyl-2(1H)-quinolin 430-730-9 - A (±)-4-[2-[[3-(4-hydroxyphenyl)-1-methylpropyl]amino]-1-hydroxyethyl]phenol hydrochloride 415-170-5 90274-24-1 Ss (±)-α-[(2-acetyl-5-methylphenyl)-amino]-2,6-dichlorobenzene-aceto-nitrile 419-290-9 Ss (1,3,4,5,6,7-hexahydro-1,3-di-oxo-2H-isoindol-2-yl)methyl (1R-trans)-2,2-dimethyl-3-(2-methylprop-1- -
A Study for Health Hazard Evaluation of Methylene Chloride Evaporated from the Tear Gas Mixture
Saf Health Work 2010;1:98-101 | DOI:10.5491/SHAW.2010.1.1.98 pISSN : 2093-7911 eISSN : 2093-7997 Case Report A Study for Health Hazard Evaluation of Methylene Chloride Evaporated from the Tear Gas Mixture Seung-Hyun PARK, Eun-Kyo CHUNG, Gwang-Yong YI, Kwang-Jae CHUNG, Jung-Ah SHIN and In-Seop LEE Department of Occupational Environment Research, Occupational Safety and Health Research Institute, KOSHA, Incheon, Korea This study explored the health hazard of those exposed to methylene chloride by assessing its atmospheric concentration when a tear gas mixture was aerially dispersed. The concentration of methylene chloride ranged from 311.1–980.3 ppm (geometric mean, 555.8 ppm), 30 seconds after the dispersion started. However, the concentration fell rapidly to below 10 ppm after dispersion was completed. The concentration during the dispersion did not surpass the National Institute for Occupational Safety and Health ‘immediately dangerous to life or health’ value of 2,300 ppm, but did exceed the American Conference of Governmental Industrial Hygienists excursion limit of 250 ppm. Since methylene chloride is highly volatile (vapor pressure, 349 mmHg at 20oC), the post- dispersion atmospheric concentration can rise instantaneously. Moreover, the o-chlorobenzylidenemalononitrile formulation of tear gas (CS gas) is an acute upper respiratory tract irritant. Therefore, tear gas mixtures should be handled with delicate care. Key Words: Methylene chloride, CS tear gas, Tear gas mixture, Health hazard evaluation Introduction Despite this long history of use, CS gas has recently come under greater scrutiny since it can be applied as a mixture that Tear gases such as o-chlorobenzylidenemalononitrile (CS), contains a suspected human carcinogen, methylene chloride. -
Department of Homeland Security (Dhs) Appendix a Chemicals of Interest (Coi)
DEPARTMENT OF HOMELAND SECURITY (DHS) APPENDIX A CHEMICALS OF INTEREST (COI) Acetaldehyde Bromine trifluoride Acetone Cyanohydrin, stabilized Bromothrifluorethylene Acetyl bromide 1,3-Butadiene Acetyl chloride Butane Acetyl iodide Butene Acetylene 1-Butene Acrolein 2-Butene Acrylonitrile 2-Butene-cis Acrylyl chloride 2-Butene-trans Allyl alcohol Butyltrichlorosilane Allylamine Calcium hydrosulfite Allyltrichlorosilane, stabilized Calcium phosphide Aluminum (powder) Carbon disulfide Aluminum Bromide, anhydrous Carbon oxysulfide Aluminum Chloride, anhydrous Carbonyl fluoride Aluminum phosphide Carbonyl sulfide Ammonia (anhydrous) Chlorine Ammonia (conc 20% or greater) Chlorine dioxide Ammonium nitrate, note #1 Chlorine monoxide Ammonium nitrate, note #2 Chlorine pentafluoride Ammonium perchlorate Chlorine trifluoride Ammonium picrate Chloroacetyl chloride Amyltrichlorosilane 2-Chloroethylchloro-methylsulfide Antimony pentafluoride Chloroform Arsenic trichloride Chloromethyl ether Arsine Chloromethyl methyl ether Barium azide 1-Chloropropylene 1,4-Bis(2-chloroethylthio)-n-butane 2-Chloropropylene Bis(2-chloroethylthio) methane Chlorosarin Bis(2-chloroethylthiomethyl)ether Chlorosoman 1,5-Bis(2-chloroethylthio)-n-pentane Chlorosulfonic acid 1,3-Bis(2-chloroethylthio)-n-propane Chromium oxychloride Boron tribromide Crotonaldehyde Boron trichloride Crotonaldehyde, (E)- Boron trifluoride Cyanogen Boron trifluoride compound with methyl Cyanogen chloride ether (1:1) Cyclohexylamine Bromine Cyclohexyltrichlorosilane Bromine chloride Cyclopropane -
List of Lists
United States Office of Solid Waste EPA 550-B-10-001 Environmental Protection and Emergency Response May 2010 Agency www.epa.gov/emergencies LIST OF LISTS Consolidated List of Chemicals Subject to the Emergency Planning and Community Right- To-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act • EPCRA Section 302 Extremely Hazardous Substances • CERCLA Hazardous Substances • EPCRA Section 313 Toxic Chemicals • CAA 112(r) Regulated Chemicals For Accidental Release Prevention Office of Emergency Management This page intentionally left blank. TABLE OF CONTENTS Page Introduction................................................................................................................................................ i List of Lists – Conslidated List of Chemicals (by CAS #) Subject to the Emergency Planning and Community Right-to-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act ................................................. 1 Appendix A: Alphabetical Listing of Consolidated List ..................................................................... A-1 Appendix B: Radionuclides Listed Under CERCLA .......................................................................... B-1 Appendix C: RCRA Waste Streams and Unlisted Hazardous Wastes................................................ C-1 This page intentionally left blank. LIST OF LISTS Consolidated List of Chemicals -
Review Article Synthesis and Reactions of Five-Membered Heterocycles Using Phase Transfer Catalyst (PTC) Techniques
Hindawi Publishing Corporation Journal of Chemistry Volume 2014, Article ID 163074, 47 pages http://dx.doi.org/10.1155/2014/163074 Review Article Synthesis and Reactions of Five-Membered Heterocycles Using Phase Transfer Catalyst (PTC) Techniques Ahmed M. El-Sayed,1 Omyma A. Abd Allah,1 Ahmed M. M. El-Saghier,1 and Shaaban K. Mohamed2,3 1 Department of Chemistry, Faculty of Science, Sohag University, Sohag 82524, Egypt 2 Chemistry and Environmental Division, Manchester Metropolitan University, Manchester M1 5GD, UK 3 Chemistry Department, Faculty of Science, Minia University, El-Minia 61519, Egypt Correspondence should be addressed to Omyma A. Abd Allah; [email protected] Received 1 May 2013; Revised 15 September 2013; Accepted 28 October 2013; Published 25 February 2014 Academic Editor: Jorge F. Fernandez-Sanchez Copyright © 2014 Ahmed M. El-Sayed et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Phase transfer catalysts (PTCs) have been widely used for the synthesis of organic compounds particularly in both liquid-liquid and solid-liquid heterogeneous reaction mixtures. They are known to accelerate reaction rates by facilitating formation of interphase transfer of species and making reactions between reagents in two immiscible phases possible. Application of PTC instead of traditional technologies for industrial processes of organic synthesis provides substantial benefits for the environment. On the basis of numerous reports it is evident that phase-transfer catalysis is the most efficient way for generation and reactions of many active intermediates. -
Less Lethal Technologies for Law Enforcement Technote, June 2019
TechNote June 2019 LESS LETHAL TECHNOLOGIES FOR LAW ENFORCEMENT The U.S. Department of Less lethal technologies are devices designed to be less likely to cause death Homeland Security (DHS) when deployed than conventional weapons like firearms. Less lethal Science and Technology technologies are used by law enforcement in two primary situations: crowd Directorate (S&T) established control and one-on-one suspect apprehension. For each of these situations, the System Assessment and Validation for Emergency technology subcategories exist based on the modalities of the technology, Responders (SAVER) Program such as chemical, kinetic and conducted energy. to assist emergency responders making Overview procurement decisions. Less lethal technologies DHS S&T’s Nation Urban grant law enforcement Security Technology Officer Presence Laboratory (NUSTL) manages officers an additional tool to the SAVER Program and de-escalate situations. In A conducts objective Multi-Method Evaluation of Verbalization assessments and validations Police Use of Force on commercial equipment and Outcomes—a study systems. These results, along commissioned by the Empty Hand with other relevant equipment National Institute of Justice Control information, are provided to the emergency response (NIJ)—authors found less community in an operationally lethal weapons reduce the Less Lethal useful form. SAVER provides rates of injuries for law information on equipment that enforcement personnel and falls within the categories offenders [1]. Compared to Lethal listed in the DHS Authorized using physical force (e.g., Equipment List. hands, fists, feet), using The SAVER Program is pepper spray or conducted supported by a network of energy weapons (e.g., stun Figure 1. NIJ Use-of-Force Continuum technical agents who perform guns) reduced the likelihood assessment and validation activities. -
Otto-Catalog-2019-20.Pdf
Lab Chemicals & More..... Otto Catalog 2019-20 1 CODE PRODUCT NAME CAS NO. PACKING RATE ` PACKING RATE ` A 1214 ABSCISIC ACID practical grade 10% 14375-45-2 100mg 2007 1gm 13059 A 1215 ABSCISIC ACID for biochemistry 99% 14375-45-2 25mg 1395 100mg 3609 500 mg 17469 A 1217 (7-AMINO CEPHALOSPORANIC ACID) 7-ACA 98% 957-68-6 1gm 2403 5gm 9396 A 1225 ACACIA 9000-01-5 500gm 504 5kg 4392 A 1226 ACACIA spray dried powder 9000-01-5 500gm 684 5kg 6309 A 1227 ACACIA GR 9000-01-5 500gm 828 5kg 7407 A 0855 ACARBOSE, >95% 56180-94-0 1 gm 18099 A 1229 ACENAPHTHENE pract 83-32-9 100gm 306 500gm 1395 5 kg 11907 A 1230 ACENAPHTHENE for synthesis 97% 83-32-9 100gm 450 500gm 1692 A 1231 ACENAPHTHENE GR for HLPC 83-32-9 100gm 1359 500gm 5533 A 1234 ACES BUFFER 99% 7365-82-4 5gm 864 25gm 2385 [N-(2-Acetamido)-2-aminoethane sulfonic acid] 100 gm 8739 A 1233 ACETALDEHYDE 20-30% solution for synthesis 75-07-0 500ml 477 5lt 4095 A 1235 ACETAMIDE for synthesis 99% 60-35-5 500 gm 801 A 1240 ACETAMIDINE CHLORIDE for synthesis 124-42-5 100gm 3159 250gm 7830 A 1242 N-(2-ACETAMIDO) IMINODIACETIC ACID (ADA BUFFER) 26239-55-4 25gm 855 100gm 2592 250 gm 5994 A 1245 ACETANILIDE for synthesis 98.5% 103-84-4 500gm 918 5kg 8289 A 1248 ACETATE BUFFER SOLUTION pH 4.6 - - - - - 500ml 180 5lt 1449 A 1250 ACETIC ACID glacial 99% 64-19-7 500ml 207 5lt 1602 A 1251 ACETIC ACID glacial GR 99%+ 64-19-7 500ml 252 5lt 1908 A 1252 ACETIC ACID GLACIAL GR 99.7% 64-19-7 500ml 315 5lt 1998 A 1253 ACETIC ACID GLACIAL EL 99.9% 64-19-7 500ml 378 5lt 2502 A 1254 ACETIC ACID 99.8% for HPLC 64-19-7 -
The Chemistry of 3-Acetyl-3, 4-Phenacylidenecoumarin Gerald Eugene Risinger Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1961 The chemistry of 3-acetyl-3, 4-phenacylidenecoumarin Gerald Eugene Risinger Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Organic Chemistry Commons Recommended Citation Risinger, Gerald Eugene, "The chemistry of 3-acetyl-3, 4-phenacylidenecoumarin " (1961). Retrospective Theses and Dissertations. 1983. https://lib.dr.iastate.edu/rtd/1983 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. This dissertation has been 62-1367 microfilmed exactly as received RISINGER, Gerald Eugene, 1932- THE CHEMISTRY OF 3-ACETYL-3,4-PHENACYLI- DENECOUMARIN. Iowa State University of Science and Technology Ph.D., 1961 Chemistry, organic University Microfilms, Inc., Ann Arbor, Michigan THE CHEMISTRY OF 3-ACETYL-3 , ^-PI-ENACYLIDENECOUKARIN by Gerald Eugene Risinger A Dissertation Submitted to the Graduate Faculty in Partial Fulfillment of The Requirements for the Degree of DOCTOR OF PHILOSOPHY Major Subject : Organic Chemistry Approved: Signature was redacted for privacy. In Charge of Major Work Signature was redacted for privacy. head of Major Department Signature was redacted for privacy. Iowa State University Of Science and Technology Ames, Iowa 1961 il TABLE OF CONTENTS PAGE I INTRODUCTION 1 II HISTORICAL 2 III DISCUSSION 49 IV SPECTRA 87 V EXPERIMENTAL 100 VI SUMMARY 116 VII LITERATURE CITED . -
Background Material: 1997-11-10 2-Cloroacetophenone As Federal
2-CHLOROACETOPHENONE 2-Chloroacetophenone is a federal hazardous air pollutant and was identified as a toxic air contaminant in April 1993 under AB 2728. CAS Registry Number: 532-27-4 COCH2Cl Molecular Formula: C8H7ClO 2-Chloroacetophenone is a colorless to gray crystalline solid. It has an odor which, in very low concentrations, resembles apple blossoms. It is practically insoluble in water but freely soluble in alcohol, benzene, acetone, petroleum ether, and carbon disulfide. When it is heated to decomposition, it emits toxic fumes of chloride (Sax, 1989). Physical Properties of 2-Chloroacetophenone Synonyms: chloromethyl phenyl ketone; mace; 2-chloro-1-phenylethanone; phenacyl chloride Molecular Weight: 154.60 Boiling Point: 244 - 245 oC Melting Point: 58 - 59 oC Vapor Pressure: 0.012 mm Hg at 20 oC Density/Specific Gravity: 1.324 at 15 oC Conversion Factor: 1 ppm = 6.32 mg/m3 (HSDB, 1991; Merck, 1989; U.S. EPA, 1994a) SOURCES AND EMISSIONS A. Sources 2-Chloroacetophenone is emitted from sources where it is used as a pharmaceutical intermediate or when used as a riot control gas (Sax, 1987). B. Emissions No emissions of 2-chloroacetophenone from stationary sources in California have been reported, based on data reported under the Air Toxics “Hot Spots” Program (AB 2588 ) (ARB, 1997b). Toxic Air Contaminant Identification List Summaries - ARB/SSD/SES September 1997 241 2-Chloroacetophenone C. Natural Occurrence No information about the natural occurrence of 2-chloroacetophenone was found in the readily- available literature. AMBIENT CONCENTRATIONS No Air Resources Board ambient concentration data exist for 2-chloroacetophenone. INDOOR SOURCES AND CONCENTRATIONS No information about the indoor sources and concentrations of 2-chloroacetophenone was found in the readily-available literature. -
Chemical Compatibility Storage Group
CHEMICAL SEGREGATION Chemicals are to be segregated into 11 different categories depending on the compatibility of that chemical with other chemicals The Storage Groups are as follows: Group A – Compatible Organic Acids Group B – Compatible Pyrophoric & Water Reactive Materials Group C – Compatible Inorganic Bases Group D – Compatible Organic Acids Group E – Compatible Oxidizers including Peroxides Group F– Compatible Inorganic Acids not including Oxidizers or Combustible Group G – Not Intrinsically Reactive or Flammable or Combustible Group J* – Poison Compressed Gases Group K* – Compatible Explosive or other highly Unstable Material Group L – Non-Reactive Flammable and Combustible, including solvents Group X* – Incompatible with ALL other storage groups The following is a list of chemicals and their compatibility storage codes. This is not a complete list of chemicals, but is provided to give examples of each storage group: Storage Group A 94‐75‐7 2,4‐D (2,4‐Dichlorophenoxyacetic acid) 94‐82‐6 2,4‐DB 609-99-4 3,5-Dinitrosalicylic acid 64‐19‐7 Acetic acid (Flammable liquid @ 102°F avoid alcohols, Amines, ox agents see SDS) 631-61-8 Acetic acid, Ammonium salt (Ammonium acetate) 108-24-7 Acetic anhydride (Flammable liquid @102°F avoid alcohols see SDS) 79‐10‐7 Acrylic acid Peroxide Former 65‐85‐0 Benzoic acid 98‐07‐7 Benzotrichloride 98‐88‐4 Benzoyl chloride 107-92-6 Butyric Acid 115‐28‐6 Chlorendic acid 79‐11‐8 Chloroacetic acid 627‐11‐2 Chloroethyl chloroformate 77‐92‐9 Citric acid 5949-29-1 Citric acid monohydrate 57-00-1 Creatine 20624-25-3 -
Dielectric Constant Chart
Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG. F CONSTANT ABS RESIN, LUMP 2.4-4.1 ABS RESIN, PELLET 1.5-2.5 ACENAPHTHENE 70 3 ACETAL 70 3.6 ACETAL BROMIDE 16.5 ACETAL DOXIME 68 3.4 ACETALDEHYDE 41 21.8 ACETAMIDE 68 4 ACETAMIDE 180 59 ACETAMIDE 41 ACETANILIDE 71 2.9 ACETIC ACID 68 6.2 ACETIC ACID (36 DEGREES F) 36 4.1 ACETIC ANHYDRIDE 66 21 ACETONE 77 20.7 ACETONE 127 17.7 ACETONE 32 1.0159 ACETONITRILE 70 37.5 ACETOPHENONE 75 17.3 ACETOXIME 24 3 ACETYL ACETONE 68 23.1 ACETYL BROMIDE 68 16.5 ACETYL CHLORIDE 68 15.8 ACETYLE ACETONE 68 25 ACETYLENE 32 1.0217 ACETYLMETHYL HEXYL KETONE 66 27.9 ACRYLIC RESIN 2.7 - 4.5 ACTEAL 21 3.6 ACTETAMIDE 4 AIR 1 AIR (DRY) 68 1.000536 ALCOHOL, INDUSTRIAL 16-31 ALKYD RESIN 3.5-5 ALLYL ALCOHOL 58 22 ALLYL BROMIDE 66 7 ALLYL CHLORIDE 68 8.2 ALLYL IODIDE 66 6.1 ALLYL ISOTHIOCYANATE 64 17.2 ALLYL RESIN (CAST) 3.6 - 4.5 ALUMINA 9.3-11.5 ALUMINA 4.5 ALUMINA CHINA 3.1-3.9 ALUMINUM BROMIDE 212 3.4 ALUMINUM FLUORIDE 2.2 ALUMINUM HYDROXIDE 2.2 ALUMINUM OLEATE 68 2.4 1 Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG. F CONSTANT ALUMINUM PHOSPHATE 6 ALUMINUM POWDER 1.6-1.8 AMBER 2.8-2.9 AMINOALKYD RESIN 3.9-4.2 AMMONIA -74 25 AMMONIA -30 22 AMMONIA 40 18.9 AMMONIA 69 16.5 AMMONIA (GAS?) 32 1.0072 AMMONIUM BROMIDE 7.2 AMMONIUM CHLORIDE 7 AMYL ACETATE 68 5 AMYL ALCOHOL -180 35.5 AMYL ALCOHOL 68 15.8 AMYL ALCOHOL 140 11.2 AMYL BENZOATE 68 5.1 AMYL BROMIDE 50 6.3 AMYL CHLORIDE 52 6.6 AMYL ETHER 60 3.1 AMYL FORMATE 66 5.7 AMYL IODIDE 62 6.9 AMYL NITRATE 62 9.1 AMYL THIOCYANATE 68 17.4 AMYLAMINE 72 4.6 AMYLENE 70 2 AMYLENE BROMIDE 58 5.6 AMYLENETETRARARBOXYLATE 66 4.4 AMYLMERCAPTAN 68 4.7 ANILINE 32 7.8 ANILINE 68 7.3 ANILINE 212 5.5 ANILINE FORMALDEHYDE RESIN 3.5 - 3.6 ANILINE RESIN 3.4-3.8 ANISALDEHYDE 68 15.8 ANISALDOXINE 145 9.2 ANISOLE 68 4.3 ANITMONY TRICHLORIDE 5.3 ANTIMONY PENTACHLORIDE 68 3.2 ANTIMONY TRIBROMIDE 212 20.9 ANTIMONY TRICHLORIDE 166 33 ANTIMONY TRICHLORIDE 5.3 ANTIMONY TRICODIDE 347 13.9 APATITE 7.4 2 Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG.