Toxicological Profile for Chloroethane
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Rhode Island Hazardous Substance List
Rhode Island Hazardous Substance List Source: T - ACGIH F - NFPA49 C - IARC Alphabetical Order C.A.S. ACGIH NFPA IARC CHEMICAL NAME 13010-47-4 C 1,-(2-Chloroethyl)-3-cyclohexyl-1-Nitrosourea 76-11-9 T 1,1,1,2-tetrachloro-2,2-difluoroethane 76-12-0 T 1,1,2,2-tetrachloro-1,2-difluoroethane 79-34-5 T 1,1,2,2-tetrachloroethane - skin 76-13-1 T 1,1,2-trichloro-1,2,2-trifluoroethane 79-00-5 T F C 1,1,2-trichloroethane - skin 594-72-9 T 1,1-Dichloro-1-nitroethane 74-34-3 T 1,1-dichloroethane 57-14-7 T 1,1-dimethylhydrazine (udmh) 96-18-4 T 1,2,3-trichloropropane 120-82-1 T 1,2,4-Trichlorobenzene 106-88-7 F 1,2-Butylene oxide 107-15-3 T F 1,2-Diaminoethane 96-12-8 C 1,2-Dibromo-3-chloropropane 106-93-4 T F C 1,2-Dibromoethane - skin 107-06-2 T F 1,2-Dichlorethane 540-59-0 T F 1,2-Dichloroethene 540-59-0 T F 1,2-Dichloroetylene 1615-80-1 C 1,2-Diethylhydrazine C 1,2-Dimethyl hydrazine - skin 106-99-0 T F 1,3-Butadiene 118-52-5 T 1,3-Dichloro-5,5-dimethylhydantoin 542-75-6 T F 1,3-Dichloropropene (cis and trans) 542-75-6 T F 1,3-Dichloropropylene 110-56-5 F 1,4-Dichlorobutane 123-91-1 T F C 1,4-Dioxane 1120-71-4 1-3-Propane sultone 110-53-2 F 1-Bromopentane 106-89-8 T F C 1-Chloro,2,3-epoxy-propane 600-25-9 T 1-Chloro-1-nitropropane 97-00-7 F 1-chloro-2,4-dinitrobenzene 543-59-9 F 1-Chloropentane 112-30-1 F 1-Decanol 111-27-3 F 1-Hexanol 141-79-7 T F 1-Isobutenyl methyl ketone 108-03-2 T F 1-Nitropropane 71-41-0 F 1-Pentanol 110-58-7 F 1-Pentylamine 111-40-0 T F 2,2'-Diaminodiethylamine 111-44-4 F 2,2'Dichlorodiethyl ether 75-99-0 T 2,2-dichloropropionic acid 556-52-5 T 2,3-Epoxy-1-propanol 93-76-5 T 2,4,5-T 95-95-4 F 2,4,5-trichlorophenol 88-06-2 F C 2,4,6-trichlorophenol 118-96-7 T F 2,4,6-Trinitro Toluene 479-95-8 T 2,4,6-Trinitrophenyl-methylnitramine 94-75-7 T 2,4-d (2,4-dichlorophenoxyacetic acid) 97-02-9 F 2,4-dinitroaniline 584-84-9 T F 2,4-Tolylene diisocyanate 108-83-8 T 2,6-Dimethyl-4-heptanone 108-83-8 T 2,6-Dimethyl-4-heptanone 128-37-0 T 2,6-Ditert. -
Chemistry 234 Chapter 16 Problem Set Electrophilic Aromatic
Chemistry 234 Chapter 16 Problem Set Electrophilic Aromatic Substitution 1) Predict the product and draw the mechanism for electrophile generation for each of the following reactions. Cl (a) 2 FeCl3 HNO3 (b) H2SO4 SO (c) 3 H2SO4 2) Explain why reaction of benzene with Br2/FeBr3 results in the product bromobenzne instead of 5,6-dibromo-1,3-cyclohexadiene. 3) Predict the product and draw the active electrophile for each reaction shown below. Cl (a) AlCl3 Cl (b) AlCl3 Cl O (c) AlCl3 Page 1 of 13 Chem. 234 – Chapter 16 Problem Set 4) Explain why each of the following substrates do not undergo Freidel-Crafts reactions. NH2 NO2 N(CH3)3 NH 5) Arrange the following benzene substituents in order of reactivity in electrophilic aromatic substitution reactions. O Cl Ph Ph N Ph Ph H O N H S Ph N Ph Ph Ph O O 6) Predict the maJor products when the following benzene derivatives are treated to nitration conditions (HNO3/H2SO4). a. O Br b. NH2 Br c. NO2 Cl 7) Write the full electron pushing mechanism for the nitration of toluene. Page 2 of 13 Chem. 234 – Chapter 16 Problem Set 8) Predict the product(s) when each of the following benzene derivatives is treated to chloroethane and AlCl3. a. Br b. NH2 Cl c. OH Br d. OH Cl Cl e. NO2 Cl Cl f. Br Br g. SO3H Page 3 of 13 Chem. 234 – Chapter 16 Problem Set 9) Predict the product(s) when the following benzene derivatives are subjected to electrophilic chlorination conditions (Cl2, FeCl3). -
United States Patent Office Patented Feb
3,794,643 United States Patent Office Patented Feb. 26, 1974 1. 2 3,794,643 aZolinedione derivatives are produced by reacting the QUINAZOLINEDONE DERIVATIVES compounds having the following general formula: Takahiro Yabuuchi, Takarazuka, and Hajime Fujimura, Akira Nakagawa, and Ryuichi Kimura, Kyoto, Japan, assignors to Hisamitsu Pharmaceutical Co., Inc., Tosu, Saga Prefecture, Japan No Drawing. Filed Apr. 20, 1971, Ser. No. 135,693 int, C. C07, 51/48 U.S. C. 260-260 8 Claims ABSTRACT OF THE DISCLOSURE O The present invention relates to novel quinazolinedione R3 R2 derivatives possessing excellent anti-inflammatory action and analgesic action, and process for the production (wherein R2 and/or Rs have the same meaning as men thereof by reacting the compounds having the following 5 tioned above) with the general formula, RX or RSO, general formula, (wherein R represents the same substances as mentioned O above), R represents lower alkyl radical, and X repre C Sents halogen atom). Consequently, the reaction of the present invention can be understood as being alkylation. 20 The abovementioned compounds used as starting reac tion materials in the present invention can be obtained in good yield by reacting N-phenylanthranilic acid or N substituted phenylanthranilic acid with urea. The quinazolinedione derivatives used as the afore Rs R 25 said starting reaction materials include 1-phenyl-2,4- (1H,3H)-quinazolinedione or 1-substituted phenyl-2,4- (1H,3H)-quinazolinedione, for example, (wherein R and/or R3 represent hydrogen atom, CFs, 1-(3'-triuuoromethylphenyl-2,4(1H,3H)- -
Exam 1 (February 23, 2004) ID# ______
Chemistry 211 Name ___________________________ Exam 1 (February 23, 2004) ID# ___________________________ 10 1. You desire to synthesize 3-ethyl-3-pentanol starting with an ester. (i) What would be the name of the ester, and what is the name for the Grignard reagent (e.g., methyl magnesium bromide)? (ii) For the carbons shown in the product, show plausible hydrocarbons that you could start with to produce the ester and the Grignard reagent (as in a retrosynthesis). 12 2. (i) Show the step-by-step process required to produce propyllithium, which requires a free radical reaction mechanism, . (ii) Show the complete reaction mechanism for reaction between propyllithium and the correct ketone to produce 3-propyl-3-pentanol. (iii) Propose a possible reaction mechanism by which dipropyl cuprate (Cu+ with two propyl groups attached) could react with ethyl bromide to produce a new hydrocarbon. (This is a thinking exercise! So, think! () 8 3. As mentioned in the text, diethyl ether, pentane, and 1-butanol have similar molar masses, but different physical properties. Boiling points are 35oC, 36oC, and 117oC, respectively. Their respective solubilities in water are 7.5g/100mL, insoluble, and 9g/100mL. (i) Draw structures for each of these compounds. (ii) Justify the observed boiling points and their solubilities. 16 4. Draw structures of the following compounds 2,3-heptanediol isopropyllithium benzylmagnesium bromide benzoic acid benzaldehylde dimethyl sulfide t-butyl methanoate dibutyl ketone 12 5. Alcohols can be oxidized to produce other compounds, and can be produced by reduction. For the reactions shown below, show the structure for the expected product (if reaction does not occur, state: No Reaction) when treated with the indicated oxidizing or reducing agents. -
Chemistry for S5 Students Short Notes & Questions with Answers & And
Chemistry for S5 students Short notes & questions with answers & and other questions to help S5 Students to revise Important Concepts: Chemical Reactions of Alkyl Halides The reaction can be broadly classified in two categories: (a) Nucleophilic substitution (b) Elimination reactions Nucleophilic substitution reactions: In this reaction a nucleophile, which is rich in electrons, attacks partial positive charge on the carbon atom bonded to halogen to replace the leaving group. Nucleophilic reactions proceed by two different mechanism: (a) Substitution nucleophilic bimolecular (SN2) (b) Substitution nucleophilic unirnolecular (SN1) The reaction follows second order kinetics No intermediate is formed. It usually requires a strong nucleophile. The order of reactivity followed as: Primary halide > Secondary halide > Tertiary halide It is carried out in polar protic solvents (water, Alcohol, acetic acid etc.). These reactions occur in two steps as shown above The order of leaving ability is: F- < Cl- < Br- < I- The order of reactivity is as shown below: Difference between E1 and E2 reaction mechanism: Attributes E1 E2 Rate law Depend on the concentration of Depends on the concentration of both substrate substrate and base Barrier Formation of carbocation None 3o>2o>> 1o Base Does not require strong base Requires strong base Stereochemistry Does not require stereochemistry Leaving group must be anti to hydrogen removed Some solved questions are given below: Question 1:Which is the correct increasing order of boiling points of the following compounds? 1-bromoethane, 1-bromopropane, 1-bromobutane, Bromobenzene (a) Bromobenzene < 1-bromobutane < 1-bromopropane < 1-bromoethane (b) Bromobenzene < 1-bromothane < 1-bromopropane < 1-bromobutane (c) 1-bromopropane < 1-bromobutane < 1-bromoethane < Bromobenzene (d) 1-bromoethane < 1-bromopropane < 1-bromobutane < Bromobenzene Solution 1: Boiling point increases with increase in size of hydrocarbon part for the same haloalkanes. -
Safety Data Sheet
SAFETY DATA SHEET 1. Identification Product identifier Jump Start® Starting Fluid Other means of identification Product Code No. 05671 (Item# 1003843) Recommended use Starting fluid Recommended restrictions None known. Manufacturer/Importer/Supplier/Distributor information Manufactured or sold by: Company name CRC Industries, Inc. Address 885 Louis Dr. Warminster, PA 18974 US Telephone General Information 215-674-4300 Technical Assistance 800-521-3168 Customer Service 800-272-4620 24-Hour Emergency 800-424-9300 (US) (CHEMTREC) 703-527-3887 (International) Website www.crcindustries.com 2. Hazard(s) identification Physical hazards Flammable aerosols Category 1 Gases under pressure Compressed gas Health hazards Skin corrosion/irritation Category 2 Carcinogenicity Category 2 Specific target organ toxicity, single exposure Category 3 narcotic effects Aspiration hazard Category 1 Environmental hazards Hazardous to the aquatic environment, acute Category 2 hazard Hazardous to the aquatic environment, Category 3 long-term hazard OSHA defined hazards Not classified. Label elements Signal word Danger Hazard statement Extremely flammable aerosol. Contains gas under pressure; may explode if heated. May be fatal if swallowed and enters airways. Causes skin irritation. May cause drowsiness or dizziness. Suspected of causing cancer. Toxic to aquatic life. Harmful to aquatic life with long lasting effects. Material name: Jump Start® Starting Fluid SDS US No. 05671 (Item# 1003843) Version #: 01 Issue date: 08-29-2017 1 / 10 Precautionary statement Prevention Obtain special instructions before use. Do not handle until all safety precautions have been read and understood. Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Do not spray on an open flame or other ignition source. -
1,2-DICHLOROETHANE 1. Exposure Data
1,2-DICHLOROETHANE Data were last reviewed in IARC (1979) and the compound was classified in IARC Monographs Supplement 7 (1987a). 1. Exposure Data 1.1 Chemical and physical data 1.1.1 Nomenclature Chem. Abstr. Serv. Reg. No.: 107-06-2 Chem. Abstr. Name: 1,2-Dichloroethane IUPAC Systematic Name: 1,2-Dichloroethane Synonym: Ethylene dichloride 1.1.2 Structural and molecular formulae and relative molecular mass Cl CH2 CH2 Cl C2H4Cl2 Relative molecular mass: 98.96 1.1.3 Chemical and physical properties of the pure substance (a) Description: Colourless liquid with a pleasant odour (Budavari, 1996) (b) Boiling-point: 83.5°C (Lide, 1995) (c) Melting-point: –35.5°C (Lide, 1995) (d) Solubility: Slightly soluble in water; miscible with ethanol, chloroform and diethyl ether (Lide, 1995; Budavari, 1996) (e) Vapour pressure: 8 kPa at 20°C (Verschueren, 1996) (f) Flash-point: 18°C, open cup (Budavari, 1996) (g) Conversion factor: mg/m3 = 4.0 × ppm 1.2 Production and use World production capacities in 1988 for 1,2-dichloroethane have been reported as follows (thousand tonnes): North America, 9445; western Europe, 9830; Japan, 3068; and other, 8351 (Snedecor, 1993). Production in the United States has been reported as follows (thousand tonnes): 1983, 5200; 1990, 6300; 1991, 6200; 1992, 6900; 1993, 8100 (United States National Library of Medicine, 1997). The total annual production in Canada in 1990 was estimated to be 922 thousand tonnes; more than 1000 thousand tonnes were produced in the United Kingdom in 1991 (WHO, 1995). –501– 502 IARC MONOGRAPHS VOLUME 71 1,2-Dichloroethane is used primarily in the production of vinyl chloride; 99% of total demand in Canada, 90% in Japan and 88% of total production in the United States are used for this purpose. -
SAFETY DATA SHEET Ethyl Chloride
SAFETY DATA SHEET Ethyl Chloride Section 1. Identification GHS product identifier : Ethyl Chloride Chemical name : chloroethane Other means of : Ethane, chloro-; Ethyl chloride; Muriatic ether; Monochloroethane; Hydrochloric ether; identification ether hydrochloric; 1-CHLOROETHANE; Ethyl chloride (Chloroethane); ethane, chloro; Monochlorethane; R 160 Product type : Liquefied gas Product use : Synthetic/Analytical chemistry. Synonym : Ethane, chloro-; Ethyl chloride; Muriatic ether; Monochloroethane; Hydrochloric ether; ether hydrochloric; 1-CHLOROETHANE; Ethyl chloride (Chloroethane); ethane, chloro; Monochlorethane; R 160 SDS # : 001023 Supplier's details : Airgas USA, LLC and its affiliates 259 North Radnor-Chester Road Suite 100 Radnor, PA 19087-5283 1-610-687-5253 24-hour telephone : 1-866-734-3438 Section 2. Hazards identification OSHA/HCS status : This material is considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200). Classification of the : FLAMMABLE GASES - Category 1 substance or mixture GASES UNDER PRESSURE - Liquefied gas CARCINOGENICITY - Category 2 AQUATIC HAZARD (LONG-TERM) - Category 3 GHS label elements Hazard pictograms : Signal word : Danger Hazard statements : Extremely flammable gas. Contains gas under pressure; may explode if heated. Suspected of causing cancer. Harmful to aquatic life with long lasting effects. May cause frostbite. May displace oxygen and cause rapid suffocation. May form explosive mixtures with air. Precautionary statements General : Read and follow all Safety Data Sheets (SDS’S) before use. Read label before use. Keep out of reach of children. If medical advice is needed, have product container or label at hand. Close valve after each use and when empty. Use equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. -
Risk Evaluation for 1-Bromopropane (N-Propyl Bromide) CASRN: 106-94-5
United States EPA Document #740-R1-8013 Environmental Protection Agency August 2020 Office of Chemical Safety and Pollution Prevention Risk Evaluation for 1-Bromopropane (n-Propyl Bromide) CASRN: 106-94-5 August 2020 TABLE OF CONTENTS TABLE OF CONTENTS ............................................................................................................. 2 LIST OF TABLES ...................................................................................................................... 10 LIST OF APPENDIX TABLES ................................................................................................ 17 LIST OF FIGURES .................................................................................................................... 17 LIST OF APPENDIX FIGURES .............................................................................................. 19 LIST OF EQUATIONS .............................................................................................................. 19 LIST OF APPENDIX EQUATIONS ........................................................................................ 20 ACKNOWLEDGEMENTS ....................................................................................................... 21 ABBREVIATIONS ..................................................................................................................... 22 EXECUTIVE SUMMARY ........................................................................................................ 30 1 INTRODUCTION................................................................................................................... -
160 'Ideal' Gases: Anaesthetics in the Heart of the Twentieth Century Ian
International Workshop on the History of Chemistry 2015 Tokyo ‘Ideal’ Gases: Anaesthetics in the Heart of the Twentieth Century Ian D. Rae University of Melbourne, Australia 1. Introduction By 1920 only three gaseous anaesthetics were widely used – nitrous oxide, diethyl ether (ether) and chloroform. The toxicity of chloroform was acknowledged, nitrous oxide did not induce deep anaesthesia, and ether was extremely inflammable, so in the 1920s there were good reasons to search for new anaesthetics. While my concern is with gaseous anaesthetics, I recognise that there were parallel developments in two related fields, that of topical or local anaesthetics, typified by the natural product cocaine and a host of synthetic substances, and injectable anaesthetics starting with opiates, then barbiturates and leading to modern materials such as propofol (2,6-diisopropylphenol). 2. Theories of anaesthetic action Hans Meyer1 noted that the anaesthetic substances were soluble in both fatty and aqueous media, proposed a general theory of anaesthesia based on the partition or distribution coefficient as a critical determinant. Meyer enunciated the following three principles that underpinned his theory: all chemically inert substances that are soluble in fats and fatty materials will produce narcosis; the line of action is in the nerve cells; the comparative strengths of substances depend on their solubility in fatty material and in water, that is, on the distribution coefficient. Charles Overton arrived at the same idea independently. Some years after completing his PhD research on cell permeability studies, Overton first presented his theory of narcosis in a lecture to the Society for Natural History in Zurich in October 1898, in a paper published the following year2 and in his book3 which included a full exposition. -
Chapter 18 Ethers and Epoxides; Thiols and Sulfides Ethers
Chapter 18 Ethers and Epoxides; Thiols and Sulfides Ethers • Ethers (R–O–R’): – Organic derivatives of water, having two organic groups bonded to the same oxygen atom © 2016 Cengage Learning 2 NAMES AND PROPERTIES OF ETHERS 3 Nomenclature: Common Names • Simple ethers are named by identifying two organic substituents and adding the word ether – Name the groups in alphabetical order – Symmetrical: Use dialkyl or just alkyl © 2016 Cengage Learning 4 Nomenclature: IUPAC Names • The more complex alkyl group is the parent name • The group with the oxygen becomes an alkoxy group © 2016 Cengage Learning 5 Nomenclature: Cyclic Ethers (Heterocycles) • Heterocyclic: Oxygen is part of the ring. O • Epoxides (oxiranes) H2C CH2 O • Oxetanes • Furans (Oxolanes) O O • Pyrans (Oxanes) O O O • Dioxanes O © 2013 Pearson Education, Inc. 6 Epoxide Nomenclature • Name the starting alkene and add “oxide” © 2013 Pearson Education, Inc. 7 Epoxide Nomenclature • The oxygen can be treated as a substituent (epoxy) on the compound • Use numbers to specify position • Oxygen is 1, the carbons are 2 and 3 • Substituents are named in alphabetical order © 2013 Pearson Education, Inc. 8 Properties of Ethers • Possess nearly the same geometry as water – Oxygen atom is sp3-hybridized – Bond angles of R–O–R bonds are approximately tetrahedral • Polar C—O bonds © 2013 Pearson Education, Inc. 9 Properties of Ethers: Hydrogen Bond • Hydrogen bond is a attractive interaction between an electronegative atom and a hydrogen atom bonded to another electronegative atom • Ethers cannot hydrogen bond with other ether molecules, so they have a lower boiling point than alcohols • Ether molecules can hydrogen bond with water and alcohol molecules • They are hydrogen bond acceptors © 2013 Pearson Education, Inc. -
Synthesis and Reactivity of Cyclopentadienyl Based Organometallic Compounds and Their Electrochemical and Biological Properties
Synthesis and reactivity of cyclopentadienyl based organometallic compounds and their electrochemical and biological properties Sasmita Mishra Department of Chemistry National Institute of Technology Rourkela Synthesis and reactivity of cyclopentadienyl based organometallic compounds and their electrochemical and biological properties Dissertation submitted to the National Institute of Technology Rourkela In partial fulfillment of the requirements of the degree of Doctor of Philosophy in Chemistry by Sasmita Mishra (Roll Number: 511CY604) Under the supervision of Prof. Saurav Chatterjee February, 2017 Department of Chemistry National Institute of Technology Rourkela Department of Chemistry National Institute of Technology Rourkela Certificate of Examination Roll Number: 511CY604 Name: Sasmita Mishra Title of Dissertation: ''Synthesis and reactivity of cyclopentadienyl based organometallic compounds and their electrochemical and biological properties We the below signed, after checking the dissertation mentioned above and the official record book(s) of the student, hereby state our approval of the dissertation submitted in partial fulfillment of the requirements of the degree of Doctor of Philosophy in Chemistry at National Institute of Technology Rourkela. We are satisfied with the volume, quality, correctness, and originality of the work. --------------------------- Prof. Saurav Chatterjee Principal Supervisor --------------------------- --------------------------- Prof. A. Sahoo. Prof. G. Hota Member (DSC) Member (DSC) ---------------------------