N-METHYLURETHANE

N-METHYLURETHANE Basic information
Product Name:N-METHYLURETHANE
Synonyms:Carbamic acid, methyl-, ethyl ester;Ethylester kyseliny methylkarbaminove;ethylesterkyselinymethylkarbaminove;ethylmethylaminoformate;EthylN-methylcarbama+e;methyl-carbamicaciethylester;N-METHYLURETHANE;ETHYL METHYLCARBAMATE
CAS:105-40-8
MF:C4H9NO2
MW:103.12
EINECS:203-295-6
Product Categories:
Mol File:105-40-8.mol
N-METHYLURETHANE Structure
N-METHYLURETHANE Chemical Properties
Boiling point 170 °C
density 1.01
refractive index 1.418-1.42
Fp 61 °C
pka13.02±0.46(Predicted)
form clear liquid
color Colorless to Almost colorless
Water Solubility 410g/L(temperature not stated)
EPA Substance Registry SystemEthyl methylcarbamate (105-40-8)
Safety Information
Hazard Codes Xn
Risk Statements 40
Safety Statements 36/37
RTECS FC2625000
HS Code 29161900
Hazardous Substances Data105-40-8(Hazardous Substances Data)
MSDS Information
ProviderLanguage
ACROS English
N-METHYLURETHANE Usage And Synthesis
Chemical PropertiesClear colorless to peach liquid
UsesN-Methylurethan is a byproduct in the synthesis of 3,5-Dimethyl-4-(methylthio)phenol (D474810), which is used as an insecticide and used the synthesis of methiocarb.
General DescriptionClear colorless liquid.
Air & Water ReactionsWater soluble.
Reactivity ProfileN-METHYLURETHANE is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.
Health HazardACUTE/CHRONIC HAZARDS: N-METHYLURETHANE may be narcotic in high concentrations. When heated to decomposition it emits toxic fumes.
Fire HazardN-METHYLURETHANE is combustible.
Safety ProfileModerately toxic by SYNS: 2-BUTANONE, OXIME 0 ETHYL METHYL subcutaneous route. Experimental teratogenic effects. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.See also CARBAMATES.
N-METHYLURETHANE Preparation Products And Raw materials
Raw materialsMethylamine-->Ethyl chloroformate
Preparation Products1-Chloro-3-Phenylacetone
N-Carbobenzyloxy-L-aspartic acid N-Carbobenzyloxy-L-alanine Z-L-PROLINE Nalpha-Cbz-L-Arginine N-Benzyloxycarbonyl-6-aminohexanoic acid N-Carbobenzyloxyglycine 5-CHLOROMETHYL-2-OXAZOLIDINONE LABOTEST-BB LT00452529 N-(tert-Butoxycarbonyl)-L-phenylalanine N-Carbethoxyphthalimide N-Cbz-L-Serine Z-AIB-OH BOC-Glycine N-CYANOACETYLURETHANE Ethyl N-piperazinecarboxylate 1-CARBOXYETHYL N-PHENYLCARBAMATE N-Cbz-L-glutamic acid N6-Cbz-L-Lysine

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