ChemicalBook--->CAS DataBase List--->105-40-8

105-40-8

105-40-8 Structure

105-40-8 Structure
IdentificationBack Directory
[Name]

N-METHYLURETHANE
[CAS]

105-40-8
[Synonyms]

Methylurethae
METHYLURETHAN
N-Methylurethan
N-Methyl uretan
N-METHYLURETHANE
ethyl methylcarate
ETHYL METHYLCARBAMATE
EthylN-methylcarbama+e
ethylmethylaminoformate
ETHYL N-METHYLCARBAMATE
Ethyl methylcarbamate,99%
methyl-carbamicaciethylester
Ethyl MethylcarbaMate, 99% 5GR
Ethyl N-Methylcarbamate
n-methylcarbamicacidethylester
METHYLCARBAMIC ACID ETHYL ESTER
n-methylcarbamicacid,ethylester
ethylesterkyselinymethylkarbaminove
Carbamic acid, methyl-, ethyl ester
Carbamic acid,N-methyl-, ethyl ester
Ethylester kyseliny methylkarbaminove
N-Methylurethane N-Methylcarbamic Acid Ethyl Ester
[EINECS(EC#)]

203-295-6
[Molecular Formula]

C4H9NO2
[MDL Number]

MFCD00041924
[MOL File]

105-40-8.mol
[Molecular Weight]

103.12
Chemical PropertiesBack Directory
[Appearance]

Clear colorless to peach liquid
[Boiling point ]

170 °C
[density ]

1.01
[refractive index ]

1.418-1.42
[Fp ]

61 °C
[form ]

clear liquid
[pka]

13.02±0.46(Predicted)
[color ]

Colorless to Almost colorless
[Water Solubility ]

410g/L(temperature not stated)
[EPA Substance Registry System]

Ethyl methylcarbamate (105-40-8)
Hazard InformationBack Directory
[Chemical Properties]

Clear colorless to peach liquid
[General Description]

Clear colorless liquid.
[Air & Water Reactions]

Water soluble.
[Reactivity Profile]

N-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 Hazard]

ACUTE/CHRONIC HAZARDS: N-METHYLURETHANE may be narcotic in high concentrations. When heated to decomposition it emits toxic fumes.
[Fire Hazard]

N-METHYLURETHANE is combustible.
[Uses]

N-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.
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

40
[Safety Statements ]

36/37
[RTECS ]

FC2625000
[HS Code ]

29161900
[Safety Profile]

Moderately 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.
[Hazardous Substances Data]

105-40-8(Hazardous Substances Data)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methylamine-->Ethyl chloroformate
[Preparation Products]

1-Chloro-3-Phenylacetone
Spectrum DetailBack Directory
[Spectrum Detail]

N-METHYLURETHANE(105-40-8)MS
N-METHYLURETHANE(105-40-8)1HNMR
N-METHYLURETHANE(105-40-8)13CNMR
N-METHYLURETHANE(105-40-8)IR1
N-METHYLURETHANE(105-40-8)IR2
N-METHYLURETHANE(105-40-8)Raman
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