N-Nitrosomethylvinylamine

Base Information

Chemical Name:N-Nitrosomethylvinylamine
CAS No.:4549-40-0
Molecular Formula:C3H6 N2 O
Molecular Weight:86.0934
Hs Code.:2928000090
NSC Number:137906
UN Number:2810,3082
UNII:4F13H2637M
Nikkaji Number:J2.217I
Wikidata:Q27155900
NCI Thesaurus Code:C44419
ChEMBL ID:CHEMBL163957
Mol file:4549-40-0.mol

Synonyms:N-nitroso-N-methylvinylamine;N-nitrosomethylvinylamine

Suppliers and Price of N-Nitrosomethylvinylamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
N-Methyl-N-nitroso-ethenamine
250 mg
$ 715.00

American Custom Chemicals Corporation
METHYLVINYLNITROSAMINE 95.00%
5MG
$ 497.46

Total 8 raw suppliers

Chemical Property of N-Nitrosomethylvinylamine

Chemical Property:

Vapor Pressure:3.63mmHg at 25°C
Refractive Index:1.5110 (estimate)
Boiling Point:151.6°Cat760mmHg
Flash Point:45.5°C
PSA：32.67000
Density:0.94g/cm³
LogP:0.74310
XLogP3:0.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:86.048012819
Heavy Atom Count:6
Complexity:61.8
Transport DOT Label:Poison

Purity/Quality:

99% ^*data from raw suppliers

N-Methyl-N-nitroso-ethenamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: Total 1 MSDS from other Authors

Useful:

Chemical Classes:Nitrogen Compounds -> Nitrosamines
Canonical SMILES:CN(C=C)N=O
Uses N-nitrosomethylvinylamine is used as a research chemical; no other uses were identified (IARC 1978, HSDB 2009). N-Methyl-N-nitroso-ethenamine is used as research reagent for base induced fragmentation to give aldehydes or ketones and smaller alkylnitrosamine

Technology Process of N-Nitrosomethylvinylamine

There total 2 articles about N-Nitrosomethylvinylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 26921-68-6
N-(2-hydroxyethyl)-N-methyl-N-nitrosamine

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 62-75-9
N-Nitrosodimethylamine

: 4549-40-0
methylvinylnitrosamine

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; tert-butyl alcohol; for 72h; Rate constant; Product distribution; Kinetics; Heating; var. solvents and temp.;
DOI:10.1021/jo00146a003