M86804
N-Methylurea
97%
Synonym(s):
1-Methylurea, N-Methylurea
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All Photos(3)
About This Item
Linear Formula:
CH3NHCONH2
CAS Number:
Molecular Weight:
74.08
Beilstein:
878189
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
crystals
SMILES string
CNC(N)=O
InChI
1S/C2H6N2O/c1-4-2(3)5/h1H3,(H3,3,4,5)
InChI key
XGEGHDBEHXKFPX-UHFFFAOYSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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L W Yousef et al.
Biochimica et biophysica acta, 984(3), 281-288 (1989-09-18)
Permeability coefficients (P) measured at various penetrant concentrations (C) by the perturbation method can be plotted to distinguish simple diffusion, simple pore kinetics and simple carrier kinetics as follows: for simple diffusion, 1/P = constant; for a simple pore, 1/P
P Vaughan et al.
Carcinogenesis, 12(2), 263-268 (1991-02-01)
Many microorganisms exhibit an adaptive response to mutagenic alkylation damage. In Escherichia coli the response is regulated by the inducible Ada protein. A sensitive immunoassay employing two anti-Ada monoclonal antibodies has been developed here to monitor low levels of induction
J Guzmán Rincón et al.
Mutation research, 412(1), 69-81 (1998-03-21)
The in vivo nitrosation capacity of third-instar larvae of Drosophila melanogaster was assessed using the wing somatic mutation and recombination test (SMART). Larvate derived from two different crosses, the standard cross (ST) and the high bioactivation cross (HB) both involving
A J Streeter et al.
Drug metabolism and disposition: the biological fate of chemicals, 18(4), 447-452 (1990-07-01)
The single-dose toxicokinetics of monomethylamine has been characterized in the rat by HPLC assay of serial blood samples. Biphasic first-order elimination was observed following an iv bolus dose of 19 mumol/kg with a terminal half-life of 19.1 +/- 1.3 min
P J Groenen et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(3), 215-225 (1988-03-01)
N-Nitroso compounds may well rank high among the genotoxic carcinogens present in our environment. Small amounts of such compounds may be formed in the human stomach after consumption of high-nitrate vegetables. Volatile nitrosamines can be conveniently determined but reliable methods
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