M86804
N-Methylurea
97%
Synonym(s):
1-Methylurea, N-Methylurea
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About This Item
Linear Formula:
CH3NHCONH2
CAS Number:
Molecular Weight:
74.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-935-0
Beilstein/REAXYS Number:
878189
MDL number:
Assay:
97%
Form:
crystals
Product Name
N-Methylurea, 97%
InChI key
XGEGHDBEHXKFPX-UHFFFAOYSA-N
InChI
1S/C2H6N2O/c1-4-2(3)5/h1H3,(H3,3,4,5)
SMILES string
CNC(N)=O
assay
97%
form
crystals
Quality Level
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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
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
V V Matveev
Tsitologiia, 31(12), 1459-1465 (1989-12-01)
Following short-term local applications of high doses of N-methyl-N-nitrozourea and 7,2-dimethylbenz(a)antracen, the intercellular adhesion in the distal colon epithelium of ice retains increased at least for a month. The magnitude of this shift and its duration ops both with moving
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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