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
Beilstein:
878189
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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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Related Categories
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
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T Gichner et al.
Mutagenesis, 3(4), 329-331 (1988-07-01)
Naturally occurring para-aminobenzoic acid (PABA) inhibited the formation of N-methyl-N-nitrosourea (MNU) from a nitrosation mixture of N-methylurea and nitrite at pH 3. The suppressive effect of PABA on the formation of MNU is higher than that of ascorbic acid. The
P Ramirez-Victoria et al.
Mutation research, 496(1-2), 39-45 (2001-09-12)
It is known that the poblano green pepper, a significant component in the Mexican diet, contains certain natural compounds such as chlorophyll, beta-carotene, and vitamins, which have antimutagenic and/or anticarcinogenic properties. Using the somatic mutation and recombination test in wing
M Nagabhushan et al.
Mutation research, 202(1), 163-169 (1988-11-01)
The effects of turmeric extract and its pure yellow pigments curcumin I, II and III were tested on the nitrosation of methylurea by sodium nitrite at pH 3.6 and 30 degrees C. The nitrosomethylurea formed was monitored by checking the
Nuzhat Gull et al.
Journal of biochemistry, 141(2), 261-268 (2006-12-19)
We report that the presence of very low concentrations (<0.1 M) of urea, a widely used chemical denaturant, induces structure formation in the water-soluble globular protein human serum albumin (HSA) at pH 7. We have presented results suggesting an almost
L S Povarov et al.
Bioorganicheskaia khimiia, 16(4), 559-568 (1990-04-01)
Derivatives of antitumour anthracycline antibiotics containing N-methylurea moiety in the carbohydrate ring were obtained by the interaction of methyl isocyanate with daunorubicin, doxorubicin, carminomycin and daunorubicin derivatives, substituted at C-13 or C-14 positions. N-Nitrosation of these compounds yielded modified anthracycline
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