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Key Documents

M86804

Sigma-Aldrich

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/REAXYS Number:
878189
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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M Kitano et al.
Japanese journal of cancer research : Gann, 88(9), 797-806 (1997-11-25)
For carcinogenic risk assessment of combinations of N-nitroso precursors in man, the effects of feeding methylurea (MU) or morpholine (Mor) plus sodium nitrite (NaNO2) were investigated using a multi-organ carcinogenesis model. In experiment 1, to initiate multiple organs, groups of
M Yamamoto et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 25(9), 663-668 (1987-09-01)
The formation of N-nitrosomethylurea (NMU) from methylurea (MU) and sodium nitrite in the guinea-pig stomach and the disappearance of NMU from the stomach were studied using a previously described method for NMU determination (Yamamoto et al. Fd Chem. Toxic. 1986
N Poklar et al.
Journal of protein chemistry, 13(3), 323-331 (1994-04-01)
The solvent denaturation of alpha-chymotrypsinogen (alpha-ctg A) in aqueous solution of urea, methyl-, N,N'-dimethyl-, ethyl-, propyl- and butylurea was studied by fluorescence measurements. Data were analyzed on the assumption of a two-state approximation to obtain the apparent equilibrium constant, Ku
Nuzhat Gull et al.
Colloids and surfaces. B, Biointerfaces, 51(1), 10-15 (2006-06-30)
The present study highlights the fact that the effect of additives (urea, monomethylurea, thiourea) on the supramolecular assemblies and proteins is strikingly similar. To investigate the effect, a viscometeric study on sphere-to-rod transition (s-->r) was undertaken in a system (3.5%
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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