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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:
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 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
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
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

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