M86804
N-Methylurea
97%
Sinônimo(s):
1-Methylurea, N-Methylurea
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About This Item
Fórmula linear:
CH3NHCONH2
Número CAS:
Peso molecular:
74.08
Beilstein:
878189
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
97%
Formulário
crystals
cadeia de caracteres SMILES
CNC(N)=O
InChI
1S/C2H6N2O/c1-4-2(3)5/h1H3,(H3,3,4,5)
chave InChI
XGEGHDBEHXKFPX-UHFFFAOYSA-N
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Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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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%
Andrew O F Jones et al.
Physical chemistry chemical physics : PCCP, 14(38), 13273-13283 (2012-08-25)
The phenomenon of solid-state proton migration within molecular complexes containing short hydrogen bonds is investigated in two dimethylurea-oxalic acid complexes. Extensive characterisation by both X-ray and neutron diffraction shows that proton migration along the hydrogen bond can be induced in
Tamara M Rodela et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 297(2), R313-R322 (2009-05-22)
Gulf toadfish (Opsanus beta) use a unique pulsatile urea excretion mechanism that allows urea to be voided in large pulses via the periodic insertion or activation of a branchial urea transporter. The precise cellular and subcellular location of the facilitated
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
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
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