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Wichtige Dokumente
M86804
N-Methylharnstoff
97%
Synonym(e):
1-Methylurea, N-Methylurea
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Alle Fotos(3)
About This Item
Lineare Formel:
CH3NHCONH2
CAS-Nummer:
Molekulargewicht:
74.08
Beilstein:
878189
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Qualitätsniveau
Assay
97%
Form
crystals
SMILES String
CNC(N)=O
InChI
1S/C2H6N2O/c1-4-2(3)5/h1H3,(H3,3,4,5)
InChIKey
XGEGHDBEHXKFPX-UHFFFAOYSA-N
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Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Nuzhat Gull et al.
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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
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
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