261394
1,1-Dimethylurea
99%
Sinónimos:
N,N-Dimethylurea
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About This Item
Fórmula lineal:
(CH3)2NCONH2
Número de CAS:
Peso molecular:
88.11
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
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Nivel de calidad
Ensayo
99%
Formulario
solid
mp
178-183 °C (lit.)
solubilidad
water: soluble 5%, clear, colorless
grupo funcional
amine
cadena SMILES
CN(C)C(N)=O
InChI
1S/C3H8N2O/c1-5(2)3(4)6/h1-2H3,(H2,4,6)
Clave InChI
YBBLOADPFWKNGS-UHFFFAOYSA-N
Información sobre el gen
human ... EPHX2(2053)
mouse ... Ephx2(13850)
Categorías relacionadas
Descripción general
Nonlinear optical properties of 1,1-dimethylurea (N,N′ dimethylurea), have been evaluated through second-harmonic generation.
Aplicación
1,1-Dimethylurea (N,N-dimethylurea) has been used in the Dowex-50W ion exchange resin-promoted synthesis of N,N′-disubstituted-4-aryl-3,4-dihydropyrimidinones.
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
dust mask type N95 (US), Eyeshields, Gloves
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Mutation research, 279(4), 275-280 (1992-06-16)
Methyl isocyanate (MIC) in aqueous solution forms methylamine (MA) and N,N'-dimethylurea (DMU). MA in buffered system further converts into its salt form, methylamine hydrochloride (MAH). Therefore, MAH and DMU were evaluated for their mutagenic activity in the in vitro Ames
W J Caspary et al.
Mutation research, 174(4), 285-293 (1986-08-01)
Methylisocyanate (MIC) induced mutagenic responses in the absence of exogenous activation in the mouse lymphoma cell forward mutation assay at concentrations as low as 8-24 microM. MIC produced predominantly small mutant colonies, suggesting the possibility of clastogenic activity. The intermediate
S Sandler et al.
Acta pharmacologica et toxicologica, 53(5), 392-400 (1983-11-01)
The possible protective effects in vitro of the hydroxyl radical scavenger dimethyl urea (6 mg/ml) and the poly(ADP-ribose)synthetase inhibitors theophylline (5 mM) and nicotinamide (0.75 mg/ml) against streptozotocin (SZ) induced deterioration of islet metabolism were investigated using isolated mouse pancreatic
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Nonlinear optical properties of N, N' dimethylurea.
Halbout JM, et al.
Applied Physics Letters, 37(10), 864-866 (2008)
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