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Merck

261394

Sigma-Aldrich

N,N-Dimethylharnstoff

99%

Synonym(e):

N,N-Dimethylurea

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25 G
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25 G
€ 86,20

About This Item

Lineare Formel:
(CH3)2NCONH2
CAS-Nummer:
Molekulargewicht:
88.11
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

€ 86,20


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Qualitätsniveau

Assay

99%

Form

solid

mp (Schmelzpunkt)

178-183 °C (lit.)

Löslichkeit

water: soluble 5%, clear, colorless

Funktionelle Gruppe

amine

SMILES String

CN(C)C(N)=O

InChI

1S/C3H8N2O/c1-5(2)3(4)6/h1-2H3,(H2,4,6)

InChIKey

YBBLOADPFWKNGS-UHFFFAOYSA-N

Angaben zum Gen

human ... EPHX2(2053)
mouse ... Ephx2(13850)

Verwandte Kategorien

Allgemeine Beschreibung

Nonlinear optical properties of 1,1-dimethylurea (N,N′ dimethylurea), have been evaluated through second-harmonic generation[1].

Anwendung

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[2].

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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G P Meshram et al.
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
J W McDonald et al.
The American review of respiratory disease, 143(4 Pt 1), 806-809 (1991-04-01)
Eugenol, an extract of cloves, has been associated with pulmonary edema when inhaled from commercially available clove cigarettes. We tested the hypothesis that eugenol directly causes lung edema through oxidant-mediated mechanisms by infusing eugenol (0.1 and 1.0 mM) into isolated
Frank F Millenaar et al.
The New phytologist, 184(1), 141-152 (2009-06-30)
Environmental challenges such as low light intensity induce differential growth-driven upward leaf movement (hyponastic growth) in Arabidopsis thaliana. However, little is known about the physiological regulation of this response. Here, we studied how low light intensity is perceived and translated
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
Nonlinear optical properties of N, N' dimethylurea.
Halbout JM, et al.
Applied Physics Letters, 37(10), 864-866 (2008)

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