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Merck
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Documentos

36574

Supelco

N,N′-Dimethylurea

PESTANAL®, analytical standard

Sinônimo(s):

1,3-Dimethylurea

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About This Item

Fórmula linear:
(CH3NH)2CO
Número CAS:
96-31-1
Peso molecular:
88.11
Beilstein:
1740672
Número CE:
202-498-7
Número MDL:
MFCD00008286
Código UNSPSC:
41116107
ID de substância PubChem:
329755404
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

descrição

(sym.)

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pb

268-270 °C (lit.)

pf

101-104 °C (lit.)

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

CNC(=O)NC

InChI

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

chave InChI

MGJKQDOBUOMPEZ-UHFFFAOYSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informações legais

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

314.6 °F - closed cup

Ponto de fulgor (°C)

157 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
BCCC2418
BCBS4651V
SZBD038XV
SZBA013XV
SZBA013X

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Yishan Chen et al.
Physical chemistry chemical physics : PCCP, 13(16), 7384-7395 (2011-03-23)
The binding behaviors of the 27-membered macrocyclic triurea 1 towards the five anions, F(-), Cl(-), Br(-), I(-) and NO(3)(-), through multiple hydrogen-bonding interactions, were investigated at the B3LYP/6-311++G(d,p)//B3LYP/6-31(1)++G(d,p) (6-31(1)++G(d,p) is a hybrid basis set; for more details see computational methods)
Anna Ronowicz et al.
Analytical biochemistry, 426(2), 91-93 (2012-04-17)
Reuse of materials in DNA hybridization-based methods has been known since the advent of Southern membranes. Array-based comparative genomic hybridization is essentially Southern hybridization with multiple probes immobilized on a solid surface. We show that comparative genomic hybridization microarrays fabricated
Dimethylurea: a radical scavenger that protects isolated pancreatic islets from the effects of alloxan and dihydroxyfumarate exposure.
L J Fischer et al.
Life sciences, 26(17), 1405-1409 (1980-04-28)
In vitro stimulation by paraquat of reactive oxygen-mediated lipid peroxidation in rat lung microsomes.
M A Trush et al.
Toxicology and applied pharmacology, 60(2), 279-286 (1981-09-15)
M M Santoro et al.
Biochemistry, 27(21), 8063-8068 (1988-10-18)
Characteristics and properties of the unfolding free energy change, delta G degrees N-U, as determined by the linear extrapolation method are assessed for the unfolding of phenylmethanesulfonyl chymotrypsin (PMS-Ct). Difference spectral measurements at 293 nm were used to define PMS-Ct
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