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Merck
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Documentos

36574

Supelco

N,N′-Dimethylurea

PESTANAL®, analytical standard

Sinónimos:

1,3-Dimethylurea

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About This Item

Fórmula lineal:
(CH3NH)2CO
Número de CAS:
96-31-1
Peso molecular:
88.11
Beilstein/REAXYS Number:
1740672
EC Number:
202-498-7
MDL number:
MFCD00008286
UNSPSC Code:
41116107
PubChem Substance ID:
329755404
NACRES:
NA.24

grade

analytical standard

Quality Level

100

description

(sym.)

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

268-270 °C (lit.)

mp

101-104 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

CNC(=O)NC

InChI

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

InChI key

MGJKQDOBUOMPEZ-UHFFFAOYSA-N

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Application

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

Legal Information

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

314.6 °F - closed cup

flash_point_c

157 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificados de análisis (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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