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Supelco

Aniline solution

certified reference material, 5000 μg/mL in methanol

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About This Item

Fórmula empírica (Notação de Hill):
C6H7N
Número CAS:
62-53-3
Peso molecular:
93.13
Código UNSPSC:
41116105

grau

certified reference material
TraceCERT®

Nível de qualidade

300

linha de produto

TraceCERT®

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

ampule of 1 mL

concentração

5000 μg/mL in methanol

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

environmental

Formato

single component solution

temperatura de armazenamento

2-8°C

InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2

chave InChI

PAYRUJLWNCNPSJ-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

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

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Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - STOT RE 2 - STOT SE 1

Órgãos-alvo

Blood, Eyes,Central nervous system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

49.5 °F - closed cup

Ponto de fulgor (°C)

9.7 °C - closed cup

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Certificados de análise (COA)

Lot/Batch Number
LRAC8992
XA16203V
LC07726
LB98108
LB85728

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Pesquise por COA

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Conghui Tang et al.
Journal of the American Chemical Society, 134(46), 18924-18927 (2012-11-08)
A novel and efficient copper-catalyzed azidation reaction of anilines via C-H activation has been developed. This method, in which the primary amine acts as a directing group by coordinating to the metal center, provides ortho azidation products regioselectively under mild
Sung Jin Bae et al.
European journal of medicinal chemistry, 57, 383-390 (2012-11-15)
We attempted to design and synthesize (E)-N-substituted benzylidene-hydroxy or methoxy-aniline derivatives and to evaluate their inhibitory effect on tyrosinase activity and anti-melanogenesis activity in murine B16F10 melanoma cells. Derivatives with a 4-methoxy- or 4-hydroxy-anilino group exerted more potent inhibition against
Wen Chen et al.
Journal of the American Chemical Society, 135(11), 4438-4449 (2013-03-02)
A series of linear and cyclic, sequence controlled, DNA-conjoined copolymers of aniline (ANi) and 2,5-bis(2-thienyl)pyrrole (SNS) were synthesized. In one approach, linear copolymers were prepared from complementary DNA oligomers containing covalently attached SNS and ANi monomers. Hybridization of the oligomers
A Subashini et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 403-408 (2013-01-01)
One of the Schiff base 4-bromo-4'dimethylamino benzylideneaniline (BDMABA) compounds was synthesized and single crystal of the material was grown by solvent evaporation method at room temperature. Molecular structure of BDMABA was confirmed by (1)H nuclear magnetic resonance and the presence
Timo Stahl et al.
Journal of the American Chemical Society, 135(4), 1248-1251 (2013-01-15)
Heterolytic splitting of the Si-H bond mediated by a Ru-S bond forms a sulfur-stabilized silicon cation that is sufficiently electrophilic to abstract fluoride from CF(3) groups attached to selected anilines. The ability of the Ru-H complex, generated in the cooperative
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