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Documentos

40542

Supelco

Aniline solution

certified reference material, 5000 μg/mL in methanol

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About This Item

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

grado

certified reference material
TraceCERT®

Nivel de calidad

300

Línea del producto

TraceCERT®

CofA

current certificate can be downloaded

envase

ampule of 1 mL

concentración

5000 μg/mL in methanol

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

environmental

formato

single component solution

temp. de almacenamiento

2-8°C

InChI

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

Clave InChI

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

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Aplicación

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

Información legal

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

Palabra de señalización

Danger

Clasificaciones de peligro

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

Órganos de actuación

Blood, Eyes,Central nervous system

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

49.5 °F - closed cup

Punto de inflamabilidad (°C)

9.7 °C - closed cup

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
LRAE0235
LRAD1971
LRAC8992
LRAC1462
XA16203V

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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
B V Subba Reddy et al.
The Journal of organic chemistry, 77(24), 11355-11361 (2012-12-05)
A domino cycloisomerization/Pictet-Spengler reaction of 2-(4-aminobut-1-yn-1-yl)aniline with aldehydes has been achieved using a AuIPrCl (5 mol %)/AgSbF(6) (10 mol %) catalytic system to produce the corresponding 1-aryl-N-tosyl-2,3,4,5-tetrahydropyrido[4,3-b] indole derivatives in good yields. This is the first report on the synthesis
Tommy Kenny et al.
Inorganic chemistry, 51(24), 13081-13095 (2012-11-23)
This work represents an effort to synthesize all four forms of polyaniline (PANI) in its organometallic versions. Polymers containing substituted 1,4-benzoquinone diimine or 1,4-diaminobenzene units in the backbone exhibiting the general structure (C≡CC(6)H(4)-N═C(6)X(4)═N-C(6)H(4)C≡C-PtL(2))(n) and (C≡CC(6)H(4)NH-C(6)X(4)-NHC(6)H(4)C≡C-PtL(2))(n) along with the corresponding model
Laya Siroos Rezaei et al.
Environmental technology, 33(19-21), 2273-2280 (2013-02-12)
Aerobic granules can be formed in sequencing batch airlift reactors (SBAR) and sequencing batch reactors (SBR). Comparing these two systems, the SBAR has excellent mixing condition, but due to a high height-to-diameter ratio (H/D), there is no performance capability at
Rongjun He et al.
Chemical communications (Cambridge, England), 49(20), 2064-2066 (2013-02-06)
Mycobacterium protein tyrosine phosphatase B (mPTPB) is essential for the survival and persistence of Mycobacterium in the host. Thus small molecule inhibitors of mPTPB are potential anti-TB agents. We developed an efficient organocatalytic multicomponent reaction (MCR) between pyrrole, formaldehyde and
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