Aniline solution

Name: Aniline solution
Brand: SUPELCO

certified reference material, 5000 μg/mL in methanol

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Fórmula empírica (notación de Hill):

C₆H₇N

Número CAS:

62-53-3

Peso molecular:

93.13

MDL number:

MFCD00007629

UNSPSC Code:

41116105

NACRES:

NA.24

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grade

certified reference material
TraceCERT^®

product line

TraceCERT^®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-8°C

SMILES string

Nc1ccccc1

InChI

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

InChI key

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

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Este artículo	51788	1036110	242284
Supelco 40542 Aniline solution	Supelco 51788 Aniline	USP 1036110 Aniline	Sigma-Aldrich 242284 Aniline
application(s) environmental	application(s) environmental	application(s) pharmaceutical	application(s) -
technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) -	technique(s) -
format single component solution	format neat	format neat	format -
Quality Level 300	Quality Level 100	Quality Level -	Quality Level 200
grade certified reference material, TraceCERT^®	grade analytical standard	grade pharmaceutical primary standard	grade ACS reagent
storage temp. 2-8°C	storage temp. -	storage temp. -	storage temp. -

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

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

pictograms

GHS02,GHS06,GHS08

signalword

Danger

hcodes

H225,H301 + H311 + H331,H370,H373,H412

pcodes

P210 - P273 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311

Hazard Classifications

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

target_organs

Blood, Eyes,Central nervous system

Clase de almacenamiento

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Copper-catalyzed C-H azidation of anilines under mild conditions.

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

C(sp3)-F bond activation of CF3-substituted anilines with catalytically generated silicon cations: spectroscopic evidence for a hydride-bridged Ru-S dimer in the catalytic cycle.

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

Synthesis of phenanthridinones via palladium-catalyzed C(sp2)-H aminocarbonylation of unprotected o-arylanilines.

Dongdong Liang et al.

Chemical communications (Cambridge, England), 49(2), 173-175 (2012-11-22)

An efficient synthesis of free (NH)-phenanthridinones through Pd-catalyzed C(sp(2))-H aminocarbonylation of unprotected o-arylanilines under an atmospheric pressure of CO has been developed. Some ortho heteroarene substituted anilines as well as N-alkyl protected o-arylanilines are also suitable substrates for this C-H

Design, synthesis, and evaluation of (E)-N-substituted benzylidene-aniline derivatives as tyrosinase inhibitors.

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

One-pot synthesis of (3-sulfopropyl methacrylate potassium)-silica hybrid monolith via thiol-ene click chemistry for CEC.

Huihui Yang et al.

Electrophoresis, 34(4), 510-517 (2012-11-23)

A novel (3-sulfopropyl methacrylate potassium)-silica hybrid monolithic column for CEC has been prepared by a simple one-pot approach based on efficient thiol-ene click chemistry. In this process, the polycondensation of hydrolyzed alkoxysilanes and in situ click reaction of vinyl groups

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