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Supelco

Aniline solution

certified reference material, 5000 μg/mL in methanol

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About This Item

Wzór empiryczny (zapis Hilla):
C6H7N
Numer CAS:
62-53-3
Masa cząsteczkowa:
93.13
Kod UNSPSC:
41116105

klasa czystości

certified reference material
TraceCERT®

Poziom jakości

300

linia produktu

TraceCERT®

Certyfikat analizy

current certificate can be downloaded

opakowanie

ampule of 1 mL

stężenie

5000 μg/mL in methanol

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

environmental

format

single component solution

temp. przechowywania

2-8°C

InChI

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

Klucz InChI

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

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Zastosowanie

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

Informacje prawne

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

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

Klasyfikacja zagrożeń

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

Organy docelowe

Blood, Eyes,Central nervous system

Kod klasy składowania

3 - Flammable liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

49.5 °F - closed cup

Temperatura zapłonu (°C)

9.7 °C - closed cup

Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number
LRAE0235
LRAD1971
LRAC8992
LRAC1462
XA16203V

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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
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
Regina Mažeikienė et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 34-40 (2013-01-30)
For the first time, chemical oxidation of aniline and N-methylaniline with dichromate as oxidant has been studied by Raman spectroscopy with 785 nm laser beam excitation, and the suitability of this technique for kinetic study of this process was demonstrated.
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
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