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442483

Supelco

Benzylamine

analytical standard

Synonyme(s) :

α-Aminotoluène

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About This Item

Formule linéaire :
C6H5CH2NH2
Numéro CAS:
100-46-9
Poids moléculaire :
107.15
Numéro Beilstein :
741984
Numéro CE :
202-854-1
Numéro MDL:
MFCD00008106
Code UNSPSC :
12000000
ID de substance PubChem :
24867867

Qualité

analytical standard

Conditionnement

ampule of 1000 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.543 (lit.)

Point d'ébullition

184-185 °C (lit.)

Pf

10 °C (lit.)

Solubilité

H2O: soluble

Densité

0.981 g/mL at 25 °C (lit.)

Application(s)

environmental

Format

neat

Température de stockage

room temp

Chaîne SMILES 

NCc1ccccc1

InChI

1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2

Clé InChI

WGQKYBSKWIADBV-UHFFFAOYSA-N

Informations sur le gène

human ... AOC3(8639)
mouse ... Aoc3(11754)

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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.

Pictogrammes

CorrosionExclamation mark
GHS05,GHS07

Mention d'avertissement

Danger

Mentions de danger

H302 + H312,H314

Classification des risques

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

149.0 °F - closed cup

Point d'éclair (°C)

65 °C - closed cup

Équipement de protection individuelle

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificats d'analyse (COA)

Lot/Batch Number
LC20962V
LC20205V
LC11574V
LC11573V
LC11500V

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Consulter la Bibliothèque de documents

Danielle M Shacklady-McAtee et al.
Organic letters, 13(13), 3490-3493 (2011-06-08)
A nickel(0) catalyst effectively mediates the cyclization of N-benzoyl aminals in the presence of a stoichiometric Lewis acid. This method enables preparation of a variety of isoindolinones with substitution on the benzoyl fragment and C-3 carbon. This reaction likely proceeds
Farid Oukacine et al.
Analytical chemistry, 84(7), 3302-3310 (2012-03-28)
A new methodology for an antibacterial assay based on capillary electrophoresis with multiple UV detection points has been proposed. The possible antibacterial activity of cationic molecules on bacteria (Gram-positive and Gram-negative) is studied by detecting the bacteria before, during, and
Erika M Milczek et al.
The FEBS journal, 278(24), 4860-4869 (2011-10-08)
The major structural difference between human monoamine oxidases A (MAO A) and B (MAO B) is that MAO A has a monopartite substrate cavity of ~550 Å(3) volume and MAO B contains a dipartite cavity structure with volumes of ~290
A Olivieri et al.
Journal of biochemical and molecular toxicology, 25(1), 26-27 (2011-02-16)
Semicarbazide-sensitive amine oxidase (SSAO) is a copper-containing enzyme that catalyzes the oxidative deamination of endogenous and exogenous primary amines. SSAO exists in mammals both as a plasma-soluble and as a membrane-bound form, and its active site is able to come
Hong Cao et al.
Organic letters, 13(1), 11-13 (2010-12-02)
A versatile synthesis of unsaturated seven-membered ring lactams has been developed. The sequence involves hydroamination of Baylis-Hillman acetate with amines, followed by intramolecular cyclocarbonylation reactions of the resulting allylamines. This process can tolerate a wide array of functional groups, and
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