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Merck
CN

13180

Benzylamine

derivatization grade (GC derivatization), LiChropur, ≥99.0%

Synonym(s):

α-Aminotoluene

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About This Item

Linear Formula:
C6H5CH2NH2
CAS Number:
Molecular Weight:
107.15
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39030404
UNSPSC Code:
23151817
EC Number:
202-854-1
MDL number:
Beilstein/REAXYS Number:
741984
Assay:
≥99.0% (GC), ≥99.0%
Form:
liquid
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grade

derivatization grade (GC derivatization)

Quality Level

assay

≥99.0% (GC), ≥99.0%

form

liquid

quality

LiChropur

technique(s)

gas chromatography (GC): suitable

refractive index

n20/D 1.543

bp

184-185 °C (lit.)

mp

10 °C (lit.)

solubility

H2O: soluble

density

0.981 g/mL at 25 °C (lit.)

SMILES string

NCc1ccccc1

InChI

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

InChI key

WGQKYBSKWIADBV-UHFFFAOYSA-N

General description

Benzylamine, a primary amine, can be used as a fluorescence derivatization agent for the sensitive and selective determination of analytes by chromatography techniques coupled with fluorescence detection.

Application

Benzylamine may be used as a derivatization agent to increase the sensitivity of 5-hydroxyindoles, catecholamines and catechols in biological samples prior to their determination using high performance liquid chromatography (HPLC) coupled with fluorescence detection.

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany


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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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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
Fei Mao et al.
Bioorganic & medicinal chemistry, 20(19), 5884-5892 (2012-09-05)
In an effort to identify novel multifunctional drug candidates for the treatment of Alzheimer's disease (AD), a series of hybrid molecules were synthesised by reacting N-(aminoalkyl)tacrine with salicylic aldehyde or derivatives of 2-aminobenzaldehyde. These compounds were then evaluated as multifunctional
Cécilia Ménard-Moyon et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(11), 3222-3227 (2011-02-11)
Carbon nanotubes (CNTs) are very promising as carriers for the delivery of bioactive molecules. The multifunctionalization of CNTs is necessary to impart multimodalities for the development of future CNT-based multipotent therapeutic constructs. In this context, we report the first example



Global Trade Item Number

SKUGTIN
13180-100ML04061838728586
13180-10X1ML04061838195487
13180-1ML-KC04061838089243
13180-500ML04061838728593