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185701

Sigma-Aldrich

Benzylamine

ReagentPlus®, 99%

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Synonym(s):
α-Aminotoluene
Linear Formula:
C6H5CH2NH2
CAS Number:
Molecular Weight:
107.15
Beilstein:
741984
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

product line

ReagentPlus®

Assay

99%

form

liquid

refractive index

n20/D 1.543 (lit.)

bp

184-185 °C (lit.)

mp

10 °C (lit.)

solubility

alcohol: miscible
diethyl ether: miscible
water: miscible

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

Gene Information

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

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1 of 4

This Item
407712131808.01812
Benzylamine ReagentPlus®, 99%

Sigma-Aldrich

185701

Benzylamine

Benzylamine purified by redistillation, ≥99.5%

Sigma-Aldrich

407712

Benzylamine

Benzylamine for GC derivatization, LiChropur™, ≥99.0%

Supelco

13180

Benzylamine

Benzylamine for synthesis

Sigma-Aldrich

8.01812

Benzylamine

form

liquid

form

liquid

form

liquid

form

liquid

refractive index

n20/D 1.543 (lit.)

refractive index

n20/D 1.543 (lit.)

refractive index

n20/D 1.543 (lit.)

refractive index

-

bp

184-185 °C (lit.)

bp

184-185 °C (lit.)

bp

184-185 °C (lit.)

bp

-

mp

10 °C (lit.)

mp

10 °C (lit.)

mp

10 °C (lit.)

mp

-42.8 °C

solubility

alcohol: miscible, diethyl ether: miscible, water: miscible

solubility

alcohol: miscible, diethyl ether: soluble, water: miscible

solubility

H2O: soluble

solubility

-

General description

Benzylamine (BnNH2) is an aromatic amine widely used for the production of organic fine chemicals and many pharmaceutical compounds. It can be prepared by the hydrogenation of benzonitrile and reductive amination of benzaldehyde using a metal catalyst.
Benzylamine undergoes oxidative deamination reaction catalyzed by benzylamine oxidase and monoamine oxidase type B.

Application

  • Benzylamine was used in modification of alkanethiol monolayers via amide and ester formation reactions for attachment onto metal electrodes.
  • It was used as carrier electrolyte for separation of alkali, alkaline earth and ammonium cations in water samples by capillary electrophoresis with indirect UV detection.
  • It was used in synthesis of cross-linked porous copolymer supports based on N-(p-vinylbenzoyl)-2-methylalanine, styrene and divinylbenzene.

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Customers Also Viewed

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Benzylamine
Heuer, Lutz
Ullmann's Encyclopedia of Industrial Chemistry (2000)
Hydrogenation of benzonitrile to benzylamine catalyzed by ruthenium hydride complexes with P- NH- NH- P tetradentate ligands: evidence for a hydridic- protonic outer sphere mechanism
Li Tianshu, et al.
Organometallics, 26(24), 5940-5949 (2007)
Aida Mohammadi et al.
Sensors (Basel, Switzerland), 18(10) (2018-10-14)
This study examines the improvements in surface-enhanced Raman scattering (SERS) performance achieved when silver nanodendritic structures are coated with various graphene-based materials, namely graphene oxide (GO), reduced graphene oxide (rGO), and graphene nanoplatelets (GNPs). The tests are performed on our
Preparation and characterization of azlactone functionalized polymer supports and their application as scavengers.
Guyomard A, et al.
Eur. Polymer J., 40(10), 2343-2348 (2004)
A benzylamine oxidase distinct from monoamine oxidase B--widespread distribution in man and rat.
R Lewinsohn et al.
Biochemical pharmacology, 27(14), 1857-1863 (1978-01-01)

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