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B25606

N-Benzylmethylamine

Name: <I>N</I>-Benzylmethylamine
Brand: ALDRICH

97%

Synonym(s):

N-Methylbenzylamine

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About This Item

Linear Formula:

C₆H₅CH₂NHCH₃

CAS Number:

103-67-3

Molecular Weight:

121.18

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891660

EC Number:

203-133-4

Beilstein/REAXYS Number:

606221

MDL number:

MFCD00008289

Assay:

97%

Form:

liquid

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Properties

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.522 (lit.)

bp

184-189 °C (lit.)

density

0.939 g/mL at 25 °C (lit.)

SMILES string

CNCc1ccccc1

InChI

1S/C8H11N/c1-9-7-8-5-3-2-4-6-8/h2-6,9H,7H2,1H3

InChI key

RIWRFSMVIUAEBX-UHFFFAOYSA-N

Description

pictograms

GHS08,GHS05

signalword

Danger

hcodes

H314,H317,H334

pcodes

P261 - P272 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

167.0 °F - closed cup

flash_point_c

75 °C - closed cup

ppe

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

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The inhibitory effect of thioproline on carcinogenesis induced by N-benzylmethylamine and nitrite.

T Tahira et al.

Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(6), 511-516 (1988-06-01)

Thioproline, which is readily nitrosated to form nitrosothioproline, is expected to act as a nitrite scavenger. The effect of thioproline as an inhibitor of the carcinogenesis induced by N-nitroso-N-benzylmethylamine precursors was examined. Two groups of male F-344 rats were given

Suitability of DTAF as a fluorescent labelling reagent for direct analysis of primary and secondary amines--spectral and chemical reactivity considerations.

R Siegler et al.

Journal of pharmaceutical and biomedical analysis, 7(1), 45-55 (1989-01-01)

DTAF has been used successfully to prepare fluorescent labelled reagents for fluorescence polarization immunoassays. Its applicability as a derivation reagent for direct fluorescence analysis of primary and secondary amines was evaluated. DTAF was shown to have spectral properties that closely

Mechanism of aryl chloride amination: base-induced oxidative addition.

L M Alcazar-Roman et al.

Journal of the American Chemical Society, 123(51), 12905-12906 (2001-12-26)

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Global Trade Item Number

SKU	GTIN
B25606-100ML	04061833426944
B25606-500ML	04061833426951
B25606-5ML	04061836823535