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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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Effect of sodium and calcium cations on the ion-exchange affinity of organic cations for soil organic matter.

Steven Droge et al.

Environmental science & technology, 46(11), 5894-5901 (2012-05-01)

Sorption of organic cations to soil organic matter was studied using dynamic column experiments with different compositions of electrolytes in aqueous eluents. The sorption affinity of the tested variety of charged compounds, including primary, secondary, and tertiary amines and quaternary

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

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

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Global Trade Item Number

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