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M31201

Sigma-Aldrich

4-Methylbenzylamine

97%

Synonym(s):

p-Xylylamine

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About This Item

Linear Formula:
CH3C6H4CH2NH2
CAS Number:
104-84-7
Molecular Weight:
121.18
Beilstein/REAXYS Number:
956670
EC Number:
203-243-2
MDL number:
MFCD00008123
UNSPSC Code:
12352100
PubChem Substance ID:
24896794
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.534 (lit.)

bp

195 °C (lit.)

mp

12-13 °C (lit.)

density

0.952 g/mL at 25 °C (lit.)

SMILES string

Cc1ccc(CN)cc1

InChI

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

InChI key

HMTSWYPNXFHGEP-UHFFFAOYSA-N

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Related Categories

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

176.0 °F - closed cup

flash_point_c

80 °C - closed cup

ppe

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

Certificates of Analysis (COA)

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Renato Pirisino et al.
British journal of pharmacology, 147(2), 218-224 (2005-11-15)
1.--4-methyl benzylamine (4-MBZ; 28 microg, 231 nmol) elicits a hyperphagic response in starved mice in contrast to the hypophagia induced by the parent compound benzylamine (BZ; 33 microg, 231 nmol) or by amphetamine (AMPH, 2 mug). 2.--In mice starved for
Nadeem Rezaq Janjua et al.
The Journal of investigative dermatology, 123(1), 57-61 (2004-06-12)
Recent in vitro and animal studies have reported estrogen-like activity of chemicals used in sunscreen preparations. We investigated whether the three sunscreens benzophenone-3 (BP-3), octyl-methoxycinnamate (OMC), and 3-(4-methylbenzylidene) camphor (4-MBC) were absorbed and influenced endogenous reproductive hormone levels in humans
J Ishida et al.
Analytical biochemistry, 184(1), 86-89 (1990-01-01)
A simple and highly sensitive method for the determination of beta-phenylethylamine in human plasma is investigated. The method employs high-performance liquid chromatography with fluorescence detection. beta-Phenylethylamine and p-methylbenzylamine (internal standard) in human plasma are isolated by cation-exchange chromatography on a
Francesc Yraola et al.
Journal of medicinal chemistry, 49(21), 6197-6208 (2006-10-13)
Structure activity relationships for semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 (SSAO/VAP-1) were studied using a library of arylalkylamine substrates, with the aim of contributing to the discovery of more efficient SSAO substrates. Experimental data were contrasted with computational docking studies, thereby

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