Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

132020

Sigma-Aldrich

2-(p-Tolyl)ethylamine

97%

Synonym(s):

4-Methylphenethylamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3C6H4CH2CH2NH2
CAS Number:
3261-62-9
Molecular Weight:
135.21
EC Number:
221-865-2
MDL number:
MFCD00008195
UNSPSC Code:
12352100
PubChem Substance ID:
24847541
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.527 (lit.)

bp

214 °C (lit.)

density

0.93 g/mL at 25 °C (lit.)

SMILES string

Cc1ccc(CCN)cc1

InChI

1S/C9H13N/c1-8-2-4-9(5-3-8)6-7-10/h2-5H,6-7,10H2,1H3

InChI key

VKJXAQYPOTYDLO-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

Related Categories

Application

2-(p-Tolyl)ethylamine was used to prepare secondary amides by amidation of sophorolipid ethyl ester.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

195.8 °F - closed cup

Flash Point(C)

91 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Benzylamine ReagentPlus®, 99%

Sigma-Aldrich

185701

Benzylamine

Sanjay K Singh et al.
The Journal of organic chemistry, 68(14), 5466-5477 (2003-07-04)
Novel enzyme-mediated synthetic routes were developed to provide a new family of sophorolipid derivatives and glycolopid-based amphiphilic monomers. These compounds are of great interest for their potential use in immunoregulation, as well as for other biological properties. In the present
Anita H Lewin et al.
Bioorganic & medicinal chemistry, 16(15), 7415-7423 (2008-07-08)
A cell line in which RD-HGA16 cells were stably transfected with the hTAAR 1 receptor was created and utilized to carry out a systematic evaluation of a series of beta-phenethylamines. Fair agreement was observed with data obtained for aryl and
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the
Minna Rahnasto et al.
Journal of medicinal chemistry, 48(2), 440-449 (2005-01-22)
The purpose of this study was to develop screening and in silico modeling methods to obtain accurate information on the active center of CYP2A6, a nicotine oxidizing enzyme. The inhibitory potencies of 26 naphthalene and 16 non-naphthalene derivatives were determined

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service