Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

726664

Sigma-Aldrich

(R)-(+)-α,4-Dimethylbenzylamine

ChiPros®, produced by BASF, 99%

Synonym(s):

(+)-1-(4-Methylphenyl)ethylamine, (+)-1-(p-Tolyl)ethylamine, (+)-p-Methyl-α-phenylethylamine, (R)-1-(4-Methylphenyl)ethylamine, (R)-1-(p-Methylphenyl)ethylamine, (R)-1-(p-Tolyl)ethanamine, (R)-4-Tolylethylamine, [(R)-(+)-1-(4-Methylphenyl)ethyl]amine

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

About This Item

Linear Formula:
CH3C6H4CH(CH3)NH2
CAS Number:
4187-38-6
Molecular Weight:
135.21
Beilstein:
3195425
MDL number:
MFCD00145202
UNSPSC Code:
12352116
PubChem Substance ID:
329764255
NACRES:
NA.22

grade

produced by BASF

Quality Level

100

Assay

99%

form

liquid

optical purity

enantiomeric excess: ≥98.5

refractive index

n20/D 1.521 (lit.)

bp

205 °C (lit.)

density

0.919 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

C[C@@H](N)c1ccc(C)cc1

InChI

1S/C9H13N/c1-7-3-5-9(6-4-7)8(2)10/h3-6,8H,10H2,1-2H3/t8-/m1/s1

InChI key

UZDDXUMOXKDXNE-MRVPVSSYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

(R)-(+)-α,4-Dimethylbenzylamine is a chiral amine.

Application

(R)-(+)-α,4-Dimethylbenzylamine reacts with 1,5-difluoro-2,4-dinitrobenzene (DFDNB) to form a chiral derivative reagent(CDR) via substitution of one fluorine atom.

Legal Information

ChiPros is a registered trademark of BASF SE

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302 + H312 + H332,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

179.6 °F - closed cup

Flash Point(C)

82 °C - closed cup

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCD5401
BCBS4682V
BCBC5230V
BCBC5230

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Synthesis of dinitrophenyl-l-Pro-N-hydroxysuccinimide ester and four new variants of Sanger's reagent having chiral amines and their application for enantioresolution of mexiletine using reversed-phase high-performance liquid chromatography.
Bhushan R and Tanwar S.
Journal of Chromatography A, 1216(30), 5769-5773 (2009)
ChiPros Chiral Amines
Aldrich Chemfiles, 11(1) null

Articles

ChiPros Chiral Amines

Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.

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