Skip to Content
MilliporeSigma
All Photos(1)

Documents

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/REAXYS Number:
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.)

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

Related Categories

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

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

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

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