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Merck
CN

726664

(R)-1-(4-甲基苯基)乙胺

ChiPros®, produced by BASF, 99%

别名:

(+)-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

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关于此项目

线性分子式:
CH3C6H4CH(CH3)NH2
化学文摘社编号:
4187-38-6
分子量:
135.21
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
329764255
MDL number:
MFCD00145202
Beilstein/REAXYS Number:
3195425

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产品名称

(R)-1-(4-甲基苯基)乙胺, ChiPros®, produced by BASF, 99%

InChI key

UZDDXUMOXKDXNE-MRVPVSSYSA-N

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

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

Quality Level

100

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相关类别

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.

General description

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

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

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

179.6 °F - closed cup

flash_point_c

82 °C - closed cup

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCD5401
BCBS4682V
BCBC5230V
BCBC5230

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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

商品

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.

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