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Merck
CN

77879

Supelco

(R)-(+)-α-甲基苄胺

for chiral derivatization, LiChropur, ≥99.0%

别名:

(R)-(+)-1-苯乙胺

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About This Item

线性分子式:
C6H5CH(CH3)NH2
CAS号:
分子量:
121.18
Beilstein:
2410916
EC 号:
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NA.22

等级

for chiral derivatization

质量水平

蒸汽压

0.5 mmHg ( 20 °C)

方案

≥99.0% (sum of enantiomers, GC)
≥99.0%

表单

liquid

旋光性

[α]20/D +30±1°, c = 10% in ethanol

光学纯度

enantiomeric ratio: ≥99.5:0.5 (GC)

质量

LiChropur

技术

HPLC: suitable

折射率

n20/D 1.526 (lit.)
n20/D 1.528

沸点

187-189 °C (lit.)

密度

0.952 g/mL at 20 °C (lit.)

储存温度

2-8°C

SMILES字符串

C[C@@H](N)c1ccccc1

InChI

1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m1/s1

InChI key

RQEUFEKYXDPUSK-SSDOTTSWSA-N

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一般描述

(R)-(+)-α-Methylbenzylamine is a high quality, useful chiral derivatization reagent for all analytical applications, specific to GC in the chiral field. It is specially selected to meet the requirements for derivatization reagents for enantiomeric excess determinations.

应用

(R)-(+)-a-Methylbenzylamine also known as (R)-(+)-1-Phenylethylamine may be used in resolution of a chiral arylalkylamine involving high-conversion enantioselective condensation with capric acid followed by hydrolysis to yield corresponding (R)-(+)-amide.

其他说明

用于测定酸对映体纯度的手性胺

推荐产品

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 1

闪点(°F)

158.0 °F - closed cup

闪点(°C)

70 °C - closed cup

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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R.W. Souter
Chromatographic Separations of Stereoisomers null
W.H. Pirkle and J. Finn et al.
Asymmetric Synthesis, 1 (1983)
Easy-on, easy-off?resolution of chiral 1-phenylethylamine catalyzed by Candida antarctica lipase B.
Torres-Gavilan, A., et al.
Tetrahedron Asymmetry, 18.22, 2621-2624 (2007)
R Moaddel et al.
Chirality, 17(8), 501-506 (2005-08-23)
A liquid chromatography stationary phase containing immobilized membranes obtained from a cell line that expresses the human organic cation transporter (hOCT1-IAM) has been used to study the binding of the enantiomers of propranolol, atenolol, pseudoephedrine, and alpha-methylbenzylamine to the immobilized
Abraham R Martin et al.
Applied microbiology and biotechnology, 76(4), 843-851 (2007-06-22)
Enzyme immobilization often improves process economics, but changes in kinetic properties may also occur. The immobilization of a recombinant thermostable (S)-aminotransferase was made by entrapment on calcium alginate-3% (w/v)-and tested with (S)-(-)-(alpha)-methylbenzylamine for acetophenone production. The best immobilization results were

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