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Merck
CN

77879

Supelco

(R)-(+)-α-甲基苄胺

for chiral derivatization, LiChropur, ≥99.0%

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别名:
(R)-(+)-1-苯乙胺
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)

检测方案

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

形式

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

bp

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

WGK

WGK 1

闪点(°F)

158.0 °F

闪点(°C)

70 °C

个人防护装备

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


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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)
Andrew M Kelly et al.
Nature protocols, 3(2), 215-219 (2008-02-16)
A three-component chiral derivatization protocol for determining the enantiopurity of chiral diols by (1)H NMR spectroscopic analysis is described here. The present approach involves the derivatization of 1,2- 1,3- and 1,4-diols with 2-formylphenylboronic acid and enantiopure alpha-methylbenzylamine. This method affords
Bartosz Lewandowski et al.
Chemical communications (Cambridge, England), (47)(47), 6399-6401 (2008-12-03)
Simple chiral aza-crown ethers based on sucrose display high enantioselectivity in complexation of phenylethylammonium chlorides.

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