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Merck
CN

70710

Supelco

(R)-(+)-1-(1-萘基)乙胺

for chiral derivatization, LiChropur, ≥99.5%

别名:

(R)-(+)-α-甲基-1-萘甲胺

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About This Item

线性分子式:
C10H7CH(CH3)NH2
CAS号:
分子量:
171.24
Beilstein:
2208025
EC 号:
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NA.22

等级

for chiral derivatization

产品线

ChiraSelect

方案

≥99.5% (sum of enantiomers, GC)
≥99.5%

表单

liquid

旋光性

[α]/D +57±2°, c = 2 in ethanol

光学纯度

enantiomeric ratio: ≥99.5:0.5 (GC)

质量

LiChropur

折射率

n20/D 1.623 (lit.)
n20/D 1.624

沸点

153 °C/11 mmHg (lit.)

密度

1.067 g/mL at 20 °C (lit.)

储存温度

2-8°C

SMILES字符串

C[C@@H](N)c1cccc2ccccc12

InChI

1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3/t9-/m1/s1

InChI key

RTCUCQWIICFPOD-SECBINFHSA-N

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一般描述

(R)-(+)-1-(1-Naphthyl)ethylamine is a chiral derivatization reagent useful for all gas chromatography (GC) applications in the chiral field. It is specially selected to meet the requirements for derivatization reagents for enantiomeric excess determinations.

其他说明

HPLC 或 NMR 检测形成酰胺的酸对映体纯度的试剂

推荐产品

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

法律信息

ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A Avgerinos et al.
Journal of chromatography, 415(1), 75-83 (1987-03-20)
A normal-phase high-performance liquid chromatographic method, using a hexane-ethyl acetate solvent system, for the determination of the enantiomeric composition of ibuprofen in human plasma is described. The method is based on the resolution of the diastereoisomeric amides formed on reaction
T.R. Hoye et al.
Tetrahedron Letters, 41, 2289-2289 (2000)
Z. Glowacki, M. Hoffmann
Phosphorus, Sulfur, and Silicon and the Related Elements, 134/135, 279-279 (1998)

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