70710
(R)-(+)-1-(1-萘基)乙胺
derivatization grade (chiral), LiChropur™, ≥99.5%
别名:
(R)-(+)-α-甲基-1-萘甲胺
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线性分子式:
C10H7CH(CH3)NH2
化学文摘社编号:
分子量:
171.24
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-425-5
Beilstein/REAXYS Number:
2208025
MDL number:
Assay:
≥99.5% (sum of enantiomers, GC), ≥99.5%
Form:
liquid
InChI key
RTCUCQWIICFPOD-SECBINFHSA-N
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
SMILES string
C[C@@H](N)c1cccc2ccccc12
grade
derivatization grade (chiral)
product line
ChiraSelect™
assay
≥99.5% (sum of enantiomers, GC), ≥99.5%
form
liquid
optical activity
[α]/D +57±2°, c = 2 in ethanol
optical purity
enantiomeric ratio: ≥99.5:0.5 (GC)
quality
LiChropur™
refractive index
n20/D 1.624
bp
153 °C/11 mmHg (lit.)
density
1.067 g/mL at 20 °C (lit.)
storage temp.
2-8°C
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General description
(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.
Legal Information
ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
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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
Z. Glowacki, M. Hoffmann
Phosphorus, Sulfur, and Silicon and the Related Elements, 134/135, 279-279 (1998)
T.R. Hoye et al.
Tetrahedron Letters, 41, 2289-2289 (2000)
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