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P5010
L-Prolinamid -hydrochlorid
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Empirische Formel (Hill-System):
C5H10N2O · HCl
CAS-Nummer:
Molekulargewicht:
150.61
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
EC Number:
255-818-2
Beilstein/REAXYS Number:
3693546
MDL number:
form
powder
SMILES string
Cl.NC(=O)[C@@H]1CCCN1
InChI
1S/C5H10N2O.ClH/c6-5(8)4-2-1-3-7-4;/h4,7H,1-3H2,(H2,6,8);1H/t4-;/m0./s1
InChI key
CSKSDAVTCKIENY-WCCKRBBISA-N
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Martin G Schmid et al.
Analytical and bioanalytical chemistry, 400(8), 2305-2316 (2011-02-15)
This article gives a short overview of the application of the principle of chiral ligand-exchange in HPLC, CE, and CEC. Since its introduction by Davankov, more than thousand articles have appeared in this field. Citing all these papers would extend
Hizuru Nakajima et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 21(1), 67-71 (2005-01-29)
The chiral separation of amino acid derivatives by ligand-exchange electrophoresis in a microchannel chip was performed for the first time. A Cu(II) complex with L-prolinamide was used as a chiral selector. The migration behaviors of eleven NBD-DL-amino acids were investigated
Li Qi et al.
Journal of separation science, 32(18), 3209-3214 (2009-08-26)
A novel method of chiral ligand-exchange CE was developed with L-amino acylamides as a chiral ligand and zinc(II) as a central ion. It has been demonstrated that these chiral complexes, such as Zn(II)-L-alaninamide, Zn(II)-L-prolinamide, and Zn(II)-L-phenylalaninamide, are suitable for use
Global Trade Item Number
| SKU | GTIN |
|---|---|
| P5010-1G | 04061825677279 |