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Merck
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P5010

Sigma-Aldrich

L-Prolinamide hydrochloride

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About This Item

Formula empirica (notazione di Hill):
C5H10N2O · HCl
Numero CAS:
42429-27-6
Peso molecolare:
150.61
Beilstein:
3693546
Numero CE:
255-818-2
Numero MDL:
MFCD00058156
Codice UNSPSC:
12352200
ID PubChem:
24898579
NACRES:
NA.26

Forma fisica

powder

Stringa SMILE

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
CSKSDAVTCKIENY-WCCKRBBISA-N

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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
Patrycja Puchalska et al.
Electrophoresis, 31(9), 1517-1520 (2010-04-28)
A new chiral stationary phase based on continuous bed (CB) technology using L-prolinamide as a chiral selector was prepared. Its ability for enantioseparation of amino acids and alpha-hydroxy acids by ligand-exchange CEC was compared with that of a CB containing

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