P5010
L-脯氨酰胺 盐酸盐
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关于此项目
经验公式（希尔记法）:
C5H10N2O · HCl
化学文摘社编号:
分子量:
150.61
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
EC Number:
255-818-2
Beilstein/REAXYS Number:
3693546
MDL number:
InChI key
CSKSDAVTCKIENY-WCCKRBBISA-N
InChI
1S/C5H10N2O.ClH/c6-5(8)4-2-1-3-7-4;/h4,7H,1-3H2,(H2,6,8);1H/t4-;/m0./s1
SMILES string
Cl.NC(=O)[C@@H]1CCCN1
form
powder
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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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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