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About This Item
經驗公式（希爾表示法）:
C5H10N2O · HCl
CAS號碼:
分子量：:
150.61
Beilstein:
3693546
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.26
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形狀
powder
SMILES 字串
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 密鑰
CSKSDAVTCKIENY-WCCKRBBISA-N
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儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
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
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
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
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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