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Merck
CN

A9377

DL-丙氨酰-DL-丙氨酸

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经验公式(希尔记法):
C6H12N2O3
化学文摘社编号:
分子量:
160.17
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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方案

≥98% (TLC)

表单

powder

颜色

white

mp

268-270 °C

储存温度

−20°C

SMILES字符串

CC(N)C(=O)NC(C)C(O)=O

InChI

1S/C6H12N2O3/c1-3(7)5(9)8-4(2)6(10)11/h3-4H,7H2,1-2H3,(H,8,9)(H,10,11)

InChI key

DEFJQIDDEAULHB-UHFFFAOYSA-N

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储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Shahab A Shamsi
Electrophoresis, 23(22-23), 4036-4051 (2002-12-14)
A review is presented to highlight several approaches for coupling capillary electrophoresis (CE) and electrospray ionization-mass spectrometry (ESI-MS) for analysis of chiral compounds. A short discussion of commercially available CE-MS instruments and interface design is followed by a detail review
Ana Maria Castilla et al.
Beilstein journal of organic chemistry, 6, 5-5 (2010-05-21)
We present here the design, synthesis, and analysis of a series of receptors for peptide ligands inspired by the hydrogen-bonding pattern of protein β-sheets. The receptors themselves can be regarded as strands 1 and 3 of a three-stranded β-sheet, with
Shifei Xia et al.
Electrophoresis, 30(16), 2837-2844 (2009-08-06)
Enantiomer of chiral dipeptides were separated by CE-ESI-MS in a bare fused-silica capillary using (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid (18C6H4) as the chiral selector. As 18C6H4 is a kind of nonvolatile chiral selector, in order to prevent from 18C6H4 into the ion-source of
Xiongwu Wu et al.
The Journal of chemical physics, 135(20), 204101-204101 (2011-12-02)
The self-guided Langevin dynamics (SGLD) is a method to accelerate conformational searching. This method is unique in the way that it selectively enhances and suppresses molecular motions based on their frequency to accelerate conformational searching without modifying energy surfaces or
Johannes G Beck et al.
Journal of the American Chemical Society, 134(29), 12125-12133 (2012-06-29)
Insufficient oral bioavailability is considered as a key limitation for the widespread development of peptides as therapeutics. While the oral bioavailability of small organic compounds is often estimated from simple rules, similar rules do not apply to peptides, and even

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