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Merck
CN

134376

丁酰胺酸

97%

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线性分子式:
H2NCOCH2CH2CO2H
化学文摘社编号:
分子量:
117.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-331-7
MDL number:
Assay:
97%
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InChI key

JDVPQXZIJDEHAN-UHFFFAOYSA-N

InChI

1S/C4H7NO3/c5-3(6)1-2-4(7)8/h1-2H2,(H2,5,6)(H,7,8)

SMILES string

NC(=O)CCC(O)=O

assay

97%

mp

153-156 °C (lit.)

functional group

amide, carboxylic acid

General description

琥珀酰胺酸可形成双核铕络合物。它可与K2PtCl4形成混合价铂蓝。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Journal of the American Chemical Society, 106(5), 1300-1303 (1984)
Vincent Michel et al.
Scientific reports, 10(1), 16430-16430 (2020-10-04)
The hair bundle of cochlear hair cells is the site of auditory mechanoelectrical transduction. It is formed by three rows of stiff microvilli-like protrusions of graduated heights, the short, middle-sized, and tall stereocilia. In developing and mature sensory hair cells
Yasuhiko Kizuka et al.
Cell chemical biology, 24(12), 1467-1478 (2017-10-17)
Fucosylation is a glycan modification critically involved in cancer and inflammation. Although potent fucosylation inhibitors are useful for basic and clinical research, only a few inhibitors have been developed. Here, we focus on a fucose analog with an alkyne group
Ye Wang et al.
Frontiers in microbiology, 8, 435-435 (2017-04-04)
Commensal non-toxigenic

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