134376
Succinamic acid
97%
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About This Item
Linear Formula:
H2NCOCH2CH2CO2H
CAS Number:
Molecular Weight:
117.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-331-7
MDL number:
Assay:
97%
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
Succinamic acid forms binuclear europium complexes. It forms mixed valent platinum blues with K2PtCl4.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis, binding sites, and spectroscopic characterizations of succinamic acid and succinimide platinum blues.
Arrizabalaga P, et al.
Journal of the American Chemical Society, 106(5), 1300-1303 (1984)
Structure and photophysical properties of europium complexes of succinamic acid and 1, 10-phenanthroline.
Zheng X-J, et al.
Polyhedron, 22(2), 323-330 (2003)
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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