514101
1,2,4-丁烷三羧酸
别名:
1,2,4-Tricarboxybutane, 3-Carboxyhexanedioic acid, NSC 60127, NSC 8447
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关于此项目
线性分子式:
HO2CCH2CH2CH(CO2H)CH2CO2H
化学文摘社编号:
分子量:
190.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Quality Level
mp
117-120 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)CCC(CC(O)=O)C(O)=O
InChI
1S/C7H10O6/c8-5(9)2-1-4(7(12)13)3-6(10)11/h4H,1-3H2,(H,8,9)(H,10,11)(H,12,13)
InChI key
LOGBRYZYTBQBTB-UHFFFAOYSA-N
Gene Information
human ... FOLH1(2346)
Application
Biological activity:
- Tetracoordinate Ni(II) binding by E. coli NikA employs His416 residue in conjunction with three carboxylate ligands from butane-1,2,4-tricarboxylate (BTC)
- Potential inhibitor of glutamate carboxypeptidase II
signalword
Warning
hcodes
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
Some Syntheses of 1, 2, 4-Butanetricarboxylic Acid1.
Lynn JW and Roberts RL.
The Journal of Organic Chemistry, 26(11), 4303-4305 (1961)
IR spectroscopy study of cyclic anhydride as intermediate for ester crosslinking of cotton cellulose by polycarboxylic acids. V. Comparison of 1, 2, 4-butanetricarboxylic acid and 1, 2, 3-propanetricarboxylic acid.
Mao Z and Yang CQ.
Journal of Applied Polymer Science, 81(9), 2142-2150 (2001)
Samad Ahadian et al.
Acta biomaterialia, 52, 81-91 (2016-12-13)
Polymer biomaterials are used to construct scaffolds in tissue engineering applications to assist in mechanical support, organization, and maturation of tissues. Given the flexibility, electrical conductance, and contractility of native cardiac tissues, it is desirable that polymeric scaffolds for cardiac
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 514101-5G | 04061831820492 |