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Merck
CN

T53503

Sigma-Aldrich

丙三羧酸

99%

别名:

1,2,3-丙三甲酸

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About This Item

线性分子式:
(HO2CCH2)2CHCO2H
CAS号:
分子量:
176.12
Beilstein:
1783567
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

99%

mp

156-161 °C (lit.)

SMILES字符串

OC(=O)CC(CC(O)=O)C(O)=O

InChI

1S/C6H8O6/c7-4(8)1-3(6(11)12)2-5(9)10/h3H,1-2H2,(H,7,8)(H,9,10)(H,11,12)

InChI key

KQTIIICEAUMSDG-UHFFFAOYSA-N

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一般描述

Tricarballylic acid also known as 1,2,3-Propanetricarboxylic acid is a small biomimetic ligand that is often used as building blocks in the synthesis of metal-organic frameworks. Additionally, it is used to produce high-value plasticizers.

应用


  • 有机酸对吡拉西坦固态多晶型相变的影响。: 考察了丙三羧酸和其它有机酸对药物吡拉西坦多晶型相变的影响,该研究与药物制剂和药物稳定性研究相关(Fan F et al., 2023)。

  • 由六重互穿三期框架形成的通道中的纳米管内含物。: 描述了含有丙三羧酸的新型材料的合成,该材料可能对聚合物生产和先进材料应用产生影响(Kusumoto S et al., 2023)。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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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访问文档库

Synthesis, chemical speciation and SOD mimic assays of tricarballylic acid--copper (II) and imidazole--tricarballylic acid--copper (II) complexes
Naso L, et al.
Journal of Inorganic Biochemistry, 103, 219-226 (2009)
Selective defunctionalization of citric acid to tricarballylic acid as a precursor for the production of high-value plasticizers
Stuyck W, et al.
Green Chemistry, 22, 7812-7822 (2020)
Robert A Yokel et al.
Nanotoxicology, 13(4), 455-475 (2019-02-08)
Ligands that accelerate nanoceria dissolution may greatly affect its fate and effects. This project assessed the carboxylic acid contribution to nanoceria dissolution in aqueous, acidic environments. Nanoceria has commercial and potential therapeutic and energy storage applications. It biotransforms in vivo.
Yana Sandlers et al.
Journal of clinical medicine, 9(2) (2020-01-26)
Nonalcoholic liver disease (NAFLD) is manifested with a wide spectrum of clinical symptoms and is closely associated with the metabolic syndrome, inflammation, and mitochondrial dysfunction. Although the mechanism of mitochondrial dysfunction in NAFLD is still not fully elucidated, multiple studies
Erica M Fatica et al.
Metabolites, 9(12) (2019-12-22)
Barth syndrome (BTHS) is an X-linked recessive multisystem disorder caused by mutations in the TAZ gene (TAZ, G 4.5, OMIM 300394) that encodes for the acyltransferase tafazzin. This protein is highly expressed in the heart and plays a significant role

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