Skip to Content
Merck
All Photos(1)

Documents

T53503

Sigma-Aldrich

Tricarballylic acid

99%

Synonym(s):

1,2,3-Propanetricarboxylic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(HO2CCH2)2CHCO2H
CAS Number:
Molecular Weight:
176.12
Beilstein:
1783567
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

mp

156-161 °C (lit.)

SMILES string

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

Looking for similar products? Visit Product Comparison Guide

General description

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.

Application


  • Effect of organic acids on the solid-state polymorphic phase transformation of piracetam.: Examines the impact of tricarballylic acid and other organic acids on the polymorphic phase transformation of the drug piracetam, relevant for pharmaceutical formulations and drug stability studies (Fan F et al., 2023).

  • Nanotubule inclusion in the channels formed by a six-fold interpenetrated, triperiodic framework.: Describes the synthesis of novel materials incorporating tricarballylic acid, which could have implications for polymer production and advanced material applications (Kusumoto S et al., 2023).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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)
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)
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.
Jennifer A Faust et al.
The journal of physical chemistry. A, 123(10), 2114-2124 (2019-03-02)
Oxidative aging alters the composition of organic aerosols over time, in turn affecting the ability of aerosols to seed cloud formation and scatter solar radiation. Here we explore the heterogeneous photooxidation of model organic particles with and without a soluble
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service