36997-31-6

Basic information

• Product Name: 1,3,5-Benzenetricarboxylic acid, trihydrazide
• CAS NO: 36997-31-6
• Molecular Formula: C9H12N6O3
• Molecular Weight: 252.233
• Mol File: 36997-31-6.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 1,3,5-Benzenetricarboxylic acid, trihydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Benzenetricarboxylic acid, trihydrazide(36997-31-6)
• EPA Substance Registry System: 1,3,5-Benzenetricarboxylic acid, trihydrazide(36997-31-6)

Safety Data

• Hazardous Substances Data: 36997-31-6(Hazardous Substances Data)

Usage

General Description

1,3,5-Benzenetricarboxylic acid, trihydrazide is a chemical compound with the molecular formula C9H15N6O6. It is a derivative of tricarboxylic acid and contains three hydrazide functional groups. 1,3,5-Benzenetricarboxylic acid, trihydrazide is used in various applications such as in the synthesis of coordination polymers, metal-organic frameworks, and as a crosslinking agent in the preparation of polymeric materials. It also has potential applications as a corrosion inhibitor and in the development of new materials for drug delivery systems. In addition, 1,3,5-Benzenetricarboxylic acid, trihydrazide has been studied for its potential antimicrobial and anti-inflammatory properties, making it a versatile chemical with a wide range of potential uses.

Upstream product

• 2672-58-4 1,3,5-tris-(methoxycarbonyl)benzene 
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Downstream Products

• 117882-60-7 benzene-1,3,5-tricarboxylic acid tris-(N'-benzenesulfonyl-hydrazide) 
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• 118927-16-5 1,3,5-tris(3,5-dimethylpyrazolyl-1-carbonyl)benzene 

Relevant articles and documents

Multifunctional properties of a star-shaped triphenylamine-benzene-1,3,5-tricarbohydrazide fluorescent molecule containing multiple flexible chains

A star-shaped triphenylamine-benzene-1,3,5-tricarbohydrazide molecule with a twisted molecular conformation was found to display amazing multifunctional optical properties. The design of peripheral triphenylamine units and a central benzene connected with hydrazide groups leads to the formation of rare polymorphic properties in the presence of multiple flexible chains. Two polymorphs with different fluorescence colors exhibited bathochromic mechanofluorochromic activities with high contrast due to a crystalline-to-amorphous transition.

Emissive intelligent supramolecular gel for highly selective sensing of Al3+ and writable soft material

A fluorine-containing acylhydrazone was newly designed and found to form gels in a mixed solvent of DMSO-ethylene glycol. The gelator could show brilliant blue light upon mixing with Al3+, which could be erased by F- ions and thus forming an erasable gel.

An acylhydrazone-based AIE organogel for the selective sensing of submicromolar level Al3+and Al(iii)-based metallogel formation to detect oxalic acid

A tripodal acylhydrazone derivative (L) was designed, synthesized, and fully characterized. Through the investigation, it had a typical bluish-green aggregation-induced emission (AIE) effect. Notably, the gelator was reported to accurately detect Al3

Redox-Active Two-Dimensional Covalent Organic Frameworks (COFs) for Selective Reductive Separation of Valence-Variable, Redox-Sensitive and Long-Lived Radionuclides

We report the first example of 2D covalent organic framework nanosheets (Redox-COF1) for the selective reduction and in situ loading of valence-variable, redox-sensitive and long-lived radionuclides (abbreviated as VRL nuclides). Compared with sorbents ba