36997-31-6

Usage

Uses

Used in Coordination Polymers and Metal-Organic Frameworks:
1,3,5-Benzenetricarboxylic acid, trihydrazide is used as a building block for the synthesis of coordination polymers and metal-organic frameworks. Its hydrazide functional groups enable the formation of stable coordination complexes with metal ions, contributing to the development of advanced materials with tailored properties for various applications.
Used as a Crosslinking Agent in Polymeric Materials:
In the polymer industry, 1,3,5-Benzenetricarboxylic acid, trihydrazide serves as an effective crosslinking agent. Its ability to form covalent bonds with other polymer chains enhances the mechanical strength, thermal stability, and chemical resistance of the resulting polymeric materials, making them suitable for diverse applications, such as coatings, adhesives, and composites.
Used as a Corrosion Inhibitor:
1,3,5-Benzenetricarboxylic acid, trihydrazide has potential applications as a corrosion inhibitor. Its hydrazide groups can form protective films on metal surfaces, preventing the penetration of corrosive agents and reducing the rate of corrosion. This property makes it a promising candidate for use in various industries, such as oil and gas, automotive, and aerospace, where corrosion protection is crucial.
Used in Drug Delivery Systems:
1,3,5-Benzenetricarboxylic acid, trihydrazide has been studied for its potential use in the development of new materials for drug delivery systems. Its ability to form stable complexes with metal ions and its potential antimicrobial and anti-inflammatory properties make it a promising candidate for the design of targeted drug delivery systems, improving the therapeutic efficacy and reducing side effects of various medications.
Used in Antimicrobial and Anti-Inflammatory Applications:
1,3,5-Benzenetricarboxylic acid, trihydrazide has shown potential antimicrobial and anti-inflammatory properties, making it a candidate for use in various applications, such as disinfectants, wound healing, and anti-inflammatory drugs. Its hydrazide functional groups can interact with bacterial cell walls or enzymes, inhibiting their growth and reducing inflammation, offering new possibilities for the treatment of infections and inflammatory conditions.

Upstream product

• 4422-95-1 1,3,5-benzene tris(carbonyl chloride) 
• 2672-58-4 1,3,5-tris-(methoxycarbonyl)benzene 
• 554-95-0 benzene-1,3,5-tricarboxylic acid 
• 4105-92-4 triethyl benzene-1,3,5-tricarboxylate 

Downstream Products

• 117882-60-7 benzene-1,3,5-tricarboxylic acid tris-(N'-benzenesulfonyl-hydrazide) 
• 118927-16-5 1,3,5-tris(3,5-dimethylpyrazolyl-1-carbonyl)benzene 
• 175791-97-6 Benzene-1,3,5-tricarboxylic acid tris(2-benzoyl>hydrazide) 
• 347165-20-2 1,3,5-benzenetricarbonyl triazide 
• 1380230-41-0 C₃₀H₂₄N₆O₉ 

Relevant academic research and scientific papers

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.

Metal-tunable nanocages as artificial chemosensors

(Figure Presented) Molecular design: Metal-tunable octahedral nanocages that act as molecular chemosensors are generated by a new strategy (the metals can be transition metals or lanthanides). Amide groups in the supramolecular structures act as guest-accessible functional sites. These interact with glucosamine molecules and function as efficient communicators to convert the recognition information into metal-tunable chromogenic and fluorogenic responses (see picture).

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.

Fabrication of conjugated polyimides with porous crosslinked networks and their application as cathodes for lithium-ion batteries

Conjugated porous polymers were successfully synthesized through dynamic covalent condensation polymerization using aromatic anhydrides and triacylhydrazine benzene. The obtained conjugated polymers with unique chemical stability, high specific surface ar

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

Organogel compound with AIE effect as well as preparation method and application of organogel compound

The invention discloses an organogel compound with an AIE effect as well as a preparation method and application of the organogel compound. An organogel compound N'1,N'3,N'5-3 ((E)-4-(diphenyl amino)benzylidene) benzene-1,3,5-tri-carbohydrazide is prepared by making 1, 3, 5-benzenetrihydrazide to react with 4-diphenylaminobenzaldehyde at the temperature of 60-100 DEG C for 20-30 hours. The structural formula of the organogel compound is shown in the specification; the organogel compound is a good gel; the organogel compound is self-assembled into a three-dimensional network structure in a chloroform solvent through non-covalent bond acting force such as Van der Waals' force, hydrogen bonds and pi-pi superposition acting force among gelator molecules, so that solvent molecules lose fluidity to form gel, and the gel has the advantage of an AIE effect. Because the triphenylamine group contained in the molecular structure of the organogel compound is an AIE group, so that the fluorescenceintensity and penetrability can be greatly improved; and the organogel compound can be used as a gel to prepare organogel with an AIE effect, so that the organogel compound is applied to the field offluorescent probes.

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

Schiff base zinc ion fluorescent probe compound as well as synthesis and application thereof

The invention discloses a Schiff base zinc ion fluorescent probe compound which is prepared by the steps: by using ethanol as a solvent and trimethyl trimellitate and hydrazine hydrate as substrates,carrying out reflux reaction at the temperature of 70-80 DEG C for 5-7 h, carrying out suction filtration, recrystallizing, and drying to obtain the product trimesoyl hydrazine; taking DMF as a solvent and trimesoyl hydrazine and 3,4-dihydroxy benzaldehyde as substrates, carrying out a reaction at the temperature of 70-100 DEG C for 6-9 h, carrying out suction filtration, washing and vacuum drying, and thus obtaining the light yellow powdery Schiff base zinc ion fluorescent probe compound. The compound can be used for specific fluorescence recognition of Zn in an aqueous solution. The method is simple in process, mild in reaction condition, short in reaction time, rapid, efficient and low in cost, the obtained product is high in yield and purity, Zn can be recognized in a high-sensitivity and high-selectivity mode, and good industrial analysis and application prospects are achieved.

Synthesis and application of Schiff base aluminium ion probe compound

The invention provides the synthesis of a Schiff base Al probe compound. A pure Schiff base Al probe compound is obtained by taking absolute ethyl alcohol as a solvent, performing reflux reaction on trimethyl 1,3,5-benzenetricarboxylate and hydraz

A pharmaceutical hydrogen-bonded covalent organic polymer for enrichment of volatile iodine

Porous organic polymers (POPs) are emerging porous materials for various applications. So far, POPs are currently synthesised by a few limited synthetic chemical reactions, leading to a lack of new structures and properties. Thus, expanding structural div