79211-41-9

Usage

Uses

Used in Research and Development:
2,4,6-Triiodobenzene-1,3,5-tricarboxylic acid is used as a research compound for exploring its unique properties and potential applications. Its specific structure with iodine and carboxylic acid functional groups makes it an interesting subject for scientific investigation.
Used in Chemical Synthesis:
In the chemical industry, 2,4,6-triiodobenzene-1,3,5-tricarboxylic acid may be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structure and functional groups can be utilized in various chemical reactions to produce desired products.
Special Considerations:
Due to the presence of iodine, a heavy halogen, in its structure, special care must be taken in handling and storing 2,4,6-triiodobenzene-1,3,5-tricarboxylic acid. Iodine can be hazardous in certain forms, and appropriate safety measures should be followed to minimize potential risks.

InChI:InChI=1/C9H3I3O6/c10-4-1(7(13)14)5(11)3(9(17)18)6(12)2(4)8(15)16/h(H,13,14)(H,15,16)(H,17,18)

Upstream product

• 19025-36-6 2,4,6-triiodomesitylene 
• 108-67-8 1,3,5-trimethyl-benzene 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 828940-27-8 1,3,5-triiodo-2,4-diacetoxymethyl-6-methyl-benzene 

Relevant academic research and scientific papers

Polyiodine-Modified 1,3,5-Benzenetricarboxylic Acid Framework Zn(II)/Cd(II) Complexes as Highly Selective Fluorescence Sensors for Thiamine Hydrochloride, NACs, and Fe3+/Zn2+

Four new complexes, [Zn(TIBTC)(DMA)]·[NH2(CH3)2] (1), [Cd(TIBTC)(H2O)]·[NH2(CH3)2]·DMA (2), [Cd2(TIBTC)(2,2′-bipy)2(HCOO)] (3), and [Cd2(DIBTC)(2,2′-bipy)2(HCOO)] (4) (H3TIBTC = 2,4,6-triiodo-1,3,5-benzenetricarboxylic acid, H3DIBTC = 2,4-diiodo-1,3,5-benzenetricarboxylic acid, 2,2′-bipy = 2,2′-bipyridine, and DMA = dimethylacetamide), were successfully synthesized and characterized by elemental analysis, powder X-ray diffraction, infrared spectroscopy, ultraviolet-visible spectroscopy, and thermogravimetric analysis. Complexes 1 and 2 are three-dimensional supramolecular network structures, while complex 4 has a two-dimensional network structure. We preliminarily studied the fluorescence properties of the complexes and found that complexes 1-3 can detect thiamine hydrochloride, NACs, and Fe3+/Zn2+ with high sensitivity and selectivity.

A family of functional Ln-organic framework constructed by iodine-substituted aromatic polycarboxylic acid for turn-off sensing of UO22+

With the rapid development of nuclear energy, one of the main constraints restricting the development of nuclear energy is the long-term safe disposal of strong uranium waste. Here it is a great significance that we use four new synthetic Ln (III)-based coordination polymers to test the uranium solution. In this study, four three-dimensional coordination polymers 1–4 (CPs-(1–4); Ln?=?Eu, Gd, Sm, Nd) were successfully synthesized through 1:1 complexation of Ln (NO3)3·6H2O with poly-carboxylic acid ligand H3TIBTC (2,4,6-Triiodo-1,3,5-benzene tricarboxylic acid) which contains substituents of the carboxylic acid group and halogen atom, respectively. Based on the ligand being excellent fluorescent properties in the solution, it prompted us to further study the fluorescence properties of the coordination polymers. Experimental results show that the coordination polymers are favorable materials for the simultaneous selective detection uranium solution from water, being potentially useful in monitoring water quality and treating uranium-wastewater.

A new stable porous Pr-organic framework constructed by multi-iodine-substituted aromatic polycarboxylates: Synthesis, characterization, and selective adsorption of dyes

Poly[tris(dimethylformamide)(μ3-2,4,6-triiodol-1,3,5-benzene tricarboxylic acid)-praseodymium (III)] {Pr(TIBTC)(DMF)3}n (1) (H3TIBTC = 2,4,6-triiodo-1,3,5-benzene tricarboxylic acid) was synthesized by the reaction of Pr(NO3)3·6H2O and H3TIBTC at 85°C in a pyrex vial. 1 was characterized by elemental analysis, IR, UV–vis, TGA, PXRD, and atomic force microscopy analytical means. Each of the central Pr ions and the three carboxyl groups from the same ligand constitute a SBU, which is then joined by a carboxyl group to form a building block. In order to further explore the functional properties of 1, we used this compound for adsorption experiments. It is found that 1 can effectively adsorb anionic dyes in aqueous solutions. In particular, there is a good adsorption efficiency for coomassie brilliant blue R-250. Therefore, 1 shows good prospects for selective adsorption of anionic dyes from wastewater solution.

METHOD FOR PRODUCING TRIIODOTRIMESIC ACID

The invention relates to a novel method for producing triiodotrimesic acid used as an intermediate product for synthesizing X-ray contrast media.

METHOD FOR PRODUCING TRIIODINE TRIMESINE ACID

The invention relates to a novel method for producing triiodine trimesine acid used as an intermediate product for the synthesis of X-ray contrast agents.

Polyiodinated aroyloxy esters

Compounds having the structure STR1 wherein Z--COO)m is the residue of a polyiodinated aromatic acid; m is 1, 2, 3 or 4; n is an integer from 1 to 20; R1 and R2 are independently H, alkyl, fluoroalkyl, cycloalkyl, aryl, aralkyl, alkoxy or aryloxy; R3 and R4 are independently H, alkyl, fluoroalkyl, cycloalkyl, aryl, aralkyl, alkoxy, aryloxy, halogen, hydroxy or acylamino; and R5 is H, alkyl, cycloalkyl, aryl, aralkyl, alkoxyalkyl or acetamidoalkyl; are useful as contrast agents in x-ray imaging compositions and methods.