Ácidos benzoicos

2,3-Diaminobenzoic acid is a benzimidazole derivative that is used in the treatment of microbial infections. It has been shown to inhibit the growth of bacteria by binding to their ribosomes and inhibiting protein synthesis. The reaction solution of 2,3-diaminobenzoic acid has fluorescence properties that can be used to detect contaminating substances. The conjugates formed with p-hydroxyphenylacetic acid are more soluble than those formed with hydroxybenzoic acid. 2,3-Diaminobenzoic acid is not very toxic and does not cause any detectable changes in enzyme activities or other biochemical parameters in short term exposure. It can be easily decomposed by sodium chloride into chlorine gas and hydrochloric acid, which are both highly reactive with water.

4-(Bromomethyl) benzoic acid (4-BA) is a chemical compound that is used as an antimicrobial agent and a reagent in organic synthesis. It has been shown to have a broad spectrum of activity against Gram-positive and Gram-negative bacteria, fungi, and protozoa. 4-BA is stable at neutral pH and can be prepared by the reaction of 2-bromobenzeneacetic acid with sodium borohydride in the presence of acetic acid. This compound reacts with nucleophiles such as imatinib, forming an iminium intermediate. The resulting product can then react with chloride or hydrogen bond to form 4-BA chloride or 4-BA hydrogen bond respectively. Magnetic resonance spectroscopy has also been used to study the magnetic properties of this compound.

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3,5-Diamino-2,4,6-triiodobenzoic acid is a metabolite of hydrochloric acid and has been used in sample preparation for roentgenographic techniques. It is also used in the preparation of methylating agents for mass spectrometric analysis. It is hydrophilic with a methyl esterification that can be activated by amines. This chemical compound is found in human urine and has been shown to have an enhanced effect on tissues when combined with hydrochloric acid.