2,4-Dihydroxybenzoic Acid Chemical Identity
2,4-Dihydroxybenzoic acid has the molecular formula C7H6O4 and the molecular weight 154.1. The ring carries a carboxylic acid group at position 1, a hydroxyl ortho to it at position 2, and a second hydroxyl para to the acid at position 4. The ortho hydroxyl forms an internal hydrogen bond with the carboxyl group, as in salicylic acid, which raises its acidity compared with the 4-hydroxy isomer and shapes its solubility. The 2,4 pattern is that of a resorcinol, meaning that the two hydroxyls sit in a 1,3 relationship on the ring.
The five other isomers include protocatechuic acid, the 3,4-isomer, and gentisic acid, the 2,5-isomer, and a name that omits the locants can refer to any of them. The natural source here is the leaf of Camellia sinensis (L.) Kuntze, in which simple phenolic acids occur beside catechins, flavonols and caffeine. 2,4-Dihydroxybenzoic acid is not a major tea constituent, and it is also produced industrially from resorcinol, so the source statement belongs next to the name. Tea is supplied in other forms: Green Tea Extract 40–98% Polyphenols, Black Tea Extract 10–40% Theaflavins and the 10:1 Green Tea Extract Powder. The 3,4-isomer is supplied as 3,4-Dihydroxybenzoic Acid 98%. The name beta-resorcylic acid reflects the resorcinol pattern of the two hydroxyls, and it is the most common alternative name for this isomer in older literature and in trade listings.












