Understanding the Chemistry of 2,3,4-Trihydroxybenzoic Acid
Chemistry is a science of transformation, and understanding the fundamental properties of chemical compounds is key to unlocking their potential. 2,3,4-Trihydroxybenzoic Acid (CAS: 610-02-6) is a prime example of a molecule whose unique chemical structure dictates its wide-ranging applications, particularly as a pharmaceutical intermediate and a specialty chemical. This article aims to provide a clearer picture of its chemical makeup and characteristics.
The compound, identified by CAS number 610-02-6, has the molecular formula C7H6O5 and a molecular weight of approximately 170.12 g/mol. Its structure features a benzene ring substituted with a carboxylic acid group (-COOH) and three hydroxyl groups (-OH) at the ortho, meta, and para positions relative to the carboxyl group. This arrangement, specifically the presence of three adjacent hydroxyl groups (a pyrogallol moiety) along with the carboxylic acid, is responsible for its distinct chemical behavior.
Typically supplied as a white to off-white powder, 2,3,4-Trihydroxybenzoic Acid is known for its high purity, often exceeding 97%. Its physical properties include a melting point of around 205 °C, with decomposition occurring at this temperature. While slightly soluble in water, its solubility can be enhanced in polar organic solvents like DMSO and methanol, as indicated by research data. These properties are important considerations for anyone looking to buy 2,3,4-Trihydroxybenzoic Acid for laboratory use or industrial processes.
The reactivity of 2,3,4-Trihydroxybenzoic Acid is significantly influenced by its hydroxyl groups. These phenolic hydroxyls can participate in various reactions, including etherification, esterification, and oxidation. The carboxylic acid group can undergo esterification, amide formation, and decarboxylation under certain conditions. This versatility makes it an indispensable intermediate in complex organic synthesis pathways. For example, its use as a pharmaceutical intermediate often involves modifying these functional groups to create desired molecular architectures for drug candidates.
Furthermore, the pyrogallol moiety is known for its antioxidant properties, acting as a radical scavenger. This inherent characteristic is a key reason why researchers and manufacturers seek out this compound. Whether used directly for its antioxidant capabilities or as a precursor for more complex molecules with similar properties, understanding this aspect is crucial.
For those in the market to purchase 2,3,4-Trihydroxybenzoic Acid, partnering with a reliable 2,3,4-Trihydroxybenzoic Acid supplier is essential. Manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. provide access to this compound with verified purity and detailed technical specifications. This commitment to quality ensures that researchers can confidently utilize 2,3,4-Trihydroxybenzoic Acid in their critical synthetic routes, whether for new drug development or advanced material formulation.
The compound, identified by CAS number 610-02-6, has the molecular formula C7H6O5 and a molecular weight of approximately 170.12 g/mol. Its structure features a benzene ring substituted with a carboxylic acid group (-COOH) and three hydroxyl groups (-OH) at the ortho, meta, and para positions relative to the carboxyl group. This arrangement, specifically the presence of three adjacent hydroxyl groups (a pyrogallol moiety) along with the carboxylic acid, is responsible for its distinct chemical behavior.
Typically supplied as a white to off-white powder, 2,3,4-Trihydroxybenzoic Acid is known for its high purity, often exceeding 97%. Its physical properties include a melting point of around 205 °C, with decomposition occurring at this temperature. While slightly soluble in water, its solubility can be enhanced in polar organic solvents like DMSO and methanol, as indicated by research data. These properties are important considerations for anyone looking to buy 2,3,4-Trihydroxybenzoic Acid for laboratory use or industrial processes.
The reactivity of 2,3,4-Trihydroxybenzoic Acid is significantly influenced by its hydroxyl groups. These phenolic hydroxyls can participate in various reactions, including etherification, esterification, and oxidation. The carboxylic acid group can undergo esterification, amide formation, and decarboxylation under certain conditions. This versatility makes it an indispensable intermediate in complex organic synthesis pathways. For example, its use as a pharmaceutical intermediate often involves modifying these functional groups to create desired molecular architectures for drug candidates.
Furthermore, the pyrogallol moiety is known for its antioxidant properties, acting as a radical scavenger. This inherent characteristic is a key reason why researchers and manufacturers seek out this compound. Whether used directly for its antioxidant capabilities or as a precursor for more complex molecules with similar properties, understanding this aspect is crucial.
For those in the market to purchase 2,3,4-Trihydroxybenzoic Acid, partnering with a reliable 2,3,4-Trihydroxybenzoic Acid supplier is essential. Manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. provide access to this compound with verified purity and detailed technical specifications. This commitment to quality ensures that researchers can confidently utilize 2,3,4-Trihydroxybenzoic Acid in their critical synthetic routes, whether for new drug development or advanced material formulation.
Perspectives & Insights
Nano Explorer 01
“This article aims to provide a clearer picture of its chemical makeup and characteristics.”
Data Catalyst One
“The compound, identified by CAS number 610-02-6, has the molecular formula C7H6O5 and a molecular weight of approximately 170.”
Chem Thinker Labs
“Its structure features a benzene ring substituted with a carboxylic acid group (-COOH) and three hydroxyl groups (-OH) at the ortho, meta, and para positions relative to the carboxyl group.”