3,5-dichloro-4-hydroxybenzoic acid
$300.00
CAS No.: 3336-41-2
Catalog No.: WLZ1386
Purity: 95%
MF: C7H4Cl2O3
MW: 207.012
Storage: 2-8 degree Celsius
SMILES: ClC=1C=C(C(=O)O)C=C(C1O)Cl
Catalog No.: WLZ1386
Purity: 95%
MF: C7H4Cl2O3
MW: 207.012
Storage: 2-8 degree Celsius
SMILES: ClC=1C=C(C(=O)O)C=C(C1O)Cl
CAS NO.: 3336-41-2; 3,5-dichloro-4-hydroxybenzoic acid. PROPERTIES: This aromatic carboxylic acid features a hydroxyl group and two chlorine substituents on a benzene ring, creating a molecule with potential antioxidant and anti-inflammatory properties. The 3,5-dichloro-4-hydroxybenzoic acid typically appears as a white crystalline powder with moderate aqueous solubility that increases with pH adjustment. Its molecular structure includes a phenolic hydroxyl group that can participate in hydrogen bonding interactions, contributing to its crystallization behavior and solubility profile. For optimal stability, this compound should be stored at 2-8 degree Celsius in a tightly sealed container away from moisture and direct light. When handling, chemists should wear appropriate personal protective equipment including nitrile gloves and safety goggles. This compound is hygroscopic and may form salts upon exposure to atmospheric moisture. In case of accidental ingestion, rinse mouth thoroughly and seek medical attention. APPLICATIONS: The 3,5-dichloro-4-hydroxybenzoic acid serves as a valuable intermediate in the synthesis of bioactive molecules, particularly in the development of anti-inflammatory agents and antioxidants. Its phenolic character makes it suitable for incorporation into compounds targeting oxidative stress-related conditions. In medicinal chemistry, this acid functions as a building block for creating prodrugs designed to improve pharmacokinetic profiles of therapeutic agents. Additionally, the compound finds utility in cosmetic formulations where its antioxidant properties can help stabilize sensitive ingredients and protect against environmental damage. Researchers utilizing this compound benefit from its versatile reactivity, enabling the creation of diverse molecular architectures for drug discovery and development.
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