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6-Hydroxynicotinic acid

Cas No. 5006-66-6
Molecular Formula
C6H5NO3
Purity. ≥99%
Molecular Weight 139.11g/mol
Properties
Chemical Name 6-Hydroxynicotinic acid
Synonyms
6-Hydroxypyridine-3-carboxylic acid, 2-Hydroxy-5-pyridinecarboxylic acid, 6-Hydroxynicotinic acid
CAS No. 5006-66-6
Molecular Formula C6H5NO3
Molecular Weight 139.11g/mol
Appearance White Powder
Storage and Shipping Conditions
Industries Pharmaceutical intermediates
Applications
1. Pharmaceutical Field (Core Applications) a. Pharmaceutical Intermediates: Used in the synthesis of anti-tuberculosis drugs, antibacterial agents, anti-inflammatory drugs, etc., serving as a key synthetic raw material for pyridine-based pharmaceuticals. b. Drug Development Tools: Act as precursors for molecular modification of drugs, aiding in the optimization of aqueous solubility, bioactivity, and metabolic stability. c. Biological Activity Research: Employed to study its potential biological functions in vivo, such as anti-inflammatory and antioxidant effects, providing a basis for the development of novel drugs. 2. Chemical and Materials Field a. Organic Synthesis Intermediates: Used in the preparation of dyes, pigments, and special polymeric materials, with their pyridine ring structure enhancing material stability. b. Coordination Chemistry Reagents: Can form complexes with metal ions, applied in the preparation of functional materials such as catalysts and ion-exchange resins. 3. Agricultural Field a. Pesticide Intermediates: Used in the synthesis of agricultural chemicals such as herbicides and fungicides, enabling targeted action against specific organisms and improving pesticide efficacy. b. Raw Materials for Plant Growth Regulators: Through structural modification, used to prepare formulations that regulate plant growth and enhance stress resistance.
Description 6-hydroxynicotinic acid is a monohydroxypyridine that is the 6-hydroxy derivative of nicotinic acid. It has a role as an Arabidopsis thaliana metabolite, a mouse metabolite and a human urinary metabolite. It is functionally related to a nicotinic acid. It is a conjugate acid of a 6-hydroxynicotinate(1-).