Description

IUPAC Name: 2-hydroxy-6-pentadecylbenzoic acid

InChI: InChI=1S/C22H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-17-15-18-20(23)21(19)22(24)25/h15,17-18,23H,2-14,16H2,1H3,(H,24,25)

InChIKey: ADFWQBGTDJIESE-UHFFFAOYSA-N

Canonical SMILES: CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O

Isomeric SMILES: CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O

Synonyms: ANACARDIC ACID; 16611-84-0; 2-Hydroxy-6-pentadecylbenzoic acid; 6-Pentadecylsalicylic acid; Ginkgolic acid C15:0; Hydroginkgolic acid; 2-Hydroxy-6-pentadecyl-benzoic acid; cyclogallipharic acid; …

Botanical Source:

Product Overview

High-purity Anacardic Acid (2-hydroxy-6-pentadecylbenzoic acid), a bioactive compound isolated from cashew nutshell liquid (CNSL), manufactured to exceptional standards for epigenetic and pharmaceutical research.

Technical Specifications

• Molecular Formula: C₂₂H₃₆O₃
• Molecular Weight: 348.5 g/mol
• Purity: ≥98% (HPLC)
• Appearance: Pale yellow to brown oil/semi-solid
• Solubility: Soluble in DMSO, ethanol, and methanol; insoluble in water

Key Features & Benefits

• Natural histone acetyltransferase (HAT) inhibitor
• Advanced purification technology
• Validated structure and activity
• Comprehensive Certificate of Analysis
• Full spectroscopic characterization

Research Applications

1. Epigenetic Research

   • HAT inhibition studies
   • Chromatin modification research
   • Gene expression regulation
   • Transcriptional control studies

2. Pharmaceutical Development

   • Anti-cancer research
   • Anti-inflammatory studies
   • Antimicrobial investigations
   • Drug discovery screening

3. Mechanism Studies

   • Cell signaling pathways
   • Protein acetylation research
   • Enzyme inhibition studies
   • Structure-activity relationships

Storage & Handling

• Store at -20°C
• Protect from light and moisture
• Avoid repeated freeze-thaw cycles
• Stock solution guidelines provided
• 24-month stability under recommended conditions

Quality Assurance

• GMP-compliant manufacturing
• Rigorous quality control
• Complete analytical documentation
• Traceable lot numbers
• Stability monitoring program

Research Support

BIORLAB provides:

• Technical consultation
• Analytical method support
• Stability data
• Custom synthesis options
• Application Guidance

Key Research Areas

1. Epigenetic Regulation

   • HAT inhibition mechanisms
   • Chromatin remodeling
   • Transcriptional regulation
   • Gene expression control

2. Cancer Research

   • Anti-proliferative mechanisms
   • Apoptosis induction
   • Cell cycle regulation
   • Drug resistance studies

3. Anti-inflammatory Studies

   • NF-κB pathway research
   • Cytokine modulation
   • Inflammatory mediators

This premium-grade Anacardic Acid is specifically designed for research institutions and pharmaceutical companies advancing therapeutic development and scientific research.

For research and development purposes only. Not for human consumption or clinical use.