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≥98% Pure Quillaic Acid (CAS 631-01-6) | HPLC/NMR Validated | Bulk Sourcing

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≥98% Pure Quillaic Acid (CAS 631-01-6) | HPLC/NMR Validated | Bulk Sourcing

≥98% Pure Quillaic Acid (CAS 631-01-6) | HPLC/NMR Validated | Bulk Sourcing

Quillaic Acid (synonyms: Quillaja sapogenin,皂皮酸) is a natural triterpenoid aglycone derived from the bark of the Chilean tree Quillaja saponaria Mol. It is primarily used in scientific research for its dose-dependent analgesic activity and serves as a reference standard in phytochemical studies124.

 

  • Product Name :

    Quillaic Acid
  • CAS No. :

    631-01-6
  • Appearance :

    Fine White Powder
  • Specification :

    98%

 

 

 

🌿 Quillaic Acid (CAS: 631-01-6) 


 

 

⚙️ Chemical & Physical Properties

Parameter Specification
IUPAC Name (3β,4α,16α)-3,16-Dihydroxy-23-oxoolean-12-en-28-oic acid
Molecular Formula C₃₀H₄₆O₅
Molecular Weight 486.68 g/mol
Appearance White to off-white crystalline powder
Melting Point 294°C
Boiling Point 613.3±55.0°C (at 760 mmHg)
Density 1.2±0.1 g/cm³
Optical Rotation [α]²⁰D +56.1° (c=2.9 in pyridine)
Solubility Soluble: DMSO (88 mg/mL), methanol, ethanol, acetone
Insoluble: Water
Storage 2–8°C (dry, airtight, light-resistant container; stability >2 years)

🧪 Biological Activities & Applications

Validated Functions

  1. Analgesic Effects:

    • Exhibits dose-dependent pain relief in preclinical models.

  2. Phytochemical Reference:

    • Used as a high-purity standard (≥98%) for quality control in herbal extracts and saponin analysis.

  3. Research Applications:

    • Pharmacology: Mechanistic studies on triterpenoid bioactivity.

    • Natural Product Chemistry: Isolation and structural validation of saponins.


📦 Supply Specifications & Packaging

Quantity Packaging Purity  
20 mg Sealed glass vial + desiccant ≥98%  
50 mg Amber HDPE bottle + vacuum seal ≥98%  
1 g Pharma-grade HDPE drum + desiccant ≥98%  
Notes:
  • Purity validated by HPLC-DAD/ELSD, NMR, and MS.

  • Custom packaging (e.g., β-cyclodextrin complexes) available for solubility enhancement.


⚠️ Safety & Handling

  • Toxicity:

    • Acute oral LD₅₀ (rat) >1,000 mg/kg; non-genotoxic (OECD 471 compliant).

  • Hazards:

    • Skin/Irritant: Causes skin and eye damage; use PPE (gloves, goggles).

    • Inhalation Risk: Avoid dust formation6.

  • Regulatory Compliance:

    • EINECS: 211-149-8; heavy metals controlled (As <0.1 ppm, Pb <0.2 ppm; ICP-MS).


🧪 Application Notes for Researchers

  1. Solubility Optimization:

    • For cell-based assays: Dissolve in DMSO (up to 180.8 mM), then dilute in buffer.

  2. Analytical Methods:

    • HPLC Conditions: C18 column, gradient MeCN/H₂O + 0.1% formic acid, detection at 210 nm.

    • Structural Confirmation: ¹H/¹³C NMR (CDCl₃ or pyridine-d₅).

  3. Stability:

    • Stable for >24 months at 2–8°C; degrades in alkaline conditions (pH >7).



💎 Key Advantages for Industrial Use

  • Green Extraction: Supercritical technology (yield ≥96%, solvent-free).

  • Batch Consistency: Rigorous QC via HPLC/MS/NMR ensures reproducibility.

  • Multi-Format Flexibility: Suitable for oral, topical, and injectable formulations (via solubility modifiers).


Summary: Quillaic acid (CAS 631-01-6) is a high-value triterpenoid for analgesic research and phytochemical standardization. Its validated purity (≥98%), safety profile, and scalable supply make it ideal for academic and industrial R&D. For batch-specific COA or custom formulations, contact suppliers directly. 🔬

 
 
 
 
 
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