Synthetic Capsaicin

Synthetic Capsaicin

Product Name: Synthetic Capsaicin
Source: Synthetic
CAS NO: 2444-46-4
Molecular Formula: C₁₇H₂₇NO₃
Molecular Weight: 293.40
Product Appearance: White to light yellow crystalline powder
Product Purity: ≥98%
Testing Method: HPLC
Packaging: 1KG/bottle & bag; 25KG/drum & bag (customizable)
Storage Method: Store in a dry, cool place away from direct sunlight and high temperatures
Shelf Life: 24 months
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Synthetic Capsaicin API Powder

Ultra-Pure TRPV1 Agonist | Bulk Pharmaceutical & Cosmetic Grade

CAS: 2444-46-4 HPLC Purity ≥ 98.0% cGMP Compliant

Product Description

We supply high-purity Bulk Synthetic Capsaicin API powder, engineered with a chemical structure identical to natural capsaicin. Unlike industrial-grade analogs or crude plant extracts, our pharmaceutical-grade capsaicin maintains a core assay purity consistently exceeding 98% via HPLC.

Key impurities are rigorously profiled and controlled to guarantee precise, reproducible bioactivity. Every production batch is manufactured under strict cGMP-compliant quality management systems, featuring comprehensive process validation and full traceability from raw materials to the final API. We are dedicated to providing fully documented, compliance-oriented core ingredients to support pharmaceutical R&D, advanced cosmetic manufacturers, and high-end dietary supplement facilities.

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Why Choose Synthetic Capsaicin API?

1. Chemical & Quality Perfection

  • Single Molecular Entity: Identical structure to natural capsaicin, avoiding the variability of complex botanical mixtures.
  • ≥98% HPLC Purity: Free from plant-derived unknown impurities, heavy metals, pigments, or pesticide residues.
  • Value: Ensures predictable drug efficacy, reproducible clinical data, and long-term shelf-life stability.

2. Unbroken Supply Chain

  • Fully Synthetic Production: Completely independent of capsicum crop cultivation.
  • Risk Mitigation: Neutralizes risks associated with climate disasters, agricultural volatility, and seasonal shortages.
  • Value: Enables large-scale, standardized, year-round continuous production with stable long-term procurement pricing.

3. Regulatory Compliance

  • cGMP Adherence: Entire synthesis process follows current Good Manufacturing Practices.
  • Documentation Support: Detailed process protocols, MOA, and quality data available.
  • Value: Streamlines regulatory submissions (IND/NDA/DMF), reducing risk in preclinical studies and accelerating time-to-market.

Technical Specifications (API Data)

Test Item Specification Limit
Appearance White to off-white crystalline powder
Assay (HPLC) ≥ 98.0%
Identification (NMR/IR) Conforms to reference structure
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%

Core Application Sectors

💊 Pharmaceutical R&D

Utilized extensively as an API in topical analgesic formulations (creams, ointments, transdermal patches) for managing neuropathic pain, osteoarthritis, and rheumatoid arthritis via TRPV1 receptor agonism.

🧴 High-End Cosmetics

Employed by advanced cosmetic manufacturers as a highly potent warming agent in microcirculation-enhancing serums, body contouring creams, and specialized scalp treatments.

🌿 Dietary Supplements

Integrated into thermogenic and metabolic support formulas, providing a standardized, heavy-metal-free alternative to crude pepper extracts.

🔬 Institutional Research

Serves as a reliable, high-purity reference standard for university laboratories conducting advanced neuropharmacological and receptor mapping studies.

Global Logistics & Packaging

Pharmaceutical Packaging
Secure Packaging
Global Shipping
Global Shipping
Payment Options
Flexible Payment

Formulation & Procurement FAQ

Q1: For drug development, is synthetic capsaicin or natural extract the better choice?
A: For high-standard pharmaceutical development, high-purity synthetic capsaicin is the superior option. It ensures a molecular structure identical to natural capsaicin but with extremely high chemical purity (≥98% HPLC). It guarantees a total absence of unknown plant-derived impurities, heavy metals, and variable agricultural analogs. This provides a solid data foundation for reproducible efficacy and regulatory submissions (e.g., DMF filings).
Q2: Does your API comply with major global pharmaceutical quality standards?
A: Yes. Our product is manufactured and controlled in strict accordance with cGMP guidelines. Our quality management system covers the entire process from starting materials to the finished product, ensuring compliance with standards such as the United States Pharmacopeia (USP) and European Pharmacopoeia (EP).
Q3: How does synthetic capsaicin compare to natural extracts in terms of safety?
A: Natural extracts inherently risk introducing residues of pesticides, toxic solvents, or variable plant analogs. Our synthetic API, refined through precise purification protocols, completely neutralizes these risks. It possesses a clear, validated impurity profile, making toxicological safety data highly predictable-a critical factor for transdermal delivery systems.
Q4: How do you ensure supply chain stability?
A: By utilizing a fully synthetic pathway, we eliminate agricultural dependency. Production is insulated from crop yields, seasonality, or climatic disasters, enabling secure, scalable, year-round supply. Every batch features a unique lot identifier accompanied by detailed Batch Production Records (BPR) and Certificates of Analysis (CoA).
HANDLING & SAFETY NOTICE

Synthetic Capsaicin is an extremely potent neurotoxin and irritant in its pure form. Handle strictly within ventilated enclosures (fume hoods/isolators) using full Personal Protective Equipment (PPE) including respiratory gear, gloves, and eye protection. For B2B industrial formulation and R&D use only. Not for direct personal use.

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