Product Overview
Ferulic Acid is a plant-derived phenolic antioxidant used to reduce free radical activity and support formulation stability by limiting oxidative degradation.
Technical Specifications
|
Category |
Key Parameter |
Specification |
|
Identity & Appearance |
Appearance |
White to light yellow crystalline powder |
|
Melting Point |
168.0°C – 172.0°C |
|
|
Purity |
Assay (HPLC, dry basis) |
≥99.0% |
|
Key Impurities |
Loss on Drying |
≤0.5% |
|
Residue on Ignition |
≤0.1% |
|
|
Heavy Metals |
Total Heavy Metals |
≤10 ppm |
|
Lead (Pb) |
≤2.0 ppm |
|
|
Arsenic (As) |
≤1.0 ppm |
|
|
Mercury (Hg) |
≤0.1 ppm |
|
|
Microbial Safety |
Total Plate Count |
≤1000 CFU/g |
|
Pathogens |
E. coli / S. aureus / P. aeruginosa: Not detected |
|
|
Stability |
Light Sensitivity |
Sensitive to light (isomerization risk) |
Source & Manufacturing Process
Botanical Source: Derived via enzymatic hydrolysis of Oryza sativa (Rice Bran) kernels.
Process Flow: Isolated through aqueous-alkaline extraction, acid precipitation, and controlled recrystallization processes.
Solvent Controls: Purified exclusively using food-grade water and ethanol.
Facility Environment: Crystallization and primary packaging performed in Class 100,000 cleanroom conditions.
Traceability: Complete batch history documented from raw biomass to final distributed lot.
Quality Assurance & Certifications
Quality Assurance
• Purity Verification: Batch HPLC testing used to confirm ≥99.0% assay consistency.
• Heavy Metal Control: ICP-MS elemental screening aligned with global cosmetic safety thresholds.
• Melting Point Validation: Determined by capillary method (168°C–172°C) to confirm crystalline integrity.
• Impurity Monitoring: Loss on drying controlled at ≤0.5% to reduce moisture-related degradation risk.
• Microbial Cleanliness: Total plate counts verified under ≤1000 CFU/g to ensure formulation stability.
Compliance & Certifications
|
Certificate / Standard |
Verification Profile |
|
ISO 9001 |
Quality management consistency. |
|
Cosmos Approved |
Natural cosmetic criteria. |
|
cGMP Guidelines |
Manufacturing practice compliance. |
|
ISO 22000 |
Food safety controls. |
|
COA |
Batch specification authentication. |
|
SGS / Eurofins |
Independent laboratory validation. |
|
Certificate / Standard |
Verification Profile |
Supply Chain & Capacity Stability
|
Operational Metric |
Core Specification & Logistics Data |
|
Annual Capacity |
500 MT |
|
Inventory Reserve |
Standard centralized buffer stock |
|
Minimum Order (MOQ) |
25 kg |
|
Bulk Lead Time |
10 – 14 business days |
|
Standard Packaging |
25 kg fiber drums |
|
Internal Protection |
Double-layer polyethylene liners |
|
Transit Protection |
Vacuum-sealed aluminum foil packaging for moisture and light protection during transport. |
FAQ
Q: Do your raw materials undergo genetic modification before chemical or enzymatic processing?
A: Processing inputs utilize non-GMO plant material backed by identity preservation documentation throughout the supply chain.
Q: How does the container design prevent the raw powder from clumping during maritime shipping?
A: Pallets combine desiccants and heat-sealed aluminum multi-layers to insulate cargo from relative humidity fluctuations during transit.
Q: Can your facility provide allergen cross-contamination statements for dietary formulation audits?
A: Production lines operate under strict allergen segregation protocols with verifiable clean-in-place records available upon request.
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