Explore our primary botanical active portfolio, verified through validated HPLC and UV spectroscopy with comprehensive batch qualification files.
The international botanical ingredient market is experiencing a profound transition from basic crude powders to fingerprint-verified bioactive compounds. Formulators no longer rely simply on generic extraction ratios; procurement now demands analytical certainty.
Global regulatory bodies require chromatographic profiling via HPLC, UPLC, and LC-MS to verify primary compounds such as Cynarin, Salicin, and Apigenin alongside secondary synergy markers.
Strict European and FDA guidelines demand ultra-low residual solvent thresholds, pesticide multi-residue screenings (500+ compounds), PAH4 compliance, and heavy metal tracking.
Consumer shift away from synthetic petrochemical extraction media has amplified demand for water-only, bio-ethanol, and Supercritical Fluid CO2 processing for clean finished claims.
Procurement departments require full audit support including batch COAs, TSE/BSE certifications, allergen declarations, non-GMO status, and environmental audit reports.
Modern herbal extract manufacturing requires strict digital engineering. Our Xi'an industrial footprint bridges sustainable wildcraft/agricultural origins with continuous intelligent extraction.
Our 6 multifunctional production lines utilize automated dynamic countercurrent extraction units. Process parameters—temperature, dynamic solvent exchange rates, and resident dwell times—are modulated via PLC systems to protect thermolabile botanical structures.
By pairing low-temperature triple-effect falling film evaporation with advanced membrane separation, we concentrate delicate active fractions without thermal degradation, ensuring superior water solubility and clarity in downstream formulations.
Finished powder isolation occurs entirely within Class 100,000 GMP-compliant cleanrooms. High-tower centrifugal spray drying produces precise bulk densities, standardized particle size distributions (80 to 200 mesh), and optimized wettability characteristics.
Standard parameters for enterprise formulators to accelerate specification matching, QA vendor approval, and regulatory compliance.
| Target Compound / Extract | Primary Marker Specification | Analytical Method | Physical Form & Solubility | Primary Industrial Sector |
|---|---|---|---|---|
| Centella Asiatica Extract | 10% - 95% Madecassoside / Asiaticoside | HPLC (Isocratic/Gradient) | Fine off-white powder / Soluble in glycols | Cosmeceuticals / Barrier Repair |
| White Willow Bark Extract | 15% - 98% Salicin | HPLC External Standard | Light yellow to white / Water-soluble | Anti-Acne / Anti-Inflammatory OTC |
| Turmeric Rhizome Extract | 95% Total Curcuminoids | HPLC / Spectrophotometry | Bright yellow crystalline / Oil dispersible | Functional Food / Joint Mobility |
| Artichoke Leaf Extract | 2.5% - 5.0% Cynarin | UV-Vis / HPLC | Fine brown powder / 100% Water dispersible | Digestive Health / Hepatic Support |
| Milk Thistle Seed Extract | 80% Silymarin (30% Silybin) | HPLC / UV (DAB/USP standard) | Yellowish-brown powder / Hydro-alcoholic | Nutraceutical Capsules / Liver Health |
| Giant Knotweed Extract | 50% - 98% Resveratrol (trans-isomer) | HPLC Reversed-Phase | Off-white crystalline powder / Alcohol soluble | Longevity Nutrients / Anti-Aging Creams |
Transforming botanical chemistry into high-performance commercial products across global market categories.
Incorporating bioactive Alpha Arbutin and Centella Asiatica into stable serum matrices. Engineered for transdermal delivery, uniform compatibility in micro-emulsions, and resistance to photo-oxidation.
Utilizing high-solubility green coffee chlorogenic acid and bromelain enzyme powders that dissolve clear without sediment, bitterness, or cloudiness across variable pH scales.
Providing high-density, free-flowing granular extracts for automated capsule filling, direct tablet compression, and sachet sachets, reducing binder demand and maintaining high active loading.
Natural secondary botanical fractions provide antioxidant stability to sensitive unsaturated lipid systems, preventing lipid peroxidation in functional nutrition products without synthetic BHT/BHA.
Direct answers addressing formulation stability, regulatory documentation, international logistics, and supplier verification.
We use multi-tier verification protocols across incoming plant batches. We cross-verify via Thin Layer Chromatography (TLC/HPTLC) for botanical identity against authentic reference specimens, followed by HPLC with photodiode array detection (PDA) to detect spiking or synthetic fortification.
Every batch includes an official Certificate of Analysis (COA) specifying residual solvents (USP <467>), heavy metals (ICP-MS), pesticide multi-residue panels, microbial enumeration (aerobic, yeast/mold, E. coli, Salmonella), alongside comprehensive SDS, non-GMO, and allergen statements.
Yes. We accommodate physical customization, including micronization down to 200 mesh for seamless suspension stability, agglomeration for reduced dusting and fast wetting, and customized solvent-free hydro-dispersion carriers.
Through direct seasonal farm-origin contracts in Shaanxi and surrounding agricultural regions, combined with our 3,000-ton capacity, we maintain steady active raw inventories. We provide predictable 12-month supply pricing agreements for contract enterprise partners.
Browse our second tier of precision-processed botanical extracts, functional pigments, and cellular defense ingredients for nutraceutical formulations.
Typical reply within one business day (UTC+8).
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