Standardized phytochemical extraction, active fraction isolation, and validated potency. Certified by ISO9001, cGMP, Halal, Kosher, and USDA Organic guidelines.
100% Organic
Supercritical CO₂
GC Standardized
High Allicin
Biotech Synthesis
Dual Extracted
High Purity PGA
Natural Vitamin C
Headquartered in Xi'an, Shaanxi, our facility operates at the nexus of the Qinling Mountain botanical corridor, delivering verified batch-to-batch phytochemical uniformity and full analytical traceability.
Phytochemical purification & solvent separation engineering
Class D cleanrooms, vacuum concentration, and spray towers
Multidisciplinary HPLC chromatographers and chemical engineers
Comprehensive factory qualification and ethical labor verification
Our systematic 8-stage line encompasses cryogenic raw material pulverization, multi-stage counter-current continuous extraction, vacuum thin-film concentration, macroporous adsorption resin fraction fractionation, industrial spray drying towers, vibro-sieving classification, pneumatic homogenizing, and automated cleanroom packaging.
We reject single-wavelength UV spectrophotometry when determining delicate active fractions. Our central testing laboratory employs Agilent High-Performance Liquid Chromatography (HPLC-DAD), Shimadzu Gas Chromatography (GC-FID/MS), Atomic Absorption Spectrophotometers (AAS), and Atomic Fluorescence Spectrometers (AFS) for precise heavy-metal detection down to parts-per-billion (ppb) thresholds.
Beyond raw active dry powders, we engineer ready-to-market finished delivery configurations: hard vegetarian HPMC capsules, multi-ingredient powder stick-sachets, custom functional beverage premixes, and dual-phase oil suspensions. We operate with scalable pilot-run thresholds starting from low MOQs up to full maritime container programs.
A strategic analytical briefing for technical directors, sourcing managers, and regulatory scientists navigating global phytochemical supply chains.
| Procurement Parameter | Legacy Sourcing Model (Brokers / Traders) | Modern Technical Factory Model (Direct Integration) | Strategic Impact on Brand Formulations |
|---|---|---|---|
| Identity Testing | TLC or UV Total Absorbance (High Risk of adulteration) | HPTLC, SEC-HPLC Fingerprinting & DNA Barcoding | Eliminates raw spiking (e.g., maltodextrin, foreign plant extracts) |
| Solvent Thresholds | Class 2/Class 3 Hydrocarbon mixtures; unmonitored | USP <467> & ICH Q3C limits; Water & Food-Grade Ethanol | Protects clean-label claims and passes stringent EU import controls |
| Contaminant Screening | Generic heavy metal spot tests (< 20 ppm colorimetry) | ICP-MS (Lead < 0.5 ppm, Arsenic < 0.2 ppm, Cadmium < 0.1 ppm) | Guarantees California Proposition 65 and FDA compliance |
| Traceability Matrix | Aggregated multi-farm batches; no geo-coordinates | Batch-specific raw provenance, harvest logs, and retention samples | Satisfies ESG corporate governance and carbon lifecycle metrics |
| Polysaccharide Validation | Phenol-Sulfuric Acid method (Vulnerable to starch fraud) | Megazyme Enzymatic Testing separating α-Glucan from β-Glucan | Validates genuine medicinal mushroom & functional fiber potency |
Discover how advanced continuous separation, super-refining, and bio-fermentation are revolutionizing the modern functional ingredient landscape.
The phased replacement of petroleum ether and hexane solvents with dense-phase carbon dioxide (scCO₂) and low-temperature butane ensures fragile lipophilic biomolecules—such as the free fatty acids in Saw Palmetto and omega fatty acids in Sea Buckthorn Berry Oil—remain 100% free of chemical degradation, isomerization, and harmful chemical residuals.
Targeted cellulase, pectinase, and protease application breaks down rigid botanical plant cell walls under moderate physiological temperatures. This enzymatic pre-digestion dramatically increases target active elution efficiency without subjecting delicate heat-sensitive compounds to high-temperature decomposition, ensuring exceptional native bioactive preservation.
Modern plant extraction increasingly integrates biosimilar microbial fermentation platforms. Advanced macromolecules like Hyaluronic Acid and Gamma Polyglutamic Acid (PGA) achieve non-animal, pharmaceutical-grade molecular uniformity and customized weight profiles impossible to harvest from natural botanical tissue alone.
Addressing volatile organoleptic properties, high hygroscopicity, and rapid gastrointestinal degradation via cyclodextrin complexation, liposomal encapsulation, and spray-congealed lipid matrices. This technology enables sulfurous compounds like those in Garlic Powder to be processed without intense pungent odors or degradation.
Precise technical guidance covering international phytosanitary compliance, analytical validation methods, and contract manufacturing logistics.
We operate a multi-tier analytical identity authentication matrix. First, botanical species are validated at intake via high-performance thin-layer chromatography (HPTLC) fingerprinting cross-referenced against USP/Ph. Eur. authentic reference standards. For high-risk botanicals susceptible to synthetic spiking (such as natural Vitamin C from Acerola or synthetic caffeine addition to tea extracts), we employ Stable Isotope Ratio Mass Spectrometry (IRMS) to confirm natural biological isotopic abundance (δ¹³C values).
Traditional UV-Vis phenol-sulfuric acid assays react indiscriminately with all hexose and pentose sugars, measuring maltodextrin carriers, grain starch residuals, and free sucrose as target active polysaccharides. In functional mushrooms like Reishi, this artificially inflates active content. We utilize the standardized Megazyme enzymatic assay system to selectively digest and quantify genuine immunological (1→3)(1→6)-β-D-glucans while filtering out non-therapeutic α-glucan starch fillers.
We monitor heavy metal limits using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Atomic Absorption Spectrophotometry (AAS). Our standard export batches comply with stringent international standards: Lead (Pb) ≤ 0.5 ppm, Arsenic (As) ≤ 0.2 ppm, Cadmium (Cd) ≤ 0.1 ppm, and Mercury (Hg) ≤ 0.05 ppm. This guarantees full compliance with California Proposition 65 limits, European Commission Regulation (EU) 2023/915, and USP <2232> dietary supplement requirements.
Our extraction facility utilizes predominantly non-toxic, USP Class 3 solvents: pure demineralized water and food-grade ethanol. In instances where specialized selective solvent systems are required, our vacuum thin-film evaporation coupled with spray congealing drives solvent residues well below the stringent requirements of USP <467> and ICH Q3C. Every batch COA includes quantitative headspace gas chromatography (GC-MS) residual solvent verification.
Standard warehouse catalog items ship within 3 to 5 business days upon PO release. Custom extraction ratios, specific granulometry milling (e.g., 200-mesh micronization), or bespoke blending projects require a 10 to 14 business-day production cycle. Standard MOQs for catalog powdered extracts start at 1 kg to 25 kg fiber drums. We supply 50g-100g pre-shipment evaluation samples complete with a lot-specific Certificate of Analysis (COA) for incoming laboratory qualification.
Every export shipment is dispatched with a complete regulatory clearance portfolio: Batch-specific COA, Material Safety Data Sheet (MSDS) conforming to OSHA/GHS, Allergen Declarations, Non-Irradiation and Non-ETO Certificates, BSE/TSE-Free Statements, Origin Traceability Certificate, and Commercial Invoices with correct HS code classification (Chapters 13, 29, or 21). Phytosanitary and Health Certificates issued by China Customs (GACC) are supplied upon request.
Initiate direct communication with our technical sales engineers in Xi'an. Request full analytical COAs, validation chromatograms, pre-shipment evaluation samples, or customized price tiers for your upcoming manufacturing run.