High-purity raw materials manufactured to the highest international quality standards.
Annual Raw Processing Capacity
Net Profit Invested in R&D
GMP Certified Production Lines
Accredited Central Laboratory
Discover how our research-driven methodology maximizes bioactive compound recovery and preservation.
Our extraction lines utilize advanced technologies such as low-temperature vacuum freeze-drying, supercritical fluid extraction, and membrane separation. This ensures the protection of heat-sensitive compounds, preserving their molecular structures and bioactivities.
Preserves aromatic profiles, cellular integrity, and nutrient concentration through precision freeze-drying systems.
Using specific solvent ratios and adsorption resins to yield standard concentrations of active molecules.
Micro-encapsulation techniques are deployed to ensure long-term shelf stability without artificial preservatives.
Why choose our manufacturing ecosystem? Scale, compliance, and technological superiority.
Our factories have passed stringent China GMP standards. All manufacturing and facilities comply with international regulations.
We hold European GMP and Certificate of Suitability (CEP) credentials for key botanical extracts, testifying to our global quality compliance.
Every phase of extraction, concentration, and spray drying is continuously monitored by automated systems, minimizing human error.
Integrating raw botanical materials into target consumer products across diverse industries.
Incorporation of soluble durian powder and energy-supportive extracts into health drinks, bakery premixes, and dairy products. These ingredients provide authentic flavors alongside dietary fibers and potassium.
Encapsulated botanical extract formulations (such as Green Tea, Grape Seed, and specialized antioxidant complexes) targeting metabolic support, liver protection, and cellular longevity.
Utilizing natural polyphenols and fruit extracts in skincare formulations to provide anti-inflammatory and skin-barrier reinforcement benefits.
State-of-the-art testing systems guaranteeing purity, compliance, and clinical-grade safety.
| Quality Control Items | Detailed Testing Parameters & Targets |
|---|---|
| Active Ingredient Analysis | Assay determination and identification (via HPLC, UHPLC, or UV-Vis) |
| Hazardous Substance Analysis | Heavy metals (Lead, Arsenic, Mercury, Cadmium, Copper) via ICP-MS, Pesticide residues (GC-MS-MS), Solvent residues (GC) |
| Microbe Analysis | Total Aerobic Microbial Count, Escherichia coli, Yeast & Mould, and target pathogen screenings |
| Raw Material Control | Botanical identification (thin layer chromatography, microscopic verification), GMO status, and traceability audits |
| Stability & Physical Analysis | Shelf-life evaluation under accelerated conditions, pH value, moisture content, ash, particle size, and bulk density |
| Instrument Model | Quantity Available | Primary Analytical Function |
|---|---|---|
| UHPLC Agilent 1290 | 2 Units | Ultra-high performance liquid chromatography for rapid active marker quantification |
| HPLC Agilent 1260 | 4 Units | High performance liquid chromatography for standard ingredient assays |
| HPLC Shimadzu LC-20AT | 2 Units | Routine identification, purity testing, and quantitative assessments |
| Shimadzu GC-2010 | 1 Unit | Gas chromatography for residual solvents and volatile pesticide analyses |
| Shimadzu AA-7000 / ICP-MS | 1 Unit | Atomic absorption spectrophotometry for trace heavy metal profiling |
Value creation through innovation, quality commitment, and community contribution.
Unlocking the physiological potential of natural resources, including premium fruits and therapeutic plants, to elevate human well-being.
Constantly optimizing extraction efficiency and production sustainability to drive down costs while maximizing product performance.
Employing cutting-edge hardware and automated control loops to establish and maintain global-grade quality stability.
Cultivating shared prosperity by fostering fair partnerships with farmers and ensuring safe, rewarding environments for our global workforce.
Get authoritative answers on industrial specifications, compliance, and bulk logistical processes.
A: We utilize low-temperature extraction techniques, such as vacuum freeze-drying and membrane filtration. These processes keep raw material temperatures within safe thresholds to prevent thermal degradation of active polyphenols and volatile oils, preserving natural bioactive properties.
A: Each shipment includes a comprehensive Certificate of Analysis (COA) containing assay results, heavy metal profiles (via ICP-MS), residual solvent evaluations (GC), pesticide screenings, and complete microbial testing. GMP, ISO, Halal, and Kosher documentations are available upon request.
A: Our regulatory affairs team continuously monitors import restrictions and safety thresholds across target markets, including the EU, North America, and APAC. We formulate and refine our products to comply with localized heavy metal, pesticide, and solvent limit guidelines.
A: Our typical MOQ for standard powders and botanical extracts is 25kg (packaged in double-layered PE bags inside food-grade fiber drums). Lead times vary from 7 to 15 working days depending on inventory status, custom specifications, and international transport arrangements.
High-purity raw materials manufactured to the highest international quality standards.
Get in touch with our technical sales team today to request product specifications, pricing, or custom formulation quotes.
Contact Us Now