Direct factory access to highly purified botanical pigments, medicinal flower components, and premium shade-grown powders verified by HPLC, UV-Vis, and ISO/SGS protocols.
Rooted in the agricultural heartland of Shaanxi Province, China, Xi'an Vexli Bio-Tech Co., Ltd. has spent over a decade establishing end-to-end integration across botanical genetics, eco-extraction, and regulatory compliance.
Vexli holds domestic intellectual property including Invention Patent ZL 2014 1 0464649.9 (specialized purification protocols) and Utility Model Patent No. 14520048 (high-efficiency solid-liquid continuous counter-current extractors), preserving thermolabile polyphenols and floral bio-actives.
Our in-house central laboratory utilizes high-performance liquid chromatography (HPLC), gas chromatography with mass spectrometry (GC-MS), and UV spectrophotometry to test each production batch against rigid pharmacopeial and clean-label monographs.
Having passed comprehensive on-site inspections conducted by SGS and international multinational food conglomerates, our manufacturing ecosystem complies fully with ISO 22000, HACCP, USDA NOP, and EU organic regulation 2018/848.
The cross-industry transition away from artificial colorants, synthetic antioxidants, and chemical flavorings has elevated floral and plant extracts into critical core ingredients across nutraceuticals, cosmeceuticals, and functional foods.
Global regulatory bodies like EFSA and the FDA are enacting stricter limits on petroleum-based food dyes (such as Red 40 and Yellow 5). Botanical pigments like natural phycocyanin, butterfly pea anthocyanins, and chlorophyllin represent the fastest growing category in functional beverage formulations, shifting procurement toward standardized color values (E-value metrics).
Traditional thermal concentration damages volatile floral aromas and delicate active compounds. The forward-looking manufacturing standard demands subcritical water extraction, ultra-low temperature vacuum evaporation, and ceramic membrane multi-stage purification to deliver maximum solubility and native bio-affinity without solvent residuals.
Formulators in Europe and North America are reducing raw material holding costs by seeking manufacturing partners that offer certified small-batch customization (starting at 1 kg), customized mesh particle sizing (from 80 to 450 mesh for instant beverage dispersion), and pre-formulated private label mixes direct from source.
To mitigate cross-border regulatory risks, procurement directors must evaluate technical parameters systematically. Below is our baseline testing methodology aligned with international pharmacopeia.
| Analytical Parameter | Standard Reference Method | Vexli Batch Compliance Specification | Clinical & Industrial Significance |
|---|---|---|---|
| Active Marker Compound Assay | HPLC-DAD / UV-Vis Spectrometry | Guaranteed Active Range (e.g. Polysaccharides ≥30%, Chlorophyllin ≥99%) | Determines true biological functionality rather than gross botanical weight. |
| Colorimetric Density (E-Value) | Spectrophotometer (1% aqueous, 1cm) | Targeted: Phycocyanin E18 – E25 (±0.5 tolerance) | Directly dictates unit dosage costs in beverage and confectionery coloring. |
| Pesticide Multi-Residue | LC-MS/MS & GC-MS/MS (BS EN 15662) | Compliant with EU Organic & US FDA zero-tolerance thresholds | Critical hurdle for entry through Rotterdam, Hamburg, and Los Angeles ports. |
| Heavy Metal Limits | ICP-MS (Inductively Coupled Plasma) | Pb ≤ 2.0 ppm, As ≤ 1.0 ppm, Cd ≤ 0.5 ppm, Hg ≤ 0.1 ppm | Guarantees safety in daily dietary supplements and infant applications. |
| Particle Dispersion (Mesh) | Analytical Sieve Shaker Analysis | Standard: 80-120 mesh; Micronized: 300-450 mesh | Regulates mouthfeel, suspension velocity, and dissolution stability in RTD drinks. |
| Microbiological Safety | Plate Count / BAM / ISO Standard | Total Plate Count ≤ 1,000 cfu/g; Salmonella & E. coli Absent | Prevents batch degradation and supports ready-to-consume food formats. |
Clear, actionable answers addressing international customs, compliance documentation, quality guarantees, and private label execution.
Unlike state-owned mills that demand multi-ton commitments, Vexli provides true R&D agility. Our standard catalog items (Matcha, Phycocyanin, Chlorophyllin, and NMN) start at an MOQ of only 1 kg. Specialized ingredients like marine collagen peptides or customized bulk blends typically start from 25 kg to 50 kg.
Every export lot includes a comprehensive Certificate of Analysis (COA) specifying the assay method, full batch traceability details, heavy metal panel, and microbiological screening. Material Safety Data Sheets (MSDS), non-GMO declarations, allergen statements, BSE/TSE statements, and IATA/IMDG transport classification sheets are standard.
We eliminate open spot market purchasing. All plant raw materials are sourced under long-term contract farming protocols in isolated sub-mountain terrains. Batch screening is executed per BS EN 15662 multi-residue pesticide methodologies through certified international testing houses like SGS.
Yes. We specialize in precision micro-pulverizing. We supply powders from granular standard 80 mesh up to ultra-fine 450 mesh (sub-35 micron), ensuring smooth mouthfeel, instant water dispersion, and non-sedimenting characteristics in cold beverages and capsule filling systems.
We support FOB (Tianjin/Qingdao/Shanghai/Guangzhou), CIF, CFR, FCA, EXW, and door-to-door Delivered Duty Paid (DDP). Multi-currency transactions are accommodated including USD, EUR, GBP, AUD, CAD, JPY, CHF, and RMB through T/T, L/C at sight, and escrow instruments.
Yes. We furnish free analytical samples (50g to 100g) for verified corporate R&D, quality assurance teams, and commercial project managers to conduct independent colorimetry, active assay testing, and pilot formulation runs prior to bulk commitment.
Consult with our biochemical engineers, request batch-specific COAs, or submit custom OEM / mesh specifications today. We respond within 12 business hours.
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