Latin Name: Withania Somnifera
CAS No.: 30655-48-2
Molecular Formula: C28H38O6
Active ingredients: Withanolide
Specification:1.5% 5% 20%
Use Part: Root
Appearance: Brown to Brownish-yellow Fine Powder
Mesh size:80 Mesh
Test Method: HPLC
- Product Description
Premium Withania Somnifera Root Powder – Natural Adaptogen for Global Formulators
Scientifically, Withania somnifera has been recognised as a member of the Solanaceae family and is a cornerstone botanical ingredient in modern functional nutrition and wellness formulations. Withania Somnifera Root Powder is made from the dried mature roots of this ancient medicinal plant. It includes standardised bioactive components which can be important for strain modulation, immunological assist and metabolic balance. The pharmaceutical-grade manner preserves clearly happening withanolides (steroidal lactones answerable for its adaptogenic outcomes), alkaloids and polysaccharides that interact synergistically to enhance physiological equilibrium. Unlike artificial substitutes and adulterants of inferior great of aerial components, real root powder supplies quantifiable efficiency that can be used in high-cease nutritional dietary supplements, useful ingredients and beauty packages where clean-label compliance is needed.
Technical Specifications
|
Parameter |
Standard Value |
Test Method |
|
Active Ingredient |
Withanolides 1.5% / 5% / 20% |
HPLC |
|
Appearance |
Brown to Brownish-yellow Fine Powder |
Visual |
|
Particle Size |
80 Mesh |
Sieve Analysis |
|
Moisture Content |
≤5.0% |
Loss on Drying |
|
Ash Content |
≤8.0% |
Gravimetric |
|
Acid Insoluble Ash |
≤1.0% |
Gravimetric |
|
Heavy Metals (Pb) |
≤2.0 ppm |
ICP-MS |
|
Arsenic (As) |
≤1.0 ppm |
ICP-MS |
|
Microbial Limits |
Total Plate Count ≤1000 cfu/g |
USP/EP |
|
Pesticide Residues |
Compliant with EU EC396 |
GC-MS/LC-MS |
|
Solvent Residue |
EU 2023/915 Standards |
GC |
|
Shelf Life |
24-36 months |
Stability Testing |
Why Choose Us?
Advanced Processing Technology
Shaanxi Rebecca Biotechnology adopts the pharmaceutical grade low-temperature drying and ultra-fine grinding technique. This retains the heat sensitive withanolides and yields homogenous particle dispersion required for tablet compression and capsule filling. Our two-stage pulverisation eliminates coarse fibre without chemical solvents.
Strict Quality Assurance
Every production batch is third party tested for 190+ pesticide residues, aflatoxins and heavy metals. In our quality control laboratory HPLC is used to verify the active constituents to ensure consistent withanolide concentrations in each shipment. ISO22000, HACCP and FSSC22000 certifications assure food safety management compliance.
Flexible Customisation Service
For example, you might need 1.5% natural whole root powder for organic blends or 20% high-purity extract for clinical-grade formulae, and we’re happy to customise to your needs. OEM/ODM services encompass customised particle size, moisture level and dosage form formulation – from water-soluble spray-dried powders to microencapsulated beadlets.
Global Supply Chain Expertise
We are completely vertically integrated from our grow partnerships all the way to finished product packaging. This allows us to offer affordable prices while maintaining traceability. Direct sourcing from arid high altitude locations guarantees superior withanolide characteristics. We also have warehouses in major markets for quick delivery and reliable supplies for large enterprises.

Complete Production Process
We manufacture to strict pharmaceutical standards to retain bioactive integrity:
Stage 1: Raw Material Inspection
The incoming roots are visually inspected and analysed by HPLC fingerprinting to validate species authenticity. Only mature roots satisfying withanolide thresholds are processed, with stems, leaves and immature specimens rejected.
Stage 2: Low-Temperature Controlled Drying
The proprietary hot-air circulation at 50-60°C lowers the moisture to less than 5% without thermal degradation of withanolides. Continuous monitoring assures the uniformity of drying within the batches.
Stage 3: Cryogenic milling
First coarse milling and then ultra fine pulverisation with the help of liquid nitrogen. Particle size 80-100 mesh. This approach prevents the formation of heat that could harm the bioactive chemicals.
Stage 4: Multi-Stage Purification
Metallic pollutants are removed using magnetic separation. Vibrating sieves and air classification are used to remove remaining fibres and large particles, assuring pharmaceutical-grade purity.
Stage 5: Mixing & Homogenising
Three-dimensional V-blenders are used to combine several production lots to standardise colour, texture and withanolide content to contract standards.
Step 6: Sterilisation by Physical Means
Steam sterilisation or gamma irradiation reduce the microbial load to <1000 cfu/g without any chemical residues and so the product remains eligible for organic certification.
Stage 7: Pharmaceutical Packaging
The fibre drums are lined with double-sealed aluminium foil bags for light protection and moisture barrier. Nitrogen flushing helps to improve shelf life by reducing oxidative discolouration.
Stage 8: Batch Release Documentation
Every batch is provided with a full Certificate of Analysis (COA) with chromatographic profiles, heavy metals report and pesticide screening findings.

Packaging & Delivery
Primary Packaging Options
· Small Volume: 1kg aluminum foil bag with resealable zipper, ideal for R&D sampling and small-batch production
· Commercial Scale: 5kg, 10kg, or 25kg double-layer food-grade PE bags with heat-sealed closure, placed inside corrugated fiber drums with desiccant packets
· Bulk Orders: 50kg PE-lined multi-wall kraft bags or 200kg steel drums with nitrogen purging for maximum stability during transit
Secondary Protection
All containers are equipped with tamper-evident seals and humidity indicators. The stretch film wrapping helps in palletization and avoids the damage during handling. Thermal blankets or refrigerated containers are included for temperature sensitive shipments as necessary.
International Logistics Network
We utilise approved international freight forwarders with door to door services. Normal lead time is 7-10 business days for air freight, 25-30 days for sea shipment. Real-time tracking and proper documentation (Phytosanitary Certificate, COA, MSDS) for seamless customs clearance in locations including North America, EU, South-east Asia and Australia.
Compliance with Regulations
Our Withania Somnifera Root Powder is USDA Organic, EU Organic, Halal and Kosher. Pre-shipment samples are available on request and bulk purchases are made after quality check. For technical or ordering information, please email info@sxrebecca.com.

FAQ
Q: Is the stuff 100% dried root without stems or adulterants?
A: Yes, only pure mature ashwagandha roots are processed, no aerial portions or additives.
Q: Are you quantifying withanolides by HPLC using marker compounds?
A: Each batch is HPLC-verified for total withanolides, including Withaferin A and Withanolide A, on the COA certificate.
Q: How do you handle pesticide residues and heavy metals?
A: Every batch is tested against over 190 EU pesticide screens and ICP-MS heavy metal tests to meet international safety criteria.
Q: Can you meet organic and clean-label requirements?
A: For sure. Physical sterilisation processes remove chemical residues and support organic certifications and natural product claims.
Contact Us
Partner with Shaanxi Rebecca Biotechnology for reliable, science-backed Withania Somnifera Root Powder that elevates your formulations. Reach out today at information@sxrebecca.com to request samples or discuss custom specifications.
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