USP Compliant Ginkgo Biloba Extract (Ginkgolic Acid ≤ 1ppm)
Latin Name: Ginkgo biloba L.
Assay: Total Ginkgo Flavone Glycosides ≥ 24.0%, Total Terpene Lactones ≥ 6.0%
Метод испытания: HPLC
Ginkgolic Acids: ≤ 1.0 ppm (Ultra-Low Acid Compliance)
Pesticide Residue: Compliant with USP & EC 396/2005 Standards
Heavy Metals: Pb ≤ 0.5 ppm, As ≤ 0.2 ppm, Cd ≤ 0.1 ppm, Hg ≤ 0.1 ppm
Certificate: BRCGS, IFS, ISO 22000, HACCP, Halal, Kosher
Sample: 10-50g Free Sample Available (For Lab R&D Testing)
- 3. Описание
- Спецификация данных
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What is USP Compliant Ginkgo Biloba Extract?
USP Compliant Ginkgo Biloba Extract (Ginkgolic Acid ≤ 1ppm) is a highly refined, premium pharmaceutical-grade botanical raw material extracted from the dried leaves of Ginkgo biloba L- да..
Green Spring Technology meticulously standardizes this natural ingredient to deliver 24.0% Ginkgo Flavone Glycosides and 6.0% Terpene Lactones by КЖПХ (HPLC), strictly adhering to current USP Monograph criteria.
Utilizing advanced multi-stage industrial purification, we successfully limit the cytotoxic and allergenic constituent to Ginkgolic Acids ≤ 1.0 ppm, far surpassing standard industry thresholds.
In high-end global nutraceutical and dietary supplement manufacturing, it serves as a fully verified, audit-ready botanical ingredient optimized for clean-label capsule filling and tableting operations.
This elite compliance-driven profile eliminates cross-border custom seizure risks, providing uncompromised supply chain security for brands targeting strict North American and European regulatory markets.
3. Технические требования
Название продукта
Экстракт порошка гинкго билобы
Название на латинском языке
Гинкго билоба л.
Кас-нет.
90045-36-6
Источник: http://www.
Лист гинкго билоба
Активные ингредиенты
Total Ginkgo Flavone Glycosides; Total Terpene Lactones
3. Технические требования
Total Ginkgo Flavone Glycosides ≥ 24.0%; Total Terpene Lactones ≥ 6.0%
Ginkgolic Acids ≤ 1.0 ppm (Ultra-Low Acid Grade) Метод испытания
HPLC
Внешний вид
Светло-желтый-коричневый мелкий порошок
Mesh Size 100% through 80 Mesh Loss on Drying ≤ 5.0% Ash Content ≤ 0.8% Heavy Metals Pb ≤ 0.5 ppm, As ≤ 0.2 ppm, Cd ≤ 0.1 ppm, Hg ≤ 0.1 ppm Microbial Safety Total Plate Count ≤ 1,000 cfu/g; Yeast & Mold ≤ 100 cfu/g Остатки пестицидов
Compliant with USP & EC 396/2005 Standards
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Ginkgolic Acid Minimization: Processed via multi-stage industrial purification to guarantee a strict limit of Ginkgolic Acids ≤ 1.0 ppm, successfully eliminating Cytotoxic risks, hypersensitivity vectors, and international customs seizure concerns.
Pesticide Residues Control: 100% compliant with both United States Pharmacopeia (USP) and European Commission (EC) No 396/2005 standards, verified through systematic batch-specific chromatography screening.
Elemental Impurities Monitoring: Tightly regulated under current USP and EP criteria using advanced ICP-MS instrumentation to enforce severe trace limits for heavy metals (Pb ≤ 0.5 ppm, As ≤ 0.2 ppm, Cd ≤ 0.1 ppm, Hg ≤ 0.1 ppm).
Global Certifications Grid: Our manufacturing infrastructure and export supply chain operations are fully backed by verified BRCGS, IFS, ISO 9001, ISO 22000, HACCP, Halal, and Kosher credentials.
Assay Purity Standardization: Active component potencies are strictly audited and verified via validated HPLC standard protocols to guarantee an authentic profile of 24.0% Ginkgo Flavone Glycosides and 6.0% Terpene Lactones.
Full Document Traceability: Every commercial volume shipment includes an instantaneous technical dossier package containing batch-specific COA, TDS, MSDS, Allergen-Free Statements, and Non-GMO Project Verification.

Key Advantages
Our USP-compliant Ginkgo Biloba extract series delivers uncompromised chemical purity and absolute regulatory compliance designed to safeguard high-end supplement manufacturing.
Ultra-Low Ginkgolic Acid Threshold: Guarantees a strict concentration of Ginkgolic Acids ≤ 1.0 ppm, completely eliminating the risk of cross-border customs rejection, cargo seizures, or adverse user hypersensitivity recalls.
Current USP Monograph Adherence: Meticulously standardized to 24.0% Flavone Glycosides and 6.0% Terpene Lactones, providing the exact fingerprint profile required for seamless validation by your corporate QC lab.
100% Authentic Botanical Origin: Verified rigorously via High-Performance Liquid Chromatography peak-ratio analysis to guarantee zero unauthorized economic adulteration or synthetic flavonoid enrichment, protecting your brand integrity.
Optimized Particle Density and Flowability: Engineered with a uniform powder structure specifically tailored for flawless high-speed mechanical capsule filling and tableting operations, drastically reducing production downtime and QA rejection rates.
Applications
Dietary Supplement Encapsulation: Perfectly optimized as a free-flowing, high-density botanical active for automated hard gelatin and veggie capsule filling production lines, ensuring excellent uniform weight distribution and zero mechanical clogging or static tracking.
Premium Nutraceutical Tableting: Functions as a highly compressible raw material variant that maintains strong particle cohesion, preventing capping, lamination, and tablet chipping while sustaining structural core integrity during industrial high-pressure compression processes.
Functional Food Enrichment: Serves as a clean-label active ingredient in high-fiber nutritional bars, healthy grain cereals, premium dark chocolates, and dry-blended meal replacement powders, offering zero off-notes or flavor degradation during thermal extrusion.
Clean-Beauty Cosmetic Matrix: Utilized as a purified botanical active in premium anti-aging creams, under-eye revitalizing serums, facial sheet masks, and hair follicle conditioning lotions, seamlessly blending into standard oil-in-water or water-in-oil cosmetic emulsions.

Why Partner With Green Spring Technology?
Partnering with Green Spring Technology secures a highly resilient, fully transparent, and audit-ready botanical ingredient supply chain aligned with your global corporate metrics.
Advanced Advanced Industrial Extraction Infrastructure: Processed via automated production configurations and precision multi-stage membrane filtration to ensure uncompromised batch uniformity and high-capacity manufacturing scale.
Bespoke Active and Physical Customization: Driven by our in-house technical laboratory to offer precision particle mesh adjustments, moisture profiling, and tailored compound standardizations to match your precise manufacturing equipment specifications.
Decade-Long Global Logistics Execution: Supported by comprehensive cross-border trade experience and audit-ready customs clearance protocols to guarantee seamless international shipping transit and zero port detention risks.
Flawless Documentation & Traceability: Every commercial volume shipment provides an instantaneous technical dossier package, supplying batch-specific COAs, independent heavy metal analysis, and complete identity preservation tracing from field cultivation to final powder.
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Download Data Sheet: COA, TDS, MSDS Please fill in the form below to receive the full technical documents via email.
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