In tandem with high-purity Sarcandra Glabra extracts, our factory manufactures, tests, and exports fully audited bio-compounds designed for global dietary supplement, functional food, and pharmaceutical formulations.
Known pharmacognostically as Herba Sarcandrae (Zhong Jie Feng or Cao Shan Hu), Sarcandra glabra (Thunb.) Nakai represents an extraordinary source of pharmacologically verified coumarins, sesquiterpenoids, and phenolic compounds.
Belonging to the primitive angiosperm family Chloranthaceae, Sarcandra glabra is an evergreen subshrub indigenous to the moist subtropical montane forests of Southern and Southwestern China (notably Jiangxi, Guangxi, Fujian, and Zhejiang provinces). Our factory sources wild-simulated, cultivated raw herb biomass harvested strictly at peak vegetative maturity in autumn. This agricultural sourcing matrix prevents deforestation, respects biodiversity, and guarantees batch-to-batch homogeneity in secondary metabolite accumulation.
The definitive pharmacopoeial reference standard for Sarcandra Glabra Extract is the hydroxycoumarin Isofraxidin (7-hydroxy-6,8-dimethoxycoumarin, CAS 486-21-5), complemented by Rosmarinic acid, Scopoletin, and Astragalin. Concurrently, complex sesquiterpene dimers (e.g., Sarcandralactones, Chloranthalactones) provide distinctive immunological, anti-inflammatory, and antimicrobial properties that cannot be duplicated by synthetic coumarin analogues.
Modern biochemical screening demonstrates that purified Sarcandra glabra fractions mediate inflammatory cascades via targeted down-regulation of nuclear factor-κB (NF-κB) phosphorylation and the downstream suppression of cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS), TNF-α, and interleukin-6 (IL-6). Furthermore, clinical oncology research supports its clinical utility in promoting megakaryocyte differentiation, elevating circulating blood platelets, and alleviating chemotherapy-induced myelosuppression.
| Analytical Parameter | Reference Test Standard | Standardized Ratio (10:1 / 20:1) | High-Potency Purified Grade |
|---|---|---|---|
| Isofraxidin Assay (HPLC) | ChP / In-house HPLC-DAD | ≥ 0.20% – 0.50% | ≥ 1.00% – 2.00% HPLC |
| Total Flavonoids (as Rutin) | UV-Vis Spectrophotometry | ≥ 4.0% – 8.0% | ≥ 10.0% – 20.0% UV |
| Total Rosmarinic Acid | Reverse-Phase HPLC | ≥ 0.50% | ≥ 1.50% – 3.00% HPLC |
| Loss on Drying / Moisture | USP <731> (105°C, 2 hrs) | ≤ 5.0% | ≤ 5.0% |
| Heavy Metals (Pb, As, Cd, Hg) | ICP-MS (USP <233>) | Pb < 2.0 ppm, As < 1.0 ppm | Heavy Metals Total < 10.0 ppm |
| Pesticide Residue Limits | GC-MS/MS (USP <561> / EC 396/2005) | Below Detection Limit / Compliant | Organic Certified Compliant |
| Total Plate Count / Yeast & Mold | USP <2021> / <2022> Microbial | < 1,000 CFU/g | < 100 CFU/g | Absence in 10g (E. Coli, Salmonella) |
Procurement teams at enterprise supplement brands, herbal cosmetic laboratories, and OTC botanical manufacturers face acute regulatory scrutiny. Here is how modern B2B buying patterns for Sarcandra Glabra Extract have evolved across North America, Europe, and Asia-Pacific.
Due to its strong bactericidal action against Streptococcus mutans, Porphyromonas gingivalis, and oral spirochetes without disturbing mucosal flora, high-purity Sarcandra Glabra is dominating premium herbal toothpaste, therapeutic mouth rinses, and gingival anti-bleeding oral gels throughout Japan, Southeast Asia, and Western Europe.
Integrative nutraceutical companies are systematically pairing Sarcandra Glabra Extract with Astragalus, Ginseng, and Chlorella Growth Factors (CGF) to formulate clean-label immune restoratives. Contract manufacturers require authenticated botanical finger-printing (HPTLC) to verify that raw supplies are entirely free from adulteration with cheaper Chloranthaceae cultivars.
Cosmeceutical developers leverage the water-soluble and lipid-carrier forms of Sarcandra Glabra to inhibit vascular endothelial hyperpermeability and treat rosacea, persistent facial erythema, and UV-mediated oxidative skin barrier breakdown. The extract's natural coumarin and flavonoid fractions exhibit remarkable synergy with Kojic Acid and Niacinamide.
Thermal degradation of thermolabile sesquiterpene lactones is the greatest vulnerability in low-tier botanical processing. ShineHerb Biotech deploys low-temperature, multi-stage countercurrent extraction coupled with automated membrane ultrafiltration and vacuum drying.
Dried Sarcandra Glabra aerial parts are cryogenic-milled to 40–60 mesh, followed by targeted pectinase incubation to disrupt botanical cell walls without hydrolyzing ester bonds.
Continuous multi-stage dynamic countercurrent extraction operating under 50°C–55°C preserves volatile terpenoids and isofraxidin from thermal oxidation and decarboxylation.
Elution through tailored food-grade adsorptive resins (AB-8 / D101) eliminates sugars, residual chlorophyll, and inorganic salts while selectively concentrating total active polyphenols.
Low-heat vacuum concentration followed by high-speed centrifugal spray drying yields 80–120 mesh free-flowing powder with instant solubility and zero clumping.
Every processing line has distinct bulk density and flowability requirements. We formulate Sarcandra Glabra powders adapted for direct compression tableting (DC grade), high-density hard gelatin/HPMC capsule filling (bulk density 0.45–0.65 g/mL), and agglomerated instant water-soluble granules suitable for sachet drink formulations without surface floatation or sediment ringing.
We supply pure, carrier-free 100% botanical extract powders, as well as customized standardized formulations blended with non-GMO tapioca maltodextrin, organic acacia fiber, or cyclodextrins for buyers seeking improved microencapsulation, shelf-life stabilization, or light protection in transparent packaging.
Importing raw botanical extracts into North America, the European Union, Australia, or the Middle East requires rigorous regulatory documentation. Our regulatory affairs team prepares complete dossier packages tailored to regional market gatekeepers.
Every export lot destined for the United States complies with FDA cGMP regulations under 21 CFR Part 111 (Dietary Supplements) and Part 117 (Preventive Controls). Documentation includes comprehensive Foreign Supplier Verification Program (FSVP) technical dossiers, verified 100% identity testing against botanical voucher specimens, and validated allergen statements.
For European buyers, our raw herb and extract products meet strict limits for Polycyclic Aromatic Hydrocarbons (PAHs: Benzo[a]pyrene and Chrysene sums < 50 ppb per EU 2015/1933), Pyrrolizidine Alkaloids (PAs per EU 2020/2040), and Mycotoxins/Aflatoxins (B1, B2, G1, G2, Ochratoxin A per EU 1881/2006). Complete Technical Data Sheets (TDS) and EU-compliant SDS are standard.
ShineHerb’s facilities maintain valid HALAL (MUI & JAKIM recognized), KOSHER (Star-K / OU compatible), and ISO 22000 certificates. Our materials are completely Non-GMO Project verifiable, 100% BSE/TSE free, and processed strictly without Ethylene Oxide (ETO) treatment or radioactive irradiation (tested via thermoluminescence).
As consumer product formulators demand smaller dosages with elevated systemic absorption, ShineHerb Biotech’s R&D team in Xi'an is pioneering advanced delivery vectors for Sarcandra Glabra's primary actives.
Hydrophobic coumarins like isofraxidin suffer from poor native aqueous dissolution in the GI tract. Our forthcoming liposomal Sarcandra Glabra formulation encases the standardized botanical extract within high-purity non-GMO sunflower phosphatidylcholine bilayers (mean vesicle diameter < 150 nm), elevating oral cellular permeability by an estimated 3.8-fold compared to unformulated powder.
Aligning with global ESG mandates and Scope 3 carbon reduction protocols, ShineHerb’s process engineering unit has developed pilot-scale Natural Deep Eutectic Solvents (NADES)—utilizing biological choline chloride and organic acids—to yield 100% petrochemical solvent-free extracts with zero volatile organic compound (VOC) emissions.
To combat morphological ambiguity among related Asian medicinal Chloranthaceae species (such as Chloranthus japonicus and Chloranthus fortunei), we have operationalized internal ITS2 and psbA-trnH genomic DNA sequence validation, ensuring absolute genetic fidelity across 100% of commercial raw herb lots before extraction.
Detailed technical, regulatory, and supply chain answers provided directly by our Chief Technology Officer and Quality Assurance Directorate.
Explore additional high-demand chemical and natural raw materials manufactured under ISO9001 and cGMP governance, shipped directly from our Xi'an industrial inventory to manufacturing partners globally.
Cut out trading company markups, secure batch-to-batch assay consistency, and obtain direct factory technical support for Sarcandra Glabra Extract. Contact our Xi'an technical sales office to request custom HPLC profiles, pricing tiers, and regulatory documentation.
Email our formulation specialists directly with target standardization levels, intended delivery forms, and volume forecasts for immediate quotation and technical turnaround within 24 hours.
Shaanxi ShineHerb Biotech Co., Ltd.
Room 10921, Building 3, Tangyan South Road, Hi-Tech Industrial Development Zone, Xi'an, Shaanxi Province, China.
Qualified enterprise buyers can schedule virtual video plant audits or request physical validation sample packs with batch COAs shipped worldwide via DHL/FedEx Express.