High-Quality Sarcandra Glabra Extract Manufacturer & Factory

Enterprise-scale botanical extraction, standardized Isofraxidin & Rosmarinic Acid active markers, HPLC-validated assays, and cGMP-compliant global manufacturing infrastructure based in the Xi'an Hi-Tech Zone.

HPLC / UV / LC-MS Batch Testing
ISO9001 · cGMP · HALAL · KOSHER
USP <561> Pesticide-Free Certified

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Sarcandra Glabra Extract: Botanical Identity, Chemical Profile & Bioactivity

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.

Botanical Taxonomy & Sustainable Harvest

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.

GAP Harvest Audits · GPS Geolocation Tracing

Primary Bioactive Markers: Isofraxidin & Phenolics

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.

HPLC Standardization: 0.20% to 2.0% Isofraxidin

Validated Mechanisms of Action

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.

Anti-Inflammatory · Thrombocytopenia Support
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)

Global Procurement Demands & Commercial Sourcing Trends

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.

1. Oral Care & Periodontal Formulations

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.

2. Immune Modulation & Platelet Support

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.

3. Dermaceutical & Cosmetic Topical Anti-Redness

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.

20+
Years Phytochemical Manufacturing
8,600m²
cGMP Cleanroom Extraction Plant
500MT
Annual Biomass Processing Capacity
100%
Lot-Specific HPLC Batch Verification

Industrial Extraction Technology & Manufacturing Workflow

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.

STEP 01

Biomass Milling & Enzymatic Pretreatment

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.

STEP 02

Low-Temperature Hydro-Ethanolic Extraction

Continuous multi-stage dynamic countercurrent extraction operating under 50°C–55°C preserves volatile terpenoids and isofraxidin from thermal oxidation and decarboxylation.

STEP 03

Macroporous Resin Column Fractionation

Elution through tailored food-grade adsorptive resins (AB-8 / D101) eliminates sugars, residual chlorophyll, and inorganic salts while selectively concentrating total active polyphenols.

STEP 04

Aseptic Spray Drying & Micro-Milling

Low-heat vacuum concentration followed by high-speed centrifugal spray drying yields 80–120 mesh free-flowing powder with instant solubility and zero clumping.

Custom Particle Engineering & Granulation

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.

Carrier Options: 100% Pure or Custom Excipients

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.

Localized Regulatory Support & International Compliance Assurance

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.

US FDA FSMA & 21 CFR Part 111

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.

European Union (EFSA & Ph. Eur.) Standards

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.

Global Cleanliness: Halal, Kosher, Non-Irradiated

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).

Technological Roadmap: Next-Generation Botanical Bioavailability

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.

1. Liposomal Phospholipid Nano-Encapsulation

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.

2. Green Deep Eutectic Solvent (DES) Extraction

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.

3. High-Throughput DNA Barcoding Verification

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.

Frequently Asked Questions for Botanical Importers & Formulators

Detailed technical, regulatory, and supply chain answers provided directly by our Chief Technology Officer and Quality Assurance Directorate.

What is the standard test method used to quantify Isofraxidin in Sarcandra Glabra Extract?
We employ reverse-phase High-Performance Liquid Chromatography (RP-HPLC) coupled with a Photo Diode Array (PDA) detector at 344 nm, utilizing a C18 column (250 mm × 4.6 mm, 5 µm). The mobile phase consists of acetonitrile and 0.1% phosphoric acid aqueous solution under isocratic or linear gradient conditions calibrated against a USP/EP certified Isofraxidin reference standard. Full chromatograms showing retention times and peak purity are supplied with every batch Certificate of Analysis (COA).
How do you prevent contamination by heavy metals and environmental toxins?
Our raw Sarcandra Glabra is harvested exclusively from monitored plantation sites situated away from industrial hubs. Every incoming biomass lot and final spray-dried powder lot is tested by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) following USP <233>. Limits conform to the most stringent international standards: Lead (Pb) < 2.0 ppm, Arsenic (As) < 1.0 ppm, Cadmium (Cd) < 1.0 ppm, and Mercury (Hg) < 0.1 ppm.
Can you provide custom extraction ratios and carrier-free specifications?
Yes. We routinely manufacture 100% pure, carrier-free Sarcandra glabra extracts (such as 10:1, 20:1, or 50:1 ratios) containing zero excipients. For specialized encapsulation, tableting, or beverage mixing lines, we can also customize bulk density, particle size (from 60 mesh to 200 mesh superfine), or introduce carriers like non-GMO maltodextrin or silica per customer master formula specifications.
What documentation is provided to support vendor qualification and audit?
We provide a complete regulatory packet comprising: Batch-specific COA, Manufacturing Flow Chart with critical control points, Technical Specification Sheet (TDS), Safety Data Sheet (SDS/MSDS conforming to GHS), Certificate of Origin (COO), BSE/TSE-Free Declaration, Non-GMO Statement, Allergen Statement, Kosher & Halal certificates, and third-party validation (e.g., Eurofins or SGS) upon request.
What is the standard lead time, packaging, and commercial shelf-life?
Catalog specifications typically ship from stock within 3 to 5 business days. Custom production campaigns require 2 to 3 weeks. Packaging is pharma-grade: inner double food-grade polyethylene liners protected by heat-sealed pharmaceutical aluminum foil bags, enclosed in 25 kg export fiber drums. The verified shelf-life is 24 months when stored unopened in a cool, dry warehouse away from direct sunlight and humidity.
Can pre-shipment testing samples be dispatched for analytical verification?
Certainly. We provide complimentary 50g–100g pre-shipment trial samples for qualified pharmaceutical, nutraceutical, and cosmetic manufacturing procurement teams. Samples are selected directly from the reserved production lot and arrive accompanied by the exact lot COA so your internal analytical chemistry team can independently confirm assay, identity, and solubility.

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Partner With a Primary Phytochemical Factory

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.

Direct Technical Inquiries

Email our formulation specialists directly with target standardization levels, intended delivery forms, and volume forecasts for immediate quotation and technical turnaround within 24 hours.

Manufacturing & R&D Headquarters

Shaanxi ShineHerb Biotech Co., Ltd.
Room 10921, Building 3, Tangyan South Road, Hi-Tech Industrial Development Zone, Xi'an, Shaanxi Province, China.

Tel: +86-133-2459-1225

Audit & Sample Ordering

Qualified enterprise buyers can schedule virtual video plant audits or request physical validation sample packs with batch COAs shipped worldwide via DHL/FedEx Express.

GMP & ISO Facility Audits Welcome