Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
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Schizandrin B

    • Product Name Schizandrin B
    • Alias SCH B
    • Einecs 210-120-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    640960

    Name Schizandrin B
    Cas Number 61281-37-6
    Molecular Formula C23H28O6
    Molecular Weight 400.46 g/mol
    Appearance White to off-white powder
    Purity ≥98% (HPLC)
    Solubility Soluble in DMSO, ethanol
    Melting Point 129-131 °C
    Storage Conditions Store at -20°C, protected from light
    Synonyms Gomisin N
    Source Extracted from Schisandra chinensis
    Chemical Structure Lignan

    As an accredited Schizandrin B factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Schizandrin B is packaged in a 100 mg amber glass vial, sealed for protection against light and moisture, with clear labeling.
    Shipping Schizandrin B is shipped in secure, sealed containers to ensure stability and prevent contamination. It is packed according to international regulations for chemical transport, typically under cooled conditions to maintain quality. All shipments include proper labeling, safety documentation, and tracking, ensuring safe and efficient delivery to the destination.
    Storage Schizandrin B should be stored in a tightly sealed container, protected from light and moisture. Keep at 2-8°C (refrigerated), avoiding excessive heat and humidity. Store in a cool, dry, and well-ventilated area, away from incompatible substances. Proper storage helps maintain its stability and quality for laboratory or research use. Always follow local regulations and material safety guidelines.
    Application of Schizandrin B

    Applications of Schizandrin B in Industrial Manufacturing

    As a dedicated manufacturer, we supply Schizandrin B to verified industrial customers seeking consistent quality for use in regulated downstream sectors. The following sections outline precise applications and integration details across key industrial segments, including pharmaceutical development, nutraceuticals, functional food additives, cosmetics formulation, and veterinary supplements.

    1. Pharmaceutical Active Ingredient Manufacturing

    Schizandrin B serves as a purified intermediate or principal bioactive for the formulation of liver-protective drugs, neuroprotective agents, and anti-inflammatory tablets or injectables. Pharmaceutical groups source this raw material to achieve quality batch productions under tightly controlled GMP conditions. Chemists reference validated monographs for identity and purity throughout the synthetic and filling process. Analytical and stability testing confirms the achievement of precise content requirements according to registered product dossiers prior to final packaging.

    Industry compliance standards

    • China Pharmacopoeia (ChP) standards for Schisandrin compounds
    • ICH Q7 GMP for active pharmaceutical ingredients
    • European Pharmacopoeia (Ph. Eur.) quality monograph, Section 04/2015:1335
    • US FDA 21 CFR Part 210/211 for finished pharmaceuticals

    Typical usage ratio

    • 0.1% – 3% (w/w) in solid-dosage forms, adjusted based on pharmacokinetic and clinical safety data
    • Variable concentration in injectables or suspensions (typically 1–5 mg per dose unit according to dosage form specifications)

    Downstream process integration

    • Dissolution into solvents during active blending
    • Granulation alongside excipients for tablet press
    • Inclusion in final API crystallization and purification steps
    • Filtration and drying prior to primary packaging

    Final product types

    • Prescription tablet and capsule drugs for hepatic support
    • Sterile injectable solutions for neurological indications
    • Combination therapy finished dosage forms
    • Herbal extract-based pharmaceuticals for clinical use

    2. Nutraceuticals & Dietary Supplement Formulation

    Contract manufacturers incorporate Schizandrin B as a standardized extract or isolated compound in nutraceutical capsules, pills, and powders intended to support hepatic, cognitive, or antioxidant health. The formulation process strictly follows regional food supplement regulations and is aligned with batch-level traceability standards for herbal and botanical products. Dosing precision, ingredient authenticity, and regulated labeling requirements drive composition and ratio adjustment during scale-up and encapsulation.

    Industry compliance standards

    • US FDA 21 CFR Part 111 Dietary Supplement GMP
    • EFSA Food Supplements Directive (2002/46/EC)
    • China National Food Safety Standard for health foods (GB 16740-2014)
    • ISO 22000 Food Safety Management System

    Typical usage ratio

    • 50–200 mg per daily serving in capsules or tablets
    • Customized blends at 0.05–0.3% (w/w) for powdered health mixes, calibrated to meet local legislation and clinical study references

    Downstream process integration

    • Dry blending with other herbal extracts before milling
    • Direct inclusion in tablet or capsule fill and compression
    • Homogenization into stick packs or sachets for powder products
    • Cold-compounding with stabilizers during liquid supplement filling

    Final product types

    • Nutritional supplement capsules and softgel pills
    • Granular sachets and ready-to-drink functional powder blends
    • Botanical extract compacts and chewable tablets
    • Multi-ingredient powders for reconstitution

    3. Functional Food and Beverage Additive Manufacturing

    Specialty food manufacturers utilize Schizandrin B as an authorized botanical ingredient for antioxidant and liver-support claims in functional beverages, health teas, or fortified snack bars. The raw material receives per-batch QC release based on food safety and purity protocols prior to wet or dry blending with carrier matrices and flavor systems. Regulatory review of finished formulations ensures compliance with regional maximum residue levels and ingredient usage guidelines for novel food substances.

    Industry compliance standards

    • GB 2760-2014 Chinese National Standard for Food Additive Use
    • EC Regulation No 1333/2008 on food additives
    • Japan Food Sanitation Act and Health Food labeling guidances
    • US FDA GRAS (Generally Recognized as Safe) notice procedure for novel botanicals

    Typical usage ratio

    • 5–30 mg per serving in ready-to-drink beverages
    • 0.005%–0.05% (w/w) in baked or extruded food matrices, subject to local maximum authorization limits

    Downstream process integration

    • Suspension in aqueous phase of beverage blending systems
    • Premixing with maltodextrin or inulin carriers for powder premixes
    • Direct dosing into kneading/blending stage for cereal and bar production
    • Infusion into liquid extracts for functional tea concentrates

    Final product types

    • Functional herbal teas and botanical beverage concentrates
    • Fortified snack bars, granolas, and healthy biscuits
    • Personalized nutrition drink sticks and superfood mixes
    • Ready-to-drink liver-support tonics

    4. Cosmetics and Personal Care Formulation

    Industrial cosmetic formulators add Schizandrin B as an antioxidant and skin-conditioning agent in creams, lotions, anti-aging serums, scalp treatments, and facial masks. Its content and purity align with cosmetic regulatory frameworks for non-pharmaceutical applications. The integration method ensures homogeneous dispersion in emulsions or gels, with compliance documented through batch-level traceability records and validated in-vitro safety studies.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • China Cosmetics Supervision and Administration Regulation (CSAR)
    • Japan Ministry of Health, Labour and Welfare Standards for Cosmetics
    • ISO 22716:2007 Cosmetics GMP

    Typical usage ratio

    • 0.01%–0.1% (w/w) in antioxidant-focused creams or serums
    • 0.05–0.2% in rinse-off products and sheet masks for topical applications, adjusted for product type and dermatological test outcomes

    Downstream process integration

    • Solubilization into the aqueous or oil phase during emulsion manufacture
    • Post-emulsification addition for temperature-sensitive formulations
    • Direct mixing with botanical extracts prior to emulsification
    • Homogenization in the final cooling stage for viscous products

    Final product types

    • Anti-aging and skin-brightening creams
    • Hydrating serums and facial ampoules
    • Scalp and hair repair conditioners
    • Sensitive skin facial masks and sheet treatments

    5. Veterinary Herbal Feed Supplement Production

    Animal nutrition manufacturers formulate herbal feed additives containing Schizandrin B to support hepatic and antioxidant functions in livestock and companion animals. Compliance with veterinary ingredient sourcing and additive registration underpins downstream integration, with content standardized by analytical testing to achieve target levels in premix and final blend. Blending and pelletizing stages are designed to preserve the ingredient’s bioactivity through finished feed production while ensuring safety for long-term animal consumption.

    Industry compliance standards

    • China Feed Additive Regulations (GB/T 21351-2008 for plant extracts)
    • EU Register of Feed Additives (Regulation (EC) No 1831/2003)
    • US FDA AAFCO ingredient definition requirements
    • ISO 22000 for feed and feed ingredient quality management

    Typical usage ratio

    • 0.02%–0.10% (w/w) in premix for swine or poultry feed
    • 10–50 mg/kg in formulated veterinary supplements, adjusted to the target animal species and regional regulations

    Downstream process integration

    • Dry blending with vitamin and mineral premixes prior to pelletizing
    • Spray application onto feed pellets after extrusion
    • Direct addition during mash feed production for young animals
    • Incorporation in liquid feed supplements during homogenization

    Final product types

    • Pelleted and extruded animal feed for poultry and swine
    • Veterinary feed supplements packed as premixes
    • Liquid multivitamin blends containing plant actives
    • Herbal drench solutions for ruminants
    Free Quote

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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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