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Cnidium Officinale Rhizome Extract

    • Product Name Cnidium Officinale Rhizome Extract
    • Alias Cnidium Officinale Extract
    • Einecs 931-321-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    389378

    botanical_name Cnidium officinale
    common_name Cnidium Officinale Rhizome Extract
    plant_part_used rhizome
    extraction_method solvent extraction
    main_active_components phthalides, ferulic acid
    appearance brownish powder
    solubility partially soluble in water
    odor aromatic, characteristic herbaceous scent
    storage_conditions cool, dry place away from direct sunlight
    typical_usage cosmetics, traditional medicine
    country_of_origin China
    cas_number 93384-43-1
    shelf_life 2 years when properly stored
    allergen_status generally non-allergenic
    preservatives_used none typically added

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

    Packing & Storage
    Packing White plastic container with a green label, labeled 'Cnidium Officinale Rhizome Extract,' 500g net weight, resealable lid, safety seal.
    Shipping Cnidium Officinale Rhizome Extract is securely packaged in airtight, moisture-proof containers to ensure product integrity during transit. The shipment is clearly labeled and follows international hazardous materials guidelines, if applicable. Express and standard shipping options are available, with tracking and temperature control provided upon request to maintain extract quality.
    Storage Cnidium Officinale Rhizome Extract should be stored in a cool, dry, and well-ventilated place, away from direct sunlight and moisture. Keep the container tightly sealed to prevent contamination and degradation. Avoid exposure to heat, and store at room temperature or as specified by the manufacturer. Ensure the extract is kept out of reach of children and incompatible substances.
    Application of Cnidium Officinale Rhizome Extract

    Applications of Cnidium Officinale Rhizome Extract in Industrial Manufacturing

    As a direct manufacturer, we supply Cnidium Officinale Rhizome Extract to specialized industrial clients across regulated sectors. The botanical extract supports precision formulation, process integration, and strict compliance in downstream applications where detailed quality and consistency are critical.

    1. Pharmaceutical Ingredient for Herbal Medications

    Pharmaceutical companies incorporate this botanical extract as an active ingredient in traditional herbal preparations targeting specific health indications. Manufacturers must verify batch-to-batch consistency through rigorous testing, as the extract's active compounds—such as ligustilide and ferulic acid—require standardized concentration within tablet, capsule, or decoction forms. Processing begins with dissolution and filtration of the extract in controlled environments, followed by blending with excipients and granulation. The extract undergoes final QC assays to validate compliance before packaging and GMP-certified release to market.

    Industry compliance standards

    • Chinese Pharmacopoeia (ChP)
    • WHO Good Manufacturing Practice (GMP) for Herbal Medicines
    • European Pharmacopoeia (Ph. Eur.) where applicable
    • ISO 17025-certified test methods for botanical identity and contaminants

    Typical usage ratio

    • 1%–8% w/w in tablet or capsule blends, based on desired active content and formulation target
    • Ratio adjusted according to monograph-prescribed dosage and extraction purity

    Downstream process integration

    • Extract is solubilized and filtered at the initial mixing step
    • Blended with starch or lactose carriers at the granulation phase
    • Enters tableting or encapsulation lines prior to final QC
    • Active content verified in finished product stability studies

    Final product types

    • Herbal tablets and capsules
    • Traditional Chinese medicine (TCM) decoction granules
    • Standardized phytopharmaceuticals for pain relief or gynecological health
    • Prescribed compounded herbal blends

    2. Functional Food and Nutraceutical Formulation

    Food manufacturers apply this extract in the development of functional foods and nutraceuticals aimed at consumer health markets demanding precise botanical origin and evidenced safety data. Utilization requires HPLC fingerprinting for active content conformance and certified absence of pesticides or heavy metals. The ingredient is homogeneously incorporated into various dosage forms, such as instant drink powders or nutritional gummies, during the pre-mixing step, where it supports label claims for botanicals. Extensive shelf-life and interaction studies validate product integrity through the distribution cycle.

    Industry compliance standards

    • GB 2760-2022 (China National Food Safety Standard – Food Additive Use)
    • FDA 21 CFR 111 (US dietary supplement GMP)
    • Novel Food Registration (EU) where required
    • ISO 22000 food safety management system

    Typical usage ratio

    • 0.2%–1.5% w/w in powder or bar formulations
    • Dosage based on permitted daily intake from safety dossiers and functional ingredient claims

    Downstream process integration

    • Incorporated at batch pre-blending, prior to carrier addition
    • Subjected to homogenization to ensure uniform active distribution
    • Extract stability confirmed in finished matrix via accelerated testing
    • Final product labeling references botanical standardization

    Final product types

    • Functional snack bars
    • Herbal instant beverage powders
    • Chewable gummies with botanical claims
    • Food supplements in sachet or stick-pack forms

    3. Topical Personal Care and Cosmetic Production

    Cosmetic manufacturers utilize the extract for high-value personal care ranges, formulating products such as skin creams and serums targeting soothing, antioxidant effects. Regulatory approvals require documented safety under the Cosmetic Ingredient Review and consistent batch analytical profiles. During emulsion preparation, the extract is solubilized in the aqueous phase at controlled temperatures, followed by integration with stabilizers and actives under vacuum homogenization. Product stability and absence of allergenic compounds are confirmed with microbatch release criteria set by international cosmetic standards.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • Cosmetic Ingredient Review (CIR) safety assessments
    • China Standards for Cosmetic Ingredient Safety (GB 7916)
    • ISO 22716 Cosmetic GMP

    Typical usage ratio

    • 0.5%–2% w/w in cream, lotion, or serum formulations
    • Optimized based on dermal toxicity, activity data, and performance testing

    Downstream process integration

    • Dissolved in deionized water during aqueous phase charging
    • Input after thickener addition to prevent precipitation
    • Vacuum homogenization achieves fine dispersion within the emulsion system
    • Batch stability and microbiological testing ensure compliance prior to filling

    Final product types

    • Botanical facial creams and hydrating gels
    • Herbal repair serums for sensitive skin
    • Body lotions with antioxidant activity claims
    • Premium bath and body treatment emulsions

    4. Veterinary Herbal Feed Additive Manufacturing

    Animal nutrition producers incorporate the extract in herbal feed additives intended to support livestock metabolic health, reduce stress, or support reproductive functions. The input must meet animal feed purity standards and exhibit consistent marker content, typically verified through HPLC or GC analysis. Mixing operations introduce the ingredient post-milling to minimize thermal degradation, and pelleting processes maintain controlled residence time for bioactive preservation. Finished feeds undergo sampling for botanical content, mycotoxin residues, and declared activity claims before bulk distribution.

    Industry compliance standards

    • FAMI-QS Code (Feed Additive and Premixtures Quality System)
    • Regulation (EC) No 1831/2003 for feed additives
    • AAFCO (US Association of American Feed Control Officials) definition and labeling standards
    • GB 13078 Safety Standard of Feed Additives (China)

    Typical usage ratio

    • 0.05%–0.3% w/w in complete feed formulations
    • Ratio adjusted based on species-specific trials and tolerance studies

    Downstream process integration

    • Added after cooling phase or prior to micro-ingredient blending
    • Ensured uniform distribution via paddle or ribbon mixers
    • Inclusion checked by NIR or rapid HPLC screening at QA checkpoints
    • Declared on feed labels as per local regulatory requirements

    Final product types

    • Herbal mineral premixes
    • Livestock concentrate feeds with botanical supports
    • Complementary animal supplement powders or blocks
    • Specialty veterinary additive blends for ruminants, swine, or poultry

    5. Natural Agrochemical Intermediate for Plant Growth Regulators

    Agrochemical formulators include this botanical extract as a natural agent in plant growth regulator blends or foliar formulations. The material must comply with agrochemical ingredient registration standards, and residue trials verify that its addition will not compromise crop safety. During batch production, the extract is solubilized prior to admixture with carrier solvents and co-formulants, controlling pH and ionic balance to ensure uniformity and stability in spraying solutions. Analytical methods evaluate degradation under UV and field exposure to assure performance and regulatory compliance in target crop applications.

    Industry compliance standards

    • FAO/WHO specifications for plant protection products
    • OECD guidelines for pesticide residue studies
    • China MARA (Ministry of Agriculture and Rural Affairs) Registration Requirements for Plant Growth Regulators
    • ISO 9001 Quality Management System in agrochemical production

    Typical usage ratio

    • 0.1%–1% w/w in foliar spray or seed treatment formulations
    • Input level determined by greenhouse and field performance evaluations

    Downstream process integration

    • Solubilized under agitation in aqueous or microemulsion concentrates
    • pH adjusted and compatibility checked with co-formulants
    • Emulsified and filtered before packaging into commercial spray products
    • Final blend stability and efficacy checked in simulated environmental trials

    Final product types

    • Natural PGR (plant growth regulator) sprays
    • Seed-coating solutions for enhanced seedling vigor
    • Integrated crop health formulations with botanical actives
    • Foliar application emulsions for fruits, vegetables, and ornamental crops
    Free Quote

    Competitive Cnidium Officinale Rhizome Extract prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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