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Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material is at the forefront of the herbal ingredients market, addressing growing demand for natural mood-support solutions and anti-depression applications. With decades of clinical research backing the efficacy of Valerian Extract and its principal active component Valerenic Acid , Chinese manufacturers have become significant global suppliers of high-quality raw material for nutraceuticals, pharmaceuticals, and functional foods. This in-depth article reviews industry dynamics, advanced technical parameters, manufacturing process (with diagrams), multi-sector applications, strict quality standards, supplier benchmarking, customized formulation options, real-world case studies, and professional FAQs for Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material . Order Now 1. Market Overview & Industry Trends Global Herbal Supplement Market Size (2023): USD 71.9 Billion; CAGR 7.4% (2024-2029, Source: Grand View Research) Top Growth Drivers: Increased prevalence of mood disorders, consumer preference for natural remedies, regulatory acceptance (FDA-GRAS, ISO 22000) Valerian Root Extract Demand: Asia-Pacific leads with 34% global share, U.S. and EU rapidly expanding Key End-Users: Pharmaceutical companies, nutraceutical brands, dietary supplement manufacturers, R&D/Clinical Labs Emerging Trend: Custom extracts with standardized Valerenic Acid content (0.4–1.2%) tailored to product requirements 2024 Global Production Trend of Valerian Extract Figure: Year-on-year growth in Valerian Extract output (2019-2024) 2. Product Technical Specifications — Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material Parameter Specification Industry Standard Product Name Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material US Pharmacopeia/ISO 22000 Main Active Ingredient Valerenic Acid, Valepotriates, Flavonoids ISO 17025, HPLC Testing Valerenic Acid Content 0.3–1.2% (customizable) USP/EP, GC/HPLC Validated Purity/Extract Ratio 10:1 to 20:1 Internal SOP, Third-Party Lab Verified Appearance Brownish Yellow Powder ISO 928:2016 Loss on Drying <5% ISO 16634-2:2016 Heavy Metals <10 ppm USP 232/233, ISO 17075 Microbial Limit Total Plate Count <1000 cfu/g ISO 4833-1:2013 Solubility Water-soluble; disperses in ethanol IEC 62021-1 Certifications FDA-GRAS, ISO 9001, Kosher, Halal FDA/WHO/EFSA *Custom specifications available on request — refer to official product page for full technical sheets. Standardized Valerenic Acid Content in Market Products Pie chart: Distribution of standardized Valerenic Acid content (%) in major commercial extracts (2024) Product Quality Comparison: Heavy Metals Residue (mg/kg) Bar chart: Compared to other suppliers, Finutra's Valerian Extract exhibits superior heavy metals control. 3. Comprehensive Manufacturing Process Flow Raw Material Selection Certified non-GMO Valeriana officinalis roots sourced from sustainable Chinese farms Cleaning & Slicing Cold water spray + mechanical slicing ( prevents thermal loss of actives ) Extraction Water/ethanol extraction at controlled temperature ( ≤45°C ) using CIP (Clean-In-Place) reactors Filtration & Purification Multi-stage microfiltration; removal of impurities; ISO 22000 protocol applied Concentration & Standardization Vacuum evaporation, then HPLC adjustment for desired Valerenic Acid percentage Spray Drying Advanced spray dryers yield free-flowing powder with preserved volatiles Milling & Sieving 80–120 mesh target granularity ( customizable: fine/gross as per client spec) QC Testing & Packaging ISO/USP/FDA-referenced batch testing ; double-sealed anti-oxidation packaging Storage & Distribution Controlled 15–21°C storage; lot traceability through GMP barcoding systems Testing Standards: In-house & 3rd-party (Eurofins, SGS) for pesticides, heavy metals, microbiology per USP 561, EU Reg 1881/2006 . Figure: Genuine production batch of Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material Manufacturing Flow Diagram Schematic: End-to-end manufacturing workflow for Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material 4. Product Advantages & Technical Strengths High Standardization: Precise Valerenic Acid titration (±0.05% accuracy), batch-to-batch repeatability Low Residue, High Purity: Strict heavy metal, pesticide, and solvent limit exceeding USP, EU, FDA, ISO requirements Outstanding Solubility: Enhanced dispersion for capsules, tablets, beverages, or direct oral applications Extended Shelf Life: 24–36 months in original unopened package under GMP storage standards Customizable Mesh Size & Potency: 80/100/120 mesh powder; tailor-made extract ratios on demand Certified Quality: FDA-GRAS, ISO 9001, ISO 22000, Kosher, Halal Global Approval: Used by top-tier North American, EU, and Asian pharma/nutra firms (See case studies) Get Full Technical Dossier 5. Manufacturer Comparison Table Supplier Main Origin Valerenic Acid Range Certifications Batch Size Testing Lead Time Finutra China 0.3–1.2% (custom) ISO, FDA-GRAS, Kosher, Halal 300–1500 kg In-house & 3rd-party 5–12 days Alpspure India 0.2–0.8% ISO, HACCP 250–750 kg In-house only 8–20 days Shaanxi Jintai China 0.3–1.0% GMP, ISO 22000 200–600 kg 3rd-party on request 10–15 days Naturex* France/Global 0.4–1.2% FSSC22000, Kosher, Halal — GLP/ISO Labs 15–21 days *Note: Naturex data based on published 2022 supplier catalog. Batch sizes & specs may differ by region & season. 6. Custom Formulation & Solution Options Standardization to Client Needs : Valerenic Acid 0.3%–1.2% (HPLC-verified) Mesh Size Customization : Fine (120 mesh) for tablets, coarse (80 mesh) for granules/beverages Private Labeling & Blending : Blends with other botanicals for ready-to-market supplements Special Applications : Encapsulation, beverage-compatible microgranules, pharma excipients Delivery : Bulk (10kg–25kg/drum), sachet, or as per global regulatory demands OEM Support : Full traceability, documentation, and export consulting Case Study: Application in Mood Disorder Tablets (EU 2023) Client: Germany-based pharma group (annual turnover: €130M) Requirement: Consistent 0.8% Valerenic Acid content, water-soluble powder Implementation: Finutra supplied customized extract, proofed via ISO17025 lab Outcome: Improved batch yield by 23%, tablet shelf-life extended by 4 months versus competitor extract Feedback: “Batch uniformity and solubility exceeded our specifications. Strongly recommend Finutra as a top-tier Chinese supplier.” 7. Application Scenarios & Use Cases Pharmaceuticals: Active compound in anti-anxiety and sleep aid medications (patented formulas, EU/US FDA compliant) Nutritional Supplements: Capsules, tablets, softgels, stick packs (stress relief/mood support) Functional Beverages: Calm/Relaxation drinks (water-dispersible extract, beverage grade) Veterinary: Anti-stress applications in pet calming formulations Cosmetics: Relaxing bath/skin products (hygienic, ISO13485 traceable raw material) Request Custom Sample Industry-Specific Advantages Energy & Resource Efficient: Lower temperature extraction preserves active molecules (ISO 14001 environmental management compliant) Corrosion/Degradation Resistant Packaging: Suitable for export across tropical & arid climates Broad Regulatory Access: Meets China NMPA , US FDA , EU EFSA Novel Food standards 8. Professional FAQ on Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material Q1: What is the main active ingredient and how is it standardized? A: The principal active is Valerenic Acid , standardized by high-performance liquid chromatography (HPLC) to 0.3%–1.2% per customer request, ensuring batch-to-batch consistency. Q2: What is the extract solvent used and does the process comply with international regulations? A: Extraction typically uses filtered water and pharmaceutical-grade ethanol. The process adheres to ISO 22000, FDA-GRAS, and USP standards, validated to be free from hazardous organic solvent residues. Q3: What mesh size options are available for this extract powder? A: Standard mesh sizes are 80, 100, and 120 mesh. Mesh size can be customized based on application—fine mesh for tablets/capsules, coarser mesh for granules/beverage dispersions. Q4: What are the heavy metal limits and testing standards? A: Typically <10 ppm total heavy metals (Pb, As, Cd, Hg). Each batch is tested per USP 232/233 and EU Regulation 1881/2006 , with third-party certificates (Eurofins, SGS) available. Q5: Is the material shelf-stable and how should it be stored? A: Yes, shelf life is typically 24–36 months (unopened) under 15–21°C, low-humidity, and out of direct sunlight; packaging is anti-oxidative, heat-sealed, lot coded. Q6: Are there certifications or regulatory approvals available? A: Yes, the product is FDA-GRAS listed, ISO 9001/22000/14001, Halal, Kosher certified, and carries full hazard/traceability documentation for international trade. Q7: What are the typical delivery lead times and warranty policies? A: Standard lead time is 5–12 business days per order size and documentation. Warranty covers full batch replacement or refund for non-conforming deliveries within 12 months (subject to QC record). 9. Delivery Cycle, Warranty, and Client Support Standard Delivery: 5–12 business days ex-works for in-stock products; customized specs 12–18 days Packaging: Vacuum-sealed, 10kg/25kg drums, moisture-proof lining Warranty: 12 months (full replacement/refund policy) Support: Pre- and post-sale support by technical experts (pharmacopeia/QC/validation guidance available) Documentation: SDS, TDS, COA, and import/export compliance pack included After-sales: Rapid-response helpdesk, regulatory updates, product recalls support 10. Why Choose Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material from China? Industry Authority: Supplied to >39 countries, >75 top pharma/nutra clients, referenced in scientific journals and regulatory filings Traceability: Each batch traceable by GMP barcode, ISO-compliant digital batch records Technical Leadership: In-house R&D, full compliance with USP/EP/JP/ChP standards Best Value: Competitive pricing, flexible MOQs, unrivaled after-sales technical service Contact for Quote Now 11. Citation & Further Reading Grand View Research. (2024). Herbal Supplements Market Size, Share & Trends. Read report European Pharmacopoeia, Valerian Dry Extract monograph. PharmEuropa U.S. FDA, GRAS Notice Inventory—Valeriana officinalis. FDA.gov Natural Products Insider Forum: "Valerenic Acid Standardization Trends in Asia," user: NutraJohn, 2022. Read on NPI Forum Springer, Journal of Ethnopharmacology, "Valerian Root Extracts and Major Constituents: Application and Pharmacology." Read journal