バレリアンエキス バレレン酸 ハーブエキス 抗うつ薬 中国原料
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 バレリアンエキス バレレン酸 ハーブエキス 抗うつ薬 中国原料.
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
2. Product Technical Specifications — バレリアンエキス バレレン酸 ハーブエキス 抗うつ薬 中国原料
| Parameter | Specification | Industry Standard |
|---|---|---|
| Product Name | バレリアンエキス バレレン酸 ハーブエキス 抗うつ薬 中国原料 | 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 |
| 外観 | 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 |
| 認定資格 | FDA-GRAS, ISO 9001, Kosher, Halal | FDA/WHO/EFSA |
Standardized Valerenic Acid Content in Market Products
Product Quality Comparison: Heavy Metals Residue (mg/kg)
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
Manufacturing Flow Diagram
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)
5. Manufacturer Comparison Table
| Supplier | Main Origin | Valerenic Acid Range | 認定資格 | Batch Size | Testing | Lead Time |
|---|---|---|---|---|---|---|
| Finutra | 中国 | 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 | 中国 | 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 |
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)
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 バレリアンエキス バレレン酸 ハーブエキス 抗うつ薬 中国原料
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 そして 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 バレリアンエキス バレレン酸 ハーブエキス 抗うつ薬 中国原料 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
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
Post time:8月 - 01 - 2025
