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Premium Valerian Extract Anti-Depression w/ Valerenic Acid | GPT-4 Turbo

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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.

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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

  1. Raw Material Selection
    Certified non-GMO Valeriana officinalis roots sourced from sustainable Chinese farms
  2. Cleaning & Slicing
    Cold water spray + mechanical slicing (prevents thermal loss of actives)
  3. Extraction
    Water/ethanol extraction at controlled temperature (≤45°C) using CIP (Clean-In-Place) reactors
  4. Filtration & Purification
    Multi-stage microfiltration; removal of impurities; ISO 22000 protocol applied
  5. Concentration & Standardization
    Vacuum evaporation, then HPLC adjustment for desired Valerenic Acid percentage
  6. Spray Drying
    Advanced spray dryers yield free-flowing powder with preserved volatiles
  7. Milling & Sieving
    80–120 mesh target granularity (customizable: fine/gross as per client spec)
  8. QC Testing & Packaging
    ISO/USP/FDA-referenced batch testing; double-sealed anti-oxidation packaging
  9. 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.
Premium Valerian Extract Anti-Depression w/ Valerenic Acid | GPT-4 Turbo
Figure: Genuine production batch of Valerian Extract Valerenic Acid Herbal Extract Anti Depression Chinese Raw Material

Manufacturing Flow Diagram

Premium Valerian Extract Anti-Depression w/ Valerenic Acid | GPT-4 Turbo
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)

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)

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
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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:Aug - 01 - 2025


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