In the dynamic nutraceutical and functional pharma ingredient markets, タンポポエキスパウダー フラボノイド 溶媒抽出 天然植物エキス has emerged as a high-performance botanical extract, offering exceptional bioactivity, purity, and multi-sectoral benefits. This comprehensive guide explores evolving industry trends, full manufacturing workflows, in-depth technical parameters, and real application cases, empowering you to make data-driven procurement and R&D decisions.
Industry Trends & Market Overview
The global タンポポエキスパウダー フラボノイド 溶媒抽出 天然植物エキス market has experienced double-digit growth across the pharmaceutical, nutraceutical, food, and personal care sectors. According to Grand View Research and Mordor Intelligence, botanical extracts featuring high-purity flavonoids show a CAGR of over 8% (2021–2027). The rise of clean label, plant-based, and preventative healthcare has fueled demand, while advanced solvent extraction techniques have raised quality, consistency, and safety benchmarks.
- 2023 global botanical extract market size: $6.8 Billion (projected $9.3B by 2027)
- Food & supplements: Largest application (45% market share)
- Main geographic drivers: North America, Europe, East Asia
Technical Parameters & Product Specifications
Below is a detailed summary table of タンポポエキスパウダー フラボノイド 溶媒抽出 天然植物エキス specifications according to leading manufacturers, featuring purity grades, main bioactive concentrations, solvent types, and compliance standards.
| Parameter | Specification | Industry Standard |
|---|---|---|
| 外観 | Light Brown to Brownish-yellow Fine Powder | QA Internal / ISO 9001:2015 |
| Main Bioactive Component | Flavonoids & Phenolic Compounds (≥8% by HPLC) | USP / EP |
| Solvent Used | Water & Ethanol (≥ 99% Residue-Free, Food Grade) | FDA GRAS / ISO 22000 |
| Total Ash | ≤6.0% | USP 281 |
| Moisture Content | ≤5.0% | ISO 6496 |
| Microbiology | Total Plate Count < 1,000 CFU/g, Negative for Pathogens | ISO 4833, ISO 16649-2 |
| Heavy Metals | Pb <2ppm; As <1ppm; Cd <1ppm; Hg <0.1ppm | USP 232 & 233 |
| Pesticide Residue | Complies with EU 396/2005 | GC/MS, LC/MS-MS validated |
| 粒子サイズ | Pharma-grade 80 mesh (≤180μm) | ANSI/ASQC Z1.4 |
| Shelf Life | 24 months in sealed packaging | Accelerated Stability: ICH Q1A |
| 認定資格 | ISO 9001, ISO 22000, HALAL, KOSHER, FDA-GMP | - |
Manufacturing Workflow: From Field to Final Powder
の タンポポエキスパウダー フラボノイド 溶媒抽出 天然植物エキス production process adopts a scientific approach to bioactive retention, safety, and traceability. Below is a stepwise diagrammatic explanation of each key stage:
Raw Dandelion Harvesting
Sustainable, residue-controlled fields; botanical species: Taraxacum officinale; traceable lots; strict sorting.
Pre-treatment & Drying
Washed, sliced, and air/spray-dried at <50°C to preserve thermolabile flavonoids.
Lab moisture/ash validation.
Lab moisture/ash validation.
溶媒抽出
Dynamic water-ethanol extraction under monitored temp. (50–65°C); advanced counter-current column system; optimized for maximal solubility.
Filtration & Concentration
Membrane ultrafiltration; vacuum concentration to remove excess solvent ensuring <0.05% residual ethanol; HPLC-test for actives.
Spray Drying & Milling
Controlled atomization; final powder milled to pharma 80 mesh; air-classifier separation; sieving and uniformity checks.
QC Inspection & Packing
Full spectrum microbial/heavy metal analysis (ISO 17025 lab); double-layer vacuum packaging with UV-opaque material; QC release.
Full Process Video Overview:
Video: Dandelion Extract Solvent Extraction Workflow – Finutra (YouTube)
Material, Manufacturing, and Quality Certification
- Origin: Non-GMO, food-grade Taraxacum officinale aerial parts & roots
- Manufacturing: Solvent (Hydroethanolic) extraction+advanced membrane ultrafiltration+GMP-controlled spray drying+pharma-grade milling
- Material Properties: Rich in flavonoids, chlorogenic acid, polyphenols; high water solubility; low odor; excellent dispersibility
- Quality Labs: On-site ISO 9001 & 17025 labs for HPLC, GC-MS, LC-MS/MS analytical verification
- Certifications: Full compliance with ISO 22000, FDA-GMP, HALAL, KOSHER, EU-pesticide & heavy metal standards
- Shelf Life: 2 years in vacuum, double barrier packaging
- Test Methods: HPLC, UV-Vis (for active compounds), Microbial, Heavy metal sets (ICP-MS)
Dandelion Extract Powder Technical Index Visualization
Technical levels: Average content from ISO and SGS-verified test reports (2023)
Global application breakdown by sector (2023, Source: Innova/Euromonitor)
Worldwide market growth (USD Million, 2018-2023, Source: Grand View Research)
Application Scenarios: Why Industry Leaders Choose Dandelion Extract Powder Flavonoids Solvent Extraction Natural Plant Extract
タンポポエキスパウダー フラボノイド 溶媒抽出 天然植物エキス delivers high bioavailability, powerful antioxidant properties, and customizable functional support for the following industries:
- Nutraceuticals: Integrative supplements, liver/kidney cleansers, immune boosters, women’s health formulas
- Pharmaceuticals: Hepatoprotective APIs, anti-inflammatory agents, diuretic and detox compounds (clinical studies: Liu et al., 2021—ref below)
- Food & Beverage: Functional beverages, wellness teas, bittering/stabilizer for healthy snacks
- Personal Care & Cosmetics: Antioxidant serums, anti-pollution creams, scalp & hair-support tonics
- Animal Healthcare: Veterinary supplements for liver and renal support in pets/ruminants
- Water Treatment/Chemical: Incorporation as green corrosion inhibitor (applied research: Wang et al., 2019—ref below)
Typical Application Case Study: Tier-1 Nutraceutical Brand
Client: A leading European health supplement group
Application: Detox and immune boosting capsule (30% of segment sales)
Customization: Bespoke 10% flavonoid grade, controlled for low bitterness, ISO 22000 and KOSHER batch certificates
Results:
Application: Detox and immune boosting capsule (30% of segment sales)
Customization: Bespoke 10% flavonoid grade, controlled for low bitterness, ISO 22000 and KOSHER batch certificates
Results:
- Product stability over 24 months (accelerated aging: per ICH Q1A)
- 99.7% pass rate on microbiology across 42 batches (2022-23, ISO 17025)
- Customer rating uplift: 4.9/5 based on >3,000 verified reviews (Trustpilot)
- Sales increase: +34% YoY after relaunch with upgraded extract
Competitive Manufacturer Comparison
| Vendor | Main Extraction Method | Flavonoid Purity (%) | Compliance Certifications | MOQ (kg) | Documentation | Shelf Life (months) |
|---|---|---|---|---|---|---|
| Finutra | Hydroethanolic Solvent, Countercurrent Extraction | 8–12 | ISO 22000, FDA-GMP, HALAL, KOSHER | 25 | Full (COA, MSDS, TDS, Allergen, Heavy Metal) | 24 |
| Herbaplant | Water Extraction - Conventional | 5–7 | HALAL, ISO 9001 | 50 | COA, MSDS (partial) | 18 |
| GreenPhyt Labs | Hydroalcoholic (Batch) Extraction | 7–9 | ISO 9001, KOSHER, Organic | 20 | COA Only | 18 |
| BioSolutio | Supercritical CO2 | 3–4 | ISO 9001, EcoCert | 5 | COA, TDS (on request) | 12 |
Customization & Formulation Support
- Flavonoid Content Customization: 8–12% or higher on request—achievable through dual-extraction and fractionation
- Particle Size Options: Standard 80 mesh (≤180μm), customizable to fine 200 mesh for RTD beverage solubility
- Carrier-free Option: Pure powder, or maltodextrin carrier for better compression
- Functional Blends: Pre-mixed with Vitamin C, prebiotics, or specific herbal actives
- Batch-specific Documentation: Full COA, TDS, MSDS, heavy metal/pesticide clearance, allergen statement, GMO-free etc.
- Regulatory Support: Compliance with FDA/EFSA/CFDA novel food dossiers
Lead time: 5–10 working days (standard batches); 14–18 days (customized grades/formulations)
Packaging: 1kg/5kg/20kg vacuum drum, with light/UV barrier, humidity indicator & tamper-evident seal
FAQ: Key Technical Questions
Q1: What is the optimal solvent for extracting flavonoids from dandelion powder?
A1: A hydroethanolic blend (typically 60–80% ethanol in water) is optimal for maximal flavonoid and phenolic extraction, balancing polarity and safety for food/pharma applications. This also enables efficient residue removal to meet EU FSA and FDA standards.
Q2: What mesh size is recommended for beverage applications?
A2: For instant or ready-to-drink applications, a finer particle size (120–200 mesh, ≤75μm) is preferred for rapid dispersion. Standard grade is 80 mesh (≤180μm) as per ANSI/ASQC Z1.4.
Q3: What are the key certifications for international export?
A3: Essential certifications include ISO 9001 (Quality Management), ISO 22000 (Food Safety), FDA-GMP, HALAL/KOSHER, and batch-specific allergen/GM statements. EU/JP market often requires pesticide clearance per EU 396/2005.
Q4: How is batch potency and consistency ensured?
A4: All lots are analyzed via HPLC (High Performance Liquid Chromatography) for total flavonoid & phenolic content, while moisture, ash, and contaminants are checked against ISO 17025-accredited lab reference methods and stability tested under ICH Q1A protocols.
Q5: What’s the typical shelf life and preferred storage conditions?
A5: Shelf life is 24 months when stored at 10–25°C, humidity <50%RH, in unopened vacuum-sealed, UV-opaque packaging. Accelerated aging is validated as per ICH Q1A, ensuring extended potency and safety.
Q6: Which test standards are used for heavy metals and pesticide residue?
A6: ICP-MS analysis is performed per USP 232/233 そして GB 5009.268. Pesticides are tested by GC/MS & LC/MS-MS as required by EU 396/2005 and local regulations.
Q7: Is your product compliant with vegan and allergen-free formulation?
A7: Yes. All タンポポエキスパウダー フラボノイド 溶媒抽出 天然植物エキス is vegan, non-GMO, gluten-free and made without the 14 major EU-listed allergens. Verified by SGS allergen screening.
Delivery Schedule, Warranty & Customer Support
- Standard Lead Time: Immediately from stock (≤25kg) or 7–12 days for manufacturer-certified custom lots
- Warranty: 24 months shelf-life guarantee for unopened original packaging; replacement or refund if not meeting COA specs
- After-sales Support: 24/7 technical/email support, dedicated account manager, lab analysis support, regulatory documentation within 48hr
- Sample Policy: Free 20–50g samples on request (via DHL/Fedex); full batch COA/MSDS provided
- Quality Complaint Rate (2023): Only 0.18% per ISO 10002 report
Authoritativeness & Industry References
- Certifications: Full ISO 9001 / 22000 certifications (verifiable); HALAL & KOSHER certified production; FDA-registered site (DUNS # info on request)
- Accreditation: All lots tested by CNAS/ISO 17025 and/or SGS laboratory partners
- Partnerships: Confirmed raw material and compliance supply to leading EU, US, and Asian supplement and pharma companies (non-disclosure covered)
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Published Research:
- Liu, X et al (2021): Experimental validation of hepatoprotective and anti-inflammatory effects of dandelion extract flavonoids (Journal of Ethnopharmacology) – read the study
- Wang T et al (2019): Application of plant polyphenols, including dandelion extract, as green corrosion inhibitors (Materials Today: Proceedings) – journal link
- Industry Forum: Discussion on raw material quality trends: ISHS Botanical Standards Forum
Further Reading:
- "Global Trends & Challenges in Botanical Extracts Market" (Nutraceutical Business Review, 2023)
- "Advances in Phytochemical Extraction for Functional Applications" (ScienceDirect, 2022)
- "Comparative Bioactivity and Quality of Commercial Dandelion Extracts" (Journal of the Science of Food and Agriculture, 2023).
- "Global Trends & Challenges in Botanical Extracts Market" (Nutraceutical Business Review, 2023)
- "Advances in Phytochemical Extraction for Functional Applications" (ScienceDirect, 2022)
- "Comparative Bioactivity and Quality of Commercial Dandelion Extracts" (Journal of the Science of Food and Agriculture, 2023).
Post time:8月 - 02 - 2025
