Choosing Dandelion Extract Powder Flavonoids Solvent Extraction Natural Plant Extract: Application Fit and Specification Checks

What Is Dandelion Extract Powder Flavonoids Solvent Extraction Natural Plant Extract?

Dandelion Extract Powder Flavonoids Solvent Extraction Natural Plant Extract is derived from Taraxacum mongolicum (Hand.-Mazz.), a botanical with a long history in traditional Chinese medicine. The extract is produced using a water and ethanol solvent system that concentrates the plant's active flavonoid compounds into a standardized, fine brown powder. Hebei Finutra Biotech Co., Ltd. supplies this ingredient to buyers in the nutraceutical, functional food, beverage, feed, and cosmeceutical sectors.

Because the source herb is rich in minerals—including calcium, potassium, magnesium, and phosphorus—and contains meaningful levels of carbohydrates and proteins, the extract carries a diverse nutritional profile in addition to its flavonoid content.

Key Specifications at a Glance

Before making a sourcing decision, buyers should confirm that the product's documented specification sheet aligns with their formulation requirements. The following parameters are drawn directly from the confirmed product data for this extract:

Additional product attributes: Non-GMO, BSE/TSE Free, Non-Irradiation, and Allergen Free.

Selection Criteria: What to Verify Before You Buy

1. Flavonoid Assay Level and Analytical Method

The confirmed specification for this product sets the flavonoid content at 5.0%, measured by UV spectrophotometry. When comparing multiple dandelion extracts, buyers should check:

• Whether the stated flavonoid percentage is measured on a dry basis or as-is basis.
• Which UV reference standard is used for calibration, since different reference compounds yield different numerical results.
• Whether your downstream formulation requires a higher standardized potency (e.g., 10% or 20%) or whether 5.0% meets your label claim and dose requirements.

Buyers targeting dietary supplement labels or functional food products with specific active compound claims should verify that the 5.0% UV-assayed value is compatible with their desired finished-product specification before ordering.

2. Extraction Solvent Compatibility

This extract uses a water and ethanol solvent system. This is relevant in several ways:

• Regulatory acceptance: Water/ethanol extraction is broadly accepted in supplement and food ingredient regulations in the US, EU, and most export markets, but buyers should verify applicable local requirements independently.
• Solubility in final formulations: Water/ethanol-extracted powders typically disperse well in water-based systems. Buyers formulating in oil-based or anhydrous systems should conduct compatibility testing.
• Residual solvent levels: Buyers in regulated markets should request a Certificate of Analysis (CoA) that includes residual ethanol data if their regulatory framework requires it.

3. Heavy Metal and Microbiological Compliance

For nutraceutical and food-grade applications, heavy metal and microbial limits are primary quality gatekeeping criteria. The confirmed specification shows:

• Total heavy metals ≤ 10 ppm, with individual limits for Pb (≤ 3 ppm), As (≤ 2 ppm), Cd (≤ 1 ppm), and Hg (≤ 1 ppm), all measured by AAS.
• Microbiological limits aligned with USP standards, including negative results for E. coli and Salmonella.

Buyers should compare these limits against the regulatory thresholds applicable in their target market (e.g., FDA dietary supplement guidelines, EU food safety regulations, or SFDA requirements). If your finished product's specification requires tighter heavy metal limits, confirm with the supplier whether tighter-spec batches are available.

4. Physical Form and Particle Size for Processing

The product is a brown fine powder with 95% passing through an 80-mesh sieve. This is relevant for:

• Capsule filling: 80-mesh powder generally flows adequately for standard capsule filling equipment.
• Tablet compression: Compressibility should be tested, as particle morphology, moisture level, and ash content all influence tablet hardness and disintegration.
• Beverage or stick pack applications: 80-mesh may still produce visible particles in clear liquid formats; buyers may require further micronization.
• Cosmeceutical blending: Uniformity and color consistency (brown) should be evaluated against finished product aesthetics.

5. Allergen, GMO, and Irradiation Status

The confirmed product is declared Non-GMO, BSE/TSE Free, Non-Irradiation, and Allergen Free. These declarations are relevant for:

• Clean-label supplement and food products targeted at consumers with allergen sensitivities.
• Markets requiring Non-GMO project verification or equivalent documentation—buyers should request supporting documentation rather than relying on product labels alone.
• Export markets with specific irradiation restrictions.

Application Fit: Where This Extract Is Appropriate

The combination of a water/ethanol solvent system, standardized flavonoid content, and nutritional mineral profile makes Dandelion Extract Powder Flavonoids Solvent Extraction Natural Plant Extract suitable for consideration in the following contexts:

Dietary Supplements Capsules, tablets, and softgels targeting digestive support, antioxidant blends, or traditional herbal formulations. The 5.0% flavonoid assay provides a defined active marker for product specification and label development.

Functional Food and Beverage Tea blends, health drinks, or food fortification where botanical extracts from traditional medicinal plants are positioned as functional ingredients. Buyers should consider taste and color impact.

Cosmeceutical Formulations Skin care and topical products that incorporate botanical antioxidants. The fine particle size facilitates blending, although solubility and stability in specific formulation bases should be tested.

Animal Feed and Aquaculture Herbal feed additives for livestock or aquaculture where plant-based bioactive ingredients are incorporated. The extract's mineral content and biological activity data (see antibacterial findings below) may be relevant to product positioning.

Supporting Scientific Context from Product Documentation

The product description references published research on Taraxacum mongolicum, noting that:

• Nutritional analysis showed moisture, carbohydrate, and protein as the primary nutrient fractions.
• Mineral elements—calcium, potassium, magnesium, and phosphorus—accounted for over 6.0% of total mineral content.
• Antibacterial activity was observed only in ethanol extracts, not aqueous extracts. The tested bacteria included Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa.

These findings support the use of ethanol-based extraction for applications where biological activity is a selection parameter. Buyers should note that this cited research pertains to the botanical species and its extracts generally; it does not constitute a health claim for any finished product. All applicable regulatory requirements for health claims must be assessed independently.

Procurement and Storage Considerations

• Pack size: Standard packing is 25 kg per drum. Buyers requiring smaller trial quantities should confirm availability with Hebei Finutra Biotech Co., Ltd. directly.
• Shelf life: Two years from manufacture date, under proper storage conditions.
• Storage requirements: Store in a cool, dry location away from direct sunlight to preserve flavonoid potency and prevent moisture uptake above the ≤ 5% loss-on-drying limit.
• Batch documentation: Request a batch-specific Certificate of Analysis covering all tabled parameters before acceptance.

When This Product May Not Be the Right Fit

This extract may not suit your requirements if:

• Your formulation requires a higher flavonoid concentration than 5.0% to meet label or efficacy targets.
• Your process requires a different particle size (finer than 80 mesh) for dissolution or aesthetic uniformity.
• Your regulatory framework imposes tighter heavy metal limits than those in the specification table.
• You need a water-only extraction (solvent-free ethanol residue) for a specific certification pathway.
• Your downstream process requires oil-soluble or liposomal delivery forms.

In any of these cases, communicate your specific requirements to Hebei Finutra Biotech Co., Ltd. to determine whether a customized specification or alternative product can be supplied.

Summary

Dandelion Extract Powder Flavonoids Solvent Extraction Natural Plant Extract from Hebei Finutra Biotech Co., Ltd. is a standardized botanical ingredient built around a 5.0% UV-assayed flavonoid specification, water/ethanol extraction, and confirmed Non-GMO, BSE/TSE Free, Non-Irradiation, and Allergen Free status. The specification table provides a clear starting point for procurement teams to verify compliance against their own application and regulatory requirements. Buyers should request a current Certificate of Analysis, confirm residual solvent data as required, and evaluate the product's particle size and color characteristics against their specific formulation needs before finalizing an order.