Resveratrol Powder | Polygonum Cuspidatum Extract Manufacturer

Polyphenol Ingredient

Resveratrol Powder | Polygonum Cuspidatum Extract Manufacturer

Resveratrol powder made from Polygonum cuspidatum root extract for dietary supplement formulations, with a defined extraction profile and analytical specification for ingredient evaluation.

Resveratrol Powder Image
Resveratrol powder from Polygonum cuspidatum root extract

Product Information

Resveratrol Powder at a Glance

Core chemical identity and botanical source information.

Nº CAS 501-36-0
Fórmula molecular C14H12O3
Peso molecular 228,24 g/mol
Plant Part Root
Fuente botánica Polygonum cuspidatum Sieb. Et Zucc.

Source & Extraction

Polygonum cuspidatum Root Extract

The ingredient is a defined root extract with a 100:1 extraction ratio and no carrier or excipient listed in the product specification.

Fuente botánica

The plant material is the root of Polygonum cuspidatum Sieb. Et Zucc., giving the ingredient a clearly defined botanical identity and plant part.

Extraction Profile

The extraction ratio is 100:1. The listed solvent system uses ethyl acetate, ethanol and water.

Especificaciones técnicas

Resveratrol Powder Specification

Analytical requirements covering active content, identity, physical characteristics, contaminants and microbiological quality.

Test Item Método Especificación Result
Active Content & Identity
Resveratrol HPLC ≥98.00% 99.23%
Emodin HPLC ≤1.0% ≤0.1%
Identificación TLC Specified by method Complies
δ13C GB/T 18932.1-2002 -30.0 to -32.0‰ -31.20‰
Propiedades físicas
Apariencia Visual Off white to white powder with bitter odour and taste Complies
Olor y sabor Visual & taste Característica Característica
Pérdida por secado GB/T 5009.3 ≤1.0% 0.12%
Sulphated Ash GB/T 5009.4 ≤0.5% 0.21%
Densidad aparente USP <616> 35.0–50.0 g/100 ml 46.1 g/100 ml
Tamaño de las partículas USP <786> 100% hasta malla 80 100% Complies
Solvent & Contaminant Controls
Ethyl Acetate USP <34> ≤10 ppm <10 ppm
Metales pesados GB/T 5009.74 ≤10 ppm <10 ppm
Pesticide Residues USP <561> Meet USP requirements Cumple con
Arsénico GB/T 5009.11 ≤2 ppm <2 ppm
Mercurio GB/T 5009.17 ≤0.1 ppm <0,1 ppm
Cadmio GB/T 5009.15 ≤1 ppm <1 ppm
Plomo GB/T 5009.12 ≤3 ppm <3 ppm
Microbiological Testing
Total Plate Count GB/T 4789.2 ≤1,000 cfu/g Complies
Yeasts & Molds GB/T 4789.15 ≤100 cfu/g Complies
E. coli GB/T 4789.3 Negativo Negativo
Salmonella GB/T 4789.4 Negativo Negativo
Staphylococcus GB/T 4789.10 Negativo Negativo

Quality & Formulation

Key Considerations for Resveratrol Powder

Source, composition and physical properties all affect how a resveratrol extract is evaluated for a finished formulation.

Composición

Active content and Emodin are measured separately, providing a clearer composition profile than a single assay value alone.

Powder Characteristics

Particle size, density, moisture and appearance are useful when assessing powder handling, blending and processing requirements.

Contaminant Controls

Residual solvent, pesticide residues, heavy metals and microbiological limits are part of the ingredient quality profile.

Application Areas

Resveratrol Powder Applications

This botanical powder can be evaluated in dry dietary supplement formats according to the needs of the finished product.

Cápsulas

A practical format where serving size, powder handling and ingredient compatibility are established during formulation.

Tabletas

Can be evaluated when blending, processing and excipient compatibility fit the tablet manufacturing process.

Mezclas en polvo

Suitable for review in dry blends and premixes where uniformity, flow, taste and moisture management matter.

Bolsitas y sobres adhesivos

Development should consider powder dispersion, taste, flow and moisture control through filling and packaging.

Gummies & Chewables

Formulation work should consider the ingredient's characteristic bitter taste and compatibility with the finished matrix.

Custom Supplement Formulas

The ingredient can be assessed against a defined specification for customized dietary supplement products.

Formulation Review

Selecting a Resveratrol Extract

A suitable grade should match the intended application, source requirements and analytical specification.

What to Review

Different resveratrol products may vary in botanical source, assay, impurity profile and physical behavior. Reviewing these points early helps align the ingredient with the finished product.

Fuente Confirm the botanical name and plant part when source-specific formulation or labeling requirements apply.
Analytical Profile Review active content, related compounds, solvent residue, contaminants and microbiological limits.
Powder Handling Consider particle size, density, flow and moisture behavior when matching the ingredient to production equipment.
Finished Formula Evaluate taste, dispersion, pH, processing conditions and stability in the actual formulation.

Specification Support

Product information can be reviewed against the ingredient requirements before sample evaluation and formulation testing.

Documentación

Resveratrol Product Documentation

Documentation supports product specification review, formulation assessment and purchasing decisions.

Certificate of Analysis

Analytical data covers composition, physical properties, contaminants and microbiological quality.

Source Information

Product information defines the botanical material, plant part, extraction ratio, solvent system and carrier status.

Métodos de ensayo

The specification uses HPLC, TLC, USP procedures and applicable GB/T methods for product evaluation.

Embalaje

25 KG / Drum

The product is packed in a drum with double plastic bags inside for storage and handling.

25 KG / Drum

Almacenamiento

Cool, Dry & Protected

  • Store in a cool and dry place.
  • Keep away from direct light and heat.
  • Do not freeze.
Resveratrol Ingredient Inquiry

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Share your required quantity, specification, application and destination so the appropriate product information can be reviewed for your project.

Especificación COA Embalaje Presupuesto

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