|
- Brand:Knowlux
- Model:Bottle/Aluminum foil bag/Drum/Customized to your needs
- Purity:98%+
- Cas:501-36-0
- Createtime: 2026-11-03
- Updatetime: 2026-11-03
| useage | research reagent |
| deliveryInfo | |
| appearance | White to off-white or slightly yellowish powder |
| aliasen | |
| supplyCapacity | 10MT/Month |
| harbor | Hongkong, Shenzhen, Shanghai |
| Sample available | yes |
| minorder | 1KG |
| Molecular Formula | C14H12O3 |
Resveratrol 98% (CAS 501-36-0) — Product Description
Document scope: Bulk ingredient specification and compliance summary
Basis: Cross-referenced against GuideChem, ChemicalBook, Sigma-Aldrich, PubChem, Made-in-China, and Alibaba listings. Discrepancies corrected.
1. Product Identity
| Parameter | Verified Value |
|---|---|
| Product Name | Resveratrol (trans-Resveratrol) |
| CAS RN | 501-36-0 |
| Synonyms | 3,4′,5-Trihydroxy-trans-stilbene; (E)-5-[2-(4-Hydroxyphenyl)ethenyl]-1,3-benzenediol |
| Molecular Formula | C14H12O3 |
| Molecular Weight | 228.24 g/mol |
| EINECS / EC Number | 610-504-8 |
| HS Code | 2932.99.0090 (China export) |
| MDL / PubChem CID | MFCD00116297 / 445154 |
Isomer note: The 98% specification refers to trans-resveratrol. Cis-resveratrol may be present as a minor impurity or degradation product. Prolonged exposure to light and heat promotes trans-to-cis isomerization; specify isomer ratio on COA where relevant.
2. Key Quality Attributes
| Attribute | Specification (Commercial Standard) |
|---|---|
| Appearance | White to off-white or slightly yellowish powder |
| Assay (HPLC) | ≥98% (trans-resveratrol) |
| Identification | Confirmed by HPLC retention time and UV spectrum; IR and MS for reference standard grade |
| Melting Point | 253–255°C (some sources cite 256–257°C) |
| Solubility | Soluble in ethanol, methanol, acetone, chloroform; sparingly soluble in water (~0.03 g/L) |
| Stability | Sensitive to light, heat, and alkaline conditions (pH >10 causes color change to pink/red) |
| Storage | ?20°C recommended for analytical standards; 2–8°C for bulk material, protected from light and moisture |
| Shelf Life | 24 months under recommended storage |
3. Regulatory and Compliance Status
United States: Resveratrol is not FDA-approved as a drug for any indication. It is marketed as a dietary supplement ingredient subject to 21 CFR Part 111 cGMP. GRAS status has been claimed for certain resveratrol ingredients in specified food applications, but GRAS status is ingredient- and use-level-specific; buyers must verify the supplier's GRAS basis rather than assuming blanket coverage. Importers are subject to FSVP requirements.
European Union: Bulk material placed on the EU market at ≥1 tonne/year requires REACH registration (EC) No 1907/2006. Cosmetic use requires safety assessment and CPNP notification under (EC) No 1223/2009. No novel food authorization exists for resveratrol as a food ingredient in the EU; suppliers should clarify the intended regulatory pathway before shipment.
China: Domestic suppliers position material as food-grade, cosmetic-grade, or pharmaceutical intermediate. Export documentation should match the destination market's intended use category.
Safety data (SDS-referenced): Oral LD50 in mouse >10,000 mg/kg (OECD 423) and >15,000 mg/kg (OECD 401); not a skin irritant or sensitizer in animal studies; Ames test negative. These data support handling under standard industrial hygiene practices, not as a hazardous substance requiring special transport classification.
4. Functional and Biological Profile
Resveratrol is a non-flavonoid polyphenolic phytoalexin produced by plants in response to stress or infection. In preclinical research it has been reported to exhibit antioxidant, anti-inflammatory, and cardiovascular-related activities, with proposed mechanisms including SIRT1 pathway modulation and inhibition of COX-1. Epidemiological associations between resveratrol intake and reduced cardiovascular risk have been suggested, but causal relationships in humans remain unestablished.
Positioning note: Commercial descriptions must not claim therapeutic efficacy for any disease. The ingredient is sold as a bulk raw material for further formulation, not as a drug. Structure/function claims for dietary supplement use must comply with applicable FDA labeling requirements and avoid disease language.
5. Supply Chain and Packaging
| Element | Recommendation |
|---|---|
| Primary Packaging | Foil inner bag with desiccant; sealed within HDPE drum or fiber carton |
| Barrier Requirement | Light and moisture protection essential; consider amber or opaque packaging |
| Labelling | Product name, CAS, assay (trans-resveratrol), isomer ratio, botanical/fermentation origin, batch, storage conditions, retest date |
| Documentation Package | COA with HPLC chromatogram, SDS, origin statement, allergen/contaminant declarations |
| Typical Commercial Pack | 1 kg/bag or 25 kg/drum |
6. Purchasing Checklist
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Confirm botanical vs. fermentation origin and request source documentation.
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Request lot-specific HPLC chromatogram with integration data; verify trans-resveratrol content and cis-isomer level.
-
Confirm storage history from supplier; material stored at ambient temperature for extended periods may show isomerization or potency loss.
-
Request SDS and toxicological summary for handling and downstream regulatory submissions.
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Verify regulatory alignment with intended market (US dietary supplement, EU cosmetic, or research use).
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Check packaging light/moisture barrier and stability data supporting the stated shelf life in the proposed packaging configuration.






