Urolithin A Manufacturer & Bulk Urolithin A Powder Supplier
Gensei cung cấp Urolithin A, còn được gọi là Uro-A, Bột Urolithin A, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one hoặc 3,8-Dihydroxy-6H-dibenzopyran-6-on, for dietary supplement capsules, tablets, gummies, sachets, drink powders, sports nutrition blends, healthy aging formulas and custom premix manufacturing. We support supplement brands and contract manufacturers with bulk supply, HPLC purity review, COA, specification review, sample coordination and global sourcing support.
Điểm nổi bật của sản phẩm
- Bulk Urolithin A raw material for dietary supplement and specialty active ingredient manufacturing
- Commonly supplied as off-white, beige or light yellow powder depending on grade and batch
- HPLC purity, identity, appearance, loss on drying and impurity profile can be reviewed according to specification and batch COA
- Suitable for capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and custom supplement premixes
- COA, bảng thông số kỹ thuật, SDS, TDS, tuyên bố về chất gây dị ứng, tuyên bố không chứa GMO và sơ đồ quy trình có sẵn cho các khách hàng đủ điều kiện
- Residual solvents, heavy metals, microbiology, solubility, particle size, stability and packaging should be reviewed before bulk purchase
- Tập trung vào việc tìm nguồn cung ứng nguyên liệu thực phẩm chức năng, không dành cho mục đích y tế, dược phẩm hay điều trị
What Is Urolithin A?
Urolithin A is a postbiotic metabolite associated with ellagitannin metabolism and is now sourced as a specialty powder ingredient for supplement manufacturing.
Urolithin A is a defined small-molecule ingredient also known as Uro-A or 3,8-Dihydroxybenzo[c]chromen-6-one. Although Urolithin A can be produced in the body from ellagitannin-rich foods depending on gut microbiota, bulk supplement-grade Urolithin A is typically evaluated as a purified ingredient with defined identity, assay and impurity controls. In B2B supplement sourcing, buyers usually evaluate Urolithin A by CAS number, chemical name, HPLC purity, assay method, appearance, residual solvents, loss on drying, heavy metals, microbiology, solubility, particle size, stability, packaging, regulatory status and destination-market label requirements.
Defined Ingredient Identity
Urolithin A sourcing should confirm CAS number, chemical name, molecular formula, assay method and batch documentation before supplier approval.
Purity & Assay Review
High-purity grades are commonly reviewed by HPLC assay, identity, loss on drying, related substances and residual solvent profile.
Tập trung vào nguồn cung cấp thực phẩm bổ sung
Gensei supports supplement brands, OEM factories and contract manufacturers with bulk Urolithin A sourcing and technical documentation.
Urolithin A Specification Options
Final specifications depend on production route, purity target, assay method, impurity controls, particle size, packaging, storage condition and destination market requirements.
| Tham số | Các phương án điển hình trong việc tìm nguồn cung ứng B2B |
|---|---|
| Danh mục sản phẩm | Urolithin A / Urolithin A Powder / Uro-A / Specialty Supplement Ingredient |
| Các từ đồng nghĩa phổ biến | Urolithin A, Uro-A, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one, 3,8-Dihydroxy-6H-dibenzopyran-6-one, Urolithin A Powder |
| Số CAS | 1143-70-0 |
| Công thức phân tử | C₁₃H₈O₄ |
| Trọng lượng phân tử | 228,20 g/mol |
| Typical Purity | High-purity options such as 98%, 99% or higher HPLC may be discussed. Final purity should be confirmed by batch COA. |
| Phương pháp thử nghiệm | HPLC assay is commonly requested for identity and purity review. Additional testing can be discussed according to market requirements. |
| Hình thức | Off-white, beige, pale yellow or light yellow powder depending on grade, process and batch condition |
| Độ hòa tan | Low water solubility is common. Buyers should test dispersibility, suspension behavior, taste and stability in the actual finished dosage format. |
| Sự phù hợp của ứng dụng | Dietary supplement capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and custom premixes |
| Stability Review | Heat, light, moisture, pH, excipient compatibility, packaging material and finished-product shelf life should be reviewed |
| Các câu hỏi thi | HPLC assay, identification, purity, loss on drying, particle size, related substances, residual solvents, heavy metals, microbiology and stability indicators upon request |
| Tài liệu | COA, specification sheet, SDS, TDS, allergen statement, non-GMO statement, vegan statement, flow chart, residual solvent report and technical files upon request |
| Đóng gói | Foil bag, aluminum bag, bottle, 1 kg sample pack, 5 kg, 10 kg, 20 kg or 25 kg carton/drum according to grade and order quantity |
| Lưu trữ | Store sealed in a cool, dry and light-protected environment. Avoid heat, moisture, direct sunlight and incompatible materials. |
Note: This table is for B2B sourcing reference. Final purity, identity, assay method, residual solvent profile, storage condition, packaging, shelf life, regulatory status and documents should be confirmed according to the actual batch and purchase agreement.
Urolithin A vs. Pomegranate Extract vs. Ellagic Acid
These ingredients are often searched together, but they differ in identity, label positioning, standardization and formulation behavior.
| Mặt hàng | Urolithin A | Pomegranate Extract | Ellagic Acid |
|---|---|---|---|
| Ingredient Positioning | Defined small-molecule ingredient with CAS number and HPLC purity review | Botanical extract usually standardized by punicalagins, polyphenols or extract ratio | Polyphenolic compound and ellagitannin-related precursor compound |
| Label Naming | Urolithin A, Uro-A or chemical name depending on documentation and market rules | Pomegranate Extract, Punica granatum extract or botanical extract name | Ellagic Acid or source extract depending on ingredient form |
| Key Buyer Check | Confirm CAS 1143-70-0, HPLC purity, residual solvents, stability, COA and market status | Confirm botanical source, extract ratio, marker assay, carrier, pesticides, heavy metals and COA | Confirm purity, source, assay method, solubility, particle size, COA and label suitability |
| Hướng dẫn sử dụng | Commonly evaluated for capsules, tablets, sachets, drink powders, gummies and specialty blends | Commonly evaluated for botanical supplement blends, capsules, tablets and powders | Commonly evaluated for polyphenol-positioned supplement formulas and botanical actives |
Ứng dụng trong thực phẩm chức năng
Gensei supplies Urolithin A mainly for supplement and specialty nutrition projects rather than medical, pharmaceutical or therapeutic applications.
Ghi chú về công thức dành cho các thương hiệu thực phẩm bổ sung
Urolithin A selection should be aligned with purity target, dosage form, solubility strategy, excipient compatibility, packaging, stability and destination market compliance.
Purity & Identity
Confirm CAS number, HPLC purity, chemical identity, related substances and batch COA before approving a supplier.
Solubility Strategy
Urolithin A may have limited water solubility, so powders, gummies and beverages should be tested for dispersion and sediment.
Residual Solvent Review
Because purified Urolithin A may involve synthetic or purification steps, residual solvents and impurities should be reviewed carefully.
Color & Taste Review
Gummies, chewables and drink powders should be tested for color impact, mouthfeel, bitterness and flavor compatibility.
Regulatory Status
Ingredient status, GRAS relevance, NDI considerations, platform policies, import rules and permitted claims should be reviewed by target market.
Tổng quan về thông tin dinh dưỡng
Final Urolithin A amount, ingredient name, serving size, warnings and other label details should be confirmed by the brand owner.
Why Choose Gensei as Your Urolithin A Supplier?
Gensei provides procurement-oriented support for supplement brands and contract manufacturers sourcing bulk Urolithin A powder.
Nguồn cung tập trung vào thực phẩm bổ sung
Our Urolithin A support is focused on capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and supplement premixes.
So sánh thông số kỹ thuật
We help match HPLC purity, identity, particle size, solubility profile, packaging and application behavior to your project.
Hỗ trợ tài liệu
COA, specification sheet, SDS, TDS, allergen statement, non-GMO statement and residual solvent reports can be provided for qualified buyers.
Phối hợp ứng dụng
We support discussion around capsules, tablets, sachets, drink powders, gummies, sports nutrition blends and custom premixes.
Hỗ trợ đặt hàng số lượng lớn
Các vấn đề liên quan đến bao bì, số lượng đặt hàng tối thiểu (MOQ), khả năng cung cấp mẫu, thời gian giao hàng và chi tiết vận chuyển có thể được thảo luận tùy theo quy mô dự án của quý khách.
Phối hợp cung ứng toàn cầu
Gensei hỗ trợ khách hàng quốc tế trong các khâu báo giá, điều phối mẫu hàng, chuẩn bị hồ sơ và lập kế hoạch vận chuyển xuất khẩu.
Kiểm soát chất lượng và lập hồ sơ
For Urolithin A raw material purchasing, HPLC assay, identity, residual solvents, batch documentation and regulatory review are essential for supplier qualification.
Bảng phân tích thành phần theo lô
Certificate of Analysis can verify key batch parameters such as HPLC assay, identification, purity, loss on drying and microbial limits.
Residual Solvent Review
Residual solvents, impurities, related substances, heavy metals and process-related parameters should be reviewed before approval.
Hồ sơ tuân thủ
SDS, TDS, allergen statement, non-GMO statement, vegan statement, flow chart and residual solvent report can support supplier approval.
Buyers should confirm Urolithin A identity, CAS number, chemical name, HPLC purity, assay method, related substances, loss on drying, residual solvents, heavy metals, microbiology, solubility, particle size, storage condition, packaging, shelf life, regulatory status and destination-market label requirements before placing bulk orders.
Quy trình đặt hàng số lượng lớn
Gensei hỗ trợ người mua nguyên liệu chuyển từ giai đoạn xem xét thông số kỹ thuật sang các giai đoạn báo giá, lấy mẫu và giao hàng.
Câu hỏi thường gặp
Các câu hỏi thường gặp từ các thương hiệu thực phẩm chức năng, nhà sản xuất OEM, nhà sản xuất gia công và các đơn vị mua nguyên liệu.
What is Urolithin A?
Urolithin A is a defined small-molecule ingredient also known as Uro-A, 3,8-Dihydroxyurolithin or 3,8-Dihydroxybenzo[c]chromen-6-one. In supplement raw material sourcing, it is commonly evaluated by identity, HPLC purity, residual solvents, heavy metals, microbiology, solubility and regulatory status.
What is the CAS number of Urolithin A?
The CAS number commonly used for Urolithin A is 1143-70-0. Buyers should confirm identity, chemical name, assay method and specification by supplier documentation and batch COA.
What is the molecular formula of Urolithin A?
The molecular formula commonly referenced for Urolithin A is C13H8O4, with molecular weight around 228.20 g/mol.
What is the difference between Urolithin A and pomegranate extract?
Urolithin A is a defined compound, while pomegranate extract is a botanical extract that may contain punicalagins, ellagic acid or other polyphenols. Buyers should compare identity, assay, marker compounds, COA and label strategy before sourcing.
What is the difference between Urolithin A and ellagic acid?
Ellagic acid is an ellagitannin-related precursor compound, while Urolithin A is a downstream metabolite associated with gut microbiota conversion. They have different chemical identities, assay methods, specifications and formulation behavior.
Is Urolithin A water soluble?
Urolithin A is generally not highly water-soluble. Finished formula performance should be tested for solubility, dispersibility, sediment, taste, active retention and stability.
What purity options are available for Urolithin A powder?
High-purity options such as 98%, 99% or higher HPLC may be available depending on grade and stock. Final purity should always be confirmed by actual batch COA.
Can Urolithin A be used in capsules or tablets?
Yes. Selected Urolithin A specifications can be evaluated for capsules and tablets when serving size, bulk density, flowability, excipient compatibility and stability are suitable.
Can Urolithin A be used in drink powders?
Urolithin A can be evaluated for drink powders, sachets and stick packs, but formulators should review solubility, dispersibility, sediment, pH, flavor compatibility and active retention.
Can Urolithin A be used in gummies?
Urolithin A can be evaluated for gummy concepts, but heat, pH, color impact, dispersion, active retention and packaging should be tested carefully before launch.
Is Urolithin A vegan?
Vegan suitability depends on production route, processing aids, carriers and manufacturing conditions. Buyers should request a vegan statement if vegan label positioning is required.
How should Urolithin A be stored?
Urolithin A should generally be stored sealed in a cool, dry and light-protected environment. Avoid heat, moisture, direct sunlight and incompatible materials.
Tôi có thể yêu cầu những tài liệu nào trước khi đặt hàng?
Qualified B2B buyers can request COA, specification sheet, SDS, TDS, allergen statement, non-GMO statement, vegan statement, flow chart, residual solvent report, stability information and other technical files depending on the selected grade.
Does Gensei supply Urolithin A for medical or pharmaceutical use?
Trang này tập trung vào việc tìm nguồn cung ứng nguyên liệu thực phẩm chức năng trong lĩnh vực B2B. Nếu dự án của quý vị liên quan đến dược phẩm, thực phẩm y tế hoặc các ứng dụng điều trị, vui lòng xác nhận riêng về tiêu chuẩn chất lượng yêu cầu, hồ sơ tài liệu và quy trình tuân thủ quy định.
Source Bulk Urolithin A from Gensei
Looking for a Urolithin A manufacturer or bulk Urolithin A powder supplier for dietary supplements? Contact Gensei to request quotation, COA, specification, HPLC purity, assay method, MOQ, sample availability and global shipping support.
Disclaimer: This product information is intended for B2B dietary supplement ingredient sourcing and formulation reference only. It is not intended to diagnose, treat, cure or prevent any disease. Urolithin A ingredient selection should be reviewed by identity, purity, assay method, residual solvents, stability, storage condition, label declaration, Supplement Facts requirements, warning statements, NDI or GRAS relevance, import requirements and destination-market regulations. Regulatory status of Urolithin A may vary by country, platform and finished-product category. Final supplement claims, dosage, labeling, warning statements, ingredient declaration, product classification and market compliance should be reviewed according to applicable regulations in the destination market.