Urolithin A Manufacturer & Bulk Urolithin A Powder Supplier
A Gensei fornece Urolitina A, também conhecido por Uro-A, Urolitina A em pó, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one ou 3,8-Dihidroxi-6H-dibenzopiran-6-ona, 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.
Destaques do produto
- 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, ficha técnica, Ficha de Segurança de Produtos (FSP), Ficha Técnica do Produto (FTP), declaração de alergénios, declaração de ausência de OGM e fluxograma disponíveis para compradores qualificados
- Residual solvents, heavy metals, microbiology, solubility, particle size, stability and packaging should be reviewed before bulk purchase
- Dedicado ao abastecimento de ingredientes para suplementos, não ao uso médico, farmacêutico ou terapêutico
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.
Urolitina 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.
Foco no abastecimento de suplementos
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.
| Parâmetro | Opções típicas para o aprovisionamento B2B |
|---|---|
| Categoria do produto | Urolithin A / Urolithin A Powder / Uro-A / Specialty Supplement Ingredient |
| Sinónimos comuns | Urolithin A, Uro-A, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one, 3,8-Dihydroxy-6H-dibenzopyran-6-one, Urolithin A Powder |
| Número CAS | 1143-70-0 |
| Fórmula molecular | C13H8O4 |
| Peso molecular | 228,20 g/mol |
| Pureza típica | High-purity options such as 98%, 99% or higher HPLC may be discussed. Final purity should be confirmed by batch COA. |
| Método de análise | HPLC assay is commonly requested for identity and purity review. Additional testing can be discussed according to market requirements. |
| Aparência | Off-white, beige, pale yellow or light yellow powder depending on grade, process and batch condition |
| Solubilidade | Low water solubility is common. Buyers should test dispersibility, suspension behavior, taste and stability in the actual finished dosage format. |
| Adequação da aplicação | 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 |
| Itens de teste | HPLC assay, identification, purity, loss on drying, particle size, related substances, residual solvents, heavy metals, microbiology and stability indicators upon request |
| Documentos | COA, specification sheet, SDS, TDS, allergen statement, non-GMO statement, vegan statement, flow chart, residual solvent report and technical files upon request |
| Embalagem | 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 |
| Armazenamento | 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.
| Artigo | Urolitina 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 |
| Verificação do comprador principal | 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 |
| Notas de aplicação | 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 |
Aplicações em suplementos alimentares
Gensei supplies Urolithin A mainly for supplement and specialty nutrition projects rather than medical, pharmaceutical or therapeutic applications.
Notas sobre a formulação para marcas de suplementos
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.
Estatuto regulamentar
Ingredient status, GRAS relevance, NDI considerations, platform policies, import rules and permitted claims should be reviewed by target market.
Análise da informação nutricional
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.
Abastecimento centrado nos suplementos
Our Urolithin A support is focused on capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and supplement premixes.
Correspondência de especificações
We help match HPLC purity, identity, particle size, solubility profile, packaging and application behavior to your project.
Suporte a documentos
COA, specification sheet, SDS, TDS, allergen statement, non-GMO statement and residual solvent reports can be provided for qualified buyers.
Correspondência de candidaturas
We support discussion around capsules, tablets, sachets, drink powders, gummies, sports nutrition blends and custom premixes.
Apoio a encomendas em grande quantidade
A embalagem, a quantidade mínima de encomenda (MOQ), a disponibilidade de amostras, o prazo de entrega e os detalhes de envio podem ser discutidos de acordo com o volume do seu projeto.
Coordenação Global do Abastecimento
A Gensei presta apoio aos compradores internacionais na elaboração de orçamentos, coordenação de amostras, documentação e planeamento de envios para exportação.
Controlo de Qualidade e Documentação
For Urolithin A raw material purchasing, HPLC assay, identity, residual solvents, batch documentation and regulatory review are essential for supplier qualification.
Lote COA
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.
Ficheiros de conformidade
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.
Processo de encomendas em grande quantidade
A Gensei ajuda os compradores de componentes a avançar da análise das especificações para a apresentação de propostas, a amostragem e o envio.
Perguntas mais frequentes
Perguntas frequentes de marcas de suplementos, fabricantes OEM, fabricantes por contrato e compradores de ingredientes.
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.
Que documentos posso solicitar antes de fazer a encomenda?
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?
Esta página centra-se no abastecimento de ingredientes para suplementos alimentares no mercado B2B. Se o seu projeto envolver aplicações farmacêuticas, alimentos médicos ou terapêuticas, por favor, confirme separadamente o grau de qualidade exigido, a documentação necessária e o processo regulamentar.
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.