Urolithin A Manufacturer & Bulk Urolithin A Powder Supplier
Gensei tedarikçisi Urolitin Aolarak da bilinir. Uro-A, Ürolitin A Tozu, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one veya 3,8-Dihidroksi-6H-dibenzopiran-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.
Ürünün Öne Çıkan Özellikleri
- 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, teknik özellik belgesi, SDS, TDS, alerjen beyanı, GDO içermez beyanı ve akış şeması, uygun alıcılar için mevcuttur
- Residual solvents, heavy metals, microbiology, solubility, particle size, stability and packaging should be reviewed before bulk purchase
- Tıbbi, farmasötik veya terapötik kullanım değil, takviye bileşenlerinin tedarikine odaklanmıştır
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.
Urolitin 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.
Belirlenmiş Malzeme Kimliği
Urolithin A sourcing should confirm CAS number, chemical name, molecular formula, assay method and batch documentation before supplier approval.
Saflık ve Analiz İncelemesi
High-purity grades are commonly reviewed by HPLC assay, identity, loss on drying, related substances and residual solvent profile.
Takviye Tedarikine Odaklanma
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.
| Parametre | B2B Tedarik için Tipik Seçenekler |
|---|---|
| Ürün Kategorisi | Urolithin A / Urolithin A Powder / Uro-A / Specialty Supplement Ingredient |
| Yaygın Eşanlamlılar | Urolithin A, Uro-A, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one, 3,8-Dihydroxy-6H-dibenzopyran-6-one, Urolithin A Powder |
| CAS Numarası | 1143-70-0 |
| Moleküler Formül | C13H8O4 |
| Moleküler Ağırlık | 228,20 g/mol |
| Tipik Saflık | High-purity options such as 98%, 99% or higher HPLC may be discussed. Final purity should be confirmed by batch COA. |
| Tahlil Yöntemi | HPLC analizi, genellikle ürünün kimliği ve saflığının doğrulanması amacıyla talep edilir. Piyasa gereksinimlerine göre ek testler de görüşülebilir. |
| Görünüş | Off-white, beige, pale yellow or light yellow powder depending on grade, process and batch condition |
| Çözünürlük | Low water solubility is common. Buyers should test dispersibility, suspension behavior, taste and stability in the actual finished dosage format. |
| Uygulama Uyumu | Dietary supplement capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and custom premixes |
| İstikrar İncelemesi | Heat, light, moisture, pH, excipient compatibility, packaging material and finished-product shelf life should be reviewed |
| Test Soruları | HPLC assay, identification, purity, loss on drying, particle size, related substances, residual solvents, heavy metals, microbiology and stability indicators upon request |
| Belgeler | Talep üzerine COA, teknik özellik belgesi, SDS, TDS, alerjen beyanı, GDO içermez beyanı, vegan beyanı, akış şeması, kalıntı çözücü raporu ve teknik dosyalar |
| Paketleme | Folyo torba, alüminyum torba, şişe, 1 kg’lık numune paketi, 5 kg, 10 kg, 20 kg veya 25 kg’lık karton/varil (ürün sınıfına ve sipariş miktarına göre) |
| Depolama | Ürünü serin, kuru ve ışıktan korunan bir ortamda kapalı halde saklayınız. Isı, nem, doğrudan güneş ışığı ve uyumsuz malzemelerden uzak tutunuz. |
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.
| Ürün | Urolitin A | Pomegranate Extract | Ellagic Acid |
|---|---|---|---|
| Malzemelerin Yerleşimi | 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 |
| Etiket Adlandırma | 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 |
| Ana Alıcı Kontrolü | 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 |
| Uygulama Notları | Genellikle kapsüller, tabletler, poşetler, içecek tozları, jelibonlar ve özel karışımlar için değerlendirilir | Commonly evaluated for botanical supplement blends, capsules, tablets and powders | Commonly evaluated for polyphenol-positioned supplement formulas and botanical actives |
Besin Takviyelerindeki Kullanım Alanları
Gensei supplies Urolithin A mainly for supplement and specialty nutrition projects rather than medical, pharmaceutical or therapeutic applications.
Takviye Markaları için Formülasyon Notları
Urolithin A selection should be aligned with purity target, dosage form, solubility strategy, excipient compatibility, packaging, stability and destination market compliance.
Saflık ve Kimlik
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.
Düzenleyici Statü
Ingredient status, GRAS relevance, NDI considerations, platform policies, import rules and permitted claims should be reviewed by target market.
Besin Değerleri İncelemesi
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.
Takviye Odaklı Tedarik
Our Urolithin A support is focused on capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and supplement premixes.
Teknik Özelliklerin Karşılaştırılması
We help match HPLC purity, identity, particle size, solubility profile, packaging and application behavior to your project.
Belge Desteği
Uygun alıcılara COA, teknik özellik belgesi, SDS, TDS, alerjen beyanı, GDO içermez beyanı ve kalıntı çözücü raporları sunulabilir.
Uygulama Eşleştirme
We support discussion around capsules, tablets, sachets, drink powders, gummies, sports nutrition blends and custom premixes.
Toplu Sipariş Desteği
Ambalaj, minimum sipariş miktarı (MOQ), numune temini, teslim süresi ve sevkiyat detayları, projenizin hacmine göre görüşülebilir.
Küresel Tedarik Koordinasyonu
Gensei, uluslararası alıcılara fiyat teklifi, numune koordinasyonu, evrak işlemleri ve ihracat sevkiyat planlaması konularında destek sağlamaktadır.
Kalite Kontrol ve Belgeleme
For Urolithin A raw material purchasing, HPLC assay, identity, residual solvents, batch documentation and regulatory review are essential for supplier qualification.
Parti COA'sı
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.
Uyum Dosyaları
SDS, TDS, alerjen beyanı, GDO içermez beyanı, vegan beyanı, akış şeması ve kalıntı çözücü raporu, tedarikçi onay sürecini destekleyebilir.
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.
Toplu Sipariş Süreci
Gensei, takviye alıcılarının teknik şartname incelemesinden teklif aşamasına, numune alma ve sevkiyata kadar tüm süreçleri tamamlamasına yardımcı olur.
Sıkça Sorulan Sorular
Takviye markaları, OEM üreticileri, fason üreticiler ve hammadde alıcılarından sıkça gelen sorular.
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.
Sipariş vermeden önce hangi belgeleri talep edebilirim?
Uygun B2B alıcılar, seçilen sınıfa bağlı olarak COA, teknik özellik belgesi, SDS, TDS, alerjen beyanı, GDO içermez beyanı, vegan beyanı, akış şeması, kalıntı çözücü raporu, stabilite bilgileri ve diğer teknik belgeleri talep edebilirler.
Does Gensei supply Urolithin A for medical or pharmaceutical use?
Bu sayfa, B2B besin takviyesi bileşenlerinin tedarikine odaklanmaktadır. Projeniz ilaç, tıbbi gıda veya terapötik uygulamaları içeriyorsa, lütfen gerekli kalite sınıfını, belgeleri ve mevzuata uygun süreci ayrı olarak teyit ediniz.
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.