Fornitore all'ingrosso di ingredienti per integratori alimentari speciali

Urolithin A Manufacturer & Bulk Urolithin A Powder Supplier

Gensei fornisce Urolitina A, noto anche come Uro-A, Urolitina A in polvere, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one o 3,8-diidrossi-6H-dibenzopiran-6-one, 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.

Urolitina A in polvere CAS 1143-70-0 HPLC Purity Review COA Support Supplement Sourcing

Caratteristiche principali del prodotto

  • 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, scheda tecnica, SDS, TDS, dichiarazione sugli allergeni, dichiarazione di assenza di OGM e diagramma di flusso disponibili per gli acquirenti qualificati
  • Residual solvents, heavy metals, microbiology, solubility, particle size, stability and packaging should be reviewed before bulk purchase
  • Dedicata all’approvvigionamento di ingredienti per integratori alimentari, non a fini medici, farmaceutici o terapeutici

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.

UA

Defined Ingredient Identity

Urolithin A sourcing should confirm CAS number, chemical name, molecular formula, assay method and batch documentation before supplier approval.

HPLC

Purity & Assay Review

High-purity grades are commonly reviewed by HPLC assay, identity, loss on drying, related substances and residual solvent profile.

B2B

Focus sull'approvvigionamento di integratori

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.

Parametro Opzioni tipiche per l'approvvigionamento B2B
Categoria di prodotto Urolithin A / Urolithin A Powder / Uro-A / Specialty Supplement Ingredient
Sinonimi comuni Urolithin A, Uro-A, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one, 3,8-Dihydroxy-6H-dibenzopyran-6-one, Urolithin A Powder
Numero CAS 1143-70-0
Formula molecolare C13H8O4
Peso molecolare 228,20 g/mol
Purezza tipica High-purity options such as 98%, 99% or higher HPLC may be discussed. Final purity should be confirmed by batch COA.
Metodo di analisi HPLC assay is commonly requested for identity and purity review. Additional testing can be discussed according to market requirements.
Aspetto Off-white, beige, pale yellow or light yellow powder depending on grade, process and batch condition
Solubilità Low water solubility is common. Buyers should test dispersibility, suspension behavior, taste and stability in the actual finished dosage format.
Adattabilità dell'applicazione Dietary supplement capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and custom premixes
Analisi della stabilità Heat, light, moisture, pH, excipient compatibility, packaging material and finished-product shelf life should be reviewed
Elementi di verifica HPLC assay, identification, purity, loss on drying, particle size, related substances, residual solvents, heavy metals, microbiology and stability indicators upon request
Documenti COA, scheda tecnica, SDS, TDS, dichiarazione sugli allergeni, dichiarazione di assenza di OGM, dichiarazione di idoneità vegana, diagramma di flusso, rapporto sui solventi residui e documentazione tecnica su richiesta
Imballaggio 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
Immagazzinamento 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.

Articolo Urolitina A Pomegranate Extract Ellagic Acid
Posizionamento degli ingredienti 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
Denominazione delle etichette 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
Verifica dei principali acquirenti 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
Note applicative 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

Applicazioni nel settore degli integratori alimentari

Gensei supplies Urolithin A mainly for supplement and specialty nutrition projects rather than medical, pharmaceutical or therapeutic applications.

Capsule Selected Urolithin A specifications can be used in capsule formulas when serving size, bulk density and flowability are suitable.
Compresse Può essere valutato per progetti di compresse in termini di compatibilità con gli eccipienti, comprimibilità, effetto cromatico e test di stabilità.
Bustine Adatto ai formati in polvere monodose, tenendo conto della dispersibilità, del gusto, della scorrevolezza della polvere e del confezionamento.
Bevande in polvere Can be evaluated for ready-to-mix powders with solubility, suspension, pH, taste and stability review.
Gomme Can be evaluated for gummy projects, but heat, pH, color, dispersion and active retention should be tested carefully.
Nutrizione sportiva Can be positioned in sports nutrition blends when final claims, dosage and market compliance are reviewed.
Healthy Aging Blends Can be combined with CoQ10, resveratrol, NMN, NAD, vitamins or botanicals after formula and compliance review.
Premix personalizzati Can support OEM supplement projects requiring a defined Urolithin A input and full documentation package.

Note sulla formulazione per i marchi di integratori alimentari

Urolithin A selection should be aligned with purity target, dosage form, solubility strategy, excipient compatibility, packaging, stability and destination market compliance.

01

Purezza e identità

Confirm CAS number, HPLC purity, chemical identity, related substances and batch COA before approving a supplier.

02

Strategia di solubilità

Urolithin A may have limited water solubility, so powders, gummies and beverages should be tested for dispersion and sediment.

03

Analisi dei solventi residui

Because purified Urolithin A may involve synthetic or purification steps, residual solvents and impurities should be reviewed carefully.

04

Color & Taste Review

Gummies, chewables and drink powders should be tested for color impact, mouthfeel, bitterness and flavor compatibility.

05

Stato normativo

Ingredient status, GRAS relevance, NDI considerations, platform policies, import rules and permitted claims should be reviewed by target market.

06

Analisi delle informazioni nutrizionali

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.

B2B

Fornitura incentrata sugli integratori

Our Urolithin A support is focused on capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and supplement premixes.

SPEC

Corrispondenza delle specifiche

We help match HPLC purity, identity, particle size, solubility profile, packaging and application behavior to your project.

COA

Assistenza sui documenti

COA, specification sheet, SDS, TDS, allergen statement, non-GMO statement and residual solvent reports can be provided for qualified buyers.

Ricerca e sviluppo

Corrispondenza delle candidature

We support discussion around capsules, tablets, sachets, drink powders, gummies, sports nutrition blends and custom premixes.

MOQ

Assistenza per ordini all'ingrosso

Le modalità di imballaggio, il quantitativo minimo ordinabile (MOQ), la disponibilità dei campioni, i tempi di consegna e i dettagli relativi alla spedizione possono essere concordati in base al volume del vostro progetto.

GLB

Coordinamento globale delle forniture

Gensei assiste gli acquirenti internazionali nella preparazione dei preventivi, nel coordinamento dei campioni, nella gestione della documentazione e nella pianificazione delle spedizioni all'estero.

Controllo qualità e documentazione

For Urolithin A raw material purchasing, HPLC assay, identity, residual solvents, batch documentation and regulatory review are essential for supplier qualification.

QC

Lotto COA

Certificate of Analysis can verify key batch parameters such as HPLC assay, identification, purity, loss on drying and microbial limits.

RS

Analisi dei solventi residui

Residual solvents, impurities, related substances, heavy metals and process-related parameters should be reviewed before approval.

DOC

Documentazione relativa alla conformità

La scheda di sicurezza (SDS), la scheda tecnica (TDS), la dichiarazione sugli allergeni, la dichiarazione di assenza di OGM, la dichiarazione vegana, il diagramma di flusso e il rapporto sui solventi residui possono costituire la documentazione necessaria per l'approvazione del fornitore.

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.

Procedura per gli ordini all'ingrosso

Gensei aiuta gli acquirenti di integratori a passare dalla revisione delle specifiche alla richiesta di preventivo, alla fornitura di campioni e alla spedizione.

1 Condividi le tue esigenze Tell us your target Urolithin A purity, application, order quantity, documentation needs, packaging needs and destination market.
2 Conferma le specifiche Our team confirms available HPLC purity, particle size, storage condition, sample availability and documentation options.
3 Verifica del certificato di autenticità (COA) e dei documenti Gli acquirenti qualificati possono richiedere il certificato di autenticità (COA), la scheda tecnica, la scheda di sicurezza (SDS), la scheda tecnica del prodotto (TDS), la dichiarazione sugli allergeni, il rapporto sui solventi residui e la relativa documentazione tecnica.
4 Preventivo e campione Forniamo informazioni relative a prezzi, quantità minima ordinabile (MOQ), tempi di consegna, disponibilità dei campioni e spedizione in base alle specifiche selezionate.
5 Ordini all'ingrosso e spedizioni Prima della consegna vengono organizzati il controllo di qualità dei lotti, l’imballaggio e il coordinamento delle spedizioni per l’esportazione.

Domande frequenti

Domande frequenti poste da marchi di integratori, produttori OEM, produttori a contratto e acquirenti di ingredienti.

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?

L'idoneità vegana dipende dal processo di produzione, dai coadiuvanti tecnologici, dagli eccipienti e dalle condizioni di produzione. Gli acquirenti dovrebbero richiedere una dichiarazione di idoneità vegana qualora sia richiesta l'apposizione dell'etichetta vegana.

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.

Quali documenti posso richiedere prima di effettuare l'ordine?

Gli acquirenti B2B qualificati possono richiedere il certificato di analisi (COA), la scheda tecnica, la scheda di sicurezza (SDS), la scheda tecnica del prodotto (TDS), la dichiarazione sugli allergeni, la dichiarazione di assenza di OGM, la dichiarazione di idoneità vegana, il diagramma di flusso, il rapporto sui solventi residui, le informazioni sulla stabilità e altra documentazione tecnica a seconda del grado selezionato.

Does Gensei supply Urolithin A for medical or pharmaceutical use?

Questa pagina è dedicata all'approvvigionamento di ingredienti per integratori alimentari nel settore B2B. Se il vostro progetto riguarda applicazioni farmaceutiche, alimenti medici o terapeutiche, vi preghiamo di verificare separatamente il grado richiesto, la documentazione necessaria e il percorso normativo.

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.

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