Bulk Specialty Supplement Ingredient Supplier

Urolithin A Manufacturer & Bulk Urolithin A Powder Supplier

겐세이 공급 우롤리틴 A로도 알려진 Uro-A, 우루리틴 A 파우더, 3,8-Dihydroxyurolithin, 3,8-Dihydroxybenzo[c]chromen-6-one 또는 3,8-디하이드록시-6H-디벤조피란-6-원, 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.

우루리틴 A 파우더 CAS 1143-70-0 HPLC 순도 검토 COA Support 보충제 조달

제품 주요 특징

  • 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
  • 자격을 갖춘 구매자에게는 COA, 사양서, SDS, TDS, 알레르기 유발 물질 표기, 비유전자변형(non-GMO) 표기 및 흐름도가 제공됩니다.
  • Residual solvents, heavy metals, microbiology, solubility, particle size, stability and packaging should be reviewed before bulk purchase
  • 의학적, 약학적 또는 치료적 용도가 아닌, 건강기능식품 원료 조달에 중점을 둡니다.

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.

우롤리틴 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

순도 및 함량 분석 검토

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

B2B

보충제 공급 현황

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.

매개변수 B2B 조달의 일반적인 옵션
제품 카테고리 Urolithin A / Urolithin A Powder / Uro-A / Specialty Supplement Ingredient
흔히 쓰이는 동의어 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 번호 1143-70-0
분자 공식 C13H8O4
분자량 228.20 g/mol
일반적인 순도 High-purity options such as 98%, 99% or higher HPLC may be discussed. Final purity should be confirmed by batch COA.
분석 방법 HPLC 분석은 일반적으로 성분 확인 및 순도 검증을 위해 의뢰됩니다. 시장 요구 사항에 따라 추가 시험에 대해 협의할 수 있습니다.
모양 Off-white, beige, pale yellow or light yellow powder depending on grade, process and batch condition
용해성 Low water solubility is common. Buyers should test dispersibility, suspension behavior, taste and stability in the actual finished dosage format.
적용 적합성 Dietary supplement capsules, tablets, gummies, sachets, drink powders, sports nutrition blends and custom premixes
안정성 검토 Heat, light, moisture, pH, excipient compatibility, packaging material and finished-product shelf life should be reviewed
시험 문제 HPLC assay, identification, purity, loss on drying, particle size, related substances, residual solvents, heavy metals, microbiology and stability indicators upon request
문서 COA, 사양서, SDS, TDS, 알레르기 유발 물질 표기, 비유전자변형(non-GMO) 표기, 비건 표기, 흐름도, 잔류 용매 분석 보고서 및 요청 시 기술 문서
패키징 포일 봉지, 알루미늄 봉지, 병, 1kg 샘플 팩, 5kg, 10kg, 20kg 또는 25kg 상자/드럼 (등급 및 주문 수량에 따라 다름)
스토리지 서늘하고 건조하며 빛이 닿지 않는 곳에 밀봉하여 보관하십시오. 열, 습기, 직사광선 및 호환되지 않는 물질과의 접촉을 피하십시오.

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.

항목 우롤리틴 A Pomegranate Extract Ellagic Acid
원료 포지셔닝 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
라벨 명명 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
주요 구매자 확인 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
응용 노트 캡슐, 정제, 소포, 음료 분말, 구미, 특수 배합 제품 등에 대해 일반적으로 평가됩니다. Commonly evaluated for botanical supplement blends, capsules, tablets and powders Commonly evaluated for polyphenol-positioned supplement formulas and botanical actives

영양보충제 분야에서의 활용

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

캡슐 Selected Urolithin A specifications can be used in capsule formulas when serving size, bulk density and flowability are suitable.
태블릿 부형제 호환성, 압축성, 색상 영향 및 안정성 시험을 포함한 정제 개념에 대해 검토할 수 있습니다.
봉지 분산성, 맛, 분말 유동성 및 포장 측면을 고려할 때 1회용 분말 제형에 적합합니다.
분말 음료 즉석 혼합용 분말의 용해도, 현탁성, pH, 맛 및 안정성 검토를 통해 평가할 수 있습니다.
구미 껌 제조 프로젝트에 적용 가능하지만, 열, pH, 색상, 분산성 및 유효 성분 유지율을 신중하게 테스트해야 합니다.
스포츠 뉴트리션 Can be positioned in sports nutrition blends when final claims, dosage and market compliance are reviewed.
건강한 노년을 위한 블렌드 Can be combined with CoQ10, resveratrol, NMN, NAD, vitamins or botanicals after formula and compliance review.
맞춤형 프리믹스 Can support OEM supplement projects requiring a defined Urolithin A input and full documentation package.

보충제 브랜드를 위한 제형 개발 지침

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

01

순수성과 정체성

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

02

Solubility Strategy

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

03

Residual Solvent Review

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

규제 현황

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

06

영양성분표 검토

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

영양제 중심 공급

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

사양

사양 일치

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

COA

문서 지원

자격을 갖춘 구매자에게는 COA, 사양서, SDS, TDS, 알레르기 유발 물질 표기, 비유전자변형(non-GMO) 표기 및 잔류 용매 분석 보고서를 제공해 드릴 수 있습니다.

연구개발

지원서 매칭

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

MOQ

대량 주문 지원

포장, 최소 주문 수량(MOQ), 샘플 제공 여부, 납기 및 배송 세부 사항은 귀사의 프로젝트 물량에 따라 협의할 수 있습니다.

GLB

글로벌 공급 조정

Gensei는 견적, 샘플 조율, 서류 준비 및 수출 선적 계획 수립을 통해 해외 구매자들을 지원합니다.

품질 관리 및 문서화

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

품질 관리

배치 COA

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

RS

Residual Solvent Review

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

DOC

규정 준수 관련 문서

SDS, TDS, 알레르기 유발 물질 표기, 비유전자변형(Non-GMO) 표기, 비건 표기, 흐름도 및 잔류 용매 보고서는 공급업체 승인을 뒷받침할 수 있습니다.

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.

대량 주문 절차

Gensei는 구매 담당자가 사양 검토 단계에서 견적, 샘플 제공 및 출하 단계로 원활하게 진행할 수 있도록 지원합니다.

1 요구 사항 공유하기 Tell us your target Urolithin A purity, application, order quantity, documentation needs, packaging needs and destination market.
2 사양 확인 저희 팀은 HPLC 순도, 입자 크기, 보관 조건, 시료 확보 가능 여부 및 문서화 옵션을 확인해 드립니다.
3 COA 및 관련 서류 검토 자격을 갖춘 구매자는 COA, 사양서, SDS, TDS, 알레르기 유발 물질 명세서, 잔류 용매 분석 보고서 및 관련 기술 문서를 요청할 수 있습니다.
4 견적 및 샘플 선택하신 사양을 바탕으로 가격, 최소 주문 수량(MOQ), 납기, 샘플 제공 여부 및 배송 정보를 안내해 드립니다.
5 대량 주문 및 배송 출하 전 일괄 품질 확인, 포장 및 수출 선적 조정이 이루어집니다.

자주 묻는 질문

보충제 브랜드, OEM 제조업체, 위탁 제조업체 및 원료 구매처에서 자주 묻는 질문.

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.

주문하기 전에 어떤 서류를 요청할 수 있나요?

자격을 갖춘 B2B 구매자는 선택한 등급에 따라 COA, 사양서, SDS, TDS, 알레르기 유발 물질 표기, 비유전자변형(non-GMO) 표기, 비건 표기, 흐름도, 잔류 용매 보고서, 안정성 정보 및 기타 기술 문서를 요청할 수 있습니다.

Does Gensei supply Urolithin A for medical or pharmaceutical use?

이 페이지는 B2B 건강기능식품 원료 조달에 중점을 두고 있습니다. 귀하의 프로젝트가 의약품, 의료용 식품 또는 치료 용도와 관련된 경우, 필요한 등급, 서류 및 규제 절차를 별도로 확인해 주시기 바랍니다.

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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