UROLITHIN A · CAS 1143-70-0

Taiyi Health urolithin A
China's first supplier of both food-grade and cosmetic-grade material

99%
MitoIgnite® oral-grade purity
10% / 80%
MitoYouth® cosmetic grade, two specifications
NMPA filed
China new cosmetic ingredient filing no. 20250106
FTO complete
Process freedom-to-operate search · available under NDA

About urolithin A

Not present in any food

Pomegranates, berries and walnuts contain only its precursors (ellagitannins), which gut bacteria convert to urolithin A in a two-step metabolism. That is why it has to be supplied as a high-purity ingredient.

Fewer people produce it as they age

Cohort studies show that the share of people who produce only urolithin A (the UM-A metabotype) falls from about 80% in childhood to about 55% after age 40, and around 10% of people produce none at all. The target population is precisely the group whose own production is declining.

The first natural molecule shown in human studies to induce mitophagy

Mechanistic studies have been published in Nature Medicine, Nature Metabolism and other journals; the scientific foundation of the category continues to be built by the global research community.

Disclaimer: this mechanism and its associated efficacy claims may not be used commercially without authorisation from the patent holder; Taiyi Health does not hold the corresponding patents.

Taiyi Health's Science Department has completed research on a new urolithin A pathway; patent filing in progress

Share of people who produce only urolithin A, declining with age
Childhood 80% Over 40 55% Non-producers ~10%

Existing third-party research on urolithin A

500+
Cumulative subjects in human studies
10
Human studies · muscle · immunity · skin · heart · exercise performance
17–22h
Plasma half-life · supports once-daily dosing
10–1000mg
Daily dose range in repeat-dose studies · all safe and well tolerated
7
Journals: Nature Metabolism · JAMA Network Open · Cell Reports Medicine · Nature Aging and others

Taiyi Health's own human studies

MitoYouth® 0.1% cream

34 volunteers aged 40+ with sensitive skin · morning and evening · 28 days
Stratum corneum hydration+28.31%
Transepidermal water loss (TEWL)−15.47%
Redness area−22.96%

TI-3N® oral combination

20 women aged 36–60 · 56 days · before-and-after comparison
Skin elasticity R2+9.61%
Under-eye wrinkle area−11.28%
Transepidermal water loss (TEWL)−17.18%

LicorPure® + MitoYouth®

4 weeks of continuous use
Transepidermal water loss (TEWL)−19.47%
Stratum corneum hydration+96.88%
Skin tone (ITA°)Improved
Human efficacy evaluations conducted by Taiyi Health's scientific laboratories and efficacy evaluation platform. Data are shared as ingredient information and do not constitute medical claims; full reports are provided in the product brochure.

Two product lines, meeting food and cosmetic quality standards respectively

ORAL GRADE

MitoIgnite®

For dietary supplements and functional foods
Purity≥99%
Dosage formsCapsules · tablets · powders · beverages
Proprietary pathway and efficacy patentsFiled
COSMETIC GRADE

MitoYouth®

NMPA new cosmetic ingredient filing 20250106 · INCI: Urolithin A
80% powderUse level 0.1–1%
10% water-dispersible (WS)Use level 1–5%
Safety dossierSafety assessment + 8 toxicology studies
In-house human efficacy evaluationSoothing · repair · hydration · skin tone

Formulation guidance

ORAL FORMULATION

Oral formulations

Dosage formsCapsules · tablets · powders · beverages
GradeMitoIgnite® 99%
Validated combination: TI-3N® (urolithin A + fisetin + ergothioneine), supported by 56-day human efficacy data; composition PCT patent filing in progress.
TOPICAL FORMULATION

Topical formulations

80% powderUse level 0.1–1%
WS water-dispersible ≥10%Use level 1–5% · can be added directly to the water phase
Validated combination: LicorPure® + MitoYouth®, supported by human efficacy data after 4 weeks of use; the 34-subject study of the 0.1% cream is itself a formulation-level validation.
01

Formulation proposal

Define the target consumer, use occasion and dosage form; oral and topical routes in parallel, with combination recommendations and claim language for the target market

02

Lab-scale sampling

Solve dispersion and stability of a poorly water-soluble active in aqueous and solid systems, and deliver samples ready for trial

03

Formulation-level validation

Stability and stress testing, system compatibility, and formulation-level human efficacy evaluation

04

ODM production

When finished products are required, Taiyi Health's ODM system takes over: formulation, sampling, validation and mass production

The intellectual property landscape for urolithin A

A complex international landscape
Using urolithin A as an ingredient means navigating a complex international IP environment: core efficacy, compositions and dosage forms are patented in the major markets, and enforcement is active. In October 2025 the originator sued 30 online sellers in U.S. federal court; in July 2026 it obtained permanent injunctions against 19 of them and a combined USD 5.3 million in damages, with the largest single award above USD 2.7 million and treble damages applied in some cases.
Directions already under patent protection
Based on continuous patent searching and analysis, the following directions are covered by third-party patents and may not be used in your product claims or formulations without authorisation: the mitophagy mechanism and its efficacy claims (muscle function · anti-ageing), skin compositions combining urolithin A with NAD precursors, sensitive-skin and anti-hair-loss applications, SIRT6 activation, and several routes that promote in-vivo production through precursors or probiotics. Continuously updated patent analysis is provided in the biweekly brief.
Process freedom-to-operate assessment complete
A freedom-to-operate search and assessment of the current manufacturing process has been completed. Qualified partners may review it under NDA.
Taiyi Health's own patents
TI-3N® three-component composition (urolithin A + fisetin + ergothioneine): PCT international search completed, U.S. national phase in progress; proprietary efficacy and pathway patents pending.
Biweekly patent analysis
Taiyi Health's Science Department, working with a U.S. law firm, reviews and summarises patent activity every two weeks in the UA Patent Biweekly.
Request the biweekly
This website does not provide legal advice, does not disclose the contents of FTO documents, and expresses no opinion on the validity or scope of any third-party patent; please rely on your own counsel for compliance decisions.

The UA Patent Biweekly

Every two weeks our patent analysis team reads the latest patent activity in the urolithin A field and writes a report that procurement and legal teams can both use, reviewed by our legal team before release. Subscription is free.

Request the product brochure · book a call

ty-sales@taiyi-nb.com

Taiyi Health's urolithin A branded-ingredient team
delivers science-backed ingredient and finished-product solutions with intellectual property risk under control

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Frequently asked questions

What is urolithin A? Is it the same as pomegranate extract?
No. Pomegranate contains only the precursors of urolithin A (ellagitannins and ellagic acid), which the gut microbiota must metabolise into urolithin A; urolithin A itself is not present in any known food. As an ingredient it is supplied as a high-purity active, CAS 1143-70-0.
Is there patent risk in sourcing urolithin A?
Yes. Patent enforcement in this category is active and the risk is real, which is why we treat IP due diligence as part of the product. We have completed an FTO assessment of the current manufacturing process and monitor patent activity continuously; key partners can discuss the details under NDA. Nothing on this site constitutes legal advice.
Is your urolithin A natural?
Urolithin A is a human gut metabolite; occurring naturally in human metabolism is a property of the molecule itself. We do not market the manufacturing process as a selling point: the product is delivered on purity, batch-to-batch consistency and a complete quality dossier, and process information is provided as part of due diligence on request.
What grades of MitoYouth® are available, and at what use levels?
Two grades: 80% (recommended use level 0.1–1%) and 10% water-dispersible WS (recommended use level 1–5%). The ingredient has completed China's new cosmetic ingredient filing (NMPA no. 20250106) and is supported by in-house human efficacy evaluation and a nine-item safety dossier.
Can you provide COAs, samples and stability data?
COAs and samples are available to qualified B2B customers on request; stability data packages are shared with partners as studies progress. Please submit your request through the form above.
What are the minimum order quantity and lead time?
Both depend on the grade and the destination market; please contact our commercial team through the form above for a quotation. Key partners also have a dedicated channel for IP discussions.