Urolithin A Powder
Urolithin A is a metabolite derived from ellagitannins, standardized to >98% purity by HPLC, presented as a light yellow powder.
Technical specification
- Specification
- 98%
- Molecular formula
- C13H8O4
- Molecular weight
- 228.2
- Form
- Powder
- Appearance
- Light yellow powder
- Test method
- HPLC
- Certifications
- ISO, HALAL, KOSHER, EU Organic, USA Organic, FDA
- Preservation condition
- 25°C, moistureproof, avoid direct sunlight
Quality parameters (COA)
| Results | Testing Items | S pecification |
|---|---|---|
| 99.54% | Purity (HPLC) | >98.0% |
| 0.17% | Water | ≤ 0.5%( Karl F ischer) |
| 0.46% | Maximum Single Impurity | ≤ 1.0% |
| 0.46% | Total impurities | ≤ 2.0% |
| N/D | (GC)/Ethyl Acetate | ≤ 0.05% |
| N/D | (GC)/Acetone | ≤ 0.05% |
| N/D | (GC)/M ethanol | ≤ 0.03% |
| N/D | (GC)dichloromethane | ≤ 0.02% |
| 22.75 ppm | Heavy metal | ≤ 300 ppm |
| Correct | Other items | HNMR correct;MS correct |
| Completely dissolved | Solubility | DMSO completely dissolved |
Description
Urolithin A is a natural metabolite produced by human gut bacteria upon consumption of ellagitannins or ellagic acid. It is presented as a light yellow powder with a purity exceeding 98%, confirmed by HPLC. The molecular formula is C13H8O4, with CAS number 1143-70-0. The product adheres to ISO, HALAL, KOSHER, EU Organic, USA Organic, and FDA standards. It is crucial for manufacturers seeking high purity and stability in their ingredients. Good solubility in DMSO ensures convenience in technological processes. Supplied with a complete set of documentation confirming quality and compliance with stated specifications. Quality control includes testing for water content, heavy metals, and residual solvents.
Applications
Used in the production of dietary supplements and functional foods, where a high-purity metabolite is required for specialized formulations.
Documents
Documents are shared on request after company verification.