Description

Urolithin D Tetramethyl Ether is a high-purity, synthetically derived polyphenol metabolite. This compound serves as a critical reference standard and research-grade intermediate for advanced biomedical and nutraceutical studies. It is primarily utilized by pharmaceutical R&D laboratories, nutraceutical formulators, and academic research institutions investigating metabolic pathways and bioactive compound synthesis.

Application

• Pharmaceutical Reference Standard: Used for the qualitative and quantitative analysis of Urolithin metabolites in drug discovery and pharmacokinetic studies.
• Nutraceutical Research Ingredient: Serves as a key intermediate in the development of advanced dietary supplements targeting cellular health and metabolism.
• Biochemical Pathway Analysis: Employed in metabolic research to study the gut microbiome's transformation of ellagitannins and ellagic acid.
• High-Purity Chemical Intermediate: Acts as a precursor in the synthesis of more complex Urolithin analogs for structure-activity relationship (SAR) studies.
• Analytical Method Development: Essential for calibrating equipment and validating HPLC, LC-MS, and other analytical methods in quality control laboratories.
• Academic and Clinical Research: Supports in-vitro and in-vivo studies exploring the potential bioactivities of Urolithin compounds.

Basic Information

Product Name	Urolithin D Tetramethyl Ether
CAS No.	146776-39-8
Molecular Formula	C20H20O6
Molecular Weight	356.37 g/mol
Synonyms	3,8,9,10-Tetramethoxy-6H-dibenzo[b,d]pyran-6-one; Urolithin D 3,8,9,10-Tetramethyl Ether; 6H-Dibenzo[b,d]pyran-6-one, 3,8,9,10-tetramethoxy-; Tetramethyl Urolithin D; 3,4,8,9-Tetramethoxy-dibenzo[b,d]pyran-6-one; Urolithin D Tetra-O-methyl Ether
EINECS	Contact for details

Quality Control

Our Urolithin D Tetramethyl Ether is produced under strict quality management protocols. Each batch undergoes rigorous analytical testing, including HPLC for purity verification and spectroscopic identification (NMR, MS). A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to ensure traceability and compliance with your research or development specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Keep the container sealed to protect this light-sensitive compound from degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms to reference spectrum
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.