Description

Amigluracil CAS NO 55696-52-1 is a high-purity pharmaceutical intermediate and research chemical. This compound is valued for its role as a key building block in the synthesis of more complex active pharmaceutical ingredients (APIs). It is primarily sought by research institutions and manufacturers in the pharmaceutical and life sciences sectors for drug discovery and development programs.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of novel therapeutic agents and active pharmaceutical ingredients (APIs).
• Biochemical Research: Used as a reference standard and reagent in metabolic pathway studies and enzymatic research.
• Academic & Institutional R&D: Serves as a key starting material for medicinal chemistry and organic synthesis projects in university and corporate laboratories.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis and scale-up projects.

Basic Information

Product Name	Amigluracil
CAS No.	55696-52-1
Molecular Formula	C9H11N3O5S
Molecular Weight	273.27 g/mol
Synonyms	1-((2S,3R,4S,5S)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-(methylsulfanyl)pyrimidine-2,4(1H,3H)-dione; 1-(β-D-Ribofuranosyl)-5-(methylthio)uracil; 5-(Methylthio)uridine; 5-Methylthiouridine; m5s2U; NSC 154020
EINECS	Contact for details

Quality Control

Our Amigluracil is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the high standards required for pharmaceutical research. A detailed Certificate of Analysis (COA) is provided with every shipment to guarantee batch-to-batch consistency and traceability.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%

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