Description

Oxetanocin is a unique nucleoside analogue characterized by its oxetane ring structure, which confers distinct biochemical properties. This compound is of significant interest in pharmaceutical research and development due to its potent antiviral and antitumor activities. It serves as a critical intermediate and reference standard for researchers in the life sciences sector, particularly those developing novel therapeutics. Industries engaged in antiviral drug discovery, oncology research, and advanced nucleotide chemistry are the primary users of this high-value compound.

Application

• Antiviral Drug Research: Serves as a key scaffold and precursor in the development of novel antiviral agents targeting viruses such as herpes simplex virus (HSV) and hepatitis B virus (HBV).
• Oncology Research: Investigated for its antitumor properties and potential use as a chemotherapeutic agent or as a building block for targeted cancer therapies.
• Biochemical Tool Compound: Used as a reference standard and probe in enzymatic studies to understand nucleoside metabolism and the mechanisms of DNA/RNA polymerases.
• Nucleoside Analogue Synthesis: Acts as a versatile intermediate for the chemical synthesis of modified nucleosides with enhanced biological stability and activity.
• Pharmaceutical Intermediate: Employed in the cGMP-compliant manufacturing of active pharmaceutical ingredients (APIs) for clinical trial materials.
• Academic & Institutional Research: Utilized in university and government laboratories for fundamental research in medicinal chemistry and molecular biology.

Basic Information

Product Name	Oxetanocin
CAS No.	103913-16-2
Molecular Formula	C8H11N5O4
Molecular Weight	241.21 g/mol
Synonyms	Oxetanocin; Oxetanocin A; OXT-A; 9-[(2R,3R,4S)-3,4-Bis(hydroxymethyl)-2-oxetanyl]adenine; 9-[(2R,3R,4S)-3,4-Bis(hydroxymethyl)oxetan-2-yl]-9H-adenine; 2-Oxetanocin; NSC 696175; AODN
EINECS	Contact for details

Quality Control

Every batch of Oxetanocin is manufactured and tested under a strict quality management system. We provide comprehensive analytical data to ensure the identity, purity, and consistency required for research and development applications. Certificates of Analysis (COA) detailing specifications such as HPLC purity, chiral purity, and residual solvent content are supplied with each shipment. Our quality commitment aligns with the standards expected for pharmaceutical intermediates and reference materials.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation. For long-term storage, consider desiccated conditions.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Chiral Purity (HPLC)	≥99.0%
Water Content (KF)	≤1.0%
Residual Solvents (GC)	Complies with ICH guidelines
Heavy Metals	<10 ppm

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