Description

Oxetanocin G is a nucleoside analogue belonging to the oxetanocin family, a class of compounds known for their unique oxetane ring structure. This compound is of significant interest in pharmaceutical research and development due to its potential biological activity. It serves as a valuable building block and reference standard for scientists in medicinal chemistry and biochemistry. Key target industries include pharmaceutical R&D, biotechnology, and academic research institutions focused on antiviral and anticancer agent discovery.

Application

• Pharmaceutical Intermediate: Serves as a key synthetic precursor in the development of novel nucleoside-based therapeutics.
• Medicinal Chemistry Research: Used as a reference standard and building block for structure-activity relationship (SAR) studies in drug discovery programs.
• Biochemical Research: Employed in enzymatic studies to investigate substrate specificity and inhibition mechanisms of nucleoside-processing enzymes.
• Antiviral Agent Development: Investigated for its potential activity against viral polymerases and as a template for designing new antiviral prodrugs.
• Academic Research: Utilized in university and institutional labs for fundamental studies on nucleic acid chemistry and analog synthesis.
• Standards & Calibration: Provides a high-purity analytical standard for quality control and method development in analytical laboratories.

Basic Information

Product Name	Oxetanocin G
CAS No.	113269-46-8
Molecular Formula	C11H15N5O5
Molecular Weight	297.27 g/mol
Synonyms	9-[(2R,3R,4S)-3,4-Dihydroxy-2-(hydroxymethyl)oxetan-2-yl]guanine; 9-[(2R,3R,4S)-3,4-Dihydroxy-2-(hydroxymethyl)oxetanyl]guanine; Oxetanocin-G; OXT-G; (2'R,3'R,4'S)-2'-Deoxy-2'-(hydroxymethyl)oxetanocin G; Guanine Oxetanocin; Oxetano-G
EINECS	Contact for details

Quality Control

Our Oxetanocin G is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, NMR and MS for structural confirmation, and residual solvent analysis. We provide a detailed Certificate of Analysis (COA) with every shipment, ensuring traceability and compliance with research-grade specifications. For custom synthesis or specific pharmacopeial standards (e.g., USP reference standard grade), please contact our technical team.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container should be kept in a desiccated environment. For long-term storage, consider storing under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms to reference standard
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Meets ICH guidelines

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