Description

Detiviciclovir is a specialized nucleoside analogue with significant pharmaceutical relevance. This high-purity compound is critical for research and development in antiviral therapies, offering a valuable building block for medicinal chemistry. It is primarily utilized by pharmaceutical manufacturers and advanced research institutions engaged in the synthesis and study of novel antiviral agents.

Application

• Pharmaceutical Intermediate: Serves as a key synthetic precursor in the development of next-generation antiviral drugs.
• Medicinal Chemistry Research: Used as a reference standard and active scaffold in structure-activity relationship (SAR) studies for antiviral activity.
• Biochemical Research: Employed in enzymatic and cellular assays to investigate mechanisms of viral inhibition.
• GMP Manufacturing: Suitable for use in controlled synthesis under Good Manufacturing Practice (GMP) conditions for active pharmaceutical ingredient (API) production.
• Reference Standard: Provides a high-purity benchmark for quality control and analytical method development in pharmaceutical labs.

Basic Information

Product Name	Detiviciclovir
CAS No.	220984-26-9
Molecular Formula	C10H13N5O4
Molecular Weight	267.24 g/mol
Synonyms	9-[(1,3-Dihydroxy-2-propoxy)methyl]guanine; DHPMG; 2-Amino-1,9-dihydro-9-[[1,3-dihydroxy-2-propoxy]methyl]-6H-purin-6-one; Detiviciclovir; 1-(2,3-Dihydroxypropoxymethyl)guanine; GW 275175X; GW-275175X
EINECS	Contact for details

Quality Control

Our Detiviciclovir is manufactured under strict quality systems to ensure batch-to-batch consistency and high purity suitable for pharmaceutical research. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to relevant industry guidelines to support our clients' regulatory and compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Water Content (KF)	≤1.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH guidelines

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