Description

Valtorcitabine is a high-purity nucleoside analog pharmaceutical intermediate of significant interest in advanced therapeutic development. Its primary value lies in its role as a key building block for the synthesis of novel antiviral and anticancer agents, enabling critical research and production. This compound is essential for pharmaceutical R&D laboratories, biotechnology firms, and manufacturers focused on creating next-generation nucleotide-based therapeutics.

Application

• Pharmaceutical Intermediate: Serves as a critical precursor in the synthesis of novel antiviral and anticancer nucleotide analogs.
• Antiviral Drug Research: Used in the development and study of new therapeutic agents targeting viral infections.
• Oncology Research: Employed as a building block for creating potential chemotherapeutic compounds and targeted cancer therapies.
• Biochemical Research: Utilized in academic and industrial laboratories for studying enzyme mechanisms, nucleotide metabolism, and cellular processes.
• Process Development & Scale-up: Integral to optimizing synthetic routes and scaling production for clinical trial material and commercial APIs.
• Reference Standard: Acts as a high-purity analytical standard for quality control and regulatory submissions in pharmaceutical manufacturing.

Basic Information

Product Name	Valtorcitabine
CAS No.	380886-95-3
Molecular Formula	C8H11FN4O4
Molecular Weight	246.20 g/mol
Synonyms	Val-L-dC; Valinocytidine; L-Valine, 2-[(2R,3S,5R)-5-(4-amino-2-oxo-1(2H)-pyrimidinyl)-2-(hydroxymethyl)tetrahydro-3-furanyl] ester; 1-(2R,3S,5R)-5-[(2S)-2-Amino-3-methylbutanoyloxymethyl]-3-hydroxytetrahydrofuran-2-yl]-5-fluoro-1,2,3,4-tetrahydropyrimidine-2,4-dione; β-L-2′-Deoxy-2′,3′-didehydro-5-fluorocytidine valinate; A compound of valine and β-L-Fd4C
EINECS	Contact for details

Quality Control

Our Valtorcitabine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity, suitable for research and pharmaceutical applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to relevant industry standards and can provide material tailored to specific project requirements, including research-grade and GMP-grade specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container sealed to protect from moisture. For long-term storage, consider storing under an inert atmosphere to ensure optimal stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Water Content (KF)	≤1.0%
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.