Description

Tenofovir Related Compound 14 is a high-purity chemical reference standard and synthetic intermediate. This compound is critical for analytical research, quality control, and process development in the pharmaceutical industry. It is primarily utilized by researchers and manufacturers involved in the synthesis and impurity profiling of antiviral active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical reference standard for analytical method development and validation.
• Impurity standard for quality control (QC) and quality assurance (QA) of Tenofovir and its prodrugs.
• Key intermediate in custom organic synthesis and process chemistry research.
• Critical material for stability studies and degradation pathway analysis.
• Used in research and development (R&D) for novel antiviral compounds.
• Essential for regulatory compliance and submission documentation.

Basic Information

Product Name	Tenofovir Related Compound 14
CAS No.	1244022-52-3
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Tenofovir Impurity 14; Tenofovir Related Substance 14; Tenofovir EP Impurity I; Tenofovir USP Related Compound 14; (R)-9-(2-Phosphonomethoxypropyl)adenine Related Compound 14; PMPA Related Compound 14; GS-1278 Related Compound 14
EINECS	Contact for details

Quality Control

Our Tenofovir Related Compound 14 is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. Certificates of Analysis (COA) with detailed chromatographic data are provided and traceable to primary reference standards.

Storage

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

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms
Identification (MS)	Conforms
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5%
Total Impurities	≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Water Content (KF)	≤ 1.0%

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