Description

Tenosiprol is a high-purity chemical compound used in advanced pharmaceutical synthesis and specialized research. Its primary value lies in its role as a key intermediate or active component in the development of novel therapeutic agents. This product is essential for pharmaceutical manufacturers, R&D laboratories, and fine chemical producers focused on innovation in drug discovery and process chemistry.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of active pharmaceutical ingredients (APIs) for various therapeutic areas.
• Biochemical Research: Used as a reagent or substrate in enzymatic studies and metabolic pathway investigations.
• Organic Synthesis: Serves as a versatile precursor for constructing complex molecular architectures in medicinal chemistry.
• Reference Standard: Employed as an analytical standard for quality control and method validation in pharmaceutical analysis.
• Process Development: Utilized in scaling up and optimizing synthetic routes for commercial pharmaceutical production.

Basic Information

Product Name	Tenosiprol
CAS No.	129336-81-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Tenosiprol; 129336-81-8; (Chemical name based on CAS); (IUPAC name based on structure); (Common research code name); (Potential trade name variant); (Abbreviated chemical alias)
EINECS	Contact for details

Quality Control

Our Tenosiprol is manufactured under a strict quality management system to ensure batch-to-batch consistency and high purity. Production adheres to cGMP guidelines where applicable, and each lot is accompanied by a comprehensive Certificate of Analysis (COA). We support our clients' regulatory needs with full traceability and documentation.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials and sources of ignition.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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