Description

Doxiproct Plus is a high-purity pharmaceutical-grade chemical compound, identified by CAS No. 76404-12-1. It is a critical active pharmaceutical ingredient (API) or advanced intermediate designed for the development and manufacturing of specialized therapeutic agents. This product is essential for pharmaceutical companies and research institutions focused on creating innovative drug formulations. Its consistent quality and reliable supply chain make it a trusted component for high-stakes production.

Application

• Pharmaceutical API Synthesis: Serves as a key building block or active ingredient in the production of prescription medications.
• Research & Development: Used in preclinical and clinical research for developing new therapeutic compounds and studying pharmacological effects.
• Veterinary Medicine: Employed in the formulation of specialized treatments for animal health.
• Controlled-Release Formulations: Utilized in the development of advanced drug delivery systems that require precise release profiles.
• Analytical Reference Standard: Acts as a certified reference material for quality control and regulatory testing in laboratories.

Basic Information

Product Name	Doxiproct Plus
CAS No.	76404-12-1
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Doxiproct; Doxiproct Plus; 76404-12-1; Doxiproct derivative; Doxiproct analog; Pharmaceutical compound 76404-12-1; Doxiproct Plus API; Doxiproct intermediate
EINECS	Contact for details

Quality Control

Every batch of Doxiproct Plus is manufactured and tested under strict quality management systems. Our products undergo rigorous quality testing to ensure compliance with industry standards, including potential alignment with ICH guidelines and GMP principles where applicable. Certificates of Analysis (COA) are available upon request, providing full transparency on purity, identity, and impurity profiles.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and 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 standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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