Description

R 112 (Pharmaceutical) is a high-purity chemical intermediate designed for advanced pharmaceutical synthesis. Its defined structure and consistent quality are critical for ensuring the integrity and efficacy of final active pharmaceutical ingredients (APIs). This product is essential for research institutions and manufacturing facilities engaged in the development and production of modern therapeutics, where stringent quality control is paramount.

Application

• Pharmaceutical Intermediate: Serves as a key building block in multi-step synthesis routes for novel active pharmaceutical ingredients (APIs).
• Process Chemistry: Used in research and development (R&D) for route scouting and optimization in drug discovery programs.
• Reference Standard: Employed as an analytical standard for method development, validation, and quality control testing in pharmaceutical laboratories.
• Precursor for Specialty Chemicals: Acts as a starting material for the synthesis of more complex, target-specific molecules in fine chemical production.

Basic Information

Product Name	R 112 (Pharmaceutical)
CAS No.	575474-82-7
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	R-112; 575474-82-7; Pharmaceutical Intermediate R112; (Chemical name based on structure to be confirmed); (IUPAC name to be confirmed); (Common research code name)
EINECS	Contact for details

Quality Control

Our R 112 (Pharmaceutical) is manufactured under a quality management system and undergoes rigorous analytical testing to ensure it meets the high standards required for pharmaceutical applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We are committed to supporting compliance with cGMP and relevant pharmacopeial guidelines where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature. The container should be kept tightly sealed to protect the integrity of the material.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
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.