Description

Analgesin is a specialized pharmaceutical intermediate and active ingredient with significant importance in the development of modern therapeutic agents. Its primary value lies in its role as a key building block for synthesizing compounds with targeted biological activity, offering researchers and manufacturers a reliable and high-purity starting material. This product is essential for pharmaceutical R&D laboratories, fine chemical synthesis facilities, and companies developing new analgesic or anti-inflammatory formulations.

Application

• Pharmaceutical Intermediate: Serves as a critical precursor in the multi-step synthesis of novel active pharmaceutical ingredients (APIs).
• Analgesic Drug Development: Used in research and production of next-generation non-steroidal anti-inflammatory drugs (NSAIDs) and other pain management medications.
• Biochemical Research: Employed as a reference standard or reagent in pharmacological studies to investigate mechanisms of action and metabolic pathways.
• Fine Chemical Synthesis: Acts as a versatile building block for creating complex organic molecules with potential therapeutic applications in various disease areas.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production of clinical trial materials and commercial drug substances.

Basic Information

Product Name	Analgesin
CAS No.	76773-82-5
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	2-Acetoxybenzoic acid 2-methoxyethyl ester; Methoxyethyl salicylate acetate; Salicylic acid acetate methoxyethyl ester; Analgesin; 76773-82-5; Methoxyethyl acetylsalicylate; Ether, methoxyethyl salicylate acetate
EINECS	Contact for details

Quality Control

Our Analgesin is manufactured under strict quality management systems to ensure batch-to-batch consistency and reliability. Each lot undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling, to meet the stringent requirements of pharmaceutical ingredient supply. Certificates of Analysis (COA) documenting full specifications and test results are provided with every shipment to support your quality assurance and regulatory compliance needs.

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). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to minimize exposure to atmospheric moisture. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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