Description

Amoxydramine Camsilate is a pharmaceutical-grade active pharmaceutical ingredient (API) and chemical intermediate. This compound is valued for its specific pharmacological activity and is a critical component in the synthesis of advanced therapeutic agents. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development of new drug formulations and clinical studies.

Application

• Pharmaceutical API: Primary active ingredient in prescription medication formulations.
• Chemical Intermediate: Key building block in the multi-step synthesis of complex drug molecules.
• Research & Development: Reference standard and material for pharmacological and pharmacokinetic studies.
• Preclinical Studies: Used in laboratory research to investigate efficacy and safety profiles.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for GMP production.

Basic Information

Product Name	Amoxydramine Camsilate
CAS No.	15350-99-9
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Amoxydramine Camsylate; Amoxydramine Camphorsulfonate; Amoxydramine (+)-10-Camphorsulfonate; 2-[(2-Dimethylaminoethoxy)phenyl]-2-methylpentyl 3-hydroxy-2-naphthoate camphorsulfonate salt; NSC 113986
EINECS	Contact for details

Quality Control

Our Amoxydramine Camsilate is produced under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to ensure traceability and compliance.

Storage

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

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%

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