Description

Medifoxamine Acid Metabolite is a key organic intermediate and reference standard of significant importance in pharmaceutical research and development. Its primary value lies in its role as a defined metabolite for analytical method development, pharmacokinetic studies, and impurity profiling. This compound is essential for researchers and quality control laboratories in the pharmaceutical, biotechnology, and contract research organization (CRO) sectors who require high-purity chemical standards to ensure drug safety and efficacy.

Application

• Pharmaceutical Reference Standard: Used as a certified standard for the identification and quantification of Medifoxamine metabolites in biological matrices and drug formulations.
• Metabolite Research: Critical for studying the metabolic pathways, pharmacokinetics, and bioavailability of Medifoxamine and related compounds.
• Impurity Profiling: Serves as a known impurity or degradation product standard to establish specifications and ensure drug purity in accordance with ICH guidelines.
• Analytical Method Development: Employed in the validation and calibration of analytical techniques such as HPLC, LC-MS, and GC-MS for accurate detection.
• Preclinical & Clinical Studies: Utilized in toxicology and clinical trial support to understand drug disposition and safety profiles.
• Chemical Synthesis Intermediate: Acts as a building block for the synthesis of more complex molecules or labeled analogs for tracer studies.

Basic Information

Product Name	Medifoxamine Acid Metabolite
CAS No.	729-89-5
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Medifoxamine Metabolite; Medifoxamine Acid; 729-89-5; Medifoxamine carboxylic acid metabolite; Medifoxamine-COOH; Medifoxamine acid derivative; Medifoxamine related compound A
EINECS	Contact for details

Quality Control

Every batch of our Medifoxamine Acid Metabolite is manufactured and tested under a strict quality management system. We provide comprehensive analytical data to support its use as a reference material. A detailed Certificate of Analysis (COA) is supplied with each shipment, reporting key parameters such as purity (by HPLC), identity confirmation (by IR or NMR), and related substance profiles. Our quality commitment ensures the material is suitable for demanding applications in regulatory and research environments.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH limits
Water Content (KF)	≤ 0.5%

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