Description

Emorfazone is a non-steroidal anti-inflammatory drug (NSAID) compound with the CAS registry number 38957-41-4. It serves as a key pharmaceutical intermediate and active ingredient in the development of analgesic and anti-inflammatory medications. This compound is primarily utilized by pharmaceutical manufacturers and research institutions engaged in drug development and synthesis.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of finished dosage forms of emorfazone-based drugs.
• Analgesic Formulations: Used in the research and production of medications designed to relieve pain.
• Anti-inflammatory Drug Development: Serves as the active pharmaceutical ingredient (API) in formulations targeting inflammation reduction.
• Reference Standard: Employed as a high-purity standard in analytical laboratories for quality control and method validation.
• Preclinical & Clinical Research: Utilized in pharmacological studies to investigate efficacy, pharmacokinetics, and safety profiles.
• Veterinary Medicine: Potential application in developing anti-inflammatory treatments for animal healthcare.

Basic Information

Product Name	Emorfazone
CAS No.	38957-41-4
Molecular Formula	C16H14N2O3
Molecular Weight	282.30 g/mol
Synonyms	4-Ethoxy-2-methyl-5-morpholino-3(2H)-pyridazinone; M-73101; Pentoil; Pentoil (pharmaceutical); Emorfazon; 5-Morpholino-4-ethoxy-2-methyl-3(2H)-pyridazinone; 4-Ethoxy-2-methyl-5-morpholin-4-yl-2H-pyridazin-3-one
EINECS	Contact for details

Quality Control

Our Emorfazone is manufactured and tested under a strict quality management system. We provide material that meets high-purity standards suitable for pharmaceutical research and development. A comprehensive Certificate of Analysis (COA), detailing identity, purity, and impurity profiles, is supplied with each batch to ensure traceability and compliance with your specifications.

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.

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% Any single impurity ≤ 1.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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