Description

Migraleve CAS NO 78168-90-8 is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for ensuring the efficacy and consistency of advanced therapeutic formulations. It is primarily required by pharmaceutical manufacturers and research institutions developing next-generation treatments.

Application

• Pharmaceutical Synthesis: A key intermediate in the production of active pharmaceutical ingredients (APIs) for specialized therapeutics.
• Neurological Research: Used in preclinical and clinical research studies targeting specific neurological pathways.
• Analytical Reference Standard: Serves as a high-purity standard for quality control and method validation in analytical laboratories.
• Formulation Development: Employed in the R&D of solid dosage forms, including tablets and capsules, requiring precise ingredient quality.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP-compliant production.

Basic Information

Product Name	Migraleve
CAS No.	78168-90-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Migraleve; 78168-90-8; 4-Amino-2-methyl-10H-thieno[2,3-b][1,5]benzodiazepine; Amthiofendyl; Amthiofendile; Amthiofendyl hydrochloride (salt form); Potential trade/proprietary names may apply.
EINECS	Contact for details

Quality Control

Our Migraleve is manufactured 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) documenting identity, purity, and related substances is provided with every shipment.

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). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥98.5%
Related Substances (HPLC)	Total impurities ≤1.5%
Single Maximum Unknown Impurity	≤0.5%
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.