Description

Gevotroline is a high-purity pharmaceutical intermediate and research chemical. This compound is of significant interest for its role in the synthesis of novel therapeutic agents, particularly within the central nervous system (CNS) domain. It is primarily utilized by research institutions, pharmaceutical development laboratories, and fine chemical manufacturers engaged in advanced drug discovery and process chemistry.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of potential antipsychotic and neuroactive drug candidates.
• Chemical Research & Development: Serves as a versatile scaffold for medicinal chemists exploring new structure-activity relationships (SAR).
• Reference Standard: Used as an analytical standard in quality control and method development for pharmaceutical analysis.
• Preclinical Studies: Employed in the preparation of compounds for biological screening and pharmacological evaluation.
• Process Chemistry Optimization: Used in scaling up and optimizing synthetic routes for target molecules in pilot plants.

Basic Information

Product Name	Gevotroline
CAS No.	107266-06-8
Molecular Formula	C16H22N2O2
Molecular Weight	274.36 g/mol
Synonyms	1-(2,3-Dihydro-1,4-benzodioxin-5-yl)-4-(2-methoxyphenyl)piperazine; GEVOTROLINE; 107266-06-8; 1-(2,3-Dihydro-1,4-benzodioxin-5-yl)-4-(2-methoxyphenyl)piperazine; 5-[4-(2-Methoxyphenyl)-1-piperazinyl]-1,4-benzodioxane
EINECS	Contact for details

Quality Control

Our Gevotroline is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the stringent requirements for research and pharmaceutical applications. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with agreed specifications.

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). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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