Description

Tametraline is a synthetic organic compound belonging to the class of substituted tetralins, identified by the CAS registry number 52760-47-1. It serves as a crucial pharmaceutical intermediate and a valuable scaffold in medicinal chemistry research for the development of novel therapeutic agents. This compound is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the synthesis of complex molecules for central nervous system (CNS) applications.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of advanced drug candidates and active pharmaceutical ingredients (APIs).
• Medicinal Chemistry Research: Used as a core scaffold for structure-activity relationship (SAR) studies and the design of new chemical entities.
• Neurological Research: Investigated for its potential pharmacological activity related to neurotransmitter systems.
• Chemical Synthesis: Employed in organic synthesis for constructing complex polycyclic frameworks in laboratory settings.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in analytical laboratories.

Basic Information

Product Name	Tametraline
CAS No.	52760-47-1
Molecular Formula	C17H19N
Molecular Weight	237.34 g/mol
Synonyms	1,2,3,4-Tetrahydro-2-methyl-9H-dibenzo[3,4:6,7]cyclohepta[1,2-c]pyridine; CP-24,441; Tametraline Hydrochloride (salt form); (±)-Tametraline; trans-(±)-Tametraline
EINECS	Contact for details

Quality Control

Our Tametraline is produced under a strict quality management system. Every batch undergoes comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with each shipment, confirming compliance with agreed specifications. We support cGMP standards for pharmaceutical intermediate applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider an inert atmosphere to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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