Description

Levoprtiline is a high-purity pharmaceutical intermediate and active ingredient of significant interest in modern medicinal chemistry. Its value lies in its role as a key building block for the synthesis of advanced therapeutic agents, requiring stringent quality control for reliable performance. This compound is essential for research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in the development and production of specialized pharmaceuticals.

Application

• Pharmaceutical Intermediate: Serves as a critical precursor in the multi-step synthesis of novel active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and the discovery of new drug candidates.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
• Fine Chemical Synthesis: A valuable building block for constructing complex molecular architectures in custom synthesis projects.

Basic Information

Product Name	Levoprtiline
CAS No.	56433-44-4
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Levoprtiline; 56433-44-4; (1R,2S)-2-(Aminomethyl)-1-phenylcyclopropan-1-ol; (1R,2S)-2-(Aminomethyl)-1-phenyl-1-cyclopropanol; Levoprtiline base
EINECS	Contact for details

Quality Control

Our Levoprtiline is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets the high standards required for pharmaceutical applications. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

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 away from incompatible materials.

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 guidelines
Water Content (KF)	≤ 0.5%

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