Description

Levometimeprazine CAS NO 1759-09-7 is a high-purity pharmaceutical intermediate and research chemical belonging to the phenothiazine class. This compound is critical for the development and synthesis of active pharmaceutical ingredients (APIs) targeting central nervous system disorders. It is primarily utilized by pharmaceutical manufacturers and advanced research institutions engaged in neuropharmacology and drug discovery.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of antipsychotic and neuroleptic drug candidates.
• Research & Development: Used in preclinical studies to investigate receptor binding and pharmacological activity related to dopamine and serotonin pathways.
• Reference Standard: Serves as a certified reference material (CRM) for analytical method development and quality control in pharmaceutical labs.
• Chemical Synthesis: Utilized in organic synthesis for creating novel phenothiazine derivatives with potential therapeutic applications.
• Academic Research: Employed in university and institutional research for studying the structure-activity relationships (SAR) of psychoactive compounds.

Basic Information

Product Name	Levometimeprazine
CAS No.	1759-09-7
Molecular Formula	C19H22N2S
Molecular Weight	310.45 g/mol
Synonyms	Levomepromazine; Methotrimeprazine; 7043 RP; Levoprome; Nozinan; Levozan; Neurocil; Veractil; (2R)-3-(2-Methoxyphenothiazin-10-yl)-N,N,2-trimethylpropan-1-amine; (-)-Methotrimeprazine
EINECS	217-166-2

Quality Control

Our Levometimeprazine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the stringent requirements for pharmaceutical research and development. Certificates of Analysis (COA) detailing all specifications are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a 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 reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5%
Single Maximum Impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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