Description

Levomethadyl Acetate Hydrochloride is a high-purity pharmaceutical intermediate and analytical reference standard. This compound is critical for research and development in medicinal chemistry, particularly in the study of opioid receptor pharmacology. It is primarily utilized by pharmaceutical manufacturers, contract research organizations (CROs), and analytical laboratories requiring precise and reliable chemical entities for synthesis and quality control processes.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis and research of specialized pharmaceutical compounds.
• Analytical Reference Standard: Used for method development, validation, and quality control testing in HPLC, GC, and other chromatographic systems.
• Medicinal Chemistry Research: Serves as a crucial reagent in preclinical studies targeting central nervous system (CNS) pathways.
• Metabolite Studies: Employed in pharmacokinetic and metabolic pathway research for related therapeutic agents.
• Impurity Standard: Acts as a certified reference material for identifying and quantifying impurities in active pharmaceutical ingredients (APIs).
• Academic & Institutional Research: Used in university and government laboratories for pharmacological and chemical research projects.

Basic Information

Product Name	Levomethadyl Acetate Hydrochloride
CAS No.	43033-72-3
Molecular Formula	C23H31NO2·HCl
Molecular Weight	389.96 g/mol
Synonyms	LAAM Hydrochloride; (-)-Methadyl Acetate Hydrochloride; Levacetylmethadol Hydrochloride; L-α-Acetylmethadol Hydrochloride; Orlaam Hydrochloride; (3S,6S)-6-(Dimethylamino)-4,4-diphenylheptan-3-yl acetate hydrochloride; L-α-Acetylmethadol Hydrochloride
EINECS	Contact for details

Quality Control

Our Levomethadyl Acetate Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling, to ensure it meets exacting standards for research and development use. Certificates of Analysis (COA) with detailed chromatographic data (HPLC/GC) are provided to guarantee traceability and batch-to-batch consistency.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture. For long-term storage, consider desiccants or inert atmosphere conditions.

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%
Water Content (KF)	≤1.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm

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