Description

Levacetylmethadol is a synthetic opioid compound with the CAS number 34433-66-4. It is a significant intermediate in pharmaceutical research and development, particularly valued for its role in the synthesis of specialized therapeutic agents. This compound is essential for research laboratories and pharmaceutical manufacturers focused on neuropharmacology and analgesic development.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of advanced opioid-based medications and research compounds.
• Analgesic Research: Used in preclinical studies to investigate mechanisms of pain relief and receptor binding profiles.
• Neuropharmacology Studies: Serves as a reference standard or active agent in studies of the central nervous system.
• Metabolite Synthesis: Employed in the preparation of metabolites for pharmacokinetic and toxicological profiling.
• Reference Standard: Utilized in analytical laboratories for method development and quality control testing via HPLC or GC.
• Chemical Synthesis: Acts as a precursor for the development of novel chemical entities with potential therapeutic activity.

Basic Information

Product Name	Levacetylmethadol
CAS No.	34433-66-4
Molecular Formula	C23H31NO2
Molecular Weight	353.50 g/mol
Synonyms	(-)-α-L-Acetylmethadol; L-α-Acetylmethadol; LAAM; Levomethadyl Acetate; Orlaam; Alphanoracetylmethadol; (3S,6S)-6-(Dimethylamino)-4,4-diphenyl-3-heptyl acetate; Nor-LAAM (referring to a metabolite)
EINECS	Contact for details

Quality Control

Our Levacetylmethadol is manufactured under strict quality systems to ensure high purity and batch-to-batch consistency. Each lot is supported by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to cGMP principles where applicable, and our analytical methods, including HPLC and GC, are validated to meet rigorous research and development standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled accordingly 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% Any single impurity ≤ 1.0%
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.