Description

(±)-Lefetamine Hydrochloride is a synthetic chemical compound belonging to the class of phenylalkylamine derivatives. This material is of significant interest in pharmaceutical research and development, particularly for its potential as a reference standard or analytical reagent. It serves a critical role for researchers and quality control laboratories in the life sciences sector requiring high-purity chemical entities for method development, validation, and pharmacological studies.

Application

• Pharmaceutical Reference Standard: Used as a certified standard for the identification, purity assessment, and quantification of lefetamine in analytical methods.
• Pharmacological Research: Serves as a key intermediate or active substance in preclinical studies investigating the effects of phenylalkylamine compounds.
• Forensic Analysis: Employed as a control substance in forensic toxicology laboratories for the detection and confirmation of related compounds.
• Method Development & Validation: Essential for developing and validating analytical protocols such as HPLC, GC-MS, or LC-MS in regulatory and R&D settings.
• Chemical Synthesis: Acts as a building block or precursor in the synthesis of more complex molecules for research purposes.
• Quality Control (QC) Testing: Used by pharmaceutical manufacturers and contract research organizations (CROs) to ensure the specificity and accuracy of their testing procedures.

Basic Information

Product Name	(±)-Lefetamine Hydrochloride
CAS No.	24301-90-4
Molecular Formula	C13H19N·HCl
Molecular Weight	225.76 g/mol
Synonyms	Lefetamine HCl; (±)-1,2-Diphenylethylamine Hydrochloride; (±)-N,α-Dimethyl-β-phenethylamine Hydrochloride; (±)-N-Methyl-1,2-diphenylethylamine Hydrochloride; (±)-N-Methyl-α-phenylphenethylamine Hydrochloride; (±)-SL-164 Hydrochloride; Racemic Lefetamine Hydrochloride; Contact for details on EINECS

Quality Control

Our (±)-Lefetamine Hydrochloride is produced and handled under strict quality management protocols. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and support our products with detailed Certificates of Analysis (COA), which include results from chromatographic and spectroscopic methods. Specifications are designed to meet the rigorous demands of research and analytical applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 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 atmospheres.

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%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%

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