Description

Lorajmine Hydrochloride is a high-purity pharmaceutical intermediate and reference standard. This compound is critical for research and development in the synthesis of specialized active pharmaceutical ingredients (APIs). It is primarily utilized by pharmaceutical manufacturers and research institutions focused on cardiovascular and neurological therapeutic areas.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of complex alkaloid-derived active pharmaceutical ingredients (APIs).
• Reference Standard: Used for analytical method development, validation, and quality control (QC) testing in pharmaceutical laboratories.
• Biochemical Research: Serves as a tool compound in pharmacological studies investigating ion channel modulation and cardiovascular effects.
• Process Development: Employed in scaling up and optimizing synthetic routes for GMP-compliant API production.

Basic Information

Product Name	Lorajmine Hydrochloride
CAS No.	40819-93-0
Molecular Formula	C22H27ClN2O2 • HCl
Molecular Weight	423.38 g/mol
Synonyms	Lorajmine HCl; Ajmaline, 17-Monochloroacetate Hydrochloride; Chloroacetylajmaline Hydrochloride; 17-Chloroacetylajmaline Hydrochloride; Ritmos Elle; Aritmina; Cardiorythmine
EINECS	Contact for details

Quality Control

Our Lorajmine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with agreed specifications. We support development and commercial projects requiring standards aligned with ICH guidelines and current Good Manufacturing Practices (cGMP).

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and purity.

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)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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