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Eleclazine (Hydrochloride) CAS NO 1448754-43-5


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CAS No.:1448754-43-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Eleclazine (Hydrochloride) CAS NO 1448754-43-5 is a high-purity, small-molecule pharmaceutical intermediate and research chemical. This compound is of significant interest for its role in the development of novel cardiac and neurological therapeutics, specifically as a late sodium current inhibitor. It is primarily utilized by pharmaceutical R&D laboratories, contract research organizations (CROs), and academic research institutions focused on ion channel modulation.

Application

  • Pharmaceutical Research & Development: Key intermediate in the synthesis of novel drug candidates targeting cardiac arrhythmias.
  • Preclinical Studies: Used in vitro and in vivo models to investigate late sodium current (INaL) blockade for conditions like long QT syndrome and atrial fibrillation.
  • Biochemical Assay Development: Serves as a reference standard and active agent in high-throughput screening (HTS) for ion channel activity.
  • Mechanism of Action (MoA) Studies: Critical tool for elucidating the pharmacological profile and selectivity of sodium channel modulators.
  • Academic Research: Employed in university labs for fundamental studies on cardiac electrophysiology and channelopathies.
  • GMP Manufacturing: Sourced as a starting material or intermediate for cGMP production of active pharmaceutical ingredients (APIs) under stringent quality protocols.

Basic Information

Product Name Eleclazine (Hydrochloride)
CAS No. 1448754-43-5
Molecular Formula C₂₀H₂₅ClN₂O₃ • HCl
Molecular Weight 397.34 g/mol (for hydrochloride salt)
Synonyms GS-6615; GS6615; Eleclazine HCl; 4-[[(3S,5R)-3,5-Dimethyl-1-piperazinyl]methyl]-N-[4-(1-methylethyl)phenyl]-2-benzothiazolamine hydrochloride; (S,R)-GS-6615 hydrochloride; Late Sodium Current Inhibitor GS-6615
EINECS Contact for details

Quality Control

Our Eleclazine (Hydrochloride) is manufactured and tested under a rigorous quality management system. Each batch is analyzed to meet high-purity standards suitable for pharmaceutical research. A comprehensive Certificate of Analysis (COA) is provided, detailing purity, identity, and impurity profiles as determined by HPLC, NMR, and MS. We support development with GMP-grade material upon request, ensuring traceability and documentation for regulatory filings.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) or as specified on the label. This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to maintain stability and purity.

Specification

Item Specification
Appearance White to off-white solid
Identification (HPLC) Conforms to reference standard
Identification (IR) Conforms to structure
Assay (HPLC) ≥98.0%
Purity (HPLC, Area%) ≥99.0%
Water Content (KF) ≤1.0%
Residual Solvents (GC) Complies with ICH Q3C
Heavy Metals <20 ppm

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

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