Description

Dimefline Hydrochloride is a pharmaceutical-grade active pharmaceutical ingredient (API) with significant therapeutic potential. This compound is valued for its precise pharmacological activity, making it a critical component in advanced pharmaceutical research and development. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development of new therapeutic agents, particularly in the areas of central nervous system and cardiovascular research. Our supply of Dimefline Hydrochloride CAS NO 2740-04-7 is characterized by high purity and batch-to-batch consistency to meet stringent R&D and production requirements.

Application

• Pharmaceutical API: Serves as the core active ingredient in the formulation of prescription medications.
• Clinical Research: Used in preclinical and clinical studies to investigate pharmacological efficacy and safety profiles.
• Reference Standard: Employed as a high-purity analytical standard in quality control laboratories for method development and validation.
• Biochemical Research: Utilized in life science research to study specific biochemical pathways and receptor interactions.
• Drug Discovery: A key intermediate or target molecule in the synthesis and screening of new chemical entities.
• Generic Drug Manufacturing: Essential for companies producing generic versions of medications containing this API, ensuring bioequivalence.

Basic Information

Item	Detail
Product Name	Dimefline Hydrochloride
CAS No.	2740-04-7
Molecular Formula	C20H21NO3 · HCl
Molecular Weight	351.85 g/mol
Synonyms	Dimefline HCl; 4-(Dimethylamino)-2-methyl-1-phenyl-2-butanol Hydrochloride; 1-Phenyl-2-methyl-4-dimethylaminobutan-2-ol Hydrochloride; Dimeflinum; Dimeflini Hydrochloridum
EINECS	Contact for details

Quality Control

Our Dimefline Hydrochloride is manufactured and tested under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. We provide a detailed Certificate of Analysis (COA) with each shipment, which includes results for identity, assay, purity, and specified impurities. Our quality protocols are designed to support compliance with cGMP and relevant pharmacopeial guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	98.0% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 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.