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Diclofensine Hydrochloride CAS NO 34041-84-4


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CAS No.:34041-84-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Diclofensine Hydrochloride CAS NO 34041-84-4 is a high-purity pharmaceutical intermediate and research chemical. It is valued for its role in the synthesis of specialized compounds and as a key reference standard in analytical development. This product is primarily utilized by pharmaceutical R&D laboratories, academic research institutions, and manufacturers of active pharmaceutical ingredients (APIs).

Application

  • Pharmaceutical Intermediate: A critical building block in the synthesis of novel therapeutic agents and active pharmaceutical ingredients (APIs).
  • Reference Standard: Used for method development, validation, and quality control in analytical laboratories (HPLC, GC-MS).
  • Biochemical Research: Employed in pharmacological and neurochemical studies to investigate specific biological pathways and receptor interactions.
  • Chemical Synthesis: Serves as a precursor or reagent in advanced organic synthesis for creating complex molecular structures.
  • Academic & Institutional Research: Utilized in universities and research institutes for experimental studies and teaching purposes.

Basic Information

Product Name Diclofensine Hydrochloride
CAS No. 34041-84-4
Molecular Formula C₁₇H₁₈ClNO₂ • HCl
Molecular Weight 340.25 g/mol
Synonyms Diclofensine HCl; 1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride; Ro 8-4650; Diclofensin Hydrochloride; 3,4-Dichloro-N-(3-phenyl-2-propenyl)benzeneethanamine Hydrochloride; 1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane, hydrochloride; (E)-N-(3,4-Dichlorocinnamyl)-N-methylamine Hydrochloride
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Quality Control

Our Diclofensine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) with detailed results from tests including assay, impurity profile, and residual solvents, supporting compliance with cGMP and ICH guidelines for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

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%
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.

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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