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Diacetolol CAS NO 69796-04-9


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CAS No.:69796-04-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Diacetolol is a key pharmaceutical intermediate and β-adrenergic blocking agent. Its significance lies in its role as a precursor in the synthesis of more complex active pharmaceutical ingredients (APIs), particularly in cardiovascular therapeutics. This compound is essential for manufacturers and research institutions in the pharmaceutical and fine chemical sectors requiring high-purity building blocks for drug development and production.

Application

  • Pharmaceutical Intermediate: Primary use as a critical building block in the synthesis of β-blocker APIs.
  • Cardiovascular Drug Research: Serves as a reference standard and starting material in R&D for new antihypertensive and antianginal agents.
  • Metabolite Studies: Used in pharmacokinetic and metabolic pathway research related to β-adrenergic antagonists.
  • Fine Chemical Synthesis: Employed in custom synthesis and process development for specialized organic compounds.
  • Analytical Standard: Provides a high-purity standard for quality control and analytical method development in pharmaceutical laboratories.

Basic Information

Product Name Diacetolol
CAS No. 69796-04-9
Molecular Formula C18H29NO5
Molecular Weight 339.43 g/mol
Synonyms Diacetolol; 1-(4-Acetylphenoxy)-3-[(1,1-dimethylethyl)amino]-2-propanol diacetate; 3'-Acetyl-4'-(2-hydroxy-3-[(1,1-dimethylethyl)amino]propoxy)acetophenone diacetate; Acebutolol metabolite diacetate; N-Acetylacebutolol; (RS)-Diacetolol; DL-Diacetolol
EINECS Contact for details

Quality Control

Our Diacetolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR spectroscopy, and residual solvent analysis. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, ensuring compliance with cGMP and relevant pharmacopeial guidelines for pharmaceutical intermediates.

Storage

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

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0%
Any single impurity ≤ 0.5%
Loss on Drying ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

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With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

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

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.