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Oxeladin CAS NO 468-61-1


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CAS No.:468-61-1

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Oxeladin is a synthetic organic compound with specific pharmacological activity. This compound is valued for its targeted action and is a key intermediate in advanced pharmaceutical synthesis. It is primarily required by research institutions and pharmaceutical manufacturers engaged in the development of therapeutic agents. We supply high-purity Oxeladin CAS NO 468-61-1 to support critical R&D and production processes globally.

Application

  • Pharmaceutical Intermediate: Serves as a crucial building block in the synthesis of specialized active pharmaceutical ingredients (APIs).
  • Biochemical Research: Used as a reference standard or investigational compound in pharmacological and metabolic studies.
  • Organic Synthesis: Acts as a versatile intermediate for constructing complex molecular architectures in medicinal chemistry.
  • Analytical Standard: Employed for method development, calibration, and quality control testing in analytical laboratories.

Basic Information

Product Name Oxeladin
CAS No. 468-61-1
Molecular Formula C18H27NO2
Molecular Weight 289.41 g/mol
Synonyms Oxeladin; Oxeladin Citrate (salt form); 2-(2-Diethylaminoethoxy)ethyl α-ethyl-α-phenylbutyrate; α-Ethyl-α-phenylbutyric acid 2-(2-diethylaminoethoxy)ethyl ester; Pectamol; Neobex; Tussefane; Tussafug
EINECS 207-418-5

Quality Control

Our Oxeladin is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation, to ensure it meets exacting standards for pharmaceutical research and development. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with every shipment.

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). Keep away from incompatible materials and sources of ignition.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Assay (HPLC) ≥ 98.5%
Related Substances (HPLC) Total impurities ≤ 1.5%
Loss on Drying ≤ 0.5%
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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Trusted Manufacturer

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

Rigorous Quality Assurance

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.