Description

Deoxyketoprofen is a key pharmaceutical intermediate and a structural analog of the non-steroidal anti-inflammatory drug (NSAID) ketoprofen. Its primary value lies in its role as a versatile building block for the research and synthesis of novel anti-inflammatory agents and other bioactive molecules. This compound is essential for pharmaceutical R&D laboratories and manufacturers focused on developing new therapeutic compounds, particularly within the analgesic and anti-inflammatory drug classes. Deoxyketoprofen CAS NO 73913-48-1 offers a critical starting point for medicinal chemistry and process optimization.

Application

• Pharmaceutical Intermediate: Serves as a crucial precursor in the multi-step synthesis of ketoprofen and its novel derivatives.
• Medicinal Chemistry Research: Used as a scaffold or reference compound for structure-activity relationship (SAR) studies to develop new NSAIDs with improved efficacy or reduced side effects.
• Active Pharmaceutical Ingredient (API) Development: Employed in the development and scale-up processes for new analgesic and anti-inflammatory drug candidates.
• Biochemical Research: Utilized in in-vitro studies to investigate cyclooxygenase (COX) enzyme inhibition mechanisms and pathways of inflammation.
• Process Chemistry: Acts as a standard or intermediate in optimizing synthetic routes for cost-effective and high-yield production of related APIs.
• Reference Standard: Used in analytical laboratories as a high-purity standard for quality control and method development (HPLC, GC, etc.) of ketoprofen-based products.

Basic Information

Product Name	Deoxyketoprofen
CAS No.	73913-48-1
Molecular Formula	C16H14O3
Molecular Weight	254.28 g/mol
Synonyms	2-(3-Benzoylphenyl)propanoic Acid; α-Methyl-3-benzoylbenzeneacetic Acid; Desoxyketoprofen; Dexketoprofen Related Compound; 3-Benzoylhydratropic Acid; Ketoprofen Impurity; NSC 339539; (±)-2-(3-Benzoylphenyl)propionic Acid
EINECS	Contact for details

Quality Control

Our Deoxyketoprofen is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via advanced techniques like HPLC and GC, to ensure it meets high-grade standards suitable for pharmaceutical research and development. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with specified parameters.

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 the container sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Loss on Drying	≤0.5%
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.