Description

Tetriprofen CAS NO 28168-10-7 is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for ensuring the quality and efficacy of final drug formulations in the pharmaceutical manufacturing process. It is primarily required by research institutions and production facilities in the pharmaceutical and fine chemical industries for the synthesis of advanced therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other active pharmaceutical ingredients (APIs).
• Active Pharmaceutical Ingredient (API): Used as the core therapeutic component in formulated drug products targeting inflammation and pain.
• Biochemical Research: Serves as a reference standard and reagent in pharmacological studies and metabolic pathway analysis.
• Fine Chemical Synthesis: Employed in advanced organic synthesis for creating complex molecules with specific chiral or structural properties.
• Veterinary Medicine: Utilized in the development of anti-inflammatory treatments for animal healthcare.

Basic Information

Product Name	Tetriprofen
CAS No.	28168-10-7
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Tetriprofen; 2-(4-Isobutylphenyl)propionic Acid (related structural analog); Ibuprofen Impurity/Intermediate; α-Methyl-4-(2-methylpropyl)benzeneacetic Acid Derivative; NSAID Intermediate; Propionic Acid Derivative; Anti-inflammatory Intermediate; Benzeneacetic Acid Derivative
EINECS	Contact for details

Quality Control

Our Tetriprofen is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with every shipment to guarantee traceability and compliance.

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). Keep away from incompatible materials such as strong oxidizing agents.

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 ≤ 1.0%
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.