Description

Tilnoprofen Arbamel is a specialized non-steroidal anti-inflammatory drug (NSAID) compound, identified by CAS No. 159098-79-0. It serves as a critical intermediate in the synthesis of advanced pharmaceutical agents, offering significant value in the development of targeted anti-inflammatory and analgesic therapies. This high-purity compound is essential for pharmaceutical R&D laboratories, fine chemical manufacturers, and academic institutions engaged in novel drug discovery and process chemistry.

Application

• Pharmaceutical Intermediate: Primary use as a key building block in the synthesis of proprietary NSAID and analgesic active pharmaceutical ingredients (APIs).
• Research & Development: Critical material for medicinal chemistry programs focused on inflammation pathways, COX enzyme inhibition, and pain management.
• Process Chemistry: Used in scale-up and optimization studies for the commercial manufacturing of related drug substances.
• Reference Standard: Serves as an analytical standard for method development, validation, and quality control in pharmaceutical analysis.
• Academic Research: Utilized in university and institutional labs for pharmacological studies and the development of new chemical entities.
• Fine Chemical Synthesis: Intermediate for creating more complex, functionalized molecules with potential therapeutic applications.

Basic Information

Product Name	Tilnoprofen Arbamel
CAS No.	159098-79-0
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Tilnoprofen Arbamel; Arbamel; 2-[4-(3-Chloro-2-methylphenyl)phenyl]propionic Acid Arbamel Ester; Tilnoprofen Intermediate; CAS 159098-79-0; Tilnoprofen Arbamel Ester; Propionic acid, 2-[4-(3-chloro-2-methylphenyl)phenyl]-, Arbamel ester
EINECS	Contact for details

Quality Control

Our Tilnoprofen Arbamel is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by spectroscopic methods (IR, NMR), and residual solvent analysis to ensure it meets exacting standards for pharmaceutical research. Certificates of Analysis (COA) documenting all test results are provided with each shipment and are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). The material should be kept under an inert atmosphere if prolonged storage is anticipated to prevent degradation.

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% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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