Description

Satigrel CAS NO 111753-73-2 is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API) of significant commercial interest. This compound is a key building block in the synthesis of advanced therapeutic agents, particularly those targeting platelet aggregation and related cardiovascular conditions. It is essential for research institutions, contract development and manufacturing organizations (CDMOs), and pharmaceutical companies engaged in the development of novel antiplatelet medications.

Application

• Pharmaceutical Intermediate: Primary use as a critical precursor in the synthesis of novel antiplatelet drugs and cardiovascular APIs.
• Active Pharmaceutical Ingredient (API): Serves as the core active component in finished dosage forms for clinical development and commercial production.
• Biochemical Research: Used in pharmacological studies to investigate mechanisms of platelet inhibition and thrombosis.
• Contract Manufacturing: Supplied to CDMOs for scale-up synthesis and process optimization under cGMP conditions.
• Reference Standard: Employed as an analytical standard for quality control, method validation, and regulatory submissions.
• Academic Research: Utilized in university and institutional labs for medicinal chemistry and drug discovery programs.

Basic Information

Product Name	Satigrel
CAS No.	111753-73-2
Molecular Formula	C14H12N2O3S
Molecular Weight	288.32 g/mol
Synonyms	Satigrel; SATIGREL; 2-(2-Methoxyphenoxy)-3-pyridinecarboxylic acid ethyl ester; Ethyl 2-(2-methoxyphenoxy)nicotinate; 2-(2-Methoxyphenoxy)nicotinic acid ethyl ester; KBT-302; KBT302; KBT 302; EINECS Contact for details

Quality Control

Our Satigrel is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Production adheres to cGMP guidelines where applicable, and the material is suitable for use in pharmaceutical development. Comprehensive analytical testing is performed, including identification, assay, and impurity profiling via advanced techniques like HPLC and GC. A Certificate of Analysis (COA) detailing all specifications and test results is provided with each 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 the container tightly sealed to protect from moisture.

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)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
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.