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Eplivanserin Mixture CAS NO 130581-13-4


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CAS No.:130581-13-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Eplivanserin Mixture CAS NO 130581-13-4 is a key chemical intermediate of significant interest in advanced pharmaceutical research and development. This compound is valued for its role in the synthesis pathway of active pharmaceutical ingredients (APIs) targeting specific neurological pathways. It is primarily utilized by research institutions, contract development and manufacturing organizations (CDMOs), and pharmaceutical companies engaged in the development of novel therapeutic agents.

Application

  • Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of complex active pharmaceutical ingredients (APIs).
  • Neurological Research: Used in preclinical and research settings for the development of compounds targeting specific receptor systems.
  • Process Development: Employed by CDMOs for route scouting, optimization, and scale-up studies for new drug candidates.
  • Reference Standard: Can be utilized as a qualitative or quantitative analytical standard in method development and quality control laboratories.
  • Chemical Synthesis: Acts as a specialized synthon in organic chemistry for constructing complex molecular architectures in medicinal chemistry programs.

Basic Information

Product Name Eplivanserin Mixture
CAS No. 130581-13-4
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Eplivanserin; Eplivanserin fumarate intermediate; 4-(2-Fluorophenyl)-6-methyl-2-piperazin-1-yl-thieno[2,3-d]pyrimidine mixture; SR 46349 mixture; SR-46349 mixture; Thienopyrimidine derivative mixture; 6-Methyl-4-(2-fluorophenyl)-2-(1-piperazinyl)thieno[2,3-d]pyrimidine mixture
EINECS Contact for details

Quality Control

Our Eplivanserin Mixture is produced and handled under a strict quality management system. Each batch undergoes comprehensive analytical testing, including identity confirmation and purity assessment, to ensure it meets the stringent requirements for pharmaceutical R&D. A Certificate of Analysis (COA) detailing specific test results 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. Keep away from incompatible materials.

Specification

Item Specification
Appearance Off-white to light yellow solid/powder
Identification (HPLC/IR) Conforms to reference standard
Assay (HPLC) ≥ 95.0%
Related Substances (HPLC) Individual impurity ≤ 1.0%; Total impurities ≤ 3.0%
Residual Solvents (GC) Complies with ICH guidelines
Loss on Drying ≤ 1.0%

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

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