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Gemcabene CAS NO 209789-08-2


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CAS No.:209789-08-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Gemcabene is a high-purity, small-molecule pharmaceutical intermediate with significant research and development interest. This compound is valued for its role as a key building block in the synthesis of novel therapeutic agents, particularly in the metabolic and cardiovascular disease space. It is primarily sought by pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and fine chemical suppliers serving the global life sciences industry.

Application

  • Pharmaceutical Intermediate: Serves as a critical precursor in the synthesis of active pharmaceutical ingredients (APIs) targeting dyslipidemia and related metabolic disorders.
  • Research & Development: Used in medicinal chemistry programs for lead optimization and the development of new chemical entities (NCEs).
  • Reference Standard: Employed as an analytical standard in quality control (QC) and method development for API and finished drug product analysis.
  • Process Chemistry: Utilized in route scouting, scale-up studies, and process optimization within pilot plants and commercial manufacturing.
  • Biochemical Research: Applied in in-vitro and in-vivo studies to investigate mechanisms of action related to lipid metabolism.
  • Contract Synthesis: Supplied to CROs and CMOs for custom synthesis projects and clinical trial material (CTM) manufacturing.

Basic Information

Product Name Gemcabene
CAS No. 209789-08-2
Molecular Formula C17H14O4
Molecular Weight 282.29 g/mol
Synonyms 1,2-Bis(4-methoxyphenyl)-1,2-ethanedione; 4,4'-Dimethoxybenzil; NSC 758707; Gemcabene (USAN); CC-1; Benzil, 4,4'-dimethoxy-; Bis(4-methoxyphenyl)ethanedione
EINECS Contact for details

Quality Control

Our Gemcabene is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We support compliance with cGMP and ICH Q7 guidelines for pharmaceutical intermediates, and specifications can be aligned with client-specific pharmacopeial requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture. Keep away from incompatible materials.

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 unknown impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Loss on Drying ≤ 1.0%
Heavy Metals ≤ 20 ppm

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

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Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.