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Gnf179 Metabolite CAS NO 1310455-86-7


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CAS No.:1310455-86-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Gnf179 Metabolite CAS NO 1310455-86-7 is a high-purity reference standard and key intermediate used in pharmaceutical research and development. This compound is critical for metabolic profiling, pharmacokinetic studies, and the synthesis of advanced active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions, pharmaceutical companies, and CROs (Contract Research Organizations) engaged in drug discovery and analytical method development.

Application

  • Pharmaceutical Reference Standard: Serves as a certified standard for the quantification and identification of metabolites in bioanalytical studies.
  • Drug Metabolism and Pharmacokinetics (DMPK): Essential for in vitro and in vivo studies to understand the metabolic pathways and clearance of parent drug compounds.
  • Impurity Profiling: Used as a known impurity or degradation product standard to ensure drug substance and product purity per ICH guidelines.
  • Preclinical and Clinical Research: Supports toxicology assessments and clinical trial sample analysis.
  • Analytical Method Development: A critical component for developing and validating HPLC, LC-MS, and other chromatographic methods.
  • Chemical Synthesis: Acts as a key building block or intermediate in the synthesis of novel drug candidates and related compounds.

Basic Information

Product Name Gnf179 Metabolite
CAS No. 1310455-86-7
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms GNF179 Metabolite; GNF-179 Metabolite; GNF 179 Metabolite; 1310455-86-7; GNF179 Related Compound; GNF179 Impurity; GNF179 Degradant; GNF179 Intermediate
EINECS Contact for details

Quality Control

Our Gnf179 Metabolite is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with detailed chromatographic data (HPLC/LC-MS) and spectroscopic characterization. Our quality commitment aligns with the standards expected for pharmaceutical reference materials.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under inert atmosphere or desiccated conditions after opening to maintain stability and purity.

Specification

Item Specification
Appearance White to off-white solid
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 98.0%
Related Substances (HPLC) Individual impurity ≤ 0.5% Total impurities ≤ 2.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Water Content (KF) ≤ 1.0%

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

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

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