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Diflunisal-D3 CAS NO 1286107-99-0


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CAS No.:1286107-99-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Diflunisal-D3 is a deuterated internal standard specifically designed for analytical applications. This compound is essential for ensuring the accuracy and reliability of quantitative mass spectrometry (MS) and liquid chromatography-mass spectrometry (LC-MS) analyses. It is primarily used by pharmaceutical research and development laboratories, contract research organizations (CROs), and quality control facilities for precise pharmacokinetic studies, bioanalytical method development, and metabolite profiling.

Application

  • Internal Standard for LC-MS/MS quantification of Diflunisal in biological matrices (plasma, serum, urine).
  • Deuterated reference material for drug metabolism and pharmacokinetics (DMPK) studies.
  • Critical component in bioanalytical method validation for regulatory submissions (FDA, EMA).
  • Use in high-precision mass spectrometry to correct for analyte loss during sample preparation and instrument variability.
  • Stable isotope-labeled standard for proteomics and metabolomics research applications.
  • Quality control and assurance in pharmaceutical manufacturing for batch consistency testing.

Basic Information

Product Name Diflunisal-D3
CAS No. 1286107-99-0
Molecular Formula C13H5D3F2O3
Molecular Weight 254.21 g/mol
Synonyms 2',4'-Difluoro-4-hydroxy-3-(trideuteriomethyl)[1,1'-biphenyl]-3-carboxylic Acid; 5-(2,4-Difluorophenyl)-2-hydroxy-3-(trideuteriomethyl)benzoic Acid; [D3]-Diflunisal; Diflunisal (phenyl-D3); Diflunisal-d3; Deuterated Diflunisal; Diflunisal Internal Standard
EINECS Contact for details

Quality Control

Our Diflunisal-D3 is manufactured under strict quality systems to ensure high chemical purity and isotopic enrichment suitable for sensitive analytical applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing results for identity, purity (HPLC), isotopic purity (D-content), and residual solvents. We support compliance with cGMP and ICH Q7 guidelines for active pharmaceutical ingredients (APIs) and reference standards.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature, 15-25°C (59-77°F). Keep the container in a dry, cool, and well-ventilated area.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (MS) Conforms to structure
Purity (HPLC) ≥ 98.0%
Isotopic Purity (D-content) ≥ 99.0 atom % D
Chemical Purity (by HPLC) ≥ 99.0%
Water Content (KF) ≤ 0.5%
Residual Solvents (GC) Complies with ICH limits

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.