Palmityl Trimethylsilyl Fumarate – High-Purity Impurity Standard for Analytical Research

 Palmityl Trimethylsilyl Fumarate is a specialized impurity reference material designed for advanced pharmaceutical and chemical research. Belonging to the Sodium Stearyl Fumarate impurity standards category, this compound plays a vital role in analytical method development, validation (AMV), quality control (QC), and regulatory submissions (ANDA, etc.).

👉 Explore the full category here: Sodium Stearyl Fumarate Impurity Standards

Product Overview

  • Product Name: Palmityl Trimethylsilyl Fumarate
  • Chemical Formula: C₂₃H₄₄O₄Si
  • Molecular Weight: 412.7 g/mol
  • Synonym: Hexadecyl (trimethylsilyl) fumarate
  • Availability: Ready-to-ship within 24 hours; custom pack sizes available
  • Documentation: Certificate of Analysis (CoA), NMR, HPLC/GC, and MS data available on request

This compound is widely used in impurity profiling and helps researchers ensure accurate detection of related substances in drug formulations. With high stability and purity, Palmityl Trimethylsilyl Fumarate is an essential tool for regulatory-compliant pharmaceutical testing.

Applications

  1. Method Development & Validation — Supports accurate identification and quantification of impurities.
  2. Quality Control (QC) Testing — Ensures consistency and safety in drug manufacturing.
  3. Regulatory Submissions — Suitable for ANDA filings and aligns with international guidelines.
  4. Research & Development — Provides insights into impurity pathways and stability studies.

Safety & Handling

As with all reference standards, this product is for laboratory use only and not intended for human or animal consumption. Always consult the Safety Data Sheet (SDS) before handling, use protective equipment (PPE), and store under recommended conditions.

Related Impurity Standards

Alongside Palmityl Trimethylsilyl Fumarate, AquigenBio also offers structurally related standards that expand the scope of impurity profiling:

These compounds, when used together, help researchers build a comprehensive impurity profile for sodium stearyl fumarate and related pharmaceutical excipients.


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