GC-MS
ANALYSIS
Gas Chromatography-Mass Spectrometry combines gas chromatography separation with mass spectrometric detection. Ideal for volatile and semi-volatile compounds. Used for identity confirmation, purity analysis, impurity profiling, and residual solvent analysis.
- 01Peptide purity verification
- 02Raw material identification
- 03Residual solvent analysis
- 04Impurity profiling
- 05Degradation product identification
GC-MS at Standard Analytica utilizes state-of-the-art instrumentation to achieve exceptional sensitivity and selectivity. Our validated methods are optimized for the analysis of peptide-related compounds and pharmaceutical intermediates.
The technique is particularly effective for characterizing volatile organic compounds, residual solvents, and low molecular weight impurities that may be present in synthetic peptide preparations.
All analyses are performed under strict GLP-compliant conditions with full system suitability verification and quality control checks throughout the analytical run.
SAMPLE INTAKE
Your sample is received, logged into our LIMS system, and assigned a unique tracking identifier. Chain-of-custody documentation is initiated.
PREPARATION
Samples are prepared according to validated protocols. For GC-MS, this typically includes dissolution, dilution, or headspace extraction depending on the analyte.
ANALYSIS
Prepared samples are injected into the GC-MS system. Separation occurs in the gas chromatograph column, followed by mass spectrometric detection and identification.
REPORTING
Results are reviewed by senior analysts, compiled into a comprehensive report with chromatograms, mass spectra, and quantitative data, then delivered to you.
SUBMIT A SAMPLE
Ready to submit a sample for GC-MS analysis? Contact our team to discuss your requirements, receive sample preparation guidelines, and initiate testing.