
High-precision separation and quantitation of volatile and semi-volatile compounds across pharmaceutical, food, and environmental matrices.
Allele Life Sciences drives high-precision GC analysis for identifying organic trace components. Utilizing advanced heated injection instrumentation, our laboratory extracts reliable data from complex matrices, quantifying biomolecules like fatty acids, metabolic sugars, and API impurities.
Converting non-volatile organics for gas-phase flow.
Supporting regulatory limits for hazard exclusions.
We guarantee that hazardous organic contaminants are absent from raw materials and APIs, promoting safe formulation development through robust LOD/LOQ validation modeling.
High-precision Gas Chromatography (GC) analysis for the identification of volatile and semi-volatile organic compounds.
Comprehensive validation including Accuracy, Repeatability, Specificity, Limit of Detection (LOD) and Limit of Quantitation (LOQ).
Accurate quantitation of derivatized biomolecules such as amino acids, fatty acids, sugars, and various metabolic products.
Precise quantification of sample additives and breakdown products to guarantee formulation stability and regulatory alignment.
Ensuring raw materials and Active Pharmaceutical Ingredients (APIs) are free from hazardous organic environmental contaminants.
Reliable analytical data applied to complex matrices across the pharmaceutical, food and beverage, and environmental sectors.
Extraction / Derivatization
Heated injection port
Capillary column transit
FID, ECD, or MS readout
Peak tracking & reports
"A powerful technique for analyzing normally non-volatile biomolecules. Once appropriately derivatized and vaporized, GC provides accurate and precise quantitation of amino acids, fatty acids, and key metabolic precursors."
Pioneering gas-phase molecular detection networks.
Advanced trace analysis
High-sensitivity detectors
Precision gas-phase flow
Volatizing biomolecules
High-throughput capacity
Chromatographic software
"Impurity profiling ensures customer trust by precisely quantifying sample additives, supporting correct labeling to satisfy the strictest regulatory criteria."
Scale of Method Execution
Routine Profiling
Fatty Acids & Sugars
Impurity & Method Dev
Download our technical handbook to explore the analytical capacity of GC derivatization, method developments, and trace volatile assays.