Volatile Organic Compounds Specific to the Pharmaceutical Manufacturing Industry by Isotope Dilution GC/MS
This method is for surveying and monitoring under the Clean Water Act. It is used to determine certain volatile organic pollutants specific to the pharmaceutical manufacturing industry (PMI) that are amenable to purge-and-trap gas chromatography/mass spectrometry (GC/MS) or direct aqueous injection GC/MS.
Stable, isotopically labeled analogs of the compounds of interest are added to the sample and the sample is purged with an inert gas at 45EC in a chamber designed for soil or water samples, as appropriate. In the purging process, the volatile compounds are transferred from the aqueous phase into the vapor phase, where they are passed into a sorbent column and trapped. After purging is completed, the trap is backflushed and heated rapidly to desorb the compounds into a gas chromatograph (GC). The compounds are separated by the GC and detected by a mass spectrometer (MS) (References 2 and 3).
–Method 1666:Volatile Organic Compounds Specific to the Pharmaceutical Manufacturing Industry by Isotope Dilution GC/MS, Revision A, July 1998
|Hold Time||All samples shall be analyzed within 14 days of collection.|
|Preservation||Samples are maintained at 4 deg C from the time of collection until analysis|
|Sample Volume||40 mL glass vial|
|Method Refernce||EPA Method RSK SOP-175|
*Please contact our project management team for more information about reporting limits and other specific project needs.
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