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55479-U

Supelco

Supel QuE QuEChERS tube

volume 15 mL, suitable for PFAS testing, pkg of 50 ea

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UNSPSC Code:
41104018
NACRES:
NB.11

product name

Supel QuE PSA/ENVI-Carb Tube 3, volume 15 mL, suitable for PFAS testing, pkg of 50 ea

reg. compliance

suitable for FDA C-010.02

Quality Level

packaging

pkg of 50 ea

volume

15 mL

application(s)

food and beverages

General description

The Supel QuE PSA/ENVI-Carb Tube 3, 15 mL (clean-up tube) is suitable for the testing workflow of 16 PFAS compounds in food according to regulated FDA method C_01.02. Prior to analysis by LC-MS/MS, a sample preparation is required by the "QuEChERS" method. The QuEChERS method (Quick, Easy, Cheap, Effective, Rugged, and Safe), has emerged as a sample prep technique popular e.g. in the area of matrix rich samples, like food product. In a first step, food sample is extracted with an aqueous miscible solvent (e.g., acetonitrile) in the presence of high amounts of extraction salts to induce liquid phase separation. Upon shaking and centrifugation, an aliquot of the organic phase is subjected to further cleanup step. The second step is facilitated by mixing bulk amounts of sorbent (e.g., Supelclean PSA, ENVI-Carb, MgSO4) with the extract. After sample cleanup, the mixture is centrifuged and the resulting supernatant can, depending on the sample, either be analyzed directly or can be subjected to further minor treatment before analysis.

Components

300 mg Supelclean PSA, 150 mg Supelclean, ENVI-Carb, 900 mg MgSO4

Legal Information

ENVI-Carb is a trademark of Sigma-Aldrich Co. LLC
Supel is a trademark of Sigma-Aldrich Co. LLC
Supelclean is a trademark of Sigma-Aldrich Co. LLC

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Articles

Discover an LC-MS/MS method for the analysis of 16 per- and polyfluoroalkyl compounds (PFAS) in milk using QuEChERS extraction technique following FDA C-010.02 guidelines.

Find more about the analysis of 16 PFAS in salmon via QuEChERS extraction and LC-MS/MS characterization following FDA Method C-010.02.

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