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54057-U

Supelco

Supelclean™ ENVI-WAX SPE Tube

suitable for PFAS testing, bed wt. 500 mg, volume 6 mL, pk of 30 ea

Synonym(s):

Supelclean™ ENVI-WAX SPE

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About This Item

UNSPSC Code:
41104018
NACRES:
NA.24

Agency

meets requirements for EPA 533
suitable for DIN 38407-42
suitable for EPA 1633
suitable for EPA 533
suitable for EPA 537.1
suitable for EPA OTM-45
suitable for GB 31604.35-2016
suitable for ISO 21675 2019
suitable for ISO 25101
suitable for ISO/CEN 15968-2010

Quality Level

100

reg. compliance

suitable for FDA C-010.02

composition

bed wt., 500 mg

packaging

pk of 30 ea

volume

6 mL

matrix

(mixed-mode polymeric)

matrix active group

WAX phase

particle size

40-60 μm

pore size

70-90 Å pore size

application(s)

environmental

separation technique

ion exchange

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General description

Supelclean™ ENVI-WAX SPE cartridges are weak anion exchange (WAX) solid phase extraction (SPE) cartridges containing mixed-mode polymeric adsorbent commonly used in sample preparation for PFAS analysis and other environmental applications. These cartridges come in 6mL, 200mg bed weight (P/N 54056-U) and 6mL, 500mg bed weight (P/N 54057-U). The 500mg bed weight cartridges are a direct equivalent to the specified SPE in method EPA 533. Other regulated methods that utilize WAX SPE cartridges are EPA 1633, ISO 25101 and ISO 21675.

Applications:

  • Environmental
  • Extraction of acidic compounds
  • PFAS

Legal Information

Supelclean is a trademark of Sigma-Aldrich Co. LLC

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
189080
188042
185666
179149
176568

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Articles

LC-MS Analysis of PFAS Compounds

LC-MS method separates 32 PFAS compounds in drinking water following EPA methods 533, 537, and 537.1. EPA 8327.

LC-MS/MS Analysis of 16 PFAS in Salmon Using QuEChERS Based on FDA Method C-010.02

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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