Cationic/zwitterionic PFAS

The introduction of these standards for emerging PFAS aims to improve the analytical methods used to detect these compounds in environmental samples.

Discover our native or mass-labelled cationic and zwitterionic PFAS standards.

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Our cationic/zwitterionic PFAS analytical standards

These individual solutions developed by Wellington Laboratories are certified standards designed specifically for the analysis of PFAS substances.

They are optimised for use with modern LC-MS/MS and GC-MS instruments.

Individual solutions are available in 1.2 mL ampoules in methanol.

Native cationic and zwitterionic PFAS standards

13C3-labelled 6:2 Fluorotelomer sulfonamide alkylbetaine standards

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High precision

These innovative solutions enable reliable identification and quantification of target compounds thanks to their exceptional purity and optimum compatibility with analytical protocols.

Designed to meet the rigorous demands of laboratories, our mixtures offer unrivalled analytical performance, ensuring reproducible results that comply with the most stringent regulatory standards. With Wellington, you benefit from reference tools for carrying out cutting-edge environmental analyses.

Certified reliability

Each batch is accompanied by a detailed certificate of analysis, attesting to the quality and purity of the compounds.

Fast delivery

France and Belgium.

Do you have a question? Contact us using the contact form. We will be delighted to advise you.

Cationic/zwitterionic PFAS individual solutions

Native cationic and zwitterionic PFAS

Native individual solutions

1.2 mL x 50ug/mL, methanol

Catalogue No.DescriptionCAS
N-AP-FBSAN-[3-(Dimethylamino)propan-1-yl]perfluoro-1-butanesulfonamide68555-77-1
N-AP-FPeSAN-[3-(Dimethylamino)propan-1-yl]perfluoro-1-pentanesulfonamide68555-78-2
N-AP-FHxSAN-(3-dimethylaminopropan-1-yl)perfluoro-1-hexanesulfonamide50598-28-2
N-AP-FOSAN-[3-(Dimethylamino)propan-1-yl]perfluoro-1-octanesulfonamide13417-01-1
N-TAmP-FHxSAN-[3-(perfluoro-1-hexanesulfonamido)propan-1-yl]-N,N,N-trimethylammonium38850-51-0
N-AP-6:2FOSA6:2 Fluorotelomer sulfonamide alkylamine (6:2 FTAA)34455-22-6
N-OxAmP-6:2FOSA6:2 Fluorotelomer sulfonamide amine oxide (6:2 FTNO, Capstone A)80475-32-7
N-CMAmP-6:2FOSAN-(carboxymethyl)-N,N-dimethyl-N-[3-(1H,1H,2H,2H-perfluoro-1-octanesulfonamido)propan-1-yl]ammonium (6:2FTAB)34455-29-3
5:3FTB2-[(4,4,5,5,6,6,7,7,8,8,8-Undecafluorooctyl)dimethylammonio]acetate171184-14-8
5:1:2FTB2-[(3,4,4,5,5,6,6,7,7,8,8,8-Dodecafluorooctyl)dimethylammonio]acetate171184-02-4

Mass-labelled cationic and zwitterionic PFASs

13C-labelled individual solution

1.2 mL x 50ug/mL, methanol

Zwitterionic/Cationic PFAS
Catalogue No.Description
M3N-CMAmP-6:2FOSA13C3-6:2 Fluorotelomer sulfonamide alkylbetaine (13C3-6:2 FTAB)

Do you have a question? Contact us using the contact form. We will be delighted to advise you.

Wellington Laboratories reagent categories

PFAS, per- polyfluoroalkyl Substances

Halogenated flame retardants, HFRs and other compounds

Polychlorinated biphenyls, PCBs

Polybrominated diphenyl ethers, PBDEs Polybrominated biphenyls, PBBs

PCDDs-PCDFs

Dioxins, Furans, PCDDs, PCDFs

Organochlorine Pesticides, OCP

Certified reference materials

Other reagents

Find out more about cationic and zwitterionic PFASs

Cationic and zwitterionic PFASs are subgroups of per- and polyfluoroalkylated substances (PFASs) that differ from the more commonly studied anionic PFASs. Cationic PFASs carry a positive charge, while zwitterionic PFASs have both positive and negative charges.

These compounds are often present in fire-fighting foams (AFFF) and can be found in soil and water contaminated by these foams.(AFFF) and can be found in soils and waters contaminated by these foams. They are less well characterised than anionic PFAS, which makes their quantification and study more complex.

Examples of cationic structures:

  • Fluorinated quaternary ammoniums
  • Protonated fluorinated alkylamines

Finally, zwitterionic PFAS behave in a particularly complex way in environmental and biological matrices , making their analytical analysis tricky.

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