Date published: 2026-4-24

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Pentafluorobenzyl chloroformate (CAS 53526-74-2)

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CAS Number:
53526-74-2
Molecular Weight:
260.55
Molecular Formula:
C8H2ClF5O2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Pentafluorobenzyl chloroformate (PFB-Cl) stands as a versatile reagent extensively employed in organic synthesis, particularly for the creation of peptides and various compounds. This compound serves as a pivotal starting material in the synthesis of peptides and other compounds, finding diverse applications within the field. In laboratory applications, Pentafluorobenzyl chloroformate is widely utilized for synthesizing peptides and other compounds. The process of synthesizing peptides and compounds involving Pentafluorobenzyl chloroformate relies on the formation of a covalent bond between the target molecule and the pentafluorobenzyl group. This reaction proceeds through a nucleophilic substitution, yielding Pentafluorobenzyl chloroformate and sodium bromide as byproducts. Typically, this reaction takes place in an aqueous solution at a temperature range of 25-30°C.


Pentafluorobenzyl chloroformate (CAS 53526-74-2) References

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  2. Gas chromatography/negative-ion chemical ionisation mass spectrometry for the quantitative analysis of morphine in human plasma using pentafluorobenzyl carbonate derivatives.  |  Leis, HJ., et al. 2002. Rapid Commun Mass Spectrom. 16: 646-9. PMID: 11921241
  3. Improved sample preparation for the quantitative analysis of paroxetine in human plasma by stable isotope dilution negative ion chemical ionisation gas chromatography-mass spectrometry.  |  Leis, HJ., et al. 2002. J Chromatogr B Analyt Technol Biomed Life Sci. 779: 353-57. PMID: 12361750
  4. Electron capture gas chromatography of tertiary amines as pentafluorobenzyl carbamates.  |  Hartvig, P., et al. 1976. Anal Chem. 48: 390-3. PMID: 1247168
  5. (S)-(-)-N-(pentafluorobenzylcarbamoyl)prolyl chloride: a chiral derivatisation reagent designed for gas chromatography/negative ion chemical ionisation mass spectrometry of amino compounds.  |  Leis, HJ. and Windischhofer, W. 2012. Rapid Commun Mass Spectrom. 26: 592-8. PMID: 22328211
  6. Derivatization reactions for use with the electron-capture detector.  |  Poole, CF. 2013. J Chromatogr A. 1296: 15-24. PMID: 23433885
  7. Pentafluorobenzyl chloroformate derivatization for enhancement of detection of amino acids or alcohols by electron capture negative ion chemical ionization mass spectrometry.  |  Simpson, JT., et al. 1995. J Am Soc Mass Spectrom. 6: 525-8. PMID: 24214307
  8. Determination of atmospheric amines by on-fiber derivatization solid-phase microextraction with 2,3,4,5,6-pentafluorobenzyl chloroformate and 9-fluorenylmethoxycarbonyl chloride.  |  Parshintsev, J., et al. 2015. J Chromatogr A. 1376: 46-52. PMID: 25542706
  9. Chloroformate derivatization for tracing the fate of Amino acids in cells and tissues by multiple stable isotope resolved metabolomics (mSIRM).  |  Yang, Y., et al. 2017. Anal Chim Acta. 976: 63-73. PMID: 28576319
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  11. Sample preparation and instrumental methods for illicit drugs in environmental and biological samples: A review.  |  Chen, X., et al. 2021. J Chromatogr A. 1640: 461961. PMID: 33582515
  12. Possibilities and limitations of tracing industrial effluents in the sea by means of capillary chromatography.  |  Josefsson, B. 1983. J Chromatogr. 279: 119-23. PMID: 6672029
  13. Analysis of amino acids in biological fluids by pentafluorobenzyl chloroformate derivatization and detection by electron capture negative ionization mass spectrometry.  |  Simpson, JT., et al. 1996. Anal Biochem. 233: 58-66. PMID: 8789147

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Pentafluorobenzyl chloroformate, 500 mg

sc-263980
500 mg
$94.00

Pentafluorobenzyl chloroformate, 1 g

sc-263980A
1 g
$173.00