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Derivatization in Analytical Chemistry

Derivatization in Analytical Chemistry

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Derivatization is one of the most widely used sample pretreatment techniques in Analytical Chemistry and Chemical Analysis. Reagent-based or reagent-less schemes offer improved detectability of target compounds, modification of the chromatographic properties and/or the stabilization of sensitive compounds until analysis. Either coupled with separation techniques or as a “stand alone” analytical procedure, derivatization offers endless possibilities in all aspects of analytical applications.

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Keywords

  • 2-naphthalenethiol
  • 96-microwell spectrophotometric assay
  • A/P ratio
  • acetazolamide
  • acetonitrile-related adducts
  • acetylenic lipids
  • amino acids
  • Analytical Chemistry
  • Biogenic Amines
  • blood plasma
  • BSTFA
  • carbonic anhydrase
  • charge-transfer reaction
  • chemical warfare agents
  • Chemistry
  • chiral metabolomics
  • chloranilic acid
  • Clams
  • creatine
  • creatinine
  • d-amino acids
  • derivatisation
  • derivatization
  • dimethyl labeling
  • double and triple bond localization
  • enantiomer separation
  • enhancement
  • esterification
  • fluorescence detection
  • fluorosurfactant-modified gold nanoparticles
  • GC-MS
  • GC–MS
  • glutamine
  • high-performance liquid chromatography
  • high-resolution mass spectrometry
  • high-throughput pharmaceutical analysis
  • homocysteine
  • homocysteine thiolactone
  • HPLC
  • HPLC-UV/Vis
  • human serum albumin
  • in-source derivatization
  • Inhibition
  • linseed oil
  • low-molecular-weight thiols
  • Lycium barbarum L.
  • Mass Spectrometry
  • Mathematics & science
  • Methylation
  • monobromobimane
  • nerve agents
  • Novichoks
  • o-phthalaldehyde
  • P/S ratio
  • pentafluorobenzyl bromide
  • pentafluoropropionic anhydride
  • pharmacokinetics
  • pigment
  • quantification
  • Reduction
  • Reference, information & interdisciplinary subjects
  • Research & information: general
  • rice water
  • sarin
  • silylation
  • sodium borohydride
  • Stability
  • sulforaphane
  • Taurine
  • TMS
  • toluene
  • Tyrosine kinase inhibitors
  • ureide
  • Validation
  • zone fluidics
  • α-lipoic acid
  • ∑D

Links

DOI: 10.3390/books978-3-0365-4255-3

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