Extreme Makeover – Derivatizations in Chromatography – Part 2 LC

Version 3

    Part 2 – Liquid Chromatography

    N. Reuter*, ACG Global Technical Support for CSD, Middelburg, The Netherlands

    Introduction

    Wikipedia defines “derivatization“ as follows:

     

    Derivatization is a technique used in chemistry, which transforms a chemical compound into a product of similar chemical structure, called a derivative.

    Generally, a specific functional group of the compound participates in the derivatization reaction and transforms the educt to a derivative of deviating reactivity, solubility, boiling point, melting point, aggregate state, or chemical composition. Resulting new chemical properties can be used for quantification or separation of the educt. Derivatization techniques are frequently employed in chemical analysis of mixtures

     

    That means derivatization is “wet“ chemistry.  Though chromatographers may not prefer this type of chemistry, it is quite often used for specific purposes, as mentioned in the first paragraph of the word definition. Something similar, but different.

     

     

    In HPLC, derivatizations can be more complex than their GC counterparts, because of the condensed state in which everything takes place. Increasing volatility is only a possible issue for LC/MS applications. Where-as all derivatizations in GC are pre-column, in HPLC you also can have post-column processes.


    Classic Pre-Column Derivatizations

    Pre-column derivatizations are carried out as off-line chemical reactions between reagent and sample prior to the injections on the HPLC column.

     

    Figure 1: Flow path of a standard HPLC analysis with pre-column derivatization.


    Chromotags

    If volatility is not the issue, then detectability is. The classic detector in HPLC is the UV detector, so com-ponents need to be UV-active to be detected. If the molecule is not, you need to insert so-called chromophores into the molecules. Reagents that do this are called chromotags.  This table lists common chromotag reagents:

                                                                                                                                                                                                   

    Reagent Abbreviation

    Full Name

    Dbs-Cl (Dabsyl chloride)

    4-Dimethylamino-azobenzene-4'-sulfonic    acid chloride

    DNBA

    3,5-Dinitrobenzyloxyamine hydrochloride

    DNBC

    3,5-Dinitrobenzoylchloride

    DNBDI

    O-(3,5-Dinitrophenylmethyl)-N,N-diisopropylthiourea

    DNPBA

    3,5-Dinitrophenylmethyl n-propylamine hydrochloride

    FDNB

    Fluoro-2,4-dinitrobenzene

    NIC

    1-Naphthylisocyanate

    Ninhydrine

    4,5-Benzo-2,2-dihydroxy-cyclopentan-1,3-dione

    PBPB

    p-Bromophenyl bromomethyl keton

    PITC

    Phenylisothiocyanate

    PNBA

    O-(p-Nitrophenylmethyl)hydroxylamine    hydrochloride

    PNBA

    O-(p-Nitrophenylmethyl)hydroxylamine    hydrochloride

    PNBDI

    O-(p-Nitrophenylmethyl)-N,N-diisopropylthiourea

    PNBPA

    p-Nitrophenylmethyl    n-propyl amin hydrochloride

    SDPNA

    N-Succinimidyl-3,5-dinitrophenylacetate

    SNPA

    N-Succinimidyl-p-nitrophenylacetate

    Table 1: Common chromotag reagents.

     

    All of these reagents carry at least one aromatic ring or even larger pi-electron systems, which are responsi-ble for the UV detection. Dabsylchloride can, for example, be used to derivatize amines, thiols, imidazoles, phenols and alcohols.

     

    Figure 2: Dabsylation of alcohols.

     

    A typical procedure is as follows:

    General procedure: Derivatives are formed within 30 minutes at room temperature or at 70 °C in 10 minutes in acetone, buffer or acetonitrile.

    Example for alcohols: Mix 1 mL of alcohol with 10 mL 100 mM sodium bicarbonate and 20 mL 10 mM dabsyl chloride, reflux for 10 minutes, cool, extract with diethylether, wash with pH 3 citrate buffer, evaporate the organic layer, reconstitute and inject an aliquot.

     

     


    Fluorotags

    Besides the standard UV detection, fluorescence detection is also often used in HPLC. Chemical reagents called fluorotags are used to introduce groups with fluorescent properties into the molecules. Table 2 shows a list of common fluorotag reagents:

                                                                                                                                                                                         

    Reagent Abbreviation

    Full Name

    AECF

    2-(9-Anthranyl)ethyl chloroformate

    BDMQ

    3-Bromomethyl-6,7-dimethoxy-1-methyl-2(1H)-quinoxalinone

    BMC    (BrMmC)

    4-Bromomethyl-7-methoxycoumarine

    BrMaC

    4-Bromomethyl-7-acetoxycoumarine

    DANS    hydrazide

    1-Dimethylaminonaphthalene-5-sulfonic    acid hydrazide, Dansyl hydrazide

    Dithiobis(amino-dimethoxybenzene

    2,2'-Dithiobis(1-amino-4,5-dimethoxybenzene)

    Dns-Cl (DANS-Cl)

    1-Dimethylaminonaphthalene-5-sulfonic acid chloride, Dansyl chloride

    EDTN

    1-Ethoxy-4-(dichloro-s-triazinyl) naphthalene

    Fluorescamine    (FLURAM)

    4-Phenylspiro(furan-2(3H),1'-phthalan)-3,3'-dione

    FMOC

    (9-fluorenyl)methyl chloroformate

    HCPI

    2-(4-Hydrazinocarbonylphenyl)-4,5-diphenylimidazole

    NBD-Cl

    7-chloro-4-nitrobenzyl-2-oxa-1,3-diazole

    NBD-F

    7-Fluoro-4-nitrobenzyl-2-oxa-1,3-diazole

    NDA

    Naphthalene dicarboxaldehyde

    OPA

    o-Phthaldialdehyde

    Table 2: List of common fluorotag reagents.

     

    (9-Fluorenyl)alkyl chloroformates, like the methyl derivative, FMOC, or the ethyl derivative, FLEC, are often used for amines and amino acids. The ethyl derivative carries an asymmetrically substituted/chiral carbon atom and is also available enantiomerically pure in both enantiomers, so that it is possible to check for both enantiomers of, for example, an amino acid due to the formation of diastereomeric derivates on an HPLC column with an achiral phase:

     

    Figure 3: Derivatization of (S)-alanine with (S)-1-(9-fluorenyl)ethyl chloroformate (FLEC).

     

    A typical procedure for chloroformate reagents is as follows:

    In the absence of water: Add 5 µL of the chloroformate to 2-10 µL of the sample in acetone in a mix-ture of acetonitrile/pyridine/alcohol (22:2:1, alcohol: methanol, ethanol or chloroethanol) and shake for some seconds. Inject.

    In the presence of water: To 50 µL of a pyridine-water solution (5:1), 50 µL acetonitrile/ethanol (2:3) and 5 µL chloroformate are added. Extraction is performed by 100 µL hexane and 200 µL water. In-ject an aliquot of the hexane layer.

     

    Fluorotags are often also chromotags due to extended aromatic systems in the reagent’s structure, but chromotags typically are not also fluorotags.

    Volatility Reagents for LC/MS

    This is about acylation reactions with perfluorinated organic acid anhydrides, like trifluoroacetic acid anhy-dride or the homologous pentafluoropropanoic and heptafluorobutanoic acid anhydrides. Acylation reactions are described in part one of this document, which was about gas chromatography.


    Post-Column Derivatizations/Online Derivatizations

    Post-column derivatizations are online chemical reactions, carried out after the separation has taken place and before the component enters the detector:

     

    Figure 4: Flow path of a standard HPLC analysis with post-column derivatization.

     

    An example for the method used in Figure 4 is the post-column fluorotag derivatization of sulfonamides [1]:

     

    Figure 5: Post-column derivatization of Sulfanilamide (blue) with benzene-1,2-dicarbaldehyde (OPA) and 2-sulfanylethanol. The exitation can be measured at 302 nm and the emission at 412 nm wavelengths.

     

    Another possibility for post-column reactions are immobilized enzyme reactors (IMERs), where an enzyme is used to catalyze certain reactions before the component goes to the detector. An example is the reaction of acetylcholine to choline and the oxidation from choline to carboxy-N,N,N-trimethylmethanaminium, an acid and hydrogen peroxide, that can be easily detected by an electrochemical detector down to low picomole/femtomole levels [2]. The first reaction (1) is catalyzed by acetylcholine esterase and the second (2) by choline oxidase, two enzymes immobilized in the IMER reactor.

     

    Figure 6: enzyme-catalzed derivatization from  acetylcholine to choline and the corresponding acid.

     

     


    Drawbacks

    If you inject a sample together with an unreacted  derivatization reagent or their reaction products, it can happen that the  baseline noise increases, but normally the detection is so specific that the  sensitivity still increases.

     

    For post-column systems you will need another pump for the  reagent and the mixing/reaction chamber.

     

    Compared to the amount of standard reagents in gas  chromatography, the amount for HPLC reagent is enormously higher and you have  lots of specific reactions for specific components. In fact, every reaction in  organic chemistry may be a derivatization reaction for HPLC components.


    Conclusions

    Derivatizations in liquid chromatography are used to:

     

    • Insert UV active groups
    • Insert fluorescent groups
    • Insert or generate electro-chemically measurable  groups
    • Enhance volatility for LC/MS applications

     


    References

    • P.  Viñas, C. L. Erroz, N.  Campillo, M. Hernández-Córdoba; ”Determination of sulfonamides in foods by  liquid chromatography with post-column fluorescence derivatization”, J.  Chromatogr. A, 726, 1996, 125-131.
    • G.  Damsma, D. Lammerts van Bueren, B. H. C. Westerink, A. S. Horn; “Determination  of acetylcholine and choline in the femtomole range by means of HPLC, a  post-column enzyme reactor, and electrochemical detection“, Chromatographia,  24(1), 1987, 827-831.

     


    Recommended Literature

    • G. Lunn, L. C. Hellwig; “Handbook of  Derivatization Reactions for HPLC”, Wiley-Intersciece, New York 1998. ISBN  978-0471164585.
    • D. R. Knapp; “Handbook of Analytical  Derivatization Reactions”, Wiley-Intersciece, New York 1979. ISBN  978-0471034698.
    • K. Blau, J. M. Halket; “Handbook of Derivatives  for Chromatography”, Wiley-Interscience, New York 1993. ISBN 978-0471926993.
    • T. Toyo'oka; “Modern Derivatization Methods for  Separation Science”, Wiley-Interscience, New York 1999. ISBN 978-0471983644.
    • S. C. Moldoveanu, V. David; “Sample Preparation  in Chromatography” (J. Chromatogr. Library Vol. 65), Elsevier Scientific,  Amsterdam 2002. ISBN 978-0444503947.