I am seeking advice from users.
I am looking into methods to quantitate some ciders for sorbic acid and benzoic acid by HPLC since the GC method requires derivatization and ether extraction. Has anyone done the LC method I am hoping to have it done by just filtering/centrifuging the cider and shooting as I have seen in vendor's applic notes, but I don't know if this will really work without sample prep. I don't want to go to SPE if not necessary since I could get sample loss.
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By Anonymous on Thursday, February 3, 2000 - 08:15 am:
I've analysed sorbic and benzoic acid on both C18 (Co-elution of peaks) and on a polar embedded phase (2 nice peaks, well separated).
If you don't use SPE then you take the risk of having interference from carbohydrates in the chromatogram. These carbohydrates may / may not damage your column.
I have also analysed acids on SDVB columns (HyperREZ XP organic Acids - ThermoQuest. You can inject the cider straight onto this column. I've injected apple juice, orange juice etc and the column behaves very well.
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By athan marion on Tuesday, February 15, 2000 - 01:01 pm:
i've analyzed for sorbic and benzoic acids in aqueous food extracts after filtering; but i'm experiencing two problems: (1) i'm getting a benzoic acid peak from water? (2) standards injected before samples differ in response from standards injected after sample extracts? i'm using a Supelco ABZ column with acetonitrile-phosphate buffer at pH 2. The good news is that the peak shapes are symetrical and retention times are stable.
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By Elana on Thursday, February 17, 2000 - 05:27 am:
i do determination of sorbic acid in dairy product.
i use column of c-18 inersil ODS 3V (GL-SCIENCES)
mobile phase of :phosphate buffer ph 6.8,methanol
80:20.the extraction of sample is by hot water than methanol ,cetrifugation and filtration ,i get very nice peak and good recovery.
i think your buffer ph is too low.
Elana
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By Anonymous on Thursday, February 17, 2000 - 07:18 am:
Sorbic and benzoic acid can be well resolved under several conditions. Fast analysis can be achieved on a 300A C18 (BioBasic 18, Keystone Scientific) column using 10/90 MeOH/0.05M KH2PO4, pH 7.0. Benzoic acid should be at about 4 minutes and sorbic at 6 minutes. It is also possible to run under ion supresion conditions for greater retention using the same column, 10/80 MeOH/0.05M KH2PO4, pH 2.5 retention times are 18 min for benzoic and 22 min for sorbic.
With fruit juices, filtering is usually adequate. However, SPE w/ a WAX (weak anion exchange)media can be used.
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By Anonymous on Thursday, February 17, 2000 - 07:21 am:
For varying peak areas, make sure that the sample loop and syringe are thoroughly flushed b/w injections, sample carry over may be to be blame.
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