-
- Posts: 5
- Joined: Thu Sep 23, 2021 7:53 pm
Advertisement
HPLC analysis of propargyl benzoate
Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
2 posts
Page 1 of 1
Hello. I am looking for suitable solvent for propagryl benzoate for hplc method with uv detection. I am using YMC Triart C8 and as mobile phase, water and methanol. In solvent it should be max 50% of organic compond, that I get nice peak shape. But I have problem that if I use 50 % Methanol or 50 % acetonitrile as solvent, my extraction is not high enough. I assume, that is because of hydrolyse of esther. If i use BHT in solvent, that not help. Please let me know, if you have any idea how to solve this.
-
- Posts: 18
- Joined: Fri May 03, 2024 1:32 pm
Hi Natasa,
I am very glad you are working with YMC columns and achieving good results on that! let's think of an extraction method. propargyl benzoate is hydrophobic with a stable logD of 2.2, it means you do not have to think of pH while running the extraction. I believe that the easiest way to work with that would be to run an extraction with a more apolar solvent with low boiling point, evaporate it completely and try to re-disolve it in your mobile phase. I used to do this for the analysis of vitamin E in blood plasma for example. extract Vitamin E from blood plasma with hexane, evaporate hexane completely, resuspend it in a water-MeOH mixture.
alternatively i'd try to enhance the extraction process - example: if you are working with a solid sample you might want to grind it to increase surface area or you can try temperature or US assisted extractions (then again there is the risk of degradation).
i hope this helps.
best regards,
I am very glad you are working with YMC columns and achieving good results on that! let's think of an extraction method. propargyl benzoate is hydrophobic with a stable logD of 2.2, it means you do not have to think of pH while running the extraction. I believe that the easiest way to work with that would be to run an extraction with a more apolar solvent with low boiling point, evaporate it completely and try to re-disolve it in your mobile phase. I used to do this for the analysis of vitamin E in blood plasma for example. extract Vitamin E from blood plasma with hexane, evaporate hexane completely, resuspend it in a water-MeOH mixture.
alternatively i'd try to enhance the extraction process - example: if you are working with a solid sample you might want to grind it to increase surface area or you can try temperature or US assisted extractions (then again there is the risk of degradation).
i hope this helps.
best regards,
Luccas Name
YMC applications specialist (LATAM)
YMC applications specialist (LATAM)
2 posts
Page 1 of 1
Who is online
In total there are 12 users online :: 0 registered, 0 hidden and 12 guests (based on users active over the past 5 minutes)
Most users ever online was 4374 on Fri Oct 03, 2025 12:41 am
Users browsing this forum: No registered users and 12 guests
Most users ever online was 4374 on Fri Oct 03, 2025 12:41 am
Users browsing this forum: No registered users and 12 guests
Latest Blog Posts from Separation Science
Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.
Subscribe to our eNewsletter with daily, weekly or monthly updates: Food & Beverage, Environmental, (Bio)Pharmaceutical, Bioclinical, Liquid Chromatography, Gas Chromatography and Mass Spectrometry.
- Follow us on Twitter: @Sep_Science
- Follow us on Linkedin: Separation Science
