Analysis and mass spectrometric characterization of the insect repellent Bayrepel and its main metabolite Bayrepel-acid☆
-
Add time:08/25/2019 Source:sciencedirect.com
Insect repellents such as N,N-diethyl-m-toluamide (DEET) which are used as protection against mosquitoes or ticks were detected in all wastewater and anthropogenically influenced surface waters analyzed. In Germany, the concentrations of DEET have constantly decreased since 1999, when DEET was substituted by Bayrepel (1-piperidinecarboxylic acid, 2-(2-hydroxyethyl), 1-methylpropyl ester; KBR 3023) in commercial insect repellent formulations. A sensitive quantitative method was developed in order to study the occurrence and fate of Bayrepel in the aquatic environment. It was thus determined that Bayrepel undergoes rapid primary aerobic biodegradation, yielding a more stable metabolite, Bayrepel-acid (1-piperidinecarboxylic acid, 1-methylpropyl ester, 2-acetic acid). In order to study the biodegradation and investigate the fate of this metabolite, Bayrepel-acid was synthesized and characterized. Various chromatographic and mass spectrometric techniques, such as gas chromatography–mass spectrometry (MS) after derivatization, liquid chromatography (LC)–electrospray ionization (ESI) MS and LC–ESI time-of-flight MS were applied.
We also recommend Trading Suppliers and Manufacturers of 1-Piperidinecarboxylic acid, 2-hydroxy-, ethyl ester (cas 111054-63-8). Pls Click Website Link as below: cas 111054-63-8 suppliers
Prev:Stereoselective Transformation of 2H-1,4-Oxazin-2-ones into 2,(2),5,5-Tri- and Tetrasubstituted Analogues of cis-5-Hydroxy-2-piperidinemethanol and cis-5-Hydroxy-6-oxo-2-piperidinecarboxylic Acid
Next:Investigation of platelet aggregation inhibitory activity by phenyl amides and esters of piperidinecarboxylic acids) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Original ArticlesN-[11C]methylpiperidine esters as acetylcholinesterase substrates: an in vivo structure–reactivity study08/27/2019
- Investigation of platelet aggregation inhibitory activity by phenyl amides and esters of piperidinecarboxylic acids08/26/2019
- Stereoselective Transformation of 2H-1,4-Oxazin-2-ones into 2,(2),5,5-Tri- and Tetrasubstituted Analogues of cis-5-Hydroxy-2-piperidinemethanol and cis-5-Hydroxy-6-oxo-2-piperidinecarboxylic Acid08/24/2019
- Synthesis of labelled compoundSynthesis of (R)-1-(4-[11C]-p-methoxyphenyl-4-phenyl-3-butenyl)-3-piperidinecarboxylic acid for positron emission tomography of the GABA uptake carrier08/23/2019
- Gram-scale, chemoselective synthesis of N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-2-oxopiperidine-3-carboxamide (HIOC)08/22/2019
-
Health and Chemical more >
-
Related Products
- 1-Piperidinecarboxylic acid, 3-(4-nitrophenoxy)-, 1,1-dimethylethyl ester
- 1-Piperidinecarboxylic acid, 4-[[[2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl]amino]carbonyl]-, 1,1-dimethylethyl ester
- 1-Piperidinecarboxylic acid, 4-benzoyl-, 1,1-dimethylethyl ester
- 1-Piperidinecarboxylic acid,4-[[4-(ethoxycarbonyl)-2-methoxyphenoxy]methyl]-, 1,1-dimethylethyles
- 1-Piperidinecarboxylic acid,4-[4-[6-amino-5-[(1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-3-pyridinyl]-1H-pyrazol-1-yl]-, 1,1-dimethylethyl ester
- Acid Black 1
- Acid Black 107
- Acid Black 168
- Acid Black 194
- Acid Black 2


