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Bioallethrin
SpectraBase Compound ID I6eOKG0owiN
InChI InChI=1S/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3
InChIKey ZCVAOQKBXKSDMS-UHFFFAOYSA-N
Mol Weight 302.41 g/mol
Molecular Formula C19H26O3
Exact Mass 302.188195 g/mol
Copyright Copyright © 2012-2025 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved.
Source of Spectrum Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences
Copyright Copyright © 2023-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum H.H.Maurer, M.Meyer, K.Pfleger, A.A. Weber / University of Saarland, D-66424 Homburg Germany
Technique GC/MS
Copyright Copyright © 2024-2025 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
Copyright Database Compilation Copyright © 2023-2025 John Wiley and Sons, Inc. Copyright © 2023-2025 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Database Compilation Copyright © 2023-2025 John Wiley and Sons, Inc. Copyright © 2023-2025 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Database Compilation Copyright © 2023-2025 John Wiley and Sons, Inc. Copyright © 2023-2025 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Database Compilation Copyright © 2023-2025 John Wiley and Sons, Inc. Copyright © 2023-2025 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Database Compilation Copyright © 2023-2025 John Wiley and Sons, Inc. Copyright © 2023-2025 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Dr. Rolf Kuehnle
Technique GC/MS
Copyright Copyright © 2016-2025  John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Copyright © 2016-2025  John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Copyright © 2016-2025  John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Copyright © 2016-2025  John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #31489
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-27228-0-0
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-1989-53838-11698
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-1989-25603-1
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SEP-27-93-Allethrin (DOI: 10.1002/jssc.200301606)
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SEP-27-94-trans-Allethrin (DOI: 10.1002/jssc.200301606)
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum AD-0-2258-0
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample McLaughlin Gormley King Company, Inc., Minneapolis, Minnesota
Technique BETWEEN SALTS
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Fluka Chemie AG, Buchs, Switzerland
Technique CAPILLARY CELL: NEAT
Copyright Copyright © 2019-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Fluka Pestanal, Sigma-Aldrich Company LLC
Source of Spectrum Forensic Spectral Research
Catalog Number 31489
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Meyer/Helfer/Weber c/o Saarland University Homburg/Saar
Technique HCD
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Meyer/Helfer/Weber c/o Saarland University Homburg/Saar
Technique HCD
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Allethrin
  • ZCVAOQKBXKSDMS-UHFFFAOYSA-N
  • ALLETHRIN CONCENTRATE 90%
  • 2,2-DIMETHYL-3-(2-METHYLPROPENYL)CYCLOPROPANECARBOXYLIC ACID, ESTER WITH 2-ALLYL-4-HYDROXY-3-METHYL-2-CYCLOPENTEN-1-ONE
  • ENT-17510
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methylpropenyl)-, ester with 2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one
  • ALLYL CINERINS
  • Bioallethrin isomer III
  • Bioallethrin isomer II
  • Bioallethrin isomer IV
  • Bioallethrin isomer I
  • Allethrin MS2
  • Bioallethrin MS2
  • Esbiothrine
  • Allethrin @
  • trans-Chrysanthemic acid, 2-methyl-2-propenyl-cyclopent-2-en-4-on-1-yl ester
  • 2,2-dimethyl-3-(2-methyl-propenyl)-cyclopropanecarboxylic acid 3-allyl-2-methyl-4-oxo-cyclopent-2-enyl ester
  • trans-2,2-dimethyl-3-(2-methyl-propenyl)-cyclopropanecarboxylic acid 3-allyl-2-methyl-4-oxo-cyclopent-2-enyl ester
  • ESBIOL <ALLETHRIN>
  • Esbiol
  • trans-Allethrin
  • (+)-Allelrethonyl (+)-cis,trans-Chrysanthemate
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propen-1-yl)-, 2-methyl-4-oxo-3-(2-propen-1-yl)-2-cyclopenten-1-yl ester
  • 3-Allyl-2-methyl-4-oxo-2-cyclopenten-1-yl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate
  • Wasp Killer II
  • Wasp stopper CF
  • Allethrin I
  • d-T-Allethrin
  • S-Bioallethrin
  • Allyl cinerin I
  • Exthrin
  • Pynamin
  • Pyresin
  • Pyresyn
  • .alpha.-DL-trans-Allethrin
  • D-trans-Allethrin
  • Pyrocide
  • Alleviate
  • Pyrethrin
  • S-trans-Bioallethrin
  • Allethrine
  • Esbiothrin
  • D-allethrin
  • Bioaletrina
  • Cinerin I allyl homolog
  • Pallethrine
  • Depallethrin
  • Allyl cinerin
  • Allyl homolog of cinerin I
  • Binamin forte
  • Pynamin-forte
  • Allethrin coil
  • Allylrethronyl DL-cis-trans-chrysanthemate
  • Esbioallethrin
  • Esdepallethrine
  • DL-3-allyl-2-methyl-4-oxocyclopent-2-enyl DL-cis trans chrysanthemate
  • Necarboxylic acid
  • (+)-trans-Allethrin
  • trans-(+)-Allethrin
  • D-allethrolone D-trans-chrysanthemumate
  • (RS)-3-Allyl-2-methyl-4-oxocyclopent-2-enyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
  • (+)-trans-Bioallethrin
  • (+-)-Allerethonyl (+-)-cis,trans-Chrysanthemate
  • D-allethrolone chrysanthemumate
  • (+)-trans-Chrysanthemumic acid ester of (+-)-Allethrolone
  • DL-2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one ester of D-trans-2,2-dimethyl-3-(2-methylpropenyl)
  • DL-2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one ester of DL cis/trans 2,2-dimethyl-3-(2-methylpropenyl)-cyclopropanecarboxylic acid
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, (1S)-2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester, (1R,3R)-
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, (1R)-2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester, (1R,3R)-rel-
  • D-allethrolone d-trans-chrysanthemate
  • 3-Allyl-2-methyl-4-oxocyclopent-2-en-1-yl (1R-(1alpha(S*),3beta))-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
  • (RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (+-)-cis,trans-chrysanthemate
  • (+)-Allethronyl (+)-trans-chrysanthemumate
  • (.+-.)-Allelrethonyl (.+-.)-cis,trans-chrysanthemate
  • Allethrolone ester of chrysanthemummonocarboxylic acid
  • 3-Allyl-2-methyl-4-oxo-2-cyclopenten-1-yl chrysanthemate
  • 3-Allyl-4-keto-2-methylcyclopentenyl chrysanthemum monocarboxylate
  • (S)-3-allyl-3-methyl-4-oxocyclopent-2-enyl (+)-trans-chrysanthemate
  • Chrysanthemummonocarboxylic acid, 3-allyl-3-methyl-4-oxo-2-cyclopenten-1-yl ester
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methylpropenyl)-, (+)-(E)-, ester with (+)-2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one
  • d-trans-(1-Methyl-2-allyl-3-oxo-1-cyclopenten-5-yl)chrysanthemumate
  • 2-Allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one ester of chrysanthemummono-carboxylic acid
  • 2-Allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one ester of 2,2-dimethyl-3-(2-methyl propenyl) cyclopropane carboxylic acid
  • 3-Allyl-4-methyl-2-oxo-3-cyclopenten-1-yl ester of 2,2-dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylic acid
  • (.+/-.)-3-Allyl-2-methyl-4-oxocyclopent-2-enyl 2,2-dimethyl-3-(2-methylprop-1-enyl) cyclopropylcarboxylate
  • 2-Cyclopenten-1-one, 2-allyl-4-hydroxy-3-methyl-, 2,2-dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylate
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopentene-1-yl ester
  • 2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylic acid (3-allyl-4-keto-2-methyl-cyclopent-2-en-1-yl) ester
  • 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid, ester with 2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one
  • 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid 2-methyl-4-oxo-3-(2-propenyl)-2- cyclopenten-1-yl ester
  • 2,2-Dimethyl-3-(2-methylprop-1-enyl)-1-cyclopropanecarboxylic acid (2-methyl-4-oxo-3-prop-2-enyl-1-cyclopent-2-enyl) ester
  • 2-Methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecar
  • 2-Methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methylpropenyl)-, ester with 2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one, trans-(.+-.)-
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester, d-trans-
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, ster with 2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one, trans-(+-)-
  • (3-allyl-2-methyl-4-oxo-cyclopent-2-en-1-yl) 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
  • (2-methyl-4-oxidanylidene-3-prop-2-enyl-cyclopent-2-en-1-yl) 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate
  • (2-methyl-4-oxo-3-prop-2-enylcyclopent-2-en-1-yl) 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate
  • MATOX
  • ESBIOL TM INTERMEDIATE 3336
  • EPA PESTICIDE CHEMICAL CODE 004001
  • EPA PESTICIDE CHEMICAL CODE 004003
  • CASWELL NO. 025
  • CCRIS 2494
  • HSDB 1511
  • FMC 249
  • NIA 249
  • EINECS 209-542-4
  • EINECS 249-013-5
  • FDA 1446
  • OMS 3045
  • ENT 16275
  • NSC 11782
  • BRN 2059862
  • RU 16121
  • RU 27436
  • AI3-17510
  • AI 3-29024
  • (RS)-3-Allyl-2-methyl-4-oxocyclopent-2-enyl-(1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)-\rcyclopropanecarboxylate
Title Journal or Book Year
Carbon-13 nuclear magnetic resonance spectra of the natural pyrethrins and related compounds Journal of the Chemical Society, Perkin Transactions 1 1975

This compound is available in the following databases:

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