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Abietic acid methyl ester
SpectraBase Compound ID CSCvLHg71oA
InChI InChI=1S/C21H32O2/c1-14(2)15-7-9-17-16(13-15)8-10-18-20(17,3)11-6-12-21(18,4)19(22)23-5/h8,13-14,17-18H,6-7,9-12H2,1-5H3/t17-,18+,20+,21+/m0/s1
InChIKey OVXRPXGVKBHGQO-UYWIDEMCSA-N
Mol Weight 316.5 g/mol
Molecular Formula C21H32O2
Exact Mass 316.24023 g/mol
Enantiomer InChIKey OVXRPXGVKBHGQO-ZFMNYDKASA-N
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Hercules, Inc., Wilmington, Delaware
Technique FILM
Copyright Copyright © 1989, 1990-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Sample Laboratory preparation
Technique Layer between CsI
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Laboratory Preparation, U. Pohl, Instiute Of Physical Chemistry, University Of Cologne
Source of Spectrum Spectra and properties provided by Professor Doctor Dieter O. Hummel
Technique Capillary film between CsI
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Hercules, Inc., Wilmington, Delaware
Technique NEAT
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample CHEM SERVICE, INC., WEST CHESTER, PENNSYLVANIA
Technique CAPILLARY CELL: NEAT
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample A. San Feliciano, J.M. Miguel Del Corral, M. Gordaliza and M.A. Salinero, Universidad De Salamanca, Salamanca, Spain Magn. Reson. Chem. 31, 841(1993)
Solvent Chloroform-d; Reference=TMS; Temperature=25C Spectrometer= Bruker WP 200 SY
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Hercules, Inc., Wilmington, Delaware
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Methanol
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Methanol
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum AD-0-5334-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum AA-0-1931-1
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum EP-8144-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum EP-0-316-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum RCM-22-3713-Table1,entry28
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Va-0-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Va-0-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Va-0-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Va-0-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Va-0-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Va-0-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum JZ-1992-2514-0
  • ABIETINSAEUREMETHYLESTER
  • (-)-ABIETIC-ACID-METHYLESTER
  • ABALYN
  • 13-ISOPROPYLPODOCARPA-7,13-DIEN-15-OIC ACID, METHYL ESTER
  • Methyl abietate, methyl ester of abietic acid
  • METHYL ESTER OF ROSIN
  • 1-PHENANTHRENECARBOXYLIC ACID, 1,2,3,4,4A,4B,5,6,10,10A-DECAHYDRO-1- 4A-DIMETHYL-7-ISOPROPYL-, METHYL ESTER
  • 13-ISOPROPYLPODOCARPA-7,13-DIEN-16-OIC ACID, METHYL ESTER
  • Methyl abietate
  • METHYL ESTER OF WOOD ROSIN
  • WOOD ROSIN, METHYL ESTER
  • PODOCARPA-7,13-DIEN-16-OIC ACID, 13-ISOPROPYL-, METHYL ESTER
  • Abietate <methyl->
  • 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, methyl ester, [1R-(1.alpha.,4a.beta.,4b.alpha.,10a.alpha.)]-
  • 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, methyl ester, (1R,4aR,4bR,10aR)-
Title Journal or Book Year
Sesterterpenoids and Diterpenoids of the Wax Excreted by a Scale Insect, Ceroplastes pseudoceriferus Journal of Natural Products 1999
The13C NMR spectrum of abietic acid and its methyl ester Organic Magnetic Resonance 1978

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