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1,6,8-Trihydroxy-3-methylanthraquinone

Compound with spectra: 18 NMR, 1 FTIR, and 9 MS (GC)

1,6,8-Trihydroxy-3-methylanthraquinone
SpectraBase Compound ID Ct3LL5ZeIpw
InChI InChI=1S/C15H10O5/c1-6-2-8-12(10(17)3-6)15(20)13-9(14(8)19)4-7(16)5-11(13)18/h2-5,16-18H,1H3
InChIKey RHMXXJGYXNZAPX-UHFFFAOYSA-N
Mol Weight 270.24 g/mol
Molecular Formula C15H10O5
Exact Mass 270.052823 g/mol

View Spectrum of 1,6,8-Trihydroxy-3-methylanthraquinone

MS (GC) Spectrum
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

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MS (GC) Spectrum
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany

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MS (GC) Spectrum
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 Biologically and Environmentally Important Organic Compounds: GCMS Library

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-0-0-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CD-558-0-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.

View Spectrum of 1,6,8-Trihydroxy-3-methylanthraquinone

MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum X4-16-117-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum H1-43-973-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QA-48-1055-10

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13C NMR Spectrum
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample F. Toma, J. C. Bouhet Org. Magn. Resonance 7, 496(1975)
Solvent Dimethyl sulfoxide-d6; Reference=TMS; Temperature=Ambient Spectrometer= Varian XL-100

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13C NMR Spectrum
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Dimethyl sulfoxide

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13C NMR Spectrum
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3/DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3/DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3:CD3OD

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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ATR-IR Spectrum
Copyright Copyright © 2018-2025 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Catalog Number 230510
  • RHMXXJGYXNZAPX-UHFFFAOYSA-N
  • EMODIN;FRACTION-I
  • EMODIN;1,3,8-TRIHYDROXY-6-METHYL-ANTHRAQUINONE
  • Emodin
  • 6-Methyl-1,3,8-trihydroxyanthraquinone
  • 1,3,8-trihydroxy-6-methylanthracene-9,10-dione
  • Frangula emodin
  • 9,10-Anthracenedione, 1,3,8-trihydroxy-6-methyl-
  • Emodin, di-TMS, isomer 1
  • Frangulic acid
  • C.I. Natural Yellow 14
  • Persian Berry Lake
  • Archin
  • Emodol
  • Schuttgelb
  • Rheum emodin
  • Anthraquinone, 6-methyl-1,3,8-trihydroxy-
  • Anthraquinone, 1,3,8-trihydroxy-6-methyl-
  • 3-Methyl-1,6,8-trihydroxyanthraquinone
  • 1,3,8-Trihydroxy-6-methylanthraquinone
  • 4,5,7-Trihydroxy-2-methylanthraquinone
  • 6-Methyl-1,3,8-trihydroxy-9,10-anthracenedione
  • 3-Methyl-1,6,8-tris(oxidanyl)anthracene-9,10-dione
  • 1,3,8-Trihydroxy-6-methyl-9,10-anthracenedione
  • 1,3,8-Trihydroxy-6-methyl-9,10-anthraquinone
  • 1,3,8-Trihydroxy-6-methylanthra-9,10-quinone
  • CCRIS 3528
  • HSDB 7093
  • EINECS 208-258-8
  • NSC 408120
  • NSC 622947
  • BRN 1888141
  • AI3-38286
  • C.I. 75440
9,10-Anthracenedione, 1,8-dihydroxy-3,6-bis(methoxymethoxy)-
RHIZOCTONIC_ACID;5-HYDROXY-2-(2-HYDROXY-6-METHOXY-4-METHYLBENZOYL)-3-METHOXYBENZOIC_ACID
Anthraquinone, 1,4-dihydroxy-6-methyl-
1-Hydroxy-8-(2-hydroxyethoxy)anthraquinone
Danthron ET
1,4,6-Trihydroxy-9,10-anthraquinone
Alizarin, al-ca lake
9,10-Anthracenedione, 1,2-dihydroxy-, diiron salt
1-HYDROXY-4-METHYLANTHRAQUINONE, SODIUM SALT
1-HYDROXY-4-METHYLANTHRAQUINONE
Title Journal or Book Year
Chemical Constituents of Caesalpinia decapetala (Roth) Alston Molecules 2013
Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography Molecules 2011
Constituents from Moghat, the Roots of Glossostemon bruguieri (Desf.) Molecules 2003
Assignment of the1H and13C NMR spectra of anthraquinone glycosides fromRhamnus frangula Magnetic Resonance in Chemistry 1998
The anthraquinones of Heterodermia obscurata Phytochemistry 1995
Anthraquinones and Phenanthroperylenequinones from Nephroma laevigatum Journal of Natural Products 1995
Pigments of Fungi, Part 8. Bianthraquinones from Dermocybe austroveneta Journal of Natural Products 1988
Emodin Glycosides from Ventilago calyculata Journal of Natural Products 1986
Isolation of hydroxyanthrones from the roots of Rumex acetosa Linn.. Agricultural and Biological Chemistry 1982
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