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D-(+)-trehalose

Compound with spectra: 5 NMR, 3 FTIR, and 1 Raman

D-(+)-trehalose
SpectraBase Compound ID ANOkAZhgPzp
InChI InChI=1S/C12H22O11/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8+,9-,10-,11-,12-/m1/s1
InChIKey HDTRYLNUVZCQOY-LIZSDCNHSA-N
Mol Weight 342.3 g/mol
Molecular Formula C12H22O11
Exact Mass 342.116212 g/mol
Enantiomer InChIKey HDTRYLNUVZCQOY-CAPXFGMSSA-N

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13C NMR Spectrum
Copyright Database Compilation Copyright © 2021-2024 John Wiley & Sons, Inc. All Rights Reserved.

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13C NMR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample E. Wenkert, E. W. Hagaman J. Org. Chem. 41, 701(1976)
Solvent Water; Reference=Dioxane; Temperature=Ambient Spectrometer= Varian XL-100

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent H2O

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1H NMR Spectrum
Copyright Database Compilation Copyright © 2021-2024 John Wiley & Sons, Inc. All Rights Reserved.

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1H NMR Spectrum
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin
Solvent D2O

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Raman Spectrum
Copyright Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number T0832

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FTIR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin
Technique KBr WAFER

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FTIR Spectrum
Copyright Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number T0832
Technique KBr1

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ATR-IR Spectrum
Copyright Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number T0832
  • alpha-D-Trehalose
  • D-Trehalose
  • TREHALOSE /A,A-TREHALOSE/
  • GLUCOPYRANOSIDE, A-D-GLUCOPYRAN- OSYL-, A-D-,
  • α,α-Trehalose
  • TREHALOSE
Hexopyranosyl hexopyranoside
.alpha.,.beta.-Trehalose
(2R,3S,4S,5R,6R)-2-methylol-6-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol
.beta.,.beta.-Trehalose
ALPHA-D-GLUCOPYRANOSYL-(1<->1)-BETA-D-GALACTOPYRANOSIDE
HDTRYLNUVZCQOY-SOIZYFOBSA-N
HDTRYLNUVZCQOY-SBAFDXSCSA-N
α,α-Trehalose
2-O-BETA-D-GLUCOPYRANOSYL-D-ARABINITOL
EPI-HETERODENDRIN;2-BETA-D-GLUCOPYRANOSYLOXY-3-METHYL-2R-BUTYRONITRILE
Heterodendrin (S)
2-O-BETA-D-GLUCOPYRANOSYL-D-GLYCERALDEHYDE-1,1-DIETHYL-ACETAL
2-O-BETA-D-GLUCOPYRANOSYL-L-GLYCERALDEHYDE-1,1-DIETHYL-ACETAL
OCT-1-EN-3-YL-BETA-GLUCOPYRANOSIDE
Title Journal or Book Year
Deuterium-induced differential isotope shift carbon-13 NMR. 1. Resonance reassignments of mono- and disaccharides Journal of the American Chemical Society 1979
Hexopyranosyl hexopyranoside
α,α-Trehalose
D-(+)-trehalose, dihydrate
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