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DL-Tryptophan
SpectraBase Compound ID BE1jhdZsKZM
InChI InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)
InChIKey QIVBCDIJIAJPQS-UHFFFAOYSA-N
Mol Weight 204.23 g/mol
Molecular Formula C11H12N2O2
Exact Mass 204.089878 g/mol
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Calbiochem, EMD Chemicals, Inc., an Affiliate of Merck KGaA, Darmstadt, Germany
Source of Spectrum Forensic Spectral Research
Catalog Number 6530
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Source of Sample Aldrich
Catalog Number 162698
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Source of Sample Winthrop Laboratories, Special Chemicals Department
Technique KBr WAFER
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Source of Sample The Matheson Company, Inc., East Rutherford, New Jersey
Technique KBr WAFER
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-0-0-0
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Source of Spectrum PG-1982-1515-0
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Source of Spectrum GT-1986-57-0
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Source of Spectrum C-85-841-22
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Source of Spectrum CM-1999-6450-0
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Source of Spectrum CM-1999-15431-0
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Source of Spectrum NP-17-9808-0
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Source of Spectrum NP-4-3098-0
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Source of Spectrum B4-0-0-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-1989-25370-0
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Source of Spectrum JZ-1992-1736-0
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Source of Spectrum CJ-0-32-0
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Source of Spectrum CK-4-256-96
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum JZ-1992-4840-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Eastman Organic Chemicals, Rochester, New York
Solvent Deuterium oxide/Deuterium chloride; Reference=Dioxane Spectrometer= Varian CFT-20
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Solvent DMSO
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Solvent D2O
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Solvent DMSO-D6
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Solvent H2O
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Solvent H2O
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Solvent DMSO-D6
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Solvent D2O
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Solvent H2O
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Solvent D2O
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Solvent H2O
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Solvent H2O
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Solvent DMSO-D6
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Solvent D2O
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Solvent H2O
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Solvent D2O
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Solvent H2O
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Solvent H2O
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Solvent H2O
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Solvent D2O
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Solvent H2O
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Solvent D2O
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Solvent D2O:DCl
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Solvent CD3OD;0.1N-NAOD
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Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O;PH=1
Copyright Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 162698
Solvent D2O & NaOD
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Solvent D2O/KOD
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Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 162698
Solvent D2O & NaOD
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Source of Sample Calbiochem, EMD Chemicals, Inc., an Affiliate of Merck KGaA, Darmstadt, Germany
Source of Spectrum Forensic Spectral Research
Catalog Number 6530
Copyright Copyright © 2017-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2017-2024 John Wiley & Sons, Inc. All Rights Reserved.
Catalog Number 162698
  • D,L-3β-Indolylalanine
  • (+/-)-α-Amino-3-indolepropionic acid
  • (+/-)-2-Amino-3-(3-indolyl)propionic acid
  • (+/-)-alpha-Amino-3-indolepropionic acid, (+/-)-2-Amino-3-(3-indolyl)propionic acid, DL-3beta-Indolylalanine
  • TRP;TRYPTOPHAN
  • L-TRYPTOPHANE
  • L-tryptophan
  • TRYPTOPHAN
  • 3-INDOLEPROPIONIC ACID, A-AMINO-,
  • TRYPTOPHAN, DL-,
  • ALANINE, 3-/3-INDOLYL/-,
  • alpha-AMINO-3-INDOLEPROPIONIC ACID
  • 3-(3-INDOLYL)ALANINE
  • A-Amino-3-indolepropanoic acid
  • 2-AMINO-3-(1H-INDOL-3-YL)-PROPIONIC ACID
  • (S)-2-ammonio-3-(1H-indol-3-yl)propanoate
  • D-TRYPTOPHANE
Title Journal or Book Year
Identificação de alguns constituintes químicos de Indigofera hirsuta Linn. (Fabaceae) por CLAE-IES-EM (TOF) e avaliação da atividade antirradicalar Química Nova 2011
Chemo-enzymatic synthesis and characterization of L-tryptophans selectively 13C-enriched or hydroxylated in the six-membered ring using transformed Escherichia coli cells Recueil des Travaux Chimiques des Pays-Bas 2010
Spectral analysis of1H coupled13C spectra of the amino acids: adaptive spectral library of amino acid13C isotopomers and positional fractional13C enrichments Magnetic Resonance in Chemistry 2008
Chlorine substituent effects for indole and tryptophan in13C NMR Journal of Heterocyclic Chemistry 1994

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