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D-Lysine monohydrochloride
SpectraBase Compound ID 2UEOoB0l2lM
InChI InChI=1S/C6H14N2O2.ClH/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H/t5-;/m1./s1
InChIKey BVHLGVCQOALMSV-NUBCRITNSA-N
Mol Weight 182.65 g/mol
Molecular Formula C6H15ClN2O2
Exact Mass 182.082205 g/mol
Parent InChIKey KDXKERNSBIXSRK-RXMQYKEDSA-N
Enantiomer InChIKey BVHLGVCQOALMSV-JEDNCBNOSA-N
Racemate InChIKey BVHLGVCQOALMSV-UHFFFAOYSA-N
Copyright Copyright © 1989, 1990-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Technique KBr-Pellet
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Fluka Chemie AG, Buchs, Switzerland
Technique KBr WAFER
Copyright Copyright © 2016-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number L07710
Technique KBr1
Copyright Copyright © 2016-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number L07710
Copyright Copyright © 2016-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number L07710
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • H-D-Lys-OH.HCl
  • (R)-2,6-Diaminohexanoic acid monohydrochloride
  • L-Lysine monohydrochloride
  • D-(-)-LYSINE, HYDROCHLORIDE
  • LYSINE, HYDROCHLORIDE, D-/MINUS/-,
  • Lysine, monohydrochloride, D-
Title Journal or Book Year
Enantioselective syntheses of isotopically labelled α-amino acids. Preparation of (ϵ-13C)-L-α-aminoadipic acid and five isotopomers of L-lysine with 13C, 15N and 2H in the δ- and ϵ-positions Recueil des Travaux Chimiques des Pays-Bas 2010

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