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MassBank Record: MSBNK-RIKEN_ReSpect-PT109980

O-Acety-L-carnitine hydrochloride, ALCAR, Levacecarnine , [(2R)-2-acetyloxy-4-hydroxy-4-oxobutyl]-trimethylazanium, (R)-3-Acetoxy-4-(trimethylammonio)butyrate, ALC, L-Carnitine acetyl ester; LC-ESI-QTOF; MS2

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-RIKEN_ReSpect-PT109980
RECORD_TITLE: O-Acety-L-carnitine hydrochloride, ALCAR, Levacecarnine , [(2R)-2-acetyloxy-4-hydroxy-4-oxobutyl]-trimethylazanium, (R)-3-Acetoxy-4-(trimethylammonio)butyrate, ALC, L-Carnitine acetyl ester; LC-ESI-QTOF; MS2
DATE: 2008.07.28
AUTHORS: Matsuda F, Suzuki M, Sawada Y, Plant Science Center, RIKEN.
LICENSE: CC BY-NC
COPYRIGHT: Copyright(C) 2009 Plant Science Center, RIKEN
COMMENT: Build 1 2009/06/24
COMMENT: Acquisition and generation of the data is financially supported in part by CREST/JST.

CH$NAME: O-Acety-L-carnitine hydrochloride
CH$NAME: ALCAR
CH$NAME: Levacecarnine
CH$NAME: [(2R)-2-acetyloxy-4-hydroxy-4-oxobutyl]-trimethylazanium
CH$NAME: (R)-3-Acetoxy-4-(trimethylammonio)butyrate
CH$NAME: ALC
CH$NAME: L-Carnitine acetyl ester
CH$COMPOUND_CLASS: CLASS1 Amino acid CLASS2 Carnitine
CH$FORMULA: C9H18NO4+
CH$EXACT_MASS: 204.246
CH$SMILES: CC(=O)OC(CC(=O)O)C[N+](C)(C)C
CH$IUPAC: InChI=1S/C9H17NO4/c1-7(11)14-8(5-9(12)13)6-10(2,3)4/h8H,5-6H2,1-4H3/p+1
CH$LINK: CAS 14992-62-2
CH$LINK: INCHIKEY RDHQFKQIGNGIED-UHFFFAOYSA-O

AC$INSTRUMENT: Q-Tof Premier, Waters
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: COLLISION_ENERGY Ramp 5-45 V
AC$MASS_SPECTROMETRY: CAPILLARY_VOLTAGE 3.0 kV
AC$CHROMATOGRAPHY: SOLVENT CH3CN/H2O

MS$FOCUSED_ION: ION_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_M/Z 204.12355

PK$SPLASH: splash10-000i-9130000000-e1b9918cf899fd3baa37
PK$NUM_PEAK: 3
PK$PEAK: m/z int. rel.int.
  85.0299 7488.0 999
  145.0539 1061.0 142
  204.1236 2527.0 337
//

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