Common name
ent_16_RS_9_epi_ST_D14_10_PhytoF
LMID
Systematic name
(S)-9-hydroxy-9-((2R,4S,5R)-4-hydroxy-5-((E)-3-hydroxypent-1-en-1-yl)tetrahydrofuran-2-yl)nonanoic acid
m/z
343.2126
Adduct / Ion
[M-H]-
Charge
-1
Ion source
ESI
Instrument
Thermo Fisher Orbitrap ID-X Tribrid
Resolution
60000
For high resolution data only
Ion mode
Negative
Collision Energy (CE)
stepped HCD collision energy 20–40–60%
Column
Kinetex C18 (100 × 2.1 mm, 1.7 µm)
Mobile phase A
H2O (0.1% HCOOH)
Mobile phase B
CH3CN (0.1% HCOOH) binary gradient at 0.5 m L/min
Retention time (min)
3.04
Amount injected
10 µL
DOI for method
Date acquired
October 2023
Submitters
Jean-Marie Galano.Ángel Sánchez Illana.Thierry Durand
Source of standard
Synthesized in-house