MassBank of North America

Spectrum SM816753 for 2,4,6-Tribromphenol

Rating: ★★★★☆

Originally submitted to the MassBank High Quality Mass Spectral Database as MassBank

SPLASH:
splash10-004i-0009000000-d4bc5a4018393fbac0dd
Submitter:
CASMI Team

Compound Information

Chemical Names

Compound Classification (provided by ClassyFire)

ClassyFire is a freely accessible computational tool that uses the ChemOnt taxonomy to classify chemical entities based on their structure. ClassyFire combines structure search, IUPAC name parsing, and evaluation of logical expressions to retrieve structural features, which are then mapped to the corresponding ChemOnt classes.

Kingdom
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Organic compounds
- Superclass
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  Benzenoids
  - Class
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    Phenols
    - Subclass
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      Halophenols
      - Intermediate Parent 1
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        Bromophenols

Compound Metadata

Name	Value
InChI Create New Query Add to Query	InChI=1S/C6H3Br3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H
InChIKey Create New Query Add to Query	BSWWXRFVMJHFBN-UHFFFAOYSA-N
molecular formula Create New Query Add to Query	C6H3Br3O
total exact mass Create New Query Add to Query	327.773401016
SMILES Create New Query Add to Query	BrC=1C=C(Br)C(O)=C(Br)C1

External Identifier	Value
cas Create New Query Add to Query	118-79-6
chebi Create New Query Add to Query	47696
kegg Create New Query Add to Query	C14454
pubchem cid Create New Query Add to Query	1483
chemspider Create New Query Add to Query	1438

Mass Spectral Metadata

Name	Value
date Create New Query Add to Query	2016.12.12
accession Create New Query Add to Query	SM816753
author Create New Query Add to Query	Krauss M, Schymanski EL, Weidauer C, Schupke H, UFZ and Eawag
license Create New Query Add to Query	CC BY
copyright Create New Query Add to Query	Copyright (C) 2016 UFZ/Eawag
publication Create New Query Add to Query	Schymanski, E. L.; Ruttkies, C.; Krauss, M.; Brouard, C.; Kind, T.; Dührkop, K.; Allen, F.; Vaniya, A.; Verdegem, D.; Böcker, S.; et al. Critical Assessment of Small Molecule Identification 2016: Automated Methods. Journal of Cheminformatics 2017, 9 (1). DOI:10.1186/s13321-017-0207-1
exact mass Create New Query Add to Query	327.7734
instrument Create New Query Add to Query	Q Exactive Plus Orbitrap Thermo Scientific
instrument type Create New Query Add to Query	LC-ESI-QFT
ms level Create New Query Add to Query	MS2
ionization Create New Query Add to Query	ESI
fragmentation mode Create New Query Add to Query	HCD
collision energy Create New Query Add to Query	35 (nominal)
resolution Create New Query Add to Query	35000
column Create New Query Add to Query	Kinetex C18 EVO 2.6 um, 2.1x50 mm, precolumn 2.1x5 mm, Phenomenex
flow gradient Create New Query Add to Query	95/5 at 0 min, 95/5 at 1 min, 0/100 at 13 min, 0/100 at 24 min
flow rate Create New Query Add to Query	300 uL/min
retention time Create New Query Add to Query	11.937 min
SOLVENT A Create New Query Add to Query	water with 0.1% formic acid
SOLVENT B Create New Query Add to Query	methanol with 0.1% formic acid
recalibrate Create New Query Add to Query	loess on assigned fragments and MS1
reanalyze Create New Query Add to Query	Peaks with additional N2/O included
whole Create New Query Add to Query	RMassBank 2.3.1
ionization mode Create New Query Add to Query	negative
spectral entropy Create New Query Add to Query	0.028194433821661917
normalized entropy Create New Query Add to Query	0.040675969855183715
precursor m/z Create New Query Add to Query	326.7661
precursor type Create New Query Add to Query	[M-H]-
mass accuracy Create New Query Add to Query	0.07655628902462139 ppm
mass error Create New Query Add to Query	-2.5015999995048332E-5 Da