MassBank of North America

Spectrum OUF00311 for Lignoceric acid

Rating: ★★★★☆

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

SPLASH:
splash10-0159-1900000000-3507c183bf018486d18f
Submitter:
Eiichiro Fukusaki

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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  Lipids and lipid-like molecules
  - Class
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    Fatty Acyls
    - Subclass
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      Fatty acids and conjugates

Compound Metadata

Name	Value
compound class Create New Query Add to Query	Natural Product
InChI Create New Query Add to Query	InChI=1S/C24H48O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26/h2-23H2,1H3,(H,25,26)
InChIKey Create New Query Add to Query	QZZGJDVWLFXDLK-UHFFFAOYSA-N
molecular formula Create New Query Add to Query	C24H48O2
total exact mass Create New Query Add to Query	368.365430776
SMILES Create New Query Add to Query	O=C(O)CCCCCCCCCCCCCCCCCCCCCCC

External Identifier	Value
cas Create New Query Add to Query	557-59-5
chebi Create New Query Add to Query	28866 31014
chemspider Create New Query Add to Query	10724
kegg Create New Query Add to Query	C08320
lipidmaps Create New Query Add to Query	LMFA01010024
pubchem Create New Query Add to Query	11197

Mass Spectral Metadata

Name	Value
accession Create New Query Add to Query	OUF00311
date Create New Query Add to Query	2016.01.19 (Created 2010.05.20, modified 2013.04.24)
license Create New Query Add to Query	CC BY-SA
author Create New Query Add to Query	Tsujimoto Y, Tsugawa H, Bamba T, Fukusaki E, engineering department, Osaka Univ.
comment Create New Query Add to Query	The chemical compound was chemically modified with N-methyl-N-trimethylsilyl-trifluoroacetamide (MSTFA) before GC-MS analysis. When it has two or more functional groups, this modification gave a mixture of the TMS derivatives having different number of TMS groups at different functional groups.
exact mass Create New Query Add to Query	368.36543
instrument Create New Query Add to Query	Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies
instrument type Create New Query Add to Query	GC-EI-TOF
ms level Create New Query Add to Query	MS1
helium flow Create New Query Add to Query	1 ml/min
ion source temperature Create New Query Add to Query	200 C
scan range m/z Create New Query Add to Query	85-500
column Create New Query Add to Query	CP-SIL 8 CB LOW BLEED/MS
injection temperature Create New Query Add to Query	230 C
oven temperature Create New Query Add to Query	80 C (Duration 2 min)-330 C (rate: 15 C/min; Duration 6 min)
retention index Create New Query Add to Query	2836.271
retention time Create New Query Add to Query	1043.988 sec
transfer line temperature Create New Query Add to Query	250 C
whole Create New Query Add to Query	ChromaTOF ver. 2.32 (LECO)
ionization mode Create New Query Add to Query	positive
spectral entropy Create New Query Add to Query	3.315954448178522
normalized entropy Create New Query Add to Query	0.6566433663490923