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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2012-09-11 21:16:33 UTC
Update Date2022-03-07 02:54:49 UTC
HMDB IDHMDB0036219
Secondary Accession Numbers
  • HMDB36219
Metabolite Identification
Common NameOctyl 2-methylbutyrate
DescriptionOctyl 2-methylbutyrate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. Based on a literature review a small amount of articles have been published on Octyl 2-methylbutyrate.
Structure
Data?1563862838
Synonyms
ValueSource
Octyl 2-methylbutyric acidGenerator
Butanoic acid, 2-methyl-, octyl esterHMDB
Butyric acid, 2-methyl-, octyl esterHMDB
FEMA 3604HMDB
N-Octyl 2-methyl butyrateHMDB
N-Octyl 2-methylbutanoateHMDB
Octyl 2-methyl butyrateHMDB
Octyl 2-methylbutanoateHMDB
Octyl 2-methyl-butanoic acidGenerator
Chemical FormulaC13H26O2
Average Molecular Weight214.3443
Monoisotopic Molecular Weight214.193280076
IUPAC Nameoctyl 2-methylbutanoate
Traditional Nameoctyl 2-methylbutanoate
CAS Registry Number29811-50-5
SMILES
CCCCCCCCOC(=O)C(C)CC
InChI Identifier
InChI=1S/C13H26O2/c1-4-6-7-8-9-10-11-15-13(14)12(3)5-2/h12H,4-11H2,1-3H3
InChI KeyBCOJVEMHTBSAOE-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty alcohol esters
Direct ParentFatty alcohol esters
Alternative Parents
Substituents
  • Fatty alcohol ester
  • Fatty acid ester
  • Carboxylic acid ester
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Disposition
Process
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0041 g/LALOGPS
logP5.18ALOGPS
logP4.71ChemAxon
logS-4.7ALOGPS
pKa (Strongest Basic)-7.1ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area26.3 ŲChemAxon
Rotatable Bond Count10ChemAxon
Refractivity63.49 m³·mol⁻¹ChemAxon
Polarizability27.64 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+154.22131661259
DarkChem[M-H]-150.27631661259
DeepCCS[M+H]+159.32330932474
DeepCCS[M-H]-155.74530932474
DeepCCS[M-2H]-193.13230932474
DeepCCS[M+Na]+168.79730932474
AllCCS[M+H]+157.832859911
AllCCS[M+H-H2O]+154.432859911
AllCCS[M+NH4]+160.932859911
AllCCS[M+Na]+161.932859911
AllCCS[M-H]-158.532859911
AllCCS[M+Na-2H]-159.932859911
AllCCS[M+HCOO]-161.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Octyl 2-methylbutyrateCCCCCCCCOC(=O)C(C)CC1653.0Standard polar33892256
Octyl 2-methylbutyrateCCCCCCCCOC(=O)C(C)CC1427.1Standard non polar33892256
Octyl 2-methylbutyrateCCCCCCCCOC(=O)C(C)CC1461.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental GC-MSGC-MS Spectrum - Octyl 2-methylbutyrate EI-B (Non-derivatized)splash10-0pbc-9200000000-deeb56bfe2fe67b6bd5a2017-09-12HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - Octyl 2-methylbutyrate EI-B (Non-derivatized)splash10-0pbc-9200000000-deeb56bfe2fe67b6bd5a2018-05-18HMDB team, MONA, MassBankView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Octyl 2-methylbutyrate GC-MS (Non-derivatized) - 70eV, Positivesplash10-052r-9200000000-4ee7b3cc663ebaf37e552017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Octyl 2-methylbutyrate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 10V, Positive-QTOFsplash10-014i-4490000000-2965fa05ba9f090627e92016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 20V, Positive-QTOFsplash10-03di-8910000000-8f5e39332126d81a137d2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 40V, Positive-QTOFsplash10-0ap3-9000000000-a76cf944220acc7656712016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 10V, Negative-QTOFsplash10-03di-2390000000-d07d78c42f7672d984f02016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 20V, Negative-QTOFsplash10-0w29-7920000000-a11a2b2a928af7bbbc502016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 40V, Negative-QTOFsplash10-0pb9-9300000000-a9e53b6bcde9e5e491c22016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 10V, Positive-QTOFsplash10-0pvr-9420000000-f99fa06f131e63d612a12021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 20V, Positive-QTOFsplash10-052r-9000000000-8cdce3b6788797c6a0d22021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 40V, Positive-QTOFsplash10-0a4i-9000000000-9e669ce7f798ea6b8ee12021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 10V, Negative-QTOFsplash10-03fr-0980000000-73da5225266cdb7ca4c92021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 20V, Negative-QTOFsplash10-0udi-2910000000-fac3c40e14301ee6b5f02021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Octyl 2-methylbutyrate 40V, Negative-QTOFsplash10-0pb9-9200000000-be38dfc5bbc5646c6d822021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Saliva
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
SalivaDetected but not QuantifiedNot QuantifiedChildren (1-13 years old)BothNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
SalivaDetected but not QuantifiedNot QuantifiedChildren (1-13 years old)BothCeliac disease details
Associated Disorders and Diseases
Disease References
Celiac disease
  1. Francavilla R, Ercolini D, Piccolo M, Vannini L, Siragusa S, De Filippis F, De Pasquale I, Di Cagno R, Di Toma M, Gozzi G, Serrazanetti DI, De Angelis M, Gobbetti M: Salivary microbiota and metabolome associated with celiac disease. Appl Environ Microbiol. 2014 Jun;80(11):3416-25. doi: 10.1128/AEM.00362-14. Epub 2014 Mar 21. [PubMed:24657864 ]
Associated OMIM IDs
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB015077
KNApSAcK IDC00030881
Chemspider ID453986
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound520455
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.