Record Information
Version1.0
Creation date2010-04-08 22:09:15 UTC
Update date2019-11-26 03:04:00 UTC
Primary IDFDB010702
Secondary Accession NumbersNot Available
Chemical Information
FooDB NameN-Hexadecanoylpyrrolidine
DescriptionN-Hexadecanoylpyrrolidine belongs to the class of organic compounds known as n-acylpyrrolidines. These are n-Acylated Pyrrolidine derivatives. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms. N-Hexadecanoylpyrrolidine has been detected, but not quantified in, green vegetables and pepper (spice). This could make N-hexadecanoylpyrrolidine a potential biomarker for the consumption of these foods. Based on a literature review a significant number of articles have been published on N-Hexadecanoylpyrrolidine.
CAS Number70974-48-0
Structure
Thumb
Synonyms
Predicted Properties
PropertyValueSource
Water Solubility0.00012 g/LALOGPS
logP6.1ALOGPS
logP6.3ChemAxon
logS-6.4ALOGPS
pKa (Strongest Basic)0.12ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area20.31 ŲChemAxon
Rotatable Bond Count14ChemAxon
Refractivity96.24 m³·mol⁻¹ChemAxon
Polarizability41.88 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Chemical FormulaC20H39NO
IUPAC name1-(pyrrolidin-1-yl)hexadecan-1-one
InChI IdentifierInChI=1S/C20H39NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-20(22)21-18-15-16-19-21/h2-19H2,1H3
InChI KeyULDNZNZTSYZQKK-UHFFFAOYSA-N
Isomeric SMILESCCCCCCCCCCCCCCCC(=O)N1CCCC1
Average Molecular Weight309.5298
Monoisotopic Molecular Weight309.303164875
Classification
Description Belongs to the class of organic compounds known as n-acylpyrrolidines. These are n-Acylated Pyrrolidine derivatives. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassPyrrolidines
Sub ClassN-acylpyrrolidines
Direct ParentN-acylpyrrolidines
Alternative Parents
Substituents
  • N-acylpyrrolidine
  • Tertiary carboxylic acid amide
  • Carboxamide group
  • Azacycle
  • Carboxylic acid derivative
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organonitrogen compound
  • Carbonyl group
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Route of exposure:

Biological location:

Source:

Role

Biological role:

Physico-Chemical Properties
Physico-Chemical Properties - Experimental
Spectra
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
Predicted GC-MSN-Hexadecanoylpyrrolidine, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positivesplash10-0002-9440000000-e1647a464e82095251ccSpectrum
Predicted GC-MSN-Hexadecanoylpyrrolidine, non-derivatized, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a4i-0009000000-8aff9701cc94cdb32c8d2015-04-25View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0ab9-9157000000-acda20e3ed455211b16e2015-04-25View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00di-9010000000-e9d1965ed982955d0a752015-04-25View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a4i-0009000000-ece7c81e9b3e46f7f16f2021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0a4i-1019000000-83f1fbd3f634c9783b742021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-01bc-9151000000-3e30cfed20bf9f64a1252021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-03di-4129000000-7e8e953d642307386cce2015-04-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0229-9422000000-97212f01e56c00343bc62015-04-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0596-9400000000-c259c507f1984097b5ca2015-04-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-03di-6009000000-cf4b8e4ead7b344f713f2021-09-23View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00di-9000000000-2e1eaf4feee0b790fb062021-09-23View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00di-9000000000-e1a52b4a67dc55fd36182021-09-23View Spectrum
NMRNot Available
ChemSpider ID216397
ChEMBL IDCHEMBL1223443
KEGG Compound IDNot Available
Pubchem Compound ID247220
Pubchem Substance IDNot Available
ChEBI IDNot Available
Phenol-Explorer IDNot Available
DrugBank IDNot Available
HMDB IDHMDB32740
CRC / DFC (Dictionary of Food Compounds) IDDFR12-Z:FOD42-X
EAFUS IDNot Available
Dr. Duke IDNot Available
BIGG IDNot Available
KNApSAcK IDC00031853
HET IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
Flavornet IDNot Available
GoodScent IDNot Available
SuperScent IDNot Available
Wikipedia IDNot Available
Phenol-Explorer Metabolite IDNot Available
Duplicate IDSNot Available
Old DFC IDSNot Available
Associated Foods
FoodContent Range AverageReference
Processing...
Biological Effects and Interactions
Health Effects / BioactivitiesNot Available
EnzymesNot Available
PathwaysNot Available
MetabolismNot Available
BiosynthesisNot Available
Organoleptic Properties
FlavoursNot Available
Files
MSDSNot Available
References
Synthesis ReferenceNot Available
General ReferenceNot Available
Content Reference— Shinbo, Y., et al. 'KNApSAcK: a comprehensive species-metabolite relationship database.' Plant Metabolomics. Springer Berlin Heidelberg, 2006. 165-181.