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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:49:22 UTC
Update Date2022-03-07 02:53:19 UTC
HMDB IDHMDB0032358
Secondary Accession Numbers
  • HMDB32358
Metabolite Identification
Common NameLauroyl diethanolamide
DescriptionLauroyl diethanolamide belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage. Thus, lauroyl diethanolamide is considered to be a fatty amide. Based on a literature review a significant number of articles have been published on Lauroyl diethanolamide.
Structure
Data?1563862254
Synonyms
ValueSource
ClindrolHMDB
Lauramide deaHMDB
Lauric diethanolamideHMDB
Lauryl diethanolamideHMDB
N,N-Bis(2-hydroxyethyl)dodecanamide, 9ci. N,N-bis(2-hydroxyethyl)lauramideHMDB
Lauramide diethanolamineMeSH
Lauric acid diethanolamideMeSH
Chemical FormulaC16H33NO3
Average Molecular Weight287.4381
Monoisotopic Molecular Weight287.246043927
IUPAC NameN,N-bis(2-hydroxyethyl)dodecanamide
Traditional NameN,N-bis(2-hydroxyethyl)dodecanamide
CAS Registry Number120-40-1
SMILES
CCCCCCCCCCCC(=O)N(CCO)CCO
InChI Identifier
InChI=1S/C16H33NO3/c1-2-3-4-5-6-7-8-9-10-11-16(20)17(12-14-18)13-15-19/h18-19H,2-15H2,1H3
InChI KeyAOMUHOFOVNGZAN-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty amides
Direct ParentN-acyl amines
Alternative Parents
Substituents
  • N-acyl-amine
  • Tertiary carboxylic acid amide
  • Carboxamide group
  • Alkanolamine
  • Carboxylic acid derivative
  • Alcohol
  • Hydrocarbon derivative
  • Primary alcohol
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Carbonyl group
  • Organic nitrogen compound
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting Point38.00 to 39.00 °C. @ 760.00 mm HgThe Good Scents Company Information System
Boiling Point443.25 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility49.91 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP4.033 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.22 g/LALOGPS
logP3.67ALOGPS
logP2.74ChemAxon
logS-3.1ALOGPS
pKa (Strongest Acidic)15.27ChemAxon
pKa (Strongest Basic)-0.064ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area60.77 ŲChemAxon
Rotatable Bond Count14ChemAxon
Refractivity82.88 m³·mol⁻¹ChemAxon
Polarizability36.16 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+173.94431661259
DarkChem[M-H]-173.05531661259
DeepCCS[M+H]+173.91130932474
DeepCCS[M-H]-170.42730932474
DeepCCS[M-2H]-206.89130932474
DeepCCS[M+Na]+182.74530932474
AllCCS[M+H]+174.432859911
AllCCS[M+H-H2O]+171.532859911
AllCCS[M+NH4]+177.132859911
AllCCS[M+Na]+177.932859911
AllCCS[M-H]-177.332859911
AllCCS[M+Na-2H]-178.232859911
AllCCS[M+HCOO]-179.432859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Lauroyl diethanolamideCCCCCCCCCCCC(=O)N(CCO)CCO3414.8Standard polar33892256
Lauroyl diethanolamideCCCCCCCCCCCC(=O)N(CCO)CCO2168.3Standard non polar33892256
Lauroyl diethanolamideCCCCCCCCCCCC(=O)N(CCO)CCO2424.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Lauroyl diethanolamide,1TMS,isomer #1CCCCCCCCCCCC(=O)N(CCO)CCO[Si](C)(C)C2431.8Semi standard non polar33892256
Lauroyl diethanolamide,2TMS,isomer #1CCCCCCCCCCCC(=O)N(CCO[Si](C)(C)C)CCO[Si](C)(C)C2487.3Semi standard non polar33892256
Lauroyl diethanolamide,1TBDMS,isomer #1CCCCCCCCCCCC(=O)N(CCO)CCO[Si](C)(C)C(C)(C)C2683.0Semi standard non polar33892256
Lauroyl diethanolamide,2TBDMS,isomer #1CCCCCCCCCCCC(=O)N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C2977.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Lauroyl diethanolamide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0zgj-8950000000-d2343f4ad1a1a66c5cae2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Lauroyl diethanolamide GC-MS (2 TMS) - 70eV, Positivesplash10-01ba-8932000000-361c517e9f981c03b5a12017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Lauroyl diethanolamide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Lauroyl diethanolamide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Lauroyl diethanolamide LC-ESI-QFT , positive-QTOFsplash10-052r-7960000000-cbf84658f45c669979de2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Lauroyl diethanolamide 50V, Positive-QTOFsplash10-004i-0790000000-3932f494d8a1f98490fa2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Lauroyl diethanolamide 20V, Positive-QTOFsplash10-004i-0090000000-d68f27e48b2fba24234d2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Lauroyl diethanolamide 10V, Positive-QTOFsplash10-000i-0090000000-350c512f0e5f956559cd2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Lauroyl diethanolamide 30V, Positive-QTOFsplash10-004i-0090000000-f4df67cbb4751daa5d2e2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Lauroyl diethanolamide 40V, Positive-QTOFsplash10-004i-0090000000-79ace3a2b10cc78706872021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Lauroyl diethanolamide 35V, Positive-QTOFsplash10-052r-7960000000-19573dabb2689e66dea62021-09-20HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 10V, Positive-QTOFsplash10-000i-1390000000-d3b6e6c20fa69b27803c2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 20V, Positive-QTOFsplash10-059i-9740000000-7da9f488a14751b7c59c2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 40V, Positive-QTOFsplash10-0btl-9300000000-951a2bdc5e782344ad572016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 10V, Negative-QTOFsplash10-000i-0190000000-acf61580b479902210b22016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 20V, Negative-QTOFsplash10-000i-2690000000-99b2d89e48be0270c43f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 40V, Negative-QTOFsplash10-0udu-9610000000-1b3cc45e3f191567a68d2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 10V, Negative-QTOFsplash10-000i-0090000000-36ecbfd1ee7ca877ebeb2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 20V, Negative-QTOFsplash10-000i-0390000000-761783819eb1ee7b57262021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 40V, Negative-QTOFsplash10-06r6-9310000000-178d7b89b1937daf35932021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 10V, Positive-QTOFsplash10-000i-0290000000-e1ead6605eb1949e75922021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 20V, Positive-QTOFsplash10-06y9-9420000000-96961d450c5df73faf272021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Lauroyl diethanolamide 40V, Positive-QTOFsplash10-052b-9100000000-e76ae67d14a26e34bce02021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB009690
KNApSAcK IDC00017077
Chemspider ID8123
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound8430
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1301071
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. (). EAFUS: Everything Added to Food in the United States.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.