TRIACETIN (GLYCEROL TRIACETATE) (CED0017600)

Record Information
Version1.0
Creation Date2016-05-19 02:29:29 UTC
Update Date2026-05-14 19:54:23 UTC
Accession NumberCHEM007721
Identification
Common NameTRIACETIN (GLYCEROL TRIACETATE)
ClassSmall Molecule
Description
TRIACETIN (GLYCEROL TRIACETATE) belongs to the triradylcglycerols, a subclass of glycerolipids within the organic compounds. This compound has the formula C9H14O6 and an average molecular weight of 218.20 g/mol. In industrial applications, it serves a wide variety of roles, acting as a solvent, biocide, film former, plasticizer, deodorizer, humectant, fragrance, and pharmaceutical. Additionally, it is utilized as a flavouring and nutrient, a surface modifier, and as processing aids not otherwise specified. The compound is found in or released from 38 recorded sources. Within electrical and electronic equipment, it is associated with antennas, amplifiers, adjustable resistors, communication cables or conductors, and conductors or conductive bodies characterised by the conductive materials, among 11 other items. It is present in household cleaning and consumer products, including bleaching agents, ash trays, cigar cigarettes, other smoking requisites, and non electric simulated smoking devices, as well as 7 other products. In the context of food, food processing and cookware, it is linked to food contact materials, food preservation, the preparation of vinegar, the preparation of wine or sparkling wine, and fermentation processes for beer, among 2 others. Other recorded sources include drinking water and water supply, indoor air via air, dust and atmospheric transport, and tents or canopies within building and construction. Recorded exposure routes for the compound include oral, inhalation, and touch.
Contaminant TypeNot Available
Chemical Structure
Synonyms
ValueSource
1,2,3-Propanetriol triacetateChEBI
1,2,3-Propanetriyl triacetateChEBI
1,2,3-TriacetoxypropaneChEBI
1,2,3-TriacetylglycerolChEBI
2-(Acetyloxy)-1-[(acetyloxy)methyl]ethyl acetateChEBI
e 1518ChEBI
e-1518ChEBI
e1518ChEBI
EnzactinChEBI
Glycerin triacetateChEBI
Glycerol triacetateChEBI
Glyceryl triacetateChEBI
TriacetinaChEBI
TriacetineChEBI
TriacetinumChEBI
Triacetyl glycerinChEBI
Triacetyl glycerineChEBI
TriacetylglycerolChEBI
1,2,3-Propanetriol triacetic acidGenerator
1,2,3-Propanetriyl triacetic acidGenerator
2-(Acetyloxy)-1-[(acetyloxy)methyl]ethyl acetic acidGenerator
Glycerin triacetic acidGenerator
Glycerol triacetic acidGenerator
Glyceryl triacetic acidGenerator
1,2,3-Propanetriol triacetate, 9ciHMDB
1,2,3-Propanetriol, 1,2,3-triacetateHMDB
1,2,3-Propanetriol, triacetateHMDB
Acetic, 1,2,3-propanetriyl esterHMDB
BlekinHMDB
EnzacetinHMDB
Estol 1581HMDB
EuzactinHMDB
FEMA 2007HMDB
FungacetHMDB
FungacetinHMDB
Glycerol triacetate tributyrinHMDB
GlypedHMDB
Kesscoflex traHMDB
Kodaflex triacetinHMDB
MotisilHMDB
Propane-1,2,3-triyl triacetateHMDB
Tri-acetinHMDB
Triacetin (1,2,3-propanetriol triacetate)HMDB
Triacetin (glycerol triacetate)HMDB
Triacetin, 8ci, ban, inn, usanHMDB
Triacetyl glycerolHMDB
VanayHMDB
Triacetyl-glycerolMeSH, HMDB
Chemical FormulaC9H14O6
Average Molecular Mass218.204 g/mol
Monoisotopic Mass218.079 g/mol
CAS Registry Number102-76-1
IUPAC Name1,3-bis(acetyloxy)propan-2-yl acetate
Traditional Nametriacetin
SMILESCC(=O)OCC(COC(C)=O)OC(C)=O
InChI IdentifierInChI=1S/C9H14O6/c1-6(10)13-4-9(15-8(3)12)5-14-7(2)11/h9H,4-5H2,1-3H3
InChI KeyURAYPUMNDPQOKB-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerolipids
Sub ClassTriradylcglycerols
Direct ParentTriacylglycerols
Alternative Parents
Substituents
  • Triacyl-sn-glycerol
  • Tricarboxylic acid or derivatives
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Organoleptic EffectsNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility11.3 g/LALOGPS
logP0.4ALOGPS
logP-0.52ChemAxon
logS-1.3ALOGPS
pKa (Strongest Basic)-6.5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity47.97 m³·mol⁻¹ChemAxon
Polarizability20.88 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyDeposition DateView
GC-MSGC-MS Spectrumsplash10-0zfs-3900000000-0e517995b789bd89015dNot AvailableView Spectrum
GC-MSGC-MS Spectrumsplash10-0007-7900000000-8dba8a82c4b9ea4fff14Not AvailableView Spectrum
GC-MSGC-MS Spectrumsplash10-0006-9100000000-4831fd0c53a09c852378Not AvailableView Spectrum
GC-MSGC-MS Spectrumsplash10-0zfs-3900000000-0e517995b789bd89015dNot AvailableView Spectrum
GC-MSGC-MS Spectrumsplash10-0007-7900000000-8dba8a82c4b9ea4fff14Not AvailableView Spectrum
GC-MSGC-MS Spectrumsplash10-0006-9100000000-4831fd0c53a09c852378Not AvailableView Spectrum
Predicted GC-MSPredicted GC-MS SpectrumNot AvailableNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-000i-0090000000-8a37824d0f2d133742dcNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-000i-0090000000-8a37824d0f2d133742dcNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0aor-0970000000-2aef4d9a7612d8dafbfeNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0006-0090000000-b38fc2a560bf20d37e0cNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0006-0090000000-b38fc2a560bf20d37e0cNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0006-0090000000-b38fc2a560bf20d37e0cNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-05mk-9710000000-f22af5cbf5889ccdd932Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-05mn-9400000000-7652606ae6706c4a9b17Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-000m-9100000000-e19f8f565c58ee733eeaNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0a4i-9410000000-298ddbbc7ca605058710Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0a4i-9600000000-200967820af7347f4ccdNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0a4i-9100000000-786d33c8b183715b60e2Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-000i-0090000000-47388b4e8c5a7aee1b2dNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-000i-0090000000-47388b4e8c5a7aee1b2dNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0aor-1970000000-5d157472f8cf1a1268a6Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-004i-0090000000-8fc8dc18b58235d1fad0Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-004i-0090000000-8fc8dc18b58235d1fad0Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-04mi-9990000000-873dc2c08186ded9c103Not AvailableView Spectrum
1D NMR13C NMR Spectrum (1D, D2O, predicted)Not AvailableNot AvailableView Spectrum
1D NMR1H NMR Spectrum (1D, D2O, predicted)Not AvailableNot AvailableView Spectrum
Toxicity Profile
Mechanism of ToxicityNot Available
Carcinogenicity (IARC Classification)Not Available
Minimum Risk LevelNot Available
SymptomsNot Available
TreatmentNot Available
Toxicity Values
Toxicity ValueUnitValue RangeOrganismDose DescriptorRoute of ExposurePredicted or ExperimentalReference
6781.0Log mg/kg[3800:12000]RatLD50oralpredictedNot Available
Health Effects
Health EffectRelationshipDirectionReference
Exposure Sources
Source IDSourceSectorReference
10InsecticidesAgriculture & land managementNot Available
19Indoor airAir, dust & atmospheric transportNot Available
115Drinking waterDrinking water & water supplyNot Available
233BrushesPersonal care & cosmeticsNot Available
490Personal care & cosmeticsNot Available
494Food contact materialsFood, food processing & cookwareNot Available
503Tents Or CanopiesBuilding & ConstructionNot Available
504Adjustable ResistorsElectrical & Electronic EquipmentNot Available
505AmplifiersElectrical & Electronic EquipmentNot Available
506AntennasElectrical & Electronic EquipmentNot Available
510Communication Cables Or ConductorsElectrical & Electronic EquipmentNot Available
511Conductors Or Conductive Bodies Characterised By The Conductive MaterialsElectrical & Electronic EquipmentNot Available
514Discharge LampsElectrical & Electronic EquipmentNot Available
516Electric Hearing AidsElectrical & Electronic EquipmentNot Available
517Electric SwitchesElectrical & Electronic EquipmentNot Available
518Electrically Stimulated Smoking DevicesElectrical & Electronic EquipmentNot Available
519ElectrodesElectrical & Electronic EquipmentNot Available
520Emergency Protective DevicesElectrical & Electronic EquipmentNot Available
521Fixed Capacitors And Their ManufactureElectrical & Electronic EquipmentNot Available
523Gas Filled Discharge Tubes With Solid CathodeElectrical & Electronic EquipmentNot Available
524Hybrid CapacitorsElectrical & Electronic EquipmentNot Available
529Power CablesElectrical & Electronic EquipmentNot Available
537Television SystemsElectrical & Electronic EquipmentNot Available
544Fermentation Processes For BeerFood, food processing & cookwareNot Available
545Food PreservationFood, food processing & cookwareNot Available
548Preparation Of VinegarFood, food processing & cookwareNot Available
549Preparation Of Wine Or Sparkling WineFood, food processing & cookwareNot Available
550Preparation Of WortFood, food processing & cookwareNot Available
552Processing MeatsFood, food processing & cookwareNot Available
554Ash TraysHousehold cleaning & consumer productsNot Available
555Bleaching AgentsHousehold cleaning & consumer productsNot Available
556Cigar CigarettesHousehold cleaning & consumer productsNot Available
559Non Electric Simulated Smoking DevicesHousehold cleaning & consumer productsNot Available
560Other Smoking RequisitesHousehold cleaning & consumer productsNot Available
561Perfumes Within Detergents And SoapsHousehold cleaning & consumer productsNot Available
562Pipe AccessoriesHousehold cleaning & consumer productsNot Available
563Soap DetergentsHousehold cleaning & consumer productsNot Available
566Tobacco PipesHousehold cleaning & consumer productsNot Available
567Tobacco Product CasesHousehold cleaning & consumer productsNot Available
568Tobacco Product Moisture ControlHousehold cleaning & consumer productsNot Available
569Tobacco Smoke FiltersHousehold cleaning & consumer productsNot Available
578Making CigarsIndustrial manufacturing & chemical processingNot Available
579Manufacture Of Iron Or SteelIndustrial manufacturing & chemical processingNot Available
580Manufacture Preparation Of Tobacco ProductsIndustrial manufacturing & chemical processingNot Available
581Paper Making MachinesIndustrial manufacturing & chemical processingNot Available
584BuoysMarine, shipping & aquacultureNot Available
589Life BuoysMarine, shipping & aquacultureNot Available
592Marine Propulsion Or SteeringMarine, shipping & aquacultureNot Available
596AcaricidesAgriculture & land managementNot Available
600Herbicides And AlgicidesAgriculture & land managementNot Available
603NematocidesAgriculture & land managementNot Available
604Pest AttractantsAgriculture & land managementNot Available
606Plant Growth RegulatorsAgriculture & land managementNot Available
609AftershavePersonal care & cosmeticsNot Available
610Aftersun ProductsPersonal care & cosmeticsNot Available
611Anti Perspirants Or Body DeoderantsPersonal care & cosmeticsNot Available
612Body Washing Or Cleaning ImplementsPersonal care & cosmeticsNot Available
613DepilatoriesPersonal care & cosmeticsNot Available
614Essential Oils Or PerfumesPersonal care & cosmeticsNot Available
615Eye Makeup ProductsPersonal care & cosmeticsNot Available
617Lip Care ProductsPersonal care & cosmeticsNot Available
618Lip Makeup ProductsPersonal care & cosmeticsNot Available
619Manicure PedicurePersonal care & cosmeticsNot Available
620Card GamesRecreation & sports surfacesNot Available
625Racing SportsRecreation & sports surfacesNot Available
630ToysRecreation & sports surfacesNot Available
632ApparelTextiles, leather & furnishingsNot Available
633Azo DyesTextiles, leather & furnishingsNot Available
638Decorating TextilesTextiles, leather & furnishingsNot Available
640Embroidering And TuftingTextiles, leather & furnishingsNot Available
642FootwearTextiles, leather & furnishingsNot Available
643HeadwearTextiles, leather & furnishingsNot Available
647Multicolour DyeingTextiles, leather & furnishingsNot Available
650Purses Luggage Hand BagsTextiles, leather & furnishingsNot Available
657Surface Finishing Of LeatherTextiles, leather & furnishingsNot Available
658Touch FastenersTextiles, leather & furnishingsNot Available
659Transfer PrintingTextiles, leather & furnishingsNot Available
662Yarns Or ThreadsTextiles, leather & furnishingsNot Available
Pathways
0 pathways

No pathways found

No metabolic pathways have been associated with this synthetic chemical

Targets
StructureProteinUniProt IDOrganismRelationshipDetails
Autotaxin structureClick to view 3D structureAutotaxinQ13822HumansPredicted (SEA)23.6662
Click to view 3D structureLysophosphatidic acid receptor 3Q9UBY5HumansPredicted (SEA)18.5281
Muscarinic acetylcholine receptor M2 structureClick to view 3D structureMuscarinic acetylcholine receptor M2P08172HumansPredicted (SEA)529.997
Muscarinic acetylcholine receptor M4 structureClick to view 3D structureMuscarinic acetylcholine receptor M4P08173HumansPredicted (SEA)411.667
Muscarinic acetylcholine receptor M1 structureClick to view 3D structureMuscarinic acetylcholine receptor M1P11229HumansPredicted (SEA)704.302
Muscarinic acetylcholine receptor M3 structureClick to view 3D structureMuscarinic acetylcholine receptor M3P20309HumansPredicted (SEA)602.786
Muscarinic acetylcholine receptor M5 structureClick to view 3D structureMuscarinic acetylcholine receptor M5P08912HumansPredicted (SEA)718.003
Click to view 3D structureArabinose 5-phosphate isomerase KdsDQ5NGP7Francisella tularensis subsp. tularensis (strain SCHU S4 / Schu 4)Predicted (SEA)0.622794
Lysophosphatidic acid receptor 1 structureClick to view 3D structureLysophosphatidic acid receptor 1Q92633HumansPredicted (SEA)35.1878
Lysophosphatidic acid receptor 2 structureClick to view 3D structureLysophosphatidic acid receptor 2Q9HBW0HumansPredicted (SEA)22.9655
Click to view 3D structurePeptidyl-glycine alpha-amidating monooxygenaseP19021HumansPredicted (SEA)196.336
Click to view 3D structureMuscarinic acetylcholine receptor M1P08482Rattus norvegicusPredicted (SEA)506.876
Click to view 3D structureMuscarinic acetylcholine receptor M2P10980Rattus norvegicusPredicted (SEA)338.644
Click to view 3D structureMuscarinic acetylcholine receptor M4P08485Rattus norvegicusPredicted (SEA)113.816
Click to view 3D structureProtein kinase C alpha typeP04409Bos taurusPredicted (SEA)2.02408
Click to view 3D structureMuscarinic acetylcholine receptor M3P08483Rattus norvegicusPredicted (SEA)256.435
Click to view 3D structure6-phosphogluconate dehydrogenase, decarboxylatingP00349Ovis ariesPredicted (SEA)1.32344
Click to view 3D structureShort transient receptor potential channel 4Q9QUQ5Mus musculusPredicted (SEA)2291.1
Click to view 3D structure1-deoxy-D-xylulose-5-phosphate synthaseB7UJP3Escherichia coli O127:H6 (strain E2348/69 / EPEC)Predicted (SEA)5.60514
Protein kinase C alpha type structureClick to view 3D structureProtein kinase C alpha typeP17252HumansPredicted (SEA)3498.0
Click to view 3D structureMitochondrial carnitine/acylcarnitine carrier proteinO43772HumansPredicted (SEA)20.8636
Click to view 3D structure6-phosphogluconate dehydrogenase, decarboxylating, putativeP31072Trypanosoma bruceiPredicted (SEA)1.47914
Lysophosphatidic acid receptor 6 structureClick to view 3D structureLysophosphatidic acid receptor 6P43657HumansPredicted (SEA)20.9414
Click to view 3D structurePutative inactive group IIC secretory phospholipase A2Q5R387HumansPredicted (SEA)61.0338
5-hydroxytryptamine receptor 2C structureClick to view 3D structure5-hydroxytryptamine receptor 2CP28335HumansPredicted (SEA)6927.41
Concentrations
Not Available
External Links
DrugBank IDNot Available
HMDB IDHMDB0029592
FooDB IDFDB000751
Phenol Explorer IDNot Available
KNApSAcK IDC00054037
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkTriacetin
Chemspider ID13835706
ChEBI ID9661
PubChem Compound ID5541
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. https://www.ncbi.nlm.nih.gov/pubmed/?term=14555416
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=23293041
3. https://www.ncbi.nlm.nih.gov/pubmed/?term=23996800
4. https://www.ncbi.nlm.nih.gov/pubmed/?term=24574778
5. Goembira F, Saka S: Optimization of biodiesel production by supercritical methyl acetate. Bioresour Technol. 2013 Mar;131:47-52. doi: 10.1016/j.biortech.2012.12.130. Epub 2012 Dec 27.
6. Brault G, Shareck F, Hurtubise Y, Lepine F, Doucet N: Isolation and characterization of EstC, a new cold-active esterase from Streptomyces coelicolor A3(2). PLoS One. 2012;7(3):e32041. doi: 10.1371/journal.pone.0032041. Epub 2012 Mar 2.
7. KARNS ME, PARKER R: The treatment of refractory fungus infections with fungacetin (triacetin). J Am Podiatry Assoc. 1959 Sep;49:411-2.
8. Cheng M, Angkawidjaja C, Koga Y, Kanaya S: Requirement of lid2 for interfacial activation of a family I.3 lipase with unique two lid structures. FEBS J. 2012 Oct;279(19):3727-37. doi: 10.1111/j.1742-4658.2012.08734.x. Epub 2012 Aug 31.
9. Malik B, Benaissa M: Determination of glucose concentration from near-infrared spectra using locally weighted partial least square regression. Conf Proc IEEE Eng Med Biol Soc. 2012;2012:6169-71. doi: 10.1109/EMBC.2012.6347402.
10. Sarkar B, Ravi V, Alexandridis P: Micellization of amphiphilic block copolymers in binary and ternary solvent mixtures. J Colloid Interface Sci. 2013 Jan 15;390(1):137-46. doi: 10.1016/j.jcis.2012.09.028. Epub 2012 Sep 26.
11. Biedermann J, Owen AJ, Schloe KT, Gassner F, Sussmuth R: Interaction between poly-3-hydroxybutyrate-co-3-hydroxyvalerate and a denitrifying Pseudomonas strain. Can J Microbiol. 1997 Jun;43(6):561-8.
12. Radomska-Soukharev A, Wojciechowska J: Microemulsions as potential ocular drug delivery systems: phase diagrams and physical properties depending on ingredients. Acta Pol Pharm. 2005 Nov-Dec;62(6):465-71.
13. Laino T, Tuma C, Moor P, Martin E, Stolz S, Curioni A: Mechanisms of propylene glycol and triacetin pyrolysis. J Phys Chem A. 2012 May 10;116(18):4602-9. doi: 10.1021/jp300997d. Epub 2012 Apr 30.
14. Inal O, Kilicarslan M, Ari N, Baykara T: In vitro and in vivo transdermal studies of atenolol using iontophoresis. Acta Pol Pharm. 2008 Jan-Feb;65(1):29-36.
15. Liu H, Venkatraman SS: Cosolvent effects on the drug release and depot swelling in injectable in situ depot-forming systems. J Pharm Sci. 2012 May;101(5):1783-93. doi: 10.1002/jps.23065. Epub 2012 Feb 8.
16. Gao Y, Li L, Zhang J, Shu W, Gao L: Simultaneous determination of triacetin, acetic ether, butyl acetate and amorolfine hydrochloride in amorolfine liniment by HPLC. Pak J Pharm Sci. 2012 Apr;25(2):389-94.
17. Emara LH, Taha NF, Badr RM, Mursi NM: Development of an osmotic pump system for controlled delivery of diclofenac sodium. Drug Discov Ther. 2012 Oct;6(5):269-77.
18. Camargo JA, Sapin A, Nouvel C, Daloz D, Leonard M, Bonneaux F, Six JL, Maincent P: Injectable PLA-based in situ forming implants for controlled release of Ivermectin a BCS Class II drug: solvent selection based on physico-chemical characterization. Drug Dev Ind Pharm. 2013 Jan;39(1):146-55. doi: 10.3109/03639045.2012.660952. Epub 2012 Mar 8.
19. Ziolek M, Burdzinski G, Douhal A: Long-living structures of photochromic salicylaldehyde azine: polarity and viscosity effects from nanoseconds to hours. Photochem Photobiol Sci. 2012 Aug;11(8):1389-400. doi: 10.1039/c2pp25081k. Epub 2012 Jun 22.
20. CAHN MM, LEVY EJ: The use of triacetin (fungacetin) in the treatment of superficial dermatomycoses. Int Rec Med Gen Pract Clin. 1959 Jun;172(6):303-9.
21. Vijayakumar KR, Gowda LR: Rice (Oryza sativa) lipase: molecular cloning, functional expression and substrate specificity. Protein Expr Purif. 2013 Mar;88(1):67-79. doi: 10.1016/j.pep.2012.11.011. Epub 2012 Nov 29.
22. Ghosh S, Strum JC, Bell RM: Lipid biochemistry: functions of glycerolipids and sphingolipids in cellular signaling. FASEB J. 1997 Jan;11(1):45-50.
23. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9.
24. 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.
25. 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.
26. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621.
27. Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.
28. The lipid handbook with CD-ROM
29. Triglycerides and Cholesterol Research