Search results for "Amine oxide"

showing 7 items of 7 documents

CCDC 907670: Experimental Crystal Structure Determination

2013

Related Article: Jochen Körber, Stefan Löffler, Dieter Schollmeyer, Udo Nubbemeyer|2013|Synthesis|45|2875|doi:10.1055/s-0033-1338519

(2-((8-Chlorodibenzo[bf]thiepin-10-yl)oxy)ethyl)dimethylamine oxide dihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Enthalpies of transfer of pentanol from water to sodium dodecylsulfate-dodecyl-dimethylamine oxide-water mixtures

1994

At a given surfactant-surfactant ratio, the enthalpies of transfer ΔH (W→W+S) of pentanol 0.03m from water to sodium dodecylsulfate (NaDS)-dodecyldimethylamine oxide-water mixtures as functions of the surfactants mixture concentration (m t) were determined. ForX NaDS=0.9, ΔH (W→W+S) increases monotonically withm t such as observed for pure surfactants. ForX NaDS=0.12 and 0.3, ΔH (W→W+S) increases withm t up to 0.12m beyond which it decreases withm t. AtX NaDS=0.6, two monotonic curves can be distinguished in the ΔH (W→W+S)vs. m t trend. Experimental data were fitted through an equation previously reported for additives in pure surfactants derived by assuming the pseudo-phase transition mode…

Aqueous solutionChemistryEnthalpyDistribution constantInorganic chemistryAnalytical chemistryMicelleAmine oxideGibbs free energychemistry.chemical_compoundsymbols.namesakePhase (matter)symbolsDimethylamineJournal of thermal analysis
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Micellization properties of cardanol as a renewable co-surfactant

2015

With the aim to improve the features of surfactant solutions in terms of sustainability and renewability we propose the use of hydrogenated natural and sustainable plant-derived cardanol as an additive to com- mercial surfactants. In the present study we demonstrated that its addition, in amounts as high as 10%, to commercial surfactants of different charge does not significantly affect surfactant properties. Conversely, the presence of hydrogenated cardanol can strongly affect spectrophotometric determination of CMC if preferential interactions with the dyes used take place. This latter evidence may be profitably exploited in surfactant manufacturing by considering that the concurrent pres…

Dynamic Laser Light Scattering.Sustainable surfactantIONIC SURFACTANTSTETRADECYLDIMETHYLAMINE OXIDEBiochemistryCardanolSurface-Active AgentsPhenolsPulmonary surfactantMoleculeOrganic chemistryFLUORESCENCEPhysical and Theoretical ChemistryMicellesCardanolCetrimoniumChemistrybusiness.industry-PotentialOrganic ChemistryWaterHYDROGENATED CARDANOLOrange OTTensiometryRenewable energyAGGREGATION NUMBERPREMICELLAR AGGREGATIONCetrimonium CompoundsSpectrophotometric determination of CMCGEMINI SURFACTANTSbusinessBEHAVIOROrganic & Biomolecular Chemistry
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CCDC 907671: Experimental Crystal Structure Determination

2013

Related Article: Jochen Körber, Stefan Löffler, Dieter Schollmeyer, Udo Nubbemeyer|2013|Synthesis|45|2875|doi:10.1055/s-0033-1338519

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(2-((8-Chloro-5-oxidodibenzo[bf]thiepin-10-yl)oxy)ethyl)dimethylamine oxide dihydrateExperimental 3D Coordinates
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CCDC 1411951: Experimental Crystal Structure Determination

2015

Related Article: R. Doroschuk|2015|Acta Crystallogr.,Sect.E:Cryst.Commun.|71|o578|doi:10.1107/S2056989015013262

Space GroupCrystallographyN-(13-Benzothiazol-2-ylmethylene)-N-methylamine oxideCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Mononuclear rearrangement of heterocycles in zwitterionic micelles of amine oxide surfactants.

2012

Abstract Rate constants for the mononuclear rearrangement (MRH) of Z -phenylhydrazones of some 5-substituted-3-benzoyl-1,2,4-oxadiazoles in water have been measured in the presence of zwitterionic micelles. The use of micellized N -tetradecyl- N , N -dimethylamineoxide (C 14 DMAO) as the reaction medium allowed to solubilize the otherwise water-insoluble oxadiazoles. Micellar rate effects were analyzed by using a simple pseudo-phase model and compared with those obtained in non-ionic micelles (Triton X-100). Evidence that both the rate of the rearrangement reaction and the binding of the substrates to the micelles are mainly governed by substrate hydrophobicity is obtained. The disagreement…

Steric effectsSpectrometry Mass Electrospray IonizationN-tetradecyl-NOctoxynolPhotochemistryMicelleMononuclear rearrangements of heterocycles (MHRs)Biomaterialschemistry.chemical_compoundSurface-Active AgentsColloid and Surface ChemistryReaction rate constantMicellar catalysiN-tetradecyl-NN-dimethylamineoxidePolymer chemistryRearrangement reactionzwitterionic micelleMicellesOxadiazolesHydrazonesSubstrate (chemistry)WaterSettore CHIM/06 - Chimica OrganicaSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmine oxideKineticschemistrySolubilitySolubilizationN-dimethylamineoxideThermodynamicsHydrophobic and Hydrophilic InteractionsMyristic AcidsDimethylaminesJournal of colloid and interface science
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Reaction of 4-acylaminomethylpyridine N-oxides with phenylbutazone in the presence of acetic anhydride

1987

medicine.drug_classInfraredOrganic ChemistryCarboxamideBiological activityNuclear magnetic resonance spectroscopyAmine oxidechemistry.chemical_compoundAcetic anhydridechemistrymedicinePhenylbutazoneOrganic chemistrymedicine.drugJournal of Heterocyclic Chemistry
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