Search results for "Saponification"

showing 10 items of 29 documents

Renewable polyol obtained by microwave-assisted alcoholysis of epoxidized soybean oil: Preparation, thermal properties and relaxation process

2019

[EN] The soybean oil polyol (SOP) use as feedstock in the polyurethane industry has been recently emphasized due to its excellent resistance to hydrolysis, which is also applicable in coatings and thermal insulation. In this article, the SOP was obtained by a very fast microwave-assisted alcoholysis of epoxidized soybean oil (ESO). The preparation method, thermal properties, and relaxation process were evaluated. High yields as opening and consumption epoxy group and selectivity of 99.8 mol%, 985 mol%, and 71.2 mol% were obtained. Through titrations, nuclear magnetic resonance and gel permeation chromatography were identified parameters as 0.32 mg KOH.g(-1) acid number, 190 mg KOH.g(-1) hyd…

Acid valuefood.ingredientMaterials scienceThermal properties02 engineering and technologyDielectric relaxation spectroscopy010402 general chemistry01 natural sciencesSoybean oilGel permeation chromatographychemistry.chemical_compoundfoodMaterials Chemistry13.- Tomar medidas urgentes para combatir el cambio climático y sus efectosPhysical and Theoretical ChemistrySoybean oil polyolSpectroscopyPolyurethane021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materials02.- Poner fin al hambre conseguir la seguridad alimentaria y una mejor nutrición y promover la agricultura sostenibleEpoxidized soybean oil08.- Fomentar el crecimiento económico sostenido inclusivo y sostenible el empleo pleno y productivo y el trabajo decente para todos12.- Garantizar las pautas de consumo y de producción sostenibles07.- Asegurar el acceso a energías asequibles fiables sostenibles y modernas para todosChemical engineeringchemistryHydroxyl valueMAQUINAS Y MOTORES TERMICOS0210 nano-technologyGlass transitionMicrowave-assisted alcoholysisSaponification
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Application of accelerated solvent extraction followed by gel performance chromatography and high-performance liquid chromatography for the determina…

2005

Accelerated solvent extraction (ASE) has been evaluated as a fast alternative to methanolic saponification for the extraction of 12 polycyclic aromatic hydrocarbons (PAHs) from mussel tissue. Several solvent systems and different operating conditions were investigated. The mixture dichloromethane-acetone (1:1, v/v) gave the best recoveries at 125 degrees C and 1500 psi, in a total time of 10 min. No yield difference was found between freeze-drying (Fd) or drying the wet mussel with diatomaceous earth (Ded) prior to extraction. The ASE method was validated using the standard reference material SRM 2977, a freeze-dried mussel tissue with naturally present organic contaminants. The performance…

Hot TemperatureTime FactorsHealth Toxicology and MutagenesisFood ContaminationToxicologyHigh-performance liquid chromatographymedia_common.cataloged_instanceAnimalsEuropean unionOrganic ChemicalsPolycyclic Aromatic HydrocarbonsChromatography High Pressure Liquidmedia_commonchemistry.chemical_classificationDetection limitChromatographyTissue ExtractsExtraction (chemistry)Public Health Environmental and Occupational HealthGeneral ChemistryMusselContaminationBivalviaHydrocarbonFreeze DryingchemistryChemistry (miscellaneous)Chromatography GelSolventsEnvironmental PollutantsSaponificationFood ScienceFood additives and contaminants
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Synthesis of optically pure alkynols

1993

Abstract (R,S)-1-alkylprop-2-yn-1-ols have been separated by a 2-step procedure, esterification with N-p-tosyl-(L)-phenylalanine (or valine), recrystallisation of the diastereomeric esters from ethanol/hexane and saponification of the optically pure esters.

Recrystallization (geology)EthanolOrganic ChemistryDiastereomerCatalysisInorganic ChemistryHexanechemistry.chemical_compoundchemistryValineOrganic chemistryPhysical and Theoretical ChemistryAliphatic compoundSaponificationTetrahedron: Asymmetry
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Patterning of a Surface Immobilized ATRP Initiator with an Inkjet Printer

2010

A new technique for patterning polymer brushes on the micrometer scale has been developed in which an inkjet printer was used to deposit droplets of acid on a surface-immobilized initiator for atom transfer radical polymerization (ATRP). The acid cleaved an ester bond in the ATRP initiator in a saponification reaction. As a result, the ATRP initiator was rendered inactive. To control the degree of defunctionalization, a new initiator containing a weak ester bond was derived from a tertiary alcohol. Comparison to an established ATRP initiator, derived from a primary alcohol, showed that the novel initiator was defunctionalized with a higher efficiency. Control of the reaction time allowed to…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationChemistryAtom-transfer radical-polymerizationOrganic ChemistryAlcoholPolymerPrimary alcoholGraftingInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryMoleculeSaponificationMacromolecules
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Convenient High Yielding Gram Scale Solution Synthesis of Methionine-Enkephalin.

1998

A simple, large-scale synthesis of a cytokine, methionine-enkephalin, Tyr-Gly-Gly-Phe-Met, has been elaborated. Classical solution peptide chemistry methods without protection of amino acid side-chain functions and 1+(2+2) segment condensation were used. A nine-step synthesis from commercial amino acid derivatives was developed with yields ranging from 86% to 99%, averaging 92%. The purity of all intermediates was found to be 99.0-100% by HPLC. The process has been used to prepare greater than 150 g quantities of the pentapeptide as a monohydrate of 100% purity. Hydantoin formation was observed during saponification of Boc-Tyr-Gly-Gly-Phe-Met-OMe and minimised.

chemistry.chemical_classificationanimal structuresintegumentary systemChemistryHydantoinPeptideGeneral ChemistryGeneral MedicinePentapeptide repeatHigh-performance liquid chromatographyChemical synthesisAmino acidchemistry.chemical_compoundDrug DiscoveryPeptide synthesisOrganic chemistrySaponificationChemical and Pharmaceutical Bulletin
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Isomerisierung von 2‐Alkoxycyclopropancarbonsäuren – Eine effektive Synthese von 4‐Oxocarbonsäuren

1983

(Z/E)-2-Alkoxycyclopropansaureester 2/3 werden aus Enolethern 1 und Diazoessigester hergestellt. Durch Verseifen entstehen die (Z/E)-2-Alkoxycyclopropancarbonsauren 4/5, welche in Wasser/Methanol Stereomutation zeigen. Diese Isomerisierung wird an (E)-2-Methoxy-2-phenyl-cyclopropancarbonsaure (5a) in deuterierten Losungsmitteln untersucht und mechanistisch interpretiert. Beim Erwarmen in Wasser/Methanol offnen sich die Verbindungen 4/5 quantitativ zu den entsprechenden 4-Oxocarbonsauren 6. Isomerisation of 2-Alkoxycyclopropanecarboxylic Acids – An Effective Synthesis of 4-Oxo Carboxylic Acids (Z/E)-2-2-Alkoxycyclopropanecarboxylic esters 2/3 were prepared from enol ethers 1 and ethyl diazoa…

Inorganic Chemistrychemistry.chemical_compoundEthyl diazoacetateChemistryOrganic chemistryMethanolMedicinal chemistryEnolIsomerizationSaponificationChemische Berichte
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Darstellung, eigenschaften und umsetzungen von polyvinylsulfofluoriden

1960

Vinylsulfofluorid wurde mit Azo-bis-isobutyronitril polymerisiert. Es wurden Polymerisationsgrade bis 390 erreicht. Die Molekulargewichte wurden durch Viskositatsmessungen an den durch Verseifung der Polyvinylsulfofluoride gewonnenen Natriumsalzen der Polyvinylsulfonsaure ermittelt. Die Polyvinylsulfofluoride wurden mit Ammoniak, aliphatischen und aromatischen Aminen umgesetzt. Dabei wurden Umsatze bis zu 80 Mol% erreicht. Vinylsulfofluoride was polymerized with azo-bis-isobutyronitrile. The degree of polymerisation was up to 390. The molecular-weights were determined by measuring the viscosity of the sodium-salts of polyvinylsulfonic acids obtained by saponification of polyvinylsulfofluori…

ViscosityAmmoniachemistry.chemical_compoundPolymerizationChemistryPolymer chemistrySaponificationDie Makromolekulare Chemie
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Levels, fingerprint and daily intake of polycyclic aromatic hydrocarbons (PAHs) in bread baked using wood as fuel

2009

Concentrations, fingerprint and daily intake of 16 PAHs in 15 bread samples baked using wood as fuel are examined in this work. Analysis was performed by GC/MS after saponification of the samples and clean up of the extract. The total concentration of the 16 analytes varies from 6 to 230 microg/kg on dry weight (d.w.). The better extraction procedure was estimated by analyzing test-samples and using different extraction methods. Additionally, for every analyzed sample, the extraction yield has been determined by the use of surrogate standards. Extraction yields were never less than 77% and in most cases almost 100%. The profiles of PAHs (percentage) are similar for all the analyzed samples …

Environmental EngineeringHealth Toxicology and MutagenesisFood ContaminationGas Chromatography-Mass SpectrometryEatingDry weightHumansEnvironmental ChemistryOrganic chemistryCookingFood sciencePolycyclic Aromatic HydrocarbonsWaste Management and Disposalchemistry.chemical_classificationPersistent organic pollutantChemistryExtraction (chemistry)BreadWoodPollutionClean-upHydrocarbonbread pahPolycyclic HydrocarbonsGas chromatography–mass spectrometrySaponification
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Characterization of the alcoholic fraction of vegetable oils by derivatization with diphenic anhydride followed by high-performance liquid chromatogr…

2008

Abstract Aliphatic and triterpene alcohols present in vegetable oils have been identified and determined by HPLC using UV–vis and MS detection after previous derivatization with diphenic anhydride. The alcoholic fraction was obtained by saponification, extraction and TLC (according to the European Union official procedure). Derivatization was performed in tetrahydrofuran in the presence of suspended grinded urea, which increases the reaction rate and yield. Derivatized extracts were chromatographed on a C8 column using gradient elution with acetonitrile/water mixtures containing 0.1% acetic acid, with UV–vis followed by negative-ion mode MS detection. Using linear discriminant analysis of t…

Resolution (mass spectrometry)Fraction (chemistry)Chemical FractionationSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryAcetic acidchemistry.chemical_compoundPlant Oilsmedia_common.cataloged_instanceEuropean unionDerivatizationChromatography High Pressure Liquidmedia_commonChromatographyEsterificationOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineModels ChemicalchemistryAlcoholsMultivariate AnalysisDibenzoxepinsSaponificationJournal of Chromatography A
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Über Hydroxy‐linolsäuremethylester und die Umsetzung von Linolsäuremethylester mit N‐Bromsuccinimid

1962

Hydroxy-linolsauremethylester wird durch selektive Reduktion von Linolsauremethylester-hydroperoxyd mit Na-Sulfit u. a. dargestellt. Die Autoxydation des Hydroxy-linolsauremethylesters verlauft nicht autokatalytisch und ist nach Aufnahme von 1 Mol Sauerstoff pro Mol Substanz nahezu beendet. Die Reaktionsprodukte sind relative niedermolekular. Die Reaktion von Linolsauremethylester mit N-Bromsuccinimid konnte durch Umsetzung des instabilen Reaktionsproduktes mit Silbernitrat weitgehend aufgeklart werden. About Hydroxy Methyl Linoleate and the Reaction of Methyl Linoleate with N-Bromosuccinimide Hydroxy methyl linoleate is prepared by selective reduction of methyl linoleate hydroperoxyde with…

AutocatalysisAutoxidationChemistryPolymer chemistrySelective reductionMethyl linoleateSaponificationFette, Seifen, Anstrichmittel
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