Search results for "Reagent"

showing 10 items of 699 documents

Improved resolution power of electrophoretic fractionation of DNA using a voltage gradient up and down application

2004

The improved resolution power of electrophoretic fractionation of DNA in a wide range of molecular masses is demonstrated using an "up and down" application of voltage gradient gel electrophoresis (VGGE). This application also allows separation of different DNA fragments which are poorly fractionated in conventional electrophoresis.

Free-flow electrophoresisGel electrophoresisElectrophoresisDNA fractionationChromatographyGel electrophoresis of nucleic acidsResolution (mass spectrometry)Voltage gradient gel electrophoresisChemistryClinical BiochemistryAnalytical chemistryFractionationDNABiochemistryELECTROPHORESIS INSTRUMENTATIONAnalytical Chemistrychemistry.chemical_compoundElectrophoresisIndicators and ReagentsDNA
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Analysis of Chemical and Biochemical Parameters of Petrol-Contaminated Soil after Biostimulation with an Enzyme Reagent

2020

This study aimed to assess the effect of petrol and the Fyre Zyme reagent on selected chemical and biochemical properties of loamy sand. The experiment was conducted under laboratory conditions. First, petrol was introduced into the soil at doses of 0 and 50 g k-1dry matter (DM). Next, 6% Fyre-Zyme enzyme reagent solution was added to the samples contaminated and uncontaminated with petrol, in the following combinations: 0 (control), once at 40 cm3 kg&ndash

Fyre-ZymeBioengineeringDehydrogenase010501 environmental scienceslcsh:Chemical technology01 natural scienceslcsh:ChemistryBiostimulationChemical Engineering (miscellaneous)lcsh:TP1-1185hydrocarbonsphosphatasesGasoline0105 earth and related environmental sciencesTotal organic carbonChemistryorganic carbonProcess Chemistry and Technologydehydrogenasessoil remediation04 agricultural and veterinary sciencesContaminationSoil contaminationnitrogen totallcsh:QD1-999ReagentEnvironmental chemistryLoam040103 agronomy & agriculture0401 agriculture forestry and fisheriesProcesses
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Multiple cross-linked hydroxypropylcellulose–succinate–salicylate: prodrug design, characterization, stimuli responsive swelling–deswelling and susta…

2015

A hydroxypropylcellulose–succinic anhydride (HPC–SAn) conjugate was synthesized homogeneously at 80 °C for 6 h under N2 in N,N-dimethylacetamide (DMA). The HPC–SAn conjugate was further covalently linked with salicylic acid (SA) drug using the versatile reagent ZrOCl2·8H2O at 80 °C for 6 h. Multiple crosslinking of the benign HPC–SAn–SA conjugate was achieved using oxalyl chloride. The resultant cross-linked prodrug (CL-HPC–SAn–SA conjugate) was characterized using different spectroscopic techniques. UV/Vis analysis of the HPC–SAn–SA conjugate has indicated that it contains 26 mg of SA per 100 mg. CL-HPC–SAn–SA showed reasonably good swelling properties in water and at different physiologic…

General Chemical EngineeringKineticsGeneral ChemistryProdrugchemistry.chemical_compoundchemistryOxalyl chlorideCovalent bondReagentmedicineOrganic chemistrySwellingmedicine.symptomSalicylic acidNuclear chemistryConjugateRSC Advances
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Investigations on isomerization and rearrangement of polycyclic arenes under oxidative conditions – Anodic versus reagent-mediated reactions

2019

Abstract Electro-organic conversions at an active molybdenum anode enable the formation of fused arenes. High chemoselectivity was achieved under anodic conditions, and a reagent-induced selectivity was observed by comparison with results of MoCl5-mediated reactions. Polycyclic arenes like phenanthrenes, triphenylenes, chrysenes, or helicenes were selectively obtained in yields up to 87% and in some cases unusual rearrangements were crucial for the product formation.

General Chemical Engineeringchemistry.chemical_elementOxidative couplingRearrangement02 engineering and technologyOxidative phosphorylation010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesElectrolysis0104 chemical sciencesAnodeAnodechemistryMolybdenumReagentElectrochemistryPhenanthrenesChemoselectivityPolycyclic arenes0210 nano-technologySelectivityIsomerizationElectrochimica Acta
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High-performance liquid chromatographic study of the regulation of phospholipid metabolism in cultured adrenocortical cells

1994

Abstract A rapid high-performance liquid chromatographic (HPLC) method for the separation of phospholipids was developed for minute samples of total lipids (ca. 200 μg). The method was applied to the study of the phospholipid metabolism in adrenocortical cell cultures. A complete separation of the different cellular phospholipid classes was achieved in 40 min. Good resolution of the phospholipid peaks was obtained, which allowed the collection of each individual class of phospholipids for further analysis of radioactivity and fatty acid composition by gas chromatography. When cells were incubated with [U-14C]glycerol or [U-14C]palmitate the bulk of the radioactivity was found in cellular ph…

GlycerolCardiolipinsPalmitatesPhospholipidHigh-performance liquid chromatographyMicechemistry.chemical_compoundTumor Cells CulturedGlycerolmedicineAnimalsCells CulturedChromatography High Pressure LiquidPhospholipidschemistry.chemical_classificationChromatographyAdrenal cortexPhosphatidylethanolaminesGeneral ChemistryMetabolismAdrenal Cortex NeoplasmsIn vitromedicine.anatomical_structurechemistryBiochemistryCell cultureAdrenal CortexPhosphatidylcholinesTetradecanoylphorbol AcetateIndicators and Reagentslipids (amino acids peptides and proteins)Polyunsaturated fatty acidJournal of Chromatography B: Biomedical Sciences and Applications
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New biodegradable hydrogels based on an acryloylated polyaspartamide cross-linked by gamma irradiation

1999

Alpha, beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA), a synthetic biocompatible macromolecule, was functionalized with glycidyl methacrylate (GMA) in order to introduce in its side chains residues having double bonds and ester groups. The copolymer (PHG), obtained from PHEA and GMA, had a degree of derivatization of 29 mol%. PHG aqueous solutions are cross-linked by gamma radiation at 0 degrees C either in the presence or absence of N,N'-methylenebisacrylamide (BIS) giving rise to new hydrogel systems. In both cases gelation occurs at quite low doses (0.26 and 0.4 kGy, respectively). The obtained networks were characterized by FT-IR spectrophotometry which confirmed that the cross-linki…

Glycidyl methacrylateMagnetic Resonance SpectroscopyMaterials scienceBiomedical EngineeringBiophysicsBiocompatible MaterialsBioengineeringIn Vitro TechniquesBiomaterialsHydrolysischemistry.chemical_compoundEnzymatic hydrolysisMaterials TestingSpectroscopy Fourier Transform InfraredPolymer chemistryCopolymerReduced viscosityAqueous solutionHydrolysisHydrogelsBiodegradation EnvironmentalCross-Linking ReagentschemistryGamma RaysSelf-healing hydrogelsPeptidesMacromoleculeJournal of Biomaterials Science, Polymer Edition
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Biodegradable hydrogels obtained by photocrosslinking of dextran and polyaspartamide derivatives

2003

The functionalization of dextran with glycidyl methacrylate (GMA) leads to the formation of a derivative that generates hydrogels for irradiation at 365nm. The effects of various polymer concentrations and irradiation times on the yield and the properties of the obtained hydrogels are reported. The networks have been characterized by FT-IR spectra, dimensional analysis and swelling measurements carried out at different pH values. In vitro studies suggest that all samples undergo a partial chemical hydrolysis, whereas the incubation with dextranases causes a total degradation whose rate depends on the degree of crosslinking. In addition, aqueous solutions of functionalized dextran have been …

Glycidyl methacrylateMaterials scienceMagnetic Resonance SpectroscopyTime FactorsPolymersUltraviolet RaysBiophysicsBiomedical EngineeringBiocompatible MaterialsBioengineeringBiomaterialschemistry.chemical_compoundContraceptive AgentsTheophyllinePolymer chemistrySpectroscopy Fourier Transform InfraredCopolymermedicineBisphenol A-Glycidyl MethacrylateDextranPolyhydroxyethyl MethacrylatePhotocrosslinkingchemistry.chemical_classificationAqueous solutionHydrolysistechnology industry and agricultureTemperatureDextransHydrogelsPolymerDrug releaseHydrogen-Ion Concentrationαβ-Poly(N-2-hydroxyethyl)-DL-aspartamideDextranCross-Linking ReagentschemistryMechanics of MaterialsSelf-healing hydrogelsDrug deliveryCeramics and CompositesSwellingmedicine.symptomPeptidesGlycidyl methacrylateBiotechnology
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Metal- and Reagent-Free Dehydrogenative Formal Benzyl-Aryl Cross-Coupling by Anodic Activation in 1,1,1,3,3,3-Hexafluoropropan-2-ol

2018

A selective dehydrogenative electrochemical functionalization of benzylic positions that employs 1,1,1,3,3,3-hexafluoropropan-2-ol (HFIP) has been developed. The electrogenerated products are versatile intermediates for subsequent functionalizations as they act as masked benzylic cations that can be easily activated. Herein, we report a sustainable, scalable, and reagent- and metal-free dehydrogenative formal benzyl-aryl cross-coupling. Liberation of the benzylic cation was accomplished through the use of acid. Valuable diarylmethanes are accessible in the presence of aromatic nucleophiles. The direct application of electricity enables a safe and environmentally benign chemical transformati…

Green chemistryChemical transformation010405 organic chemistryChemistryArylGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesMetalchemistry.chemical_compoundNucleophileReagentvisual_artvisual_art.visual_art_mediumSurface modificationAngewandte Chemie International Edition
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Inside Back Cover: Metal- and Reagent-Free Dehydrogenative Formal Benzyl-Aryl Cross-Coupling by Anodic Activation in 1,1,1,3,3,3-Hexafluoropropan-2-o…

2018

Green chemistryChemistryArylGeneral ChemistryElectrochemistryMedicinal chemistryCatalysisAnodeCoupling (electronics)Metalchemistry.chemical_compoundvisual_artReagentvisual_art.visual_art_mediumAngewandte Chemie International Edition
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Imidazolium and Potassium Hydrogen Carbonate Salts as Ecofriendly Organocatalysts for Oxazolidinone Synthesis

2016

International audience; Although oxazolidinones are valuable intermediate compounds for industrial applications, no synthetic method is suitable for their production on a large scale owing to the use of reagents/catalysts that are hazardous or toxic to human health or ecotoxic for the environment. In this manuscript, we describe new and efficient catalysts, that is, the nontoxic hydrogen carbonate anion in combination with a potassium or diisobutylimidazolium ([iBu(2)IM]) countercation, for the conversion of -amino alcohols into cyclic oxazolidinones in high yields of 69 to 90%. Depending on the catalytic conditions, both catalysts could be easily recovered from the crude reaction products …

Green chemistryHydrogenPotassiumchemistry.chemical_elementHomogeneous catalysisantibacterial agentsHeterocyclesamino-alcohols010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencescatalystsCatalysisefficientchemistry.chemical_compounddioxide[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistry[CHIM]Chemical SciencesSustainable chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganocatalysisOrganic Chemistry[CHIM.CATA]Chemical Sciences/CatalysisHomogeneous catalysis0104 chemical scienceschemistryCyclizationOrganocatalysisReagentderivativesCarbonateacid
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