Search results for "Acetonitriles"

showing 9 items of 59 documents

Multi-scale optimisation vs. genetic algorithms in the gradient separation of diuretics by reversed-phase liquid chromatography

2019

Abstract Multi-linear gradients are a convenient solution to get separation of complex samples by modulating carefully the gradient slope, in order to accomplish the local selectivity needs for each particular solute cluster. These gradients can be designed by trial-and-error according to the chromatographer experience, but this strategy becomes quickly inappropriate for complex separations. More evolved solutions imply the sequential construction of multi-segmented gradients. However, this strategy discards part of the search space in each step of the construction and, again, cannot deal properly with very complex samples. When the complexity is too large, the only valid alternative for fi…

Work (thermodynamics)AcetonitrilesScale (descriptive set theory)010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistrySet (abstract data type)DiureticsSubdivisionChromatography Reverse-PhaseChromatographyChemistryElutionbusiness.industry010401 analytical chemistryOrganic ChemistryWaterGeneral MedicineFunction (mathematics)0104 chemical sciencesDistribution (mathematics)SolventsbusinessAlgorithmAlgorithmsLevel of detailJournal of Chromatography A
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Peak capacity estimation in isocratic elution.

2008

Peak capacity (i.e. maximal number of resolved peaks that fit in a chromatographic window) is a theoretical concept with growing interest, but based on a situation rarely met in practice. Real chromatograms tend to have uneven distributions, with overlapped peaks and large gaps. The number of resolved compounds should, therefore, be known from estimations. Several equations have been reported for this purpose based on three perspectives, namely, the intuitive approach (peak capacity as the size of the retention time window measured in peak width units), which assumes peaks with the same width, and the outlines of Giddings and Grushka, which consider changes in peak width with retention time…

Work (thermodynamics)Isocratic elutionChromatographyAcetonitrilesChemistryOrganic ChemistryMean valueAdrenergic beta-AntagonistsChromatography liquidSodium Dodecyl SulfateGeneral MedicineModels TheoreticalBiochemistryAnalytical ChemistrySkewnessPhase compositionDiureticsRetention timeMicellesChromatography LiquidJournal of chromatography. A
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Effect of buffer nature and concentration on the chromatographic performance of basic compounds in the absence and presence of 1-hexyl-3-methylimidaz…

2019

Abstract In reversed-phase liquid chromatography, the performance for basic compounds is affected by the interaction of the protonated (cationic) species with the anionic free silanols on the alkyl-bonded stationary phases. Using aqueous-organic mobile phases in the absence of additives, the retention may be too high, and the peaks be broad and asymmetric. The performance is improved by addition to the mobile phase of ionic liquids, from which 1-hexyl-3-methylimidazolium chloride ([C6MIm][Cl]) has especially good characteristics. A recent report has also revealed that the use of the phosphate system as buffer, at varying concentration and pH, may have a significant role in the chromatograph…

buffer systemsAcetonitrilesAdrenergic beta-AntagonistsIonic LiquidsProtonationBuffers010402 general chemistry01 natural sciencesBiochemistryChlorideAnalytical Chemistryionic liquidschemistry.chemical_compoundreversed-phase liquid chromatographyBoratesmedicineFormateβ-Adrenoceptor antagonistsChromatography High Pressure LiquidChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryCationic polymerizationImidazolesWatersilanol effectGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationPhosphate0104 chemical sciencesSilanolchemistryIonic liquidSolventsmedicine.drug
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Silanol suppressing potency of alkyl-imidazolium ionic liquids on C18 stationary phases

2011

Residual silanols on C18 columns yield undesirable slow-kinetics ion-exchange interactions with positively charged basic compounds that result in asymmetrical peaks, low efficiencies and long retention times. The purity of the silica employed as supporting material, and the technique used to form the bonded phase, which varies with the brand and manufacturer, give rise to different amounts of residual silanols in the packings, and consequently, different chromatographic performance. One of the most efficient and widespread strategies to reduce or even eliminate the different performance among columns is the addition of a reagent to the mobile phase to block the silanol sites. However, the i…

chemistry.chemical_classificationAcetonitrilesChromatographyTetrafluoroborateAdrenergic beta-AntagonistsOrganic ChemistryImidazolesIonic LiquidsGeneral MedicineSilanesBiochemistryAnalytical Chemistrychemistry.chemical_compoundSilanolAdsorptionchemistryYield (chemistry)ReagentPhase (matter)Ionic liquidAlkylChromatography LiquidJournal of Chromatography A
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Pyrrolo[3,4-e][1,2,3]triazolo[1,5-a]pyrimidine and pyrrolo[3,4-d] [1,2,3]triazolo[1,5-a]pyrimidine. New tricyclic ring systems of biological interest

2000

Derivatives of the new ring system pyrrolo[3,4-e][1,2,3] triazolo[1,5-a]pyrimidine 6 were prepared in high yields in one step by reaction of 3-azidopyrrole 3 and substituted acetonitriles. Compound 6b rearranged, upon heating in dimethyl sulfoxide in the presence of water, to pyrrolo[3,4-d][1,2,3]triazolo-[1,5-a]pyrimidine 7.

chemistry.chemical_classificationchemistry.chemical_compoundAcetonitrileschemistryPyrimidineDimethyl sulfoxideStereochemistryOrganic ChemistryRing (chemistry)TricyclicD-1Journal of Heterocyclic Chemistry
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ChemInform Abstract: Pyrrolo[3,4-e][1,2,3]triazolo[1,5-a]pyrimidine and Pyrrolo[3,4-d][1,2,3]triazolo[1,5-a]pyrimidine. New Tricyclic Ring Systems of…

2001

Derivatives of the new ring system pyrrolo[3,4-e][1,2,3] triazolo[1,5-a]pyrimidine 6 were prepared in high yields in one step by reaction of 3-azidopyrrole 3 and substituted acetonitriles. Compound 6b rearranged, upon heating in dimethyl sulfoxide in the presence of water, to pyrrolo[3,4-d][1,2,3]triazolo-[1,5-a]pyrimidine 7.

chemistry.chemical_classificationchemistry.chemical_compoundAcetonitrileschemistryPyrimidineStereochemistryDimethyl sulfoxideTriazole derivativesGeneral MedicineRing (chemistry)D-1TricyclicChemInform
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An Unexpected Three-Component Condensation Leading to Amino- (3-oxo-2,3-dihydro-1H-isoindol-1-ylidene)- acetonitriles

2004

The reaction of 2-carboxybenzaldehyde with primary amines in the presence of cyanide leads to the formation of 2-substituted amino(3-oxo-2,3-dihydro-1H-isoindol-1-ylidene)acetonitriles. These compounds originate from the condensation of 2-carboxybenzaldehyde with the amine and two molecules of hydrogen cyanide and represent a novel class of isoindolinones.

chemistry.chemical_compoundAcetonitrilesBicyclic moleculeChemistryCyanideOrganic ChemistryHydrogen cyanideMoleculeAmine gas treatingOrganic synthesisCondensation reactionMedicinal chemistryThe Journal of Organic Chemistry
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An Unexpected Three-Component Condensation Leading to Amino(3-oxo-2,3-dihydro-1H-isoindol-1-ylidene)acetonitriles.

2005

The reaction of 2-carboxybenzaldehyde with primary amines in the presence of cyanide leads to the formation of 2-substituted amino(3-oxo-2,3-dihydro-1H-isoindol-1-ylidene)acetonitriles. These compounds originate from the condensation of 2-carboxybenzaldehyde with the amine and two molecules of hydrogen cyanide and represent a novel class of isoindolinones.

chemistry.chemical_compoundPrimary (chemistry)AcetonitrileschemistryStereochemistryCyanideCondensationHydrogen cyanideMoleculeAmine gas treatingGeneral MedicineMedicinal chemistryChemInform
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Mucosa-dependent muscarinic liberation of prostaglandins from rat isolated trachea.

1995

1. The present study examined whether cholinoceptor stimulation modulates the release of arachidonic acid-derived mediators from rat isolate tracheae. 2. Tracheae were preincubated with [3H]-arachidonic acid and the outflow of 3H-compounds was determined. Acetylcholine and the muscarinic agonist, carbachol but not nicotine, increased the rate of tritium outflow maximally by about 30%. The M3 receptor-preferring antagonist rho-fluoro-hexahydrosiladiphenidol was more effective than pirenzepine and methoctramine in antagonizing the effect of acetylcholine. 3. High performance liquid chromatography analysis (methanol gradient) of the released 3H-compounds showed that one peak, co-eluting with […

medicine.medical_specialtyCarbacholAcetonitrilesMuscarinic AntagonistsIn Vitro TechniquesMuscarinic AgonistsMuscarinic agonistRats Sprague-Dawleychemistry.chemical_compoundPiperidinesInternal medicineMuscarinic acetylcholine receptormedicineMethoctramineAnimalsDrug InteractionsAcetylcholine receptorPharmacologyArachidonic AcidDose-Response Relationship DrugMuscarinic acetylcholine receptor M1PirenzepineAcetylcholineRatsTracheaEndocrinologychemistryProstaglandinslipids (amino acids peptides and proteins)FemaleAcetylcholinemedicine.drugResearch Article
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