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Methanol
Kinds of Methanol Terms modified by Methanol Selected AbstractsChiral stationary phases for separation of intermedine and lycopsamine enantiomers from Symphytum uplandicumJOURNAL OF SEPARATION SCIENCE, JSS, Issue 2 2010Rahul S. Pawar Abstract Enantioseparation of the pyrrolizidine alkaloid isomers intermedine and lycopsamine, isolated from Symphytum uplandicum, is discussed. The separatory power of two immobilized carbohydrate-based chiral HPLC columns, Chiralpak IA and IC, in different chromatographic conditions is compared. The study demonstrated the importance of solvent and column selection while developing such chiral HPLC separation methods. The baseline HPLC separation of the two alkaloid isomers in preparatory scale is reported for the first time. The optimized separations were achieved on a Chiralpak IA column with mobile phases of ACN/methanol (80:20) and methanol/methyl- t -butyl ether (90:10), both containing 0.1% diethylamine. [source] Preparation of novel ZSM-5 zeolite-filled chitosan membranes for pervaporation separation of dimethyl carbonate/methanol mixturesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007Bingbing Liu Abstract Novel mixed matrix membranes were prepared by incorporating ZSM-5 zeolite into chitosan polymer for the pervaporative separation of dimethyl carbonate (DMC) from methanol. These membranes were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD) to assess their morphology, intermolecular interactions, and crystallinity. Sorption studies indicated that the degree of swelling for zeolite-filled membranes increased with zeolite content in the membrane increasing and the separation selectivity of DMC/methanol was dominated by solubility selectivity rather than diffusivity selectivity. The characteristics of these membranes for separating DMC/methanol mixtures were investigated by varying zeolite content, feed composition, and operating temperature. The pervaporation separation index (PSI) showed that 5 wt % of ZSM-5 zeolite-filled membrane gave the optimum performance in the PV process. From the temperature-dependent permeation values, the Arrhenius activation parameters were estimated. The resulting lower activation energy values obtained for zeolite-filled membranes contribute to the framework of the zeolite. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] First synthesis and x-ray crystal structure of hexahydrobenzo[b]pyrido[3,4,5- de]-1,6-naphthyridinesJOURNAL OF HETEROCYCLIC CHEMISTRY, Issue 6 2005Leonid G. Voskressensky The reaction of 10-carboxamido tetrahydrobenzo[b][1,6]naphthyridines 1-3 with activated terminal alkynes in DMF/methanol resulted with the formation of hexahydrobenzo[b]pyrido[3,4,5- de]-1,6-naph-thyridines 7-10 - representatives of a new heterocyclic system. [source] CHRACTERIZATION AND 1,1-DIPHENYL-2-PICRYLHYDRAZYL RADICAL SCAVENGING ACTIVITY OF METHANOL AND SUPERCRITICAL CARBON DIOXIDE EXTRACTS FROM LEAVES OF ADINANDRA NITIDAJOURNAL OF FOOD BIOCHEMISTRY, Issue 4 2008BENGUO LIU ABSTRACT Leaves of Adinandra nitida are consumed in southern China as health tea (Shiyacha) and as herbal medicine. In this study, the methanol and supercritical fluid extracts from leaves of A. nitida were obtained by traditional solvent extraction and supercritical carbon dioxide extraction, respectively. Both the extracts showed high 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity. By using ultraviolet-visible spectrometry (UV), infrared spectrometry (IR), nuclear magnetic resonance, electrospray ionization mass spectrometry (ESI-MS), high-performance liquid chromatography-ESI/MS, the main bioactive constituents in the methanol extract (ME) were identified as camellianin A, camellianin B, apigenin. By analysis of gas chromatography-mass spectrometry, a total of 16 compounds accounting for 98.79% of the supercritical fluid extract (SFE) were identified as ,-sitosterol, vitamin E, ,-tocopherol and so on. These compounds found in ME and SFE could contribute to the DPPH radical scavenging performance of the extracts in this study. PRACTICAL APPLICATION Adinandra nitida is a kind of particular wild plant in South China. Few reports have been published about it in the world. In this study, the methanol and supercritical fluid extracts from leaves of A. nitida were respectively obtained by two kinds of industrially significant methods, traditional solvent extraction and supercritical carbon dioxide extraction. By using ultraviolet-visible spectrometry (UV), infrared spectrometry (IR), nuclear magnetic resonance, electrospray ionization mass spectrometry (ESI-MS), high-performance liquid chromatography-ESI/MS, gas chromatography-MS, the main bioactive constituents in the two extracts were identified as flavonoids and plant sterols. Both the extracts showed high 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity and this activity of the flavonoid-rich methanol extract was 10 times more than that of butylated hydroxytoluene. These results showed that leaves of A. nitida is a new kind of natural antioxidant-rich, flavonoid-rich plant source with great commercial interest in the food and phytopharmaceutical market. [source] ChemInform Abstract: Magnesium/Methanol: An Effective Reducing Agent for Chemoselective Reduction of Pyrimidine-2(1H)-ones.CHEMINFORM, Issue 34 2009Kamaljit Singh Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] The Determination of Methanol Using an Electrolytically Fabricated Nickel Microparticle Modified Boron Doped Diamond ElectrodeELECTROANALYSIS, Issue 5 2010Kathryn Abstract A nickel modified boron doped diamond (Ni-BDD) electrode and nickel foil electrode were used in the determination of methanol in alkaline solutions. The Ni-BDD electrode was electrodeposited from a 1,mM Ni(NO3)2 solution (pH,5), followed by repeat cycling in KOH. Subsequent analysis utilised the Ni(OH)2/NiOOH redox couple to electrocatalyse the oxidation of methanol. Methanol was determined to limits of 0.3,mM with a sensitivity of 110,nA/mM at the Ni-BDD electrode. The foil electrode was less sensitive achieving a limit of 1.6,mM and sensitivity of 27,nA/mM. SEM analysis of the electrodes found the Ni-BDD to be modified by a quasi-random microparticle array. [source] Electroreduction of Oxygen and Electrooxidation of Methanol at Carbon and Single Wall Carbon Nanotube Supported Platinum ElectrodesELECTROANALYSIS, Issue 10 2008Ahmad, Nozad Golikand Abstract The present research aimed at investigating the electrocatalytic properties and the electrochemical deposition of Pt nanoparticles on carbon powder, carbon nanotube and preparation of carbon and single wall carbon nanotube supported platinum electrodes. The Pt nanoparticles were synthesized by electroreduction of hexachloroplatinic acid in aqueous solution at ,200,mV. Electrocatalytic properties of the modified electrodes for oxygen reduction were investigated by cyclic voltammetry in O2 saturated solution containing 0.1,M HClO4. Methanol electrooxidation at the modified surfaces in 0.5,M HCLO4 was studied by cyclic voltammetry. The corresponding results showed that the Pt/SWCNT/GC electrode exhibits more improved catalytical activity than the Pt/C/GC electrode. [source] Dehydrogenation of Hydridoirida-,-diketones in Methanol: The Selective Formation of Mono- and Dinuclear Acyl ComplexesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 20 2010Roberto Ciganda Abstract The hydridoirida-,-diketone [IrH{(PPh2(o -C6H4CO))2H}Cl] (1) reacts with diimines (NN) or with pyridine (py) in refluxing methanol to undergo dehydrogenation. The reactions afford selectively the cis -acyl, trans -phosphane isomers of the cationic [Ir(PPh2(o -C6H4CO))2(NN)]+ {NN = 2,2,-bipyridine (2); R,N=C(CH3),C(CH3)=N,R, [R = R, = NH2 (3); R = R, = OH (4); R = OH, R, = NH2 (5)]} or neutral [IrCl(PPh2(o -C6H4CO))2(py)] (6) derivatives. The reactions are faster for ligands containing amino substituents. Refluxing 1 in MeOH affords the formation of an equimolar mixture of dimercationic species [Ir2(,-Cl)(,-PPh2(o -C6H4CO))2(PPh2(o -C6H4CO))2]+ (7a and 7b) containing two acyls and a chloride as bridging groups. The isomers could be separated by fractional precipitation. Compound [3]Cl, containing amino substituents in the imino functionalities, catalyses the hydrogen transfer from 2-propanol to cyclohexanone to afford cyclohexanol. All the complexes were fully characterised spectroscopically. Single crystal X-ray diffraction analysis was performed on complexes 6 and [7b]ClO4. [source] Optical Measurements of Platinum Based Electrocatalysts for the Electrooxidation of Methanol,FUEL CELLS, Issue 1-2 2003K. Gruber Abstract In a combinatorial electrochemistry experiment quinine was used as a pH sensitive fluorescing indicator to detect the catalytic activity of methanol oxidation catalysts. During electrochemical experiments the surface of the electrode array was monitored with a CCD camera. The dependence of the intensity of the fluorescence on the applied potential was used as an analytical tool; to investigate the electrochemical performance of Pt based electrocatalysts, for the electrooxidation of methanol, in both short and long term tests. [source] Electro-Oxidation of Methanol and Ethanol on Poly(3,4-Ethylenedioxythiophene) with Dispersed Pt, Pt + Sn, and Pt + Pb Particles,FUEL CELLS, Issue 1-2 2003S. Biallozor Abstract The influence of tin and lead additives on the catalytic activity of platinum particles dispersed on a poly(3,4-dioxyethylenethiophene) (PEDT) layer deposited on gold or steel towards anodic oxidation of methanol and ethanol was studied. It was found that these additives increase the rate of anodic oxidation of both alcohols. It was also found that the electro-catalytic properties of PEDT depend on the kind of support used for its deposition. The authors have shown that these additives (Pb and Sn) increase the rate of anodic oxidation of both alcohols on platinum deposited on PEDT, but tin was evidently more effective than lead. In the presence of Sn, the steady-state current density of methanol oxidation increases about 100 times, while Pb only promotes the platinum catalyst activity by about 2 times. In the authors opinion the most probable mechanism for the tin promotion effect seems to be a homogenous catalytic reaction with the participation of the Sn (IV) and Sn (II) ions as mediators. [source] CFD modelling and experimental investigation of an ejector refrigeration system using methanol as the working fluidINTERNATIONAL JOURNAL OF ENERGY RESEARCH, Issue 2 2001S. B. Riffat Abstract This paper presents results of computational fluid dynamic (CFD) analysis and experimental investigation of an ejector refrigeration system using methanol as the working fluid. The CFD modelling was used to investigate the effect of the relative position of the primary nozzle exit within the mixing chamber on the performance of the ejector. The results of the CFD were used to obtain the optimum geometry of the ejector, which was then used to design, construct and test a small-scale experimental ejector refrigeration system. Methanol was used as the working fluid, as it has the advantage of being an ,environmentally friendly' refrigerant that does not contribute to global warming and ozone layer depletion. In addition, use of methanol allows the ejector refrigeration system to produce cooling at temperatures below the freezing point of the water, which of course would not be possible with a water ejector refrigeration system. CFD results showed that positioning the nozzle exit at least 0.21 length of the mixing chamber throat's diameter upstream of the entrance of the mixing chamber gave better performance than pushing it into the mixing chamber. Experimental values of coefficient of performance (COP) between 0.2 and 0.4 were obtained at operating conditions achievable using low-grade heat such as solar energy and waste heat. Copyright © 2001 John Wiley & Sons, Ltd. [source] Evaluation of pre-heating and extraction solvents in antioxidant and antimicrobial activities of garlic, and their application in fresh pork pattiesINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 2 2010Sung Y. Park Summary The objectives of this study were to screen the optimum conditions for antioxidant and antimicrobial activities of garlic as affected by pre-heating and different extraction solvents, and to evaluate the antioxidant and antimicrobial effects of these extracts in ground meat during refrigerated storage. Methanol extracted garlic had a greater total phenolic content, 1,1-diphenyl-2-picrylhydrazyl (DPPH)-radical scavenging activity and reducing power than water extracted one (P < 0.05), whereas the latter had a greater yield and iron chelating ability than the former (P < 0.05). Moreover, water extract from fresh garlic (WEFG) and methanol extract from heated garlic (MEHG) produced an inhibition zone against Escherichia coli O157:H7 and Listeria monocytogenes. The addition of garlic extracts (WEFG, MEHG and their combinations WEFMEHG)) to pork patties decreased the pH, hunter a values (redness), thiobarbituric acid substances values and the number of total plate count and Enterobacteriaceae (P < 0.05), while the hunter b values (yellowness) increased (P < 0.05). Results of this study indicated that the use of the garlic extracts was able to control lipid oxidation and microbial growth in pork patties. [source] A High-Yield, Liquid-Phase Approach for the Partial Oxidation of Methane to Methanol using SO3 as the OxidantADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 9 2005Sudip Mukhopadhyay Abstract A direct approach for producing methanol from methane in a three-step, liquid phase process is reported. In the first step, methane is reacted with SO3 to form methanesulfonic acid (MSA) at 75,°C using a free-radical initiator and MSA as the solvent. Urea-H2O2 in combination with RhCl3 is found to be the most effective initiator (57% conversion of SO3; 7.2% conversion of CH4). MSA is then oxidized by SO3 at 160,°C in a second step to produce a mixture containing methyl bisulfate and some methyl methanesulfonate (87% conversion of MSA). In the third step, the mixture of methyl bisulfate and methyl methanesulfonate is hydrolyzed in the presence of an organic solvent, to produce an organic phase containing methanol and an aqueous phase containing sulfuric acid and some MSA (63% conversion of methyl bisulfate; 72% conversion of methyl methanesulfonate). Overall, 58% of the MSA (of which 23% is derived from methane) is converted to methanol. [source] Solubility and phase separation of poly(L,D -lactide) copolymersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008Marja Rissanen Abstract In this study, the solubility and precipitation properties of medical-grade stereocopolymers were investigated. The solubility of the polymers was tested with eight different organic solvents and four nonsolvents. The solubility of poly(L,D -lactide) stereocopolymers was highly dependent on the L/D ratio of the copolymer. The phase-separation ability was tested by cloud-point titration with a solvent and a nonsolvent. The solvent was in all cases dichloromethane, and the nonsolvents were n -hexane, methanol, ethanol, and isopropyl alcohol. The results showed that n -hexane was the most efficient nonsolvent. Methanol and ethanol showed quite similar precipitation properties. Isopropyl alcohol was the least efficient nonsolvent of those studied. Also, the L/D ratio of the copolymer had an effect on the precipitation properties. The precipitation happened most easily when the L content was high. The molecular weight of the copolymer had only a slight effect on the phase separation. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Pervaporation separation of sodium alginate/chitosan polyelectrolyte complex composite membranes for the separation of water/alcohol mixtures: Characterization of the permeation behavior with molecular modeling techniquesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007Sang-Gyun Kim Abstract Polyelectrolyte complex (PEC) membranes were prepared by the complexation of protonated chitosan with sodium alginate doped on a porous, polysulfone-supporting membrane. The pervaporation characteristics of the membranes were investigated with various alcohol/water mixtures. The physicochemical properties of the permeant molecules and polyion complex membranes were determined with molecular modeling methods, and the data from these methods were used to explain the permeation of water and alcohol molecules through the PEC membranes. The experimental results showed that the prepared PEC membranes had an excellent pervaporation performance in most aqueous alcohol solutions and that the selectivity and permeability of the membranes depended on the molecular size, polarity, and hydrophilicity of the permeant alcohols. However, the aqueous methanol solutions showed a permeation behavior different from that of the other alcohol solutions. Methanol permeated the prepared PEC membranes more easily than water even though water molecules have stronger polarity and are smaller than methanol molecules. The experimental results are discussed from the point of view of the physical properties of the permeant molecules and the membranes in the permeation state. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2634,2641, 2007 [source] Thermal analysis of polymer,water interactions and their relation to gas hydrate inhibitionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007Manika Varma-Nair Abstract Gas hydrates formed in oil production pipelines are crystalline solids where hydrocarbon gas molecules such as methane, propane, and their mixtures are trapped in a cagelike structure by hydrogen-bonded water molecules to form undesirable plugs. Methanol and glycol are currently used to prevent these plugs via thermodynamic inhibition. Small amounts of water-soluble polymers may provide an alternate approach for preventing gas hydrates. In this study, we expand the fundamental understanding of water,polymer systems with differential scanning calorimetry. Nonfreezable bound water was used to quantify polymer,water interactions and relate them to the chemical structure for a series of polymers, including acrylamides, cyclic lactams, and n -vinyl amides. For good interactions, the water structure needs to be stabilized through hydrophobic interactions. An increased hydrophobicity of the pendant group also appears to favor polymer performance as a gas hydrate inhibitor. Good inhibitors, such as poly(diethyl acrylamide) and poly(N -vinyl caprolactam), also show higher heat capacities, which indicate higher hydrophobicity, than poor performers such as polyzwitterions, in which hydrophilicity dominated. The phase behavior and thermodynamic properties of dilute polymer solutions were also evaluated through measurements of the heat of demixing and lower critical solution temperature. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2642,2653, 2007 [source] Preparation and use of a mesoporous silicate material for the removal of tetramethyl ammonium hydroxide (TMAH) from aqueous solutionJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 12 2001Brian P Kelleher Abstract A cubic mesoporous silicate (CMS) was prepared, characterised, and assessed as an adsorbent for tetramethyl ammonium hydroxide (TMAH) from aqueous solution. The adsorption process was studied as a function of temperature and time. Sorption closely followed the Langmuir model. The adsorption of TMAH on CMS was endothermic and kinetic studies suggest that the overall rate of adsorption was pseudo-second-order. Pore diffusion effects contribute to limiting the overall rate of adsorption while at lower initial TMAH concentrations, film diffusion becomes more important. Desorption studies were carried out using water and methanol. Methanol was the superior desorbing agent. © 2001 Society of Chemical Industry [source] FRUIT BRANDY PRODUCTION BY BATCH COLUMN DISTILLATION WITH REFLUXJOURNAL OF FOOD PROCESS ENGINEERING, Issue 1 2005MICHAEL J. CLAUS ABSTRACT The relationship between the operating parameters of batch fruit spirits column stills with reflux and the congener (trace compounds that provide flavors and aromas) concentrations in resulting fruit spirits has not been widely studied. Congener concentrations were determined in three different collection fractions, or "cuts," during batch distillation. Acetaldehyde and ethyl acetate were found in higher concentrations in the head cut, first overhead fraction, of the distillation and have lower boiling points relative to ethanol. 1-Propanol and isoamyl alcohol (isopentanol) were present in higher concentrations in the tail cut, third or final fraction, of the distillation and have boiling points that are higher than ethanol. Methanol has a unique concentration profile as it has higher concentrations in both the head and tail cuts, but a lower concentration in the heart cut, the middle fraction which is the desired product of the distillation. Methanol was of particular interest because the distillate must adhere to governmental regulations that limit its concentration in the product. Operating-condition parameters that were studied include the number of trays used in the distillation as well as the use of a "catalytic converter," a high surface, copper-packing material thought to catalyze formation of cyanide-containing compounds allowing them to be separated from the distillate. The effect of the number of trays used in a distillation on the concentration of ethanol and the congeners, methanol, acetaldehyde, ethyl acetate, 1-propanol and isoamyl alcohol in the final distilled spirits product is presented. An additional result of acetaldehyde production at the copper surface of the catalytic converter was also discovered in the analysis of the data. [source] Reduction of Levels of Volatile Components Associated with the "Beany" Flavor in Soymilk by Lactobacilli and StreptococciJOURNAL OF FOOD SCIENCE, Issue 3 2005Trenna D. Blagden ABSTRACT: Methanol, acetaldehyde, ethanol, and hexanal were the 4 major volatiles detected in unfermented soymilk. Eight of the cultures of lactobacilli or streptococci completely eliminated hexanal in the soymilk during fermentation. However, there were considerable variations in the effects of the cultures on the other 3 compounds. All 8 caused significant reduction in levels of methanol. Streptococcus thermophilus OSU-2 was the only culture that significantly lowered the concentration of ethanol in the soymilk. All except Lactobacillus acidophilus C19 and Lactobacillus casei E5 significantly lowered the level of acetaldehyde. Of the cultures tested, L. acidophilus L1 offered the best potential for producing fermented soymilk with an improved volatile profile. [source] Simultaneous determination of carotenoids, tocopherols, and ,-oryzanol in crude rice bran oil by liquid chromatography coupled to diode array and mass spectrometric detection employing silica C30 stationary phasesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 14 2005Wolfgang Stöggl Abstract Crude rice bran oil contains tocopherols (vitamin E), carotenoids (vitamin A), and phytosterols, which possess antioxidant activities and show promising effects as preventive and therapeutic agents. The aim of this work was to establish methods and to compare C18 and C30 silica stationary phases in order to separate and detect tocopherols, carotenoids, and ,-oryzanol in one single run. Comparing RP-LC on silica C18 and C30, higher resolution between all target compounds was obtained using the C30 stationary phase. Methanol was used as eluent and the elution strength was increased by the addition of tert -butyl methyl ether for highly hydrophobic analytes such as ,-oryzanol. Detection was accomplished by diode array detection from 200 to 500 nm. Absorbance maxima were found at 295 nm for tocopherols, 324 nm for ,-oryzanol, and 450 nm for carotenoids. Furthermore, compounds were characterized and identified on the basis of their UV-spectra. Both RP systems were coupled to MS (LC-MS) by using an atmospheric pressure chemical ionization interface. [source] High-performance thin layer chromatographic analysis of anti-inflammatory triterpenoids from Boswellia serrata Roxb.PHYTOCHEMICAL ANALYSIS, Issue 6 2001K. Krohn Abstract A rapid and simple high-performance thin layer chromatographic (HPTLC) method was developed for the simultaneous quantitative estimation of the biologically active triterpenoids ,-boswellic acid, 3- O -acetyl-,-boswellic acid, 11-keto-,-boswellic acid and 3- O -acetyl-11-keto-,-boswellic acid from the gum resin of Boswellia serrata. The assay combines the isolation and separation of boswellic acid derivatives on silica gel 60F254 -HPTLC plates with spot visualisation and scanning at 250,nm. Methanol was found to be the most appropriate solvent for the exhaustive extraction of boswellic acid derivatives. Copyright © 2001 John Wiley & Sons, Ltd. [source] Cardiovascular effects of the methanol and dichloromethanol extracts from Mentha suaveolens Ehrh.PHYTOTHERAPY RESEARCH, Issue 5 2001Dr R. Bello Abstract Methanol and dichloromethanol extracts of the leaves and stems of Mentha suaveolens Ehrh. have been tested for their effects on resting arterial blood pressure, heart rate and noradrenaline induced hypertension. Both extracts administered by i.v. bolus to urethane anaesthetized normotensive rats reduced the mean arterial blood pressure and heart rate, while only the dichloromethanol extract prevented the noradrenaline induced hypertension. Copyright © 2001 John Wiley & Sons, Ltd. [source] Assessment of acetone as an alternative to acetonitrile in peptide analysis by liquid chromatography/mass spectrometryRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 14 2009Ria Fritz Acetonitrile as a solvent used in liquid chromatography/mass spectrometry (LC/MS) of peptides and proteins is a relatively toxic solvent (LD50 oral; rat; 2,460,mg/kg) compared to alternatives like methanol (LD50 oral; rat; 5,628,mg/kg) and acetone (LD50 oral; rat; 5,800,mg/kg). Strategies to minimize its consumption in LC are either to reduce the inner diameter of the column or replace acetonitrile with a suitable alternative. Methanol is often recommended to replace acetonitrile in peptide analysis. In this study however, the main focus lies on another alternative solvent for LC/MS of peptides; acetone. A number of model proteins were tryptically digested and the peptide solutions were analyzed on a linear trap quadrupole (LTQ) mass spectrometer. The performances of acetonitrile, methanol and acetone were compared according to the quality of the chromatograms obtained and identification of the peptides using the BioWorksÔ software developed by Thermo Scientific. In accordance to the elutropic series, acetone was found to significantly reduce the retention times of peptides separated by C18 column material with regard to acetonitrile while methanol led to increased retention times. Acetone was the superior solvent to methanol for most of the tested model proteins reaching similar sequence coverage and numbers of identified peptides as acetonitrile. We therefore propose acetone as an alternative to acetonitrile in LC/MS of peptides. Copyright © 2009 John Wiley & Sons, Ltd. [source] Eins ist zu wenig, drei sind zuviel: Oxidation von Methan an Dikupferzentren,ANGEWANDTE CHEMIE, Issue 38 2010Dr. Richard Was ist das aktive Zentrum? Und wo ist es? Metallionengehalt und -verteilung der bakteriellen membrangebundenen Methanmonooxygenase pMMO waren trotz des Vorliegens von Protein-Kristallstrukturen lange umstritten. Eine neue Studie scheint nun Klarheit zu schaffen: Ein Dikupferzentrum vermittelt die Oxidation von Methan zu Methanol. Die ungewöhnliche Umgebung dieses aktiven Zentrums wirft aber viele Fragen zur Kupfer-Disauerstoff-(Bio)Chemie auf. [source] Enhancing by Weakening: Electrooxidation of Methanol on Pt3Co and Pt Nanocubes,ANGEWANDTE CHEMIE, Issue 38 2010Dr. Hongzhou Yang Beladene Würfel: Pt3Co- und Pt-Nanowürfel hoher Qualität und ähnlicher Größe wurden durch langsames Reduzieren der Metallvorstufen bei hohen Temperaturen hergestellt. Laut Cyclovoltammetrie- und Chronoamperometrie-Messungen ist die Stromdichte der Methanoloxidation an den Pt3Co-Nanowürfeln viel höher (siehe Bild). Diese größere katalytische Aktivität wurde mit der langsameren und schwächeren Adsorption von CO an Pt3Co erklärt. [source] Chemistry on Single Atoms: Spontaneous Hydrogen Production from Reactions of Transition-Metal Atoms with Methanol at Cryogenic Temperatures,ANGEWANDTE CHEMIE, Issue 7 2010Guanjun Wang Wichtig für Methanol-Brennstoffzellen: Bei der Reaktion von Atomen früher Übergangsmetalle im Grundzustand mit Methanol in einer Argonmatrix entstehen spontan Diwasserstoff und Methoxidsalze M(OMe)2 (M=Sc, Ti, V, Nb). Die Befunde belegen, dass selbst bei tiefen Temperaturen Wasserstoff direkt durch die Umsetzung von Metallatomen im Grundzustand mit Methanol produziert werden kann. [source] Diversification of RTH-Type Zeolite and Its Catalytic Application,ANGEWANDTE CHEMIE, Issue 52 2009Toshiyuki Yokoi Dr. Metall macht's möglich: RTH-Zeolithe (siehe Bild) haben eine attraktive poröse Struktur, ihre Zusammensetzung lässt sich aber nur bedingt variieren. Metallosilicate mit RTH-Topologie sind nun über zwei Wege zugänglich; bei einem davon kann sogar auf strukturbestimmende Agentien verzichtet werden. So erhaltene Al-haltige RTH-Zeolithe waren wirksame Katalysatoren für die hoch selektive Umwandlung von Methanol in Propen. [source] Feste Katalysatoren für die selektive Niedertemperaturoxidation von Methan zu Methanol,ANGEWANDTE CHEMIE, Issue 37 2009Regina Palkovits Dr. Fünfmal gut: Die Titelreaktion gelang an Katalysatoren auf der Basis triazinbasierter Polymere, die durch Trimerisierung von 2,6-Dicyanpyridin in einer ZnCl2 -Schmelze hergestellt wurden und Bipyridin-Struktureinheiten zur Koordination von Platin aufweisen. Die Katalysatoren zeigen hohe Aktivität und können leicht vom Reaktionsgemisch abgetrennt sowie mindestens fünfmal ohne signifikanten Aktivitätsverlust wiederverwendet werden. [source] Ocular Changes after Intravitreal Injection of Methanol, Formaldehyde, or Formate in RabbitsBASIC AND CLINICAL PHARMACOLOGY & TOXICOLOGY, Issue 2 2001Yoriko Hayasaka One hundred ,l of 1% methanol, 1% or 0.1% formaldehyde, or 1% formate was injected in the vitreous cavity of the right eyes of rabbits. The eyes were examined by biomicroscopy and ophthalmoscopy weekly. One month after injection, the eyes were enucleated and examined histologically. One week after treatment the animals that received 0.1% formaldehyde showed retinal vessel dilation, and the rabbits that received 1% formaldehyde showed mild posterior subcapsular cataract and retinal vessel dilation and haemorrhages. One month after treatment, the animals that received 0.1% or 1% formaldehyde developed mild posterior subcapsular cataract and retinal lesions. Animals that received 1% methanol or 1% formate showed nearly normal optical media and fundi. Histologically disorganized retina and optic nerve were seen in eyes that received 0.1% or 1% formaldehyde. Eyes that received 1% methanol or 1% formate appeared histologically normal. Our findings indicate that intravitreal injection of formaldehyde causes retinal and optic nerve damage, while methanol and formate are not or less toxic to ocular tissues. [source] Lipophilicity of some guaianolides isolated from two endemic subspecies of Amphoricarpos neumayeri (Asteraceae) from MontenegroBIOMEDICAL CHROMATOGRAPHY, Issue 3 2009Abubaker A. B. Atrrog Abstract In this study 10 guaianolide-type sesquiterpene , -lactones named amphoricarpolides, isolated from the aerial parts of two endemic subspecies of Amphoricarpos neumayeri (ssp. neumayeri and ssp. murbeckii Bo,njak), were investigated by means of reversed-phase thin-layer chromatography. Methanol,water and tetrahydrofuran,water binary mixtures were used as mobile phase in order to determine lipophilicity parameters R and C0. Some of the investigated compounds were screened for their cytotoxic activity against HeLa and B16 cells. Chromatographically obtained lipophilicity parameters were correlated with calculated logP values and IC50 values. Principal component analysis identified the dominant pattern in the chromatographically obtained data. Copyright © 2008 John Wiley & Sons, Ltd. 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