Search results for "Reaction product"

showing 10 items of 20 documents

3,3?,5,5?-Tetramethylbenzidme for the colorimetric determination of manganese in water

1998

Manganese can be determined by colorimetry with previous oxidation of Mn(II) in a strong basic medium, using 3,3′,5,5′-tetramethylbenzidine as a chromogenic reagent. The molar absorptivity of the reaction product is 3.4 × 104 mol−1l cm−1l, the detection limit 3 ng/ml, the RSD (0.5 mg/l,n = 8) 0.9% and the calibration range (1-cm cells) 0.02–0.8 mg/1 V(V), Cr(VI) and Co(II) are the most significant interferences. The new method was compared with an AAS procedure (air-acetylene flame) with previous solvent extraction and also with a colorimetric method for the determination of manganese in sea and drinking water.

Detection limitchemistryStereochemistryChromogenicReagentchemistry.chemical_elementSeawaterManganeseMolar absorptivityColorimetryAnalytical ChemistryReaction productNuclear chemistryMikrochimica Acta
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2018

Chardonnay wines from Burgundy, obtained from musts with three levels of clarification (Low, Medium and High) during two consecutive vintages (2009 and 2010) and for two kinds of closures (screw caps and synthetic coextruded closures) were analyzed chemically and sensorially. Three bottles per turbidity level were opened in 2015 in order to assess the intensity of the reductive and/or oxidative aromas (REDOX sensory scores) by a trained sensory panel. The chemical analyses consisted in polyphenols and colloids quantification, followed by a proteomic characterization. For the two vintages, the REDOX sensory scores appeared to be driven both by the type of closure and to a lesser extent by th…

0301 basic medicinebusiness.product_categoryGrape reaction productdigestive oral and skin physiology010401 analytical chemistryfood and beveragesGeneral ChemistryOxidative phosphorylation01 natural sciencesSensory analysis0104 chemical sciencesTyrosol03 medical and health scienceschemistry.chemical_compound030104 developmental biologychemistryPolyphenolWhite WineBottleFood sciencebusinessMacromoleculeFrontiers in Chemistry
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Über die zersetzung von hydroperoxyden durch katalase und durch lebereiweißfraktionen

1959

Es werden Herstellung und Eigenschaften einer Eiweisfraktion aus Rinderleber beschrieben, die auf Wasserstoffperoxyd, athyl-, Isopropyl- und tert.-Butylhydroperoxyd zersetzende Wirkung ausubt. Der fur das Zustandekommen der Zersetzungsreaktion der drei letzgenannten Peroxyde notwendige Acceptor wird als athanol identifiziert. Die Eiweisfraktion wird bezuglich ihrer Eigenschaften mit einer kristallisierten Katalase verglichen und aus dem Ergebnis der Schlus gezogen, das sie mit Katalase identisch ist. Als Reaktionsprodukt der enzymatisch katalysierten Reaktion zwischen tert.-Butylhydroperoxyd und athanol wurde Acetaldehyd nachgewiesen. The preparation and properties of an albumen fraction fr…

chemistry.chemical_compoundEthanolchemistrybiologyCatalasePolymer chemistryAcetaldehydebiology.proteinHydrogen peroxideMedicinal chemistryChemical decompositionIsopropylReaction productDie Makromolekulare Chemie
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Alkaline haematin D-575, a new tool for the determination of haemoglobin as an alternative to the cyanhaemiglobin method. I. description of the method

1984

A new method for the rapid and accurate measurement of haemoglobin has been developed as an alternative to the conventional cyanhaemiglobin method. This method is based on the conversion of all haeme, haemoglobin, and haemiglobin species into a stable end product by an alkaline solution of a non-ionic detergent ('AHD reagent'). The reaction product, designated as alkaline haematin D-575, is extremely stable and shows a characteristic absorption peak at 575 nm. As compared to the cyanhaemiglobin method, the determination of haemoglobin by alkaline haematin D-575 offers several advantages such as (1) extreme stability of the AHD reagent and the conversion product, (2) decreased conversion tim…

ChromatographyHemeproteinOctoxynolChemistryStereochemistrySmokingBiochemistry (medical)Clinical BiochemistryHemeGeneral MedicineHydrogen-Ion ConcentrationBiochemistryHaematinPolyethylene GlycolsReaction productPhotometryHemoglobinschemistry.chemical_compoundBasic solutionReagentHeminHumansHemoglobinClinica Chimica Acta
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2-Methyl-4-phenyl-3,4-dihydro­quinazoline

2011

The title compound, C15H14N2, was formed during the lithiation of 2-methylquinazoline with phenyllithium followed by hydrolysis of the intermediate lithium 2-methyl-4-phenyl-4H-quinazolin-3-ide. NMR spectra as well as single-crystal X-ray structural data indicate that the reaction product to have the same structure in chloroform solution as in the crystalline state. The phenyl substituent is twisted out of the plane of the 3,4-dihydroquinazoline ring system by 86.47 (7)°. In the crystal, intermolecular N—H...N interactions connect the molecules into infinite chains.

Substituentchemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic PapersReaction productlcsh:ChemistryNMR spectra databaseCrystalHydrolysischemistry.chemical_compoundCrystallographylcsh:QD1-999chemistryQuinazolineGeneral Materials ScienceLithiumta116Acta Crystallographica Section E: Structure Reports Online
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Dialkyl(butadiene)cyclopentadienylmolybdenum(III) Complexes. Synthesis, Characterization, and Reactivity

2000

International audience; Treatment of CpMo(η4-diene)Cl2 (diene = 1,3-butadiene, C4H6, 1‘; isoprene, C5H8, 1‘ ‘; 2,3-dimethyl-1,3-butadiene, C6H10, 1‘ ‘) in diethyl ether at low temperature with 2 equiv of alkylmagnesium RMgX reagents affords the corresponding dialkyl complexes CpMo(η4-1,3-diene)R2 (2, 2‘, 2‘ ‘, R = CH3, a; CH2Ph, b; CH2SiMe3, c). These species are isolable in moderate yields and have been fully characterized by EPR, elemental analyses, and cyclic voltammetry. They all show a reversible reduction process at relatively low potentials and an irreversible oxidation. The structure of 2‘ ‘a was confirmed by single-crystal X-ray diffraction. The mixed complex CpMo(η4-C4H6)Cl(CH3), …

DieneStereochemistryReaction productsLigands010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compound[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryRedistribution (chemistry)Redox reactionsPhysical and Theoretical ChemistryIsoprene010405 organic chemistryLigandArylOrganic ChemistryAlkyls0104 chemical scienceschemistryReagentCyclic voltammetryDiethyl etherElectron paramagnetic resonance spectroscopyOrganometallics
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Role of Alkyl Substituent and Solvent on the Structural, Thermal, and Magnetic Properties of Binary Radical Salts of 1,2,3,5-Dithia- or Diselenadiazo…

2022

The synthesis, structural, thermal, and magnetic properties of a series of simple binary organic salts based on the radical anion of 7,7,8,8-tetracyanoquinodimethane (TCNQ) and 4-(N-alkylpyridinium-3-yl)-1,2,3,5-dithiadiazolyl (DTDA), 1R (R = Et, Pr, Bu), radical cations and their heavier selenium analogues (DSDA), 2R, are described. Single-crystal X-ray structural analyses reveal that short alkyl substituents on the pyridinium moiety of DTDA/DSDA cations lead to crystallization of isostructural acetonitrile (MeCN) solvates 1Et·MeCN, 1Pr·MeCN, 2Et·MeCN, and 2Pr·MeCN with trans-cofacial DTDA radical cation and eclipsed-cofacial TCNQ radical anion dimers. A slight increase in the substituent …

anionitsuolatreaction productssaltskationitGeneral Materials ScienceGeneral ChemistryoligomersCondensed Matter PhysicsanionscationsCrystal Growth & Design
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Population of neutron-rich nuclei around 48ca with deep inelastic collisions

2009

The deep inelastic reaction 48Ca+64Ni at 6 MeV/A has been studied using the CLARA–PRISMA setup. Angular distributions for pure elastic scattering and total cross-sections of the most relevant transfer channels have been measured. The experimental results are compared with predictions from a semiclassical model, showing good agreement for the presently analyzed few neutrons transfer channels. The decay of the most intense reaction products has also been studied, giving indications of the population of states with very short lifetimes. Gadea Raga, Andrés, Gadea.Andres@ific.uv.es

Neutron-rich nucleiReacción InelásticaUNESCO::FÍSICAUNESCO::FÍSICA::Nucleónica::Física de partículasInelastic collision Neutron-rich nuclei Reaction products Semiclassical model Transfer channel; Angular distribution; CalciumReaction productsCanales de transmisiónSemiclassical modelCLARA–PRISMAReacción Inelástica ; CLARA–PRISMA ; Distribuciones angulares ; Secciones cruzadas ; Modelo semiclásico ; Canales de transmisión ; Muy corta vidaInelastic collisionDistribuciones angularesdeep inelastic reaction; semiclassical model; closed shell nuceli:FÍSICA [UNESCO]:FÍSICA::Nucleónica::Física de partículas [UNESCO]Muy corta vidaTransfer channelSecciones cruzadasCalciumAngular distributionModelo semiclásico
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Variances in the Level of COX-2 and iNOS in Different Grades of Endometrial Cancer.

2019

Background:Many experimental studies have demonstrated the importance of COX-2 in the tumor angiogenesis. Inducible iNOS is responsible for a high and stable level of nitric oxide and is expressed in response to pro-inflammatory factors.Objective:The aim of this study was to evaluate the expression of COX-2 and iNOS at the protein level and to assess their potential prognostic significance in patients with endometrial cancer.Methods:The study group consisted of 45 women with endometrial cancer divided according to the degree of histological differentiation i.e. G1, 17; G2, 15; G3, 13. The control group consisted of 15 women without neoplastic changes. The expression of studied proteins was …

0301 basic medicineTumor angiogenesisAngiogenesisPharmaceutical ScienceNitric Oxide Synthase Type IINitric oxideAndrologyangiogenesis03 medical and health scienceschemistry.chemical_compound0302 clinical medicineEndometrial cancerMedicineHumansIn patientAgedmolecular markerbiologybusiness.industryEndometrial cancerProtein levelCOX-2Middle Agedneoplastic changesmedicine.diseasePrognosisReaction productEndometrial NeoplasmsiNOS030104 developmental biologychemistryPolyclonal antibodiesCyclooxygenase 2030220 oncology & carcinogenesisbiology.proteinFemaleNeoplasm GradingbusinessBiotechnologyCurrent pharmaceutical biotechnology
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Deoxygenative Divergent Synthesis : En Route to Quinic Acid Chirons

2020

The installation of vicinal mesylate and silyl ether groups in a quinic acid derivative generates a system prone for stereoselective borane-catalyzed hydrosilylation through a siloxonium intermediate. The diversification of the reaction conditions allowed the construction of different defunctionalized fragments foreseen as useful synthetic fragments. The selectivity of the hydrosilylation was rationalized on the basis of deuteration experiments and computational studies. peerReviewed

Hydrosilylation010402 general chemistry01 natural sciencesBiochemistrySilyl etherchemistry.chemical_compoundredox reactionsPhysical and Theoretical Chemistryhapetus-pelkistysreaktioorgaaniset yhdisteeteetteritkemiallinen synteesi010405 organic chemistryreaction productsOrganic ChemistryhydrosilylationQuinic acidCombinatorial chemistry0104 chemical sciencesbond cleavageetherschemistryStereoselectivitySelectivityDivergent synthesisDerivative (chemistry)Vicinal
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