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Quinin

In the following decades, chemists tried to utilize more and more the knowledge on reactions which had already been gained. A number of landmark syntheses represent the change to modern chemistry, such as the synthesis of the estrogenic steroid equilenin (W. Bachmann, 1939), of pyridoxine (K. Folkers, 1939), and of quinine (R.B. Woodward, W. von E. Doering, 1944) [23]. [Pg.568]

Supplement (combined with Volumes XXIV and 1936 3458-3793 methane, 25. Pyrimidine, 89. Pyrazine, 91. Nicotine, 110. Dipyridyl, 199. Phenanthroline, 227. Hydroxy compounds, 348 Cinchonine, 424. Quinine, 511. Indigo white, i... [Pg.1124]

Many alkaloids such as nicotine and quinine contain two (or more) nitrogen atoms The nitrogens... [Pg.924]

Acridine orange hydrochloride Ethanol 0.54 Quinine sulfate 0.58 Anthracene... [Pg.717]

Fluorescein, ethyl ester O.lNNaOH 0.99 Quinine sulfate 0.99 POPOP... [Pg.717]

Thymol Acetanilide, antipyrine, camphor, chlorohydrate, menthol, quinine sulfate, ure-thene... [Pg.1212]

Description of Method. Quinine is an alkaloid used in treating malaria (it also is found in tonic water). It is a strongly fluorescent compound in dilute solutions of H2SO4 (f = 0.55). The excitation spectrum of quinine shows two absorption bands at 250 nm and 350 nm, and the emission spectrum shows a single emission band at 450 nm. Quinine is rapidly excreted from the body in urine and is easily determined by fluorescence following its extraction from the urine sample. [Pg.431]

Chloride ion is known to quench the intensity of quinine s fluorescent emission. For example, the presence of 100 ppm NaCI (61 ppm Ch) gives an emission intensity that is only 83% of that without chloride, whereas the presence of 1000 ppm NaCI (610 ppm Ch) gives a fluorescent emission that is only 29% as intense. The concentration of chloride in urine typically ranges from 4600 to 6700 ppm Ch. Flow is an interference from chloride avoided in this procedure ... [Pg.431]

Extracting the aqueous urine sample with a mixture of chloroform and isopropanol separates the quinine and chloride, with the chloride remaining in the urine sample. [Pg.431]

Samples of urine that do not contain quinine still contain a small amount of fluorescent material after the extraction steps. Flow can the quantitative procedure described earlier be modified to take this into account ... [Pg.431]

One approach is to prepare a sample blank using urine known to be free of quinine. The fluorescent signal for the sample blank is subtracted from the urine sample s measured fluorescence. [Pg.432]

The fluorescent emission for quinine at 450 nm can be induced using an excitation frequency of either 250 nm or 350 nm. The fluorescent quantum efficiency is known to be the same for either excitation wavelength, and the UV absorption spectrum shows that 250 is greater than 350- Nevertheless, fluorescent emission intensity is greater when using 350 nm as the excitation wavelength. Speculate on why this is the case. [Pg.432]

With the introduction of improved analytical techniques, starting around 1817, the evaluation of dmgs began and, over a span of about 10 years, strychnine (13, R = H), emetine (14), bmcine (13, R = OCH3), piperine (15), caffeine (16), quinine (17, R = OCH3), colchicine (4), cinchonidine (17,... [Pg.531]

A persistent idea is that there is a very small number of flavor quaUties or characteristics, called primaries, each detected by a different kind of receptor site in the sensory organ. It is thought that each of these primary sites can be excited independently but that some chemicals can react with more than one site producing the perception of several flavor quaUties simultaneously (12). Sweet, sour, salty, bitter, and umami quaUties are generally accepted as five of the primaries for taste sucrose, hydrochloric acid, sodium chloride, quinine, and glutamate, respectively, are compounds that have these primary tastes. Sucrose is only sweet, quinine is only bitter, etc saccharin, however, is slightly bitter as well as sweet and its Stevens law exponent is 0.8, between that for purely sweet (1.5) and purely bitter (0.6) compounds (34). There is evidence that all compounds with the same primary taste characteristic have the same psychophysical exponent even though they may have different threshold values (24). The flavor of a complex food can be described as a combination of a smaller number of flavor primaries, each with an associated intensity. A flavor may be described as a vector in which the primaries make up the coordinates of the flavor space. [Pg.3]

Fig. 1. Quinine knines from primary intermediates couple with secondary intermediates to form viscous colors. Fig. 1. Quinine knines from primary intermediates couple with secondary intermediates to form viscous colors.

See other pages where Quinin is mentioned: [Pg.21]    [Pg.338]    [Pg.338]    [Pg.338]    [Pg.924]    [Pg.574]    [Pg.715]    [Pg.717]    [Pg.717]    [Pg.717]    [Pg.894]    [Pg.947]    [Pg.947]    [Pg.430]    [Pg.431]    [Pg.431]    [Pg.432]    [Pg.836]    [Pg.836]    [Pg.836]    [Pg.836]    [Pg.836]    [Pg.61]    [Pg.368]    [Pg.548]    [Pg.549]    [Pg.551]    [Pg.161]    [Pg.2]    [Pg.3]    [Pg.4]    [Pg.11]    [Pg.255]   
See also in sourсe #XX -- [ Pg.448 ]




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2.6- diisopropylphenylcarbamoyl-quinine

Absorption of quinine

Addition quinine

Aldehydes quinine

Alkaloids quinine

Amantadine Quinine

Amine catalysts, primary quinine-derived

Anesthesia quinine

Antacids with quinine

Antimalarial alkaloid quinine synthesis

Artemether Quinine

Astemizole Quinine

C9-epi-quinine

Chiral quinine

Chiral quinine/quinidine

Cimetidine with quinine

Cinchona alkaloids quinine

Cinchona bark, quinine from

Cinchona tree quinine

Cinchonism quinine causing

Colds, quinine

Desipramine Quinine

Diels-Alder reaction quinine

Digestion, quinine

Doxycycline Quinine

Emission Spectra of 9,10-Diphenylanthracene, Quinine Sulfate, and Fluorescein

Epi Quinine

Epoxides synthesis, quinine

Ethyl quininate

Flecainide Quinine

Fluvoxamine Quinine

Formal synthesis of quinine

Gliclazide Quinine

Halofantrine Quinine

Halofantrine with quinine

Headache quinine

Hormonal) Quinine

Isoniazid Quinine

Ketones quinine

Look up the names of both individual drugs and their drug groups to access full information Quinine

Lumefantrine Quinine

Malaria quinine

Mefloquine Quinine

Michael addition quinine

NSAIDs) Quinine

Natural product synthesis Quinine

Organocatalysts quinine

Oxidants quinine

Phase quinine-derived

Phenprocoumon Quinine

Plasma quinine concentrations

Polymeric catalysts, quinine

Primaquine Quinine

Pseudoenantiomeric quinine-derived

Pseudoenantiomeric quinine-derived catalyst

Pyrrolo-quinoline quinine

Pyrroloquinoline quinine

Pyruvic acid Quinine

Quinine

Quinine 172 Sodium chloride

Quinine 216 Verapamil

Quinine Aluminium hydroxide

Quinine Antacids

Quinine Antidiabetics

Quinine Carbamazepine

Quinine Cimetidine

Quinine Cinchona

Quinine Constitution

Quinine Coumarins

Quinine Cyclosporine

Quinine Digoxin

Quinine Grapefruit juice

Quinine Ketoconazole

Quinine Michael reactions

Quinine Phenobarbital

Quinine Phenytoin

Quinine Quinidine

Quinine Ranitidine

Quinine Rifampicin

Quinine Rifampin

Quinine Smoking

Quinine Stork

Quinine Sulfate A Classic Drug

Quinine Synthesis

Quinine Tobacco

Quinine Warfarin

Quinine acetate

Quinine acetylsalicylate

Quinine acid

Quinine adverse effects

Quinine aldol reaction

Quinine alkaloids Cinchona Bark

Quinine alkaloids Quinidine

Quinine analogs

Quinine analogues

Quinine and

Quinine and Cinchonine

Quinine and congeners

Quinine antimalarial

Quinine antimalarial agent

Quinine antimalarial drug

Quinine antipyretic action

Quinine biological activity

Quinine bisulfate

Quinine bisulphate

Quinine catalysis

Quinine catalysts, addition with

Quinine catalytic reactions

Quinine chemical structure

Quinine chemistry

Quinine chiral selectors

Quinine cinchona tree, bark

Quinine cinchonism

Quinine colloids

Quinine compounds

Quinine conjugate addition

Quinine contact dermatitis

Quinine contraindications

Quinine copolymerization

Quinine curve

Quinine cyclization

Quinine dehydrogenase

Quinine derivatives

Quinine diastereoselectivity

Quinine diffusion

Quinine dihydrochloride

Quinine discovery

Quinine dosage

Quinine dosage forms

Quinine drug reaction

Quinine early history

Quinine enantioselectivity

Quinine epoxide synthesis

Quinine fever

Quinine for Treatment of Malaria

Quinine formal

Quinine gluconate

Quinine hydrochloride

Quinine hydrogen sulfate

Quinine hydrolysis

Quinine in tonic water

Quinine injection

Quinine interactions

Quinine ketone reduction

Quinine market

Quinine organic cation transport

Quinine oxidase

Quinine pH dependent fluorescence

Quinine partial synthesis

Quinine pharmacokinetics

Quinine pharmacological effects

Quinine phosphate with

Quinine poisoning with

Quinine pregnancy

Quinine preparations

Quinine quinotoxine

Quinine reaction

Quinine reaction with

Quinine reconstitution from

Quinine salts

Quinine skeletal muscle

Quinine stationary phase

Quinine stereochemistry

Quinine structure

Quinine sulfate

Quinine sulfate dihydrate

Quinine sulfinates

Quinine sulphate

Quinine tablets

Quinine taste

Quinine tests)

Quinine thiourea catalyst

Quinine thiourea derivatives

Quinine thrombocytopenia with

Quinine total synthesis

Quinine toxicity

Quinine tree

Quinine types

Quinine ventricular arrhythmias caused

Quinine with mefloquine

Quinine with tetracycline

Quinine, Dimethyl

Quinine, absorption

Quinine, dihydroasymmetric dihydroxylation

Quinine, enzymic oxidation

Quinine, fluorescence

Quinine, fluorophore

Quinine, natural product

Quinine, quinidine and cinchonine synthesis pathway

Quinine, radical addition

Quinine, taste properties

Quinine-acrylonitrile copolymer

Quinine-clindamycin

Quinine-derived catalyst

Quinine-derived catalysts Michael addition

Quinine-derived thiourea catalyst

Quinine-induced thrombocytopenia

Quinine-squaramide

Quinine-tetracycline

Quinine/quinidine-based catalysts

Quinine: Cinchonan-9-ol, 6 -methoxy

Quinine: analysis

Quinines reaction with carboxylic acids

Quininic acid

Reduction quinine

Respiratory quinines

Retina quinine

Sesquiterpene quinines

Squaramides, quinine-derived

Stereoselective elimination quinine

Stereoselective synthesis of quinin

Subject Quinine

Tert-butylcarbamoyl)quinine selector

Thiourea catalysts quinine-based

Thiourea quinine/quinidine-derived

Thiourea-based organocatalysts quinine-derived

Tonic water, quinine

Tryptophan quinine

Wild quinine

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