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Dive into the research topics where H.Sanke Gowda is active.

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Featured researches published by H.Sanke Gowda.


Talanta | 1966

Chlorpromazine hydrochloride as a new redox indicator in vanadametry.

H.Sanke Gowda; R. Shakunthala

Chlorpromazine hydrochloride is proposed as an indicator in the vanadametric titration of iron(II) and molybdenum(V). It gives a sharp, reversible colour change from green to violet at the equivalence point. It has advantages over the diphenylamine class of indicators. Its redox and transition potentials are reported.


Microchemical Journal | 1983

Tungstophosphoric acid as a new reagent for the spectrophotometric determination of phenothiazines

P. G. Ramappa; H.Sanke Gowda; Anant N. Nayak

Abstract A simple and rapid spectrophotometric method for the determination of phenothiazines based on the formation of a colored compound between tungstophosphoric acid and phenothiazines is described. The proposed method is successfully employed for the determination of phenothiazine drugs in various pharmaceutical products.


Microchemical Journal | 1980

Spectrophotometric studies on platinum-promethazine hydrochloride complex.

H.Sanke Gowda; K. A. Padmaji

Abstract Promethazine hydrochloride forms a yellowish-green complex with platinum(IV) in sodium acetate-hydrochloric acid buffer containing copper catalyst. The complex has an absorption maximum at 406 nm with molar absorptivity 1.001 × 104 liters mol−1 cm−1. The sensitivity of the reaction is 19.5 ng/cm2 for log I ° I = 0.001 . Beers law is valid over the range 0.5–7.5 ppm of platinum(IV) with optimum concentration range 0.8-7.3 ppm. Continuous variations, mole ratio, and slope ratio methods indicate 1:1 composition for the complex. The effects of pH, time, temperature, order of addition of reagents, reagent concentration, and interferences from various ions are reported.


Journal of Inorganic and Nuclear Chemistry | 1981

Magnetic, spectral and thermal studies of copper(II) phenothiazine complexes

H.Sanke Gowda; Jayarama

Abstract Complexes of copper(II) with eight phenothiazines have been prepared. Probable structures for the complexes have been proposed on the basis of elemental analysis and conductometric, spectral, thermogravimetric and magnetic susceptibility data.


Talanta | 1979

N-Substituted phenothiazines as redox indicators in bromatometry

H.Sanke Gowda; S. Akheel Ahmed

Diethazine hydrochloride, butaperazine dimaleate, trifluoperazine hydrochloride, promethazine hydrochloride, prochlorperazine maleate and chlorpromazine hydrochloride have been studied as indicators in bromate titration of quinol, metol and ascorbic acid. They give a very sharp reversible colour change at the equivalence point. Their formal potentials have been determined. A simple but accurate method for the estimation of quinol and metol is reported.


Analytica Chimica Acta | 1979

Rapid spectrophotometric determination of phenothiazines with molybdophosphoric acid

H.Sanke Gowda; P. G. Ramappa; Anant N. Nayak

Abstract A simple and rapid spectrophotometric method for the determination of six phenothiazines can be based on the formation of a coloured compound between molybdophosphoric acid and phenothiazines. The i.r. and e.s.r. spectra of the coloured compounds showed that molybdophosphoric acid oxidizes phenothiazines to a radical cation with which it then forms a coloured compound. The proposed method is employed for the determination of phenothiazines in pharmaceutical preparations. Calibration graphs are linear over ranges of about 100–2000 μg of the phenothiazine.


Analytica Chimica Acta | 1978

N-substituted phenothiazines as indicators in titrations with chloramine-T

H.Sanke Gowda; S. Akheel Ahmed

Abstract Trifluoperazine dihydrochloride, butaperazine dimaleate, promethazine hydrochloride, diethazine hydrochloride, prochlorperazine maleate and chlorpromazine hydrochloride have been studied as redox indicators in titrations of hydroquinone, metol and ascorbic acid with chloramine-T. The end-points obtained are sharper than with conventional indicators. The molar absorptivities of the oxidized indicators are reported. Simple but accurate methods for the determination of hydroquinone and metol are described.


Microchemical Journal | 1985

Prochlorperazine bismethanesulfonate: Sensitive and selective reagent for the spectrophotometric determination of microgram amounts of osmium

A.Thimme Gowda; N.M.Made Gowda; H.Sanke Gowda

Abstract Prochlorperazine bismethanesulfonate (PCPMS) is proposed as a new sensitive and selective reagent for the spectrophotometric determination of microgram amounts of osmium. PCPMS forms a red-colored species with osmium(VIII) or osmium(VI) instantaneously at room temperature in 5 M phosphoric acid medium. The red species exhibits maximum absorbance at 529 nm. Beers law is valid over the concentration range 0.05–3.6 ppm for osmium(VIII) and 0.15–6.4 ppm for osmium(VI). Sandells sensitivity of the reaction is 2.89 nm cm−2 for osmium(VIII) and 4.24 ng cm−2 for osmium(VI). The effects of time, temperature, acidity, order of addition of reagents, reagent concentration, and diverse ions are investigated. The application of the proposed method in the determination of osmium content in synthetic ores has been explored.


Analytica Chimica Acta | 1983

Propericiazine as a reagent for the spectrophotometric determination of ruthenium(III)

A.Thimme Gowda; H.Sanke Gowda; N.M.Made Gowda

Abstract Propericiazine forms an orange-red species with ruthenium(III) immediately in 6–8 M phosphoric or hydrochloric acid or 4.5–5.5 M sulphuric acid. The absorption maximum is at 511 nm and the molar absorptivity is 1.1 × 10 4 1 mol −1 cm −1 . Beers Law is obeyed over the range 0.2–9.4 mg 1 −1 (optimum range 0.5–9.0 mg 1 −1 ). Interferences are described. The method is used to determine ruthenium in synthetic zinc–magnesium alloy and uranium alloy (fuel) solutions.


Microchemical Journal | 1985

Rapid spectrophotometric determination of cerium(IV), arsenic(III), and nitrite with perphenazine

H.Sanke Gowda; A.Thimme Gowda; N.M.Made Gowda

Abstract Perphenazine dihydrochloride, PPN, is proposed as a new reagent for the spectrophotometric determination of cerium(IV), arsenic(III), and nitrite. The reagent forms a red-colored species with cerium(IV) instantaneously in 3.5–5.5 M phosphoric acid medium. The red species exhibits maximum absorbance at 516 nm. A 15-fold molar excess of PPN is necessary for the full development of the color intensity. Beers law is obeyed over the cerium concentration range 0.4–20 ppm and Sandells sensitivity is found to be 0.016 μg/ cm2. The effects of acidity, time, order of addition of reagents, temperature, reagent concentration, and diverse ions are reported. The proposed method offers the advantages of good sensitivity, simplicity, rapidity, selectivity, and a wider range of determination without the need for heating or extraction. Arsenic(III) and nitrite are also indirectly determined. The method is extended to the determination of cerium content in synthetic mixture corresponding to misch metal.

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N.M.Made Gowda

University of Texas Medical Branch

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Jayarama

University of Mysore

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