Colorimetric Determination of Trace Amount of Copper in Boiler Water.

A sensitive colorimetric determination of fluoride in drinking water has been developed using a polymeric zirconium complex of 5-(2-Carboxyphenylazo)-8-Hydroxyquinoline as fluoride reagents. The method allowed a reliable determination of fluoride in range of (0.0-1.5) mg L-1. The molar absorptivity of the complex formation is 7695 ± 27 L mol-1 cm-1 at 460 nm. The sensitivity, detection limit, quantitation limit, and percentage recovery for 1.0 mg L-1 fluoride for the proposed method were found to be 0.353 ± 0.013 μg mL-1, 0.1 mg L-1, 0.3 mg L-1, and 101.7 ± 4.1, respectively.

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Colorimetric Determination of Amoxicillin in Pure and some Pharmaceutical Formulations Via Reaction with Potassium Permanganate as Oxidant Reagent

International Journal of Pharmaceutical Quality Assurance ◽

10.25258/ijpqa.10.2.2 ◽

2019 ◽

Vol 10 (02) ◽

Author(s):

Abbas Shebeeb Al-kadumi ◽

Sahar Rihan Fadhel ◽

Mohammed Abdullah Ahmed ◽

Luma Amer Musa

Keyword(s):

Potassium Permanganate ◽

Pharmaceutical Preparations ◽

Pharmaceutical Formulations ◽

Atomic Emission ◽

Basic Medium ◽

Photometric Method ◽

Colorimetric Determination ◽

Spectrophotometric Methods ◽

Label Claim

We proposed two simple, rapid, and convenient spectrophotometric methods are described for the determination of Amoxicillin in bulk and its pharmaceutical preparations. They are based on the measurement of the flame atomic emission of potassium ion (in first method) and colorimetric determination of the green colored solution for manganite ion at 610 nm formed after reaction of Amoxicillin with potassium permanganate as oxidant agent (in the second method) in basic medium. The working conditions of the methods were investigated and optimized. Beer's law plot showed a good correlation in the concentration range of 5-45 μg/ml. The detection limits and relative standared deviations were (2.573, 2.814 μg/ml) (2.137, 2.498) for the flame emission photometric method and (1.844, 2.016 μg/ml) (1.645,1.932) for colorimetric methods for capsules and suspensions respectively. The methods were successfully applied to the determination of Amoxicillin in capsules and suspensions, and the obtained results were in good agreement with the label claim. No interference was observed from the commonly encountered additives and expectancies.

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Spectrophotometric and Colorimetric Determination of Pharmaceutical by Oxidative Coupling Reaction: A Review

Systematic Reviews in Pharmacy ◽

10.31838/srp.2020.4.91 ◽

2020 ◽

Vol 11 (04) ◽

Keyword(s):

Oxidative Coupling ◽

Coupling Reaction ◽

Colorimetric Determination ◽

Oxidative Coupling Reaction

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Synthesis and solvatochromic studies of 2- amino-3-phenolazo1-(4-sulfophenyl)-3-methyi-5-pyrozolone and use it for the determination of trace amount of Nickel (II) in blood samples

International Journal of Bioassays ◽

10.21746/ijbio.2016.10.001 ◽

2016 ◽

Vol 5 (10) ◽

pp. 4920

Author(s):

Amar M. Ali ◽

Hussain. J. Mohammed*

Keyword(s):

Stability Constant ◽

Trace Amount ◽

Benzenesulfonic Acid ◽

Determination Method ◽

Blood Samples ◽

Determination Of Nickel ◽

Normal Human ◽

The Stability ◽

Normal Human Blood

A new, simple, sensitive and rapid spectrophotometric method is proposed for the determination of trace amount of Nickel (II). The method is based on the formation of a 1:2 complex with 4-(4-((2-hydroxy-6-nitrophenyl) diazenyl) -3-methyl-5-oxo-2, 5-dihydro-1H-pyrazol-1-yl) benzenesulfonic acid (2-ANASP) as a new reagent is developed. The complex has a maximum absorption at 516 nm and εmax of 1. 84 X 105 L. mol-1. cm-1. A linear correlation (0. 25 – 4. 0μg. ml-1) was found between absorbance at λmax and concentration. The accuracy and reproducibility of the determination method for various known amounts of Nickel (II) were tested. The results obtained are both precise (RSD was 1. 2 %) and accurate (relative error was 0. 787 %). The effect of diverse ions on the determination of Nickel (II) to investigate the selectivity of the method were also studied. The stability constant of the product was 0. 399 X 106 L. mol-1. The proposed method was successfully applied to the analysis of diabetes blood and normal human blood.

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