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Colorimetric analysis is a method of determining the concentration of a chemical element or chemical compound in a solution with the aid of a color reagent. It is applicable to both organic compounds and inorganic compounds and may be used with or without an enzymatic stage.
Determination of iron by a colorimetric method Determination of iron by a colorimetric method, top view. Nessler cylinders (also named color comparison cylinders or color comparing cylinders) are laboratory tubes with a fixed volume, made of glass with optically plane bottom. On the walls, there are marks of the nominal stroke volume (usually ...
Colorimetric assays use reagents that undergo a measurable color change in the presence of the analyte. They are widely used in biochemistry to test for the presence of enzymes, specific compounds, antibodies, hormones and many more analytes. For example, para-Nitrophenylphosphate is converted into a yellow product by alkaline phosphatase enzyme.
In histology, histopathology, and clinical pathology, Perls Prussian blue is a commonly used method to detect the presence of iron in tissue or cell samples. [ 1 ] : 235 [ 2 ] [ 3 ] [ 4 ] Perls Prussian Blue derives its name from the German pathologist Max Perls (1843–1881), who described the technique in 1867. [ 2 ]
Wet chemistry techniques can be used for qualitative chemical measurements, such as changes in color (colorimetry), but often involves more quantitative chemical measurements, using methods such as gravimetry and titrimetry. Some uses for wet chemistry include tests for: [citation needed] pH (acidity, alkalinity) concentration
A colorimeter is a device used in colorimetry that measures the absorbance of particular wavelengths of light by a specific solution. [1] [2] It is commonly used to determine the concentration of a known solute in a given solution by the application of the Beer–Lambert law, which states that the concentration of a solute is proportional to the absorbance.
Ammonium thiocyanate can also be used to determine the iron content in soft drinks by colorimetry. Ammonium thiocyanate may also be used to separate quinidine, from liquors, after the isolation of quinine from the neutral, aqueous, sulphate solution. The salt is added to the hot solution and the gummy solid that forms is strained off from the ...
Bial's reagent consists of 0.4 g orcinol, 200 ml of concentrated hydrochloric acid and 0.5 ml of a 10% solution of ferric chloride. [2] Bial's test is used to distinguish pentoses from hexoses; this distinction is based on the color that develops in the presence of orcinol and iron (III) chloride.