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Phenolphthalein is slightly soluble in water and usually is dissolved in alcohols in experiments. It is a weak acid, which can lose H + ions in solution. The nonionized phenolphthalein molecule is colorless and the double deprotonated phenolphthalein ion is fuchsia. Further proton loss in higher pH occurs slowly and leads to a colorless form.
Solution: The main components of a universal indicator, in the form of a solution, are thymol blue, methyl red, bromothymol blue, and phenolphthalein. This mixture is important because each component loses or gains protons depending upon the acidity or alkalinity of the solution being tested. It is beneficial to use this type of universal ...
An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.
A solution of phenol red is used as a pH indicator, often in cell culture. Its color exhibits a gradual transition from yellow (λ max = 443 nm [2]) to red (λ max = 570 nm [3]) over the pH range 6.8 to 8.2. Above pH 8.2, phenol red turns a bright pink color. [4] [5]
Manufacturers provide a material safety data sheet (MSDS; also 'safety data sheet', SDS) for each hazardous chemical they produce. MSDSs are typically used and affixed by regulation at worksites handling those chemicals. An MSDS includes workplace health aspects, restrictions, emergency numbers, and other safety information. [14]
Ferroxyl indicator, or rust indicator, is a solution containing potassium hexacyanoferrate(III), phenolphthalein and sodium chloride. It turns blue in the presence of Fe 2+ ions, and pink in the presence of hydroxide (OH −) ions. It can be used to detect metal oxidation, and is often used to detect rusting in various situations.
This is typically achieved by boiling an alkaline solution of phenolphthalein with powdered zinc, which reduces the phenolphthalein into phenolphthalin. Upon reduction, the very intense pink color of the cationic form of phenolphthalein fades to a faint yellow color. It is this form of phenolphthalein that is present in Kastle–Meyer test kits.
The compound has uses ranging from medicine to laboratory syntheses of chemically similar compounds. o-Cresophthalein has been used to derive polyamides and polyimides, colorimetrically estimate calcium in serum, and predict amount of time to wait before blood collection after a patient receives gadodiamide.