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Phenolphthalein (/ fɛˈnɒl (f) θəliːn / [citation needed]feh-NOL (F)-thə-leen) is a chemical compound with the formula C 20 H 14 O 4 and is often written as " HIn ", " HPh ", " phph " or simply " Ph " in shorthand notation. Phenolphthalein is often used as an indicator in acid–base titrations. For this application, it turns colorless in ...
In biochemistry, naturally occurring phenols are natural products containing at least one phenol functional group. [1][2][3] Phenolic compounds are produced by plants and microorganisms. [4] Organisms sometimes synthesize phenolic compounds in response to ecological pressures such as pathogen and insect attack, UV radiation and wounding. [5]
The Kastle–Meyer test is a presumptive blood test, first described in 1903, in which the chemical indicator phenolphthalein is used to detect the possible presence of hemoglobin. It relies on the peroxidase -like activity of hemoglobin in blood to catalyze the oxidation of phenolphthalin (the colorless reduced form of phenolphthalein) into ...
Phthalide. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Phthalide is an organic chemical compound with the molecular formula C 8 H 6 O 2. It is a white solid and the simplest benzo lactone. It is prepared from hydroxymethylbenzoic acid.
Hazard pictograms are one of the key elements for the labelling of containers under the GHS, along with: [2] an identification of the product; a signal word – either Danger or Warning – where necessary. hazard statements, indicating the nature and degree of the risks posed by the product. precautionary statements, indicating how the product ...
U.S. Army Public Health Center Toxicology Lab technician assessing samples. Toxicology testing, also known as safety assessment, or toxicity testing, is the process of determining the degree to which a substance of interest negatively impacts the normal biological functions of an organism, given a certain exposure duration, route of exposure, and substance concentration.
Chemical structure and properties. Phenol red exists as a red crystal that is stable in air. Its solubility is 0.77 grams per liter (g/L) in water and 2.9 g/L in ethanol. [1] It is a weak acid with p Ka = 8.00 at 20 °C (68 °F). A solution of phenol red is used as a pH indicator, often in cell culture.
5 OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. Phenol – the simplest of the phenols Chemical structure of salicylic acid, the active metabolite of aspirin. Phenols are both synthesized industrially and produced by plants and microorganisms. [2]