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Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils. It is slightly soluble in water (2 ml per 100 ml of H 2 O), but miscible with most organic solvents.
2-Phenylphenol is a precursor to 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, a commercial fire retardant. The sodium salt of orthophenyl phenol, sodium orthophenyl phenol, is a preservative, used to treat the surface of citrus fruits. [5] Orthophenyl phenol is also used as a fungicide in food packaging and may migrate into the contents. [6]
Phenylethanol may refer to: 1-Phenylethanol; 2-Phenylethanol (phenethyl alcohol) This page was last edited on 22 October 2023, at 17:24 (UTC). Text is available ...
This page was last edited on 16 November 2007, at 13:39 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
TCEP is often used as a reducing agent to break disulfide bonds within and between proteins as a preparatory step for gel electrophoresis.. Compared to the other two most common agents used for this purpose (dithiothreitol and β-mercaptoethanol), TCEP has the advantages of being odorless, a more powerful reducing agent, an irreversible reducing agent (in the sense that TCEP does not ...
1-Phenylethanol is the organic compound with the formula C 6 H 5 CH(OH)CH 3. It is one of the most commonly available chiral alcohols. It is a colorless liquid with a mild gardenia-hyacinth scent. [4] Phenylethanol is an aromatic alcohol, it has the role of mouse metabolite.
Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. [1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds.
2.0 g paraformaldehyde; 25 ml distilled water; 1M sodium hydroxide 2 to 4 drops; 50% glutaraldehyde 5.0 ml; 0.2M cacodylate buffer, pH 7.4, 20.0 ml; Mix the paraformaldehyde with 25 ml of distilled water in a 125 ml Erlenmeyer flask. Heat to 60 °C on a stir plate. When moisture forms on the sides of flask, add sodium hydroxide and stir until ...
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