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  2. Precursor chemicals - Wikipedia

    en.wikipedia.org/wiki/Precursor_chemicals

    Drug precursors, also referred to as precursor chemicals or simply precursors, are substances used to manufacture illicit drugs.Most precursors also have legitimate commercial uses and are legally used in a wide variety of industrial processes and consumer products, such as medicines, flavourings, and fragrances.

  3. Phenylacetic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylacetic_acid

    Phenylacetic acid (conjugate base phenylacetate), also known by various synonyms, is an organic compound containing a phenyl functional group and a carboxylic acid functional group. It is a white solid with a strong honey-like odor. Endogenously, it is a catabolite of phenylalanine.

  4. Phenyl alkanoic acids - Wikipedia

    en.wikipedia.org/wiki/Phenyl_alkanoic_acids

    Phenylacetic, 3-phenylpropanoic and 3-phenylpropenoic acids are found in propolis, mammalian exocrine secretions or plant fragrances. During a systematic study of the lipids from seeds of the plant Araceae, [1] the presence of 13-phenyltridecanoic acid as a major component (5-16% of total fatty acids)was discovered. Other similar compounds but ...

  5. Phenyl acetate - Wikipedia

    en.wikipedia.org/wiki/Phenyl_acetate

    Phenyl acetate is the ester of phenol and acetic acid.It can be produced by reacting phenol with acetic anhydride or acetyl chloride.. Phenyl acetate can be separated into phenol and an acetate salt, via saponification: heating the phenyl acetate with a strong base, such as sodium hydroxide, will produce phenol and an acetate salt (sodium acetate, if sodium hydroxide were used).

  6. These espresso machine tablets are how I keep my fancy ... - AOL

    www.aol.com/lifestyle/these-espresso-machine...

    Better-tasting espresso. After using the tablets, your machine will be cleared of odor-causing residue, limescale, and oily build-up, leaving you with better-tasting espresso.

  7. Willgerodt rearrangement - Wikipedia

    en.wikipedia.org/wiki/Willgerodt_rearrangement

    An example with modified reagents (sulfur, concentrated ammonium hydroxide and pyridine) is the conversion of acetophenone to 2-phenylacetamide and phenylacetic acid [5] The Willgerodt rearrangement using acetophenone

  8. Methyl phenylacetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_phenylacetate

    Methyl phenylacetate is an organic compound that is the methyl ester of phenylacetic acid, with the structural formula C 6 H 5 CH 2 CO 2 CH 3. It is a colorless liquid that is only slightly soluble in water, but soluble in most organic solvents. Methyl phenylacetate has a strong odor similar to honey.

  9. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    Anthranilic acid, its esters, and its salts methaqualone and analogues Benzyl cyanide: phenylacetic acid, phenylacetone, amphetamine: Ephedrine, its salts, optical isomers, and salts of optical isomers methamphetamine: Ergonovine and its salts lysergic acid diethylamide: Ergotamine and its salts lysergic acid diethylamide