Novel (3,5-di-tert-butyl-2-hydroxy-phenylcarbamoyl)-alkanoic acids as potent antioxidants was written by Lodyato, Vladimir I.;Yurkova, Irina L.;Sorokin, Viktor L.;Shadyro, Oleg I.;Dolgopalets, Vladimir I.;Kisel, Mikhail A.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2004.Recommanded Product: 12-Methoxy-12-oxododecanoic acid This article mentions the following:
A series of novel phenolic antioxidants, e.g., I, of amphiphilic structure has been synthesized. Investigations into the influence of aliphatic spacer length and nature of a hydrophilic anchor on the antioxidant activity allowed elucidating certain structure requirements for the membrane-addressed antioxidant designing. In the experiment, the researchers used many compounds, for example, 12-Methoxy-12-oxododecanoic acid (cas: 3903-40-0Recommanded Product: 12-Methoxy-12-oxododecanoic acid).
12-Methoxy-12-oxododecanoic acid (cas: 3903-40-0) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 12-Methoxy-12-oxododecanoic acid
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics