Inhibitory properties of 1,3-propanediols in cutting fluids was written by Bennett, E. O.;Gannon, J. E.;Bennett, D. L.. And the article was included in Tribology International in 1983.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:
Preservative properties and compatibility studies of 1,3-propanediol-based cutting fluid additives are reported for a number of compounds Compatibilities of some of the title preservatives with EDTA [60-00-4] are reported; in addition, compatibilities are also given for 2-nitro-2-ethyl-1,3-propanediol (I) [597-09-1] with other cutting fluid preservatives, a number of alkanolamines and amines, and a number of com. cutting fluids. I was compatible with EDTA, showed no antagonism with other preservatives (except for Triadine 10 [72103-18-5]), combined well with C2-4 alkanolamines and butylamines, and generally improved inhibition of a number of com. fluids. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts