Tick-repellent investigations at Bull’s Island, S.C., 1948 was written by Cole, Moses M.;Smith, Carroll N.. And the article was included in Journal of Economic Entomology in 1949.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:
cf. C.A. 44, 1641i; King, C.A. 43, 9349a. Various repellents, applied to regulation U.S. army fatigue uniforms, were tested in areas heavily infested with lone star ticks (Amblyomma americanum). The Bu ester of 3,4-dihydro-2,2-dimethyl-4-oxo-1,2H-pyran-6-carboxylic acid (Indalone) (I), 2-phenoxyethyl isobutyrate, hexyl mandelate, and Et β-phenylhydracrylate were most effective and safe for use on the human skin or on clothing. I was the most consistently effective of these compounds Outstanding in effectiveness alone were 2-[2-(2-ethylhexyloxy)ethoxy]ethanol (II) and N-amyl-α-butoxyacetamide, 2-butyl-2-ethyl-1,3-propanediol, and di-Me cis-bicyclo[2.2.1]-5-heptene-2,3-dicarboxylate (III). Some of these caused some skin irritation. Acetone solutions of I produced better impregnation of garments than I emulsions; the solutions and emulsions of II and III gave about equal impregnation. I and II powders protected uniforms through a single wearing. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Name: 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. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Name: 2-Butyl-2-ethylpropane-1,3-diol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts