The author of 《Transition potentials of some triphenylmethane dyes redox indicators》 were Belcher, R.; Brazier, J. N.; Stephen, W. I.. And the article was published in Talanta in 1965. Synthetic Route of C10H14O2 The author mentioned the following in the article:
The transition ranges of 3 triphenylmethane dye redox indicators have been redetermined The figures found in 1F H2SO4 are appreciably higher than earlier values; the new figures are more in accord with the behavior of these indicators when compared with 2,2′-dipyridyl and substituted ferroins. At high acidities the indicators function in the dichromate-Fe(II) system. In a HClO4 medium the figures are significantly higher and fall into a range which accounts for the fact that all 3 dyes function as indicators with hexaperchloratocerate(IV) titrant. The potentials of ferroin and is derivatives are apparently unaffected by change of medium. The experimental process involved the reaction of 4-Butylbenzene-1,2-diol(cas: 2525-05-5Synthetic Route of C10H14O2)
4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Synthetic Route of C10H14O2
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts