In 1966,Polimery (Warsaw, Poland) included an article by Mleziva, Josef. Formula: C10H14O2. The article was titled 《Inhibitors of the copolymerization of unsaturated polyester resins》. The information in the text is summarized as follows:
The effect of 32 inhibitors (p-quinones, hydroquinones, pyrocatechols, pyrogallols, and naphthols) was studied in 3 polymerization mixture (fumaric acid in %, maleic acid in %, modifying acid, glycol and telomerization agent given): (mixture A) 29.1, 1.7, phthalic acid (I), ethylene glycol (II), methylcyclohexanol (III); (mixture B) 21.1, 1.3, I, II, III; (mixture C) 24.3, 2.1, adipic acid, diethylene glycol, -. The polyesters had 51, 49.4, and 30.8 acid number, resp. The polymerization was performed at 20° in the dark, in sunlight, in regular lamp light, or at 110° and then the polyesters were cured at 20° in presence of 3% methylcyclohexanol peroxide and 1% Co naphthenate. Best results were obtained with 2,5-dichloro-p-benzoquinone.4-Butylbenzene-1,2-diol(cas: 2525-05-5Formula: C10H14O2) was used in this study.
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.Formula: C10H14O2 Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities.
Referemce:
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Alcohols – Chemistry LibreTexts