[{"data":1,"prerenderedAt":23},["ShallowReactive",2],{"notifications-general-sl":3,"compound-IBF-sl":4},"Laboratorij bo zaradi počitnic od 22. julija do 10. avgusta 2026 obratoval po spremenjenem delovnem času. Rezultate analiz lahko pričakujete v enem tednu do deset dni od prejema vzorca. Prosimo za razumevanje.",{"name":5,"shortname":6,"synonyms":7,"cas":8,"molMass":9,"pubchemLink":10,"structure":11,"important":12,"synthetic":13,"compoundClass":14,"asociationImage":17,"summarySet":18,"compoundEffectSet":22},"Isobornyl formate","IBF","Isobornyl methanoate, Isoborneol, formate","1200-67-5",182.26,"https:\u002F\u002Fpubchem.ncbi.nlm.nih.gov\u002Fcompound\u002FIsobornyl-formate","science\u002Fstructures\u002FIBF.png",true,false,{"id":15,"description":16},"1","Terpenoids","",[19],{"summaryText":20,"language":21},"\u003Cp>Isobornyl formate, also known as 2-isobornyl formate, is an organic compound with the chemical formula C\u003Csub>12\u003C\u002Fsub>H\u003Csub>20\u003C\u002Fsub>O\u003Csub>2\u003C\u002Fsub>. It is derived from isobornyl alcohol and formic acid. Isobornyl formate belongs to a class of compounds known as esters, which are formed by the reaction of an alcohol with an organic acid. It is a component of the essential oil from pine needles (from the family \u003Ci>Pinaceae\u003C\u002Fi>) and primarily responsible for its odor.\u003C\u002Fp>\u003Cp>Isobornyl formate may find applications in research and development, particularly in the study of ester chemistry and its potential uses in fragrance, flavor, and chemical industries.\u003Cbr>\u003C\u002Fp>",null,[],1785925860327]