[{"data":1,"prerenderedAt":23},["ShallowReactive",2],{"notifications-general-it":3,"compound-PHELA-it":4},"A causa delle vacanze estive, il laboratorio seguirà un orario modificato dal 22 luglio al 9 agosto 2026. I risultati delle analisi saranno disponibili entro 7-10 giorni dal ricevimento del campione. Grazie per la comprensione.",{"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},"alpha-Phellandrene","PHELA","a-Phellandrene","99-83-2",136.24,"https:\u002F\u002Fpubchem.ncbi.nlm.nih.gov\u002Fcompound\u002FR_-_-_-alpha-Phellandrene","science\u002Fstructures\u002Falpha-Phellandrene_5jBjtJh.png",true,false,{"id":15,"description":16},"1","Terpenoids","science\u002Fimages\u002Falpha-phelandrene.jpeg",[19],{"summaryText":20,"language":21},"\u003Cp>α-phellandrene is an organic compound, classified as a cyclic monoterpene. The compound belongs to the group oh phellandrenes, which also includes β-phellandrene, a structural isomer. In α-phellandrene, both double bonds are endocyclic and in β-phellandrene, one of them is exocyclic. Both are insoluble in water, but miscible with diethyl ether. \u003C\u002Fp>\u003Cp>α-Phellandrene was named after \u003Ci>Eucalyptus phellandra\u003C\u002Fi>, from which it was isolated. The phellandrenes are used in fragrances because of their pleasing aromas. α-Phellandrene can form hazardous peroxides with air at elevated temperature. \u003C\u002Fp>\u003Cp>Phellandrene produces a minty, woody, and mildly citrus aromatic profile and it is easily absorbed, making it a fairly common additive to a host of cosmetic products. It has also been a staple in holistic Eastern medicine for a long time, used for its antifungal and antibacterial properties. \u003Cbr>\u003C\u002Fp>",null,[],1785925851213]