[{"data":1,"prerenderedAt":31},["ShallowReactive",2],{"notifications-general-en":3,"compound-TERP-en":4},"Due to summer holidays, the laboratory will operate on a revised schedule from July 22 to August 9, 2026. Analysis results may take 7 to 10 days from sample receipt. Thank you for your understanding.",{"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},"Terpineol","TERP","alpha-TERPINEOL, p-Menth-1-en-8-ol","98-55-5",154.25,"https:\u002F\u002Fpubchem.ncbi.nlm.nih.gov\u002Fcompound\u002F17100","science\u002Fstructures\u002FTERP.png",true,false,{"id":15,"description":16},"1","Terpenoids","science\u002Fimages\u002FKardamom_Winter_in_den_Beskiden_K6GtWqU.jpeg",[19],{"summaryText":20,"language":21},"\u003Cp>Terpineols are a class of terpenoids, a terpene-like compounds that are modified by the addition of a functional group. Terpineols have been isolated from a variety of sources such as cardamom, cajuput oil, pine oil, and petitgrain oil. Four isomers exist: α-, β-, γ-terpineol, and terpinen-4-ol, with α- isomer being the most abundant one. Although it is naturally occurring, terpineol is commonly manufactured from alpha-pinene, which is hydrated in the presence of sulfuric acid while the alternative route starts from limonene.\u003C\u002Fp>\u003Cp>α-terpineol has a fresh, floral, and slightly herbal scent, making it a valuable ingredient in perfumes, colognes, and fragrances. It adds a pleasant, calming note to scented products. It is also found in some over-the-counter and prescription medications, primarily in cough syrups and topical ointments, for its potential soothing and respiratory benefits.\u003Cbr>\u003C\u002Fp>",null,[23,28],{"effectName":24,"LiteratureReferences":27},{"effectName":25,"effectType":26},"SWEET","A_3","Goldleaf Primary Terpenes Chart",{"effectName":29,"LiteratureReferences":27},{"effectName":30,"effectType":26},"FLORAL",1785925828203]