1-Nonanol

changed 477208308 1-Nonanol 1-Nonanol.png skin-invert-image Skeletal formula 1-Nonanol-3D-vdW.png bg-transparent Space-filling model Nonan-1-ol 1-NonanolPelargonic alcoholNonyl alcoholn-Nonyl alcohol NnOHn-NnOHnNnOHnNnOH correct chemspider correct EBI 35986 8574 correct FDA NGK73Q6XMC correct kegg C14696 1/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3 ZWRUINPWMLAQRD-UHFFFAOYAC CCCCCCCCCO correct EBI 24563 correct chemspider 1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3 correct chemspider ZWRUINPWMLAQRD-UHFFFAOYSA-N correct CAS 143-08-8 correct drugbank DB03143 OCCCCCCCCC 8914 9 20 1 Colorless liquid 0.83 g/cm3490177 -6 214 0.13 g/L 07 09 Warning 315 319 411 264 264+265 273 280 302+352 305+351+338 321 332+317 337+317 362+364 391 501 1 2 0 96 3560 mg/kg (oral, rat) Food and Cosmetics Toxicology 11 95–115 1973 10.1016/0015-6264(73)90065-5 4716134 Opdyke DL Monographs on fragrance raw materials 14680 mg/kg (dermal, rabbit) 2-Nonanol, 1-Octanol, 1-Decanol alcohols Pelargonic acid 1-Nonanolˈ n oʊ n ə n ɒ l is a straight chain fatty alcohol with nine carbon atoms and the molecular formula CH3(CH2)8OH. It is a colorless oily liquid with a citrus odor similar to citronella oil. Nonanol occurs naturally in orange oil. The primary use of nonanol is in the manufacture of artificial lemon oil. Various esters of nonanol, such as nonyl acetate, are used in perfumery and flavors. Nonanols More common than 1-nonanol are its many isomers, including isononyl alcohol, which are typically produced by hydroformylation of octenes. Isomeric octenes are produced by dimerization of butenes. These alcohol mixtures are used as solvents in paints and as precursors to plasticizers.10.1002/14356007.a01_279.pub2 Alcohols, Aliphatic Ullmann's Encyclopedia of Industrial Chemistry 2013 Falbe Jürgen Bahrmann Helmut Lipps Wolfgang Mayer Dieter Frey Guido D. 978-3-527-30385-4 Toxicity The LD50 (oral, rats) is about 2.98 g/kg. References Category:Fatty alcohols Category:Primary alcohols Category:Nonanols