1-Nonanol

{{chembox

| Watchedfields = changed

| verifiedrevid = 477208308

| Name = 1-Nonanol

| ImageFile = 1-Nonanol.png

| ImageName = Skeletal formula

| ImageFile1 = 1-Nonanol-3D-vdW.png

| ImageName1 = Space-filling model

| PIN = Nonan-1-ol

| OtherNames = 1-Nonanol
Pelargonic alcohol
Nonyl alcohol
n-Nonyl alcohol

|Section1={{Chembox Identifiers

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChEBI_Ref = {{ebicite|correct|EBI}}

| ChEBI = 35986

| ChemSpiderID = 8574

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = NGK73Q6XMC

| KEGG_Ref = {{keggcite|correct|kegg}}

| KEGG = C14696

| InChI = 1/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3

| InChIKey = ZWRUINPWMLAQRD-UHFFFAOYAC

| SMILES1 = CCCCCCCCCO

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| ChEMBL = 24563

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChI = 1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = ZWRUINPWMLAQRD-UHFFFAOYSA-N

| CASNo_Ref = {{cascite|correct|CAS}}

| CASNo = 143-08-8

| DrugBank_Ref = {{drugbankcite|correct|drugbank}}

| DrugBank = DB03143

| SMILES = OCCCCCCCCC

| PubChem = 8914

}}

|Section2={{Chembox Properties

| C=9 | H=20 | O=1

| Appearance = Colorless liquid

| Density = 0.83 g/cm³{{GESTIS|ZVG=490177}}

| MeltingPtC = -6

| MeltingPt_ref =

| BoilingPtC = 214

| BoilingPt_ref =

| Solubility = 0.13 g/L}}

|Section3={{Chembox Hazards

| MainHazards =

| NFPA-H = 1

| NFPA-F = 2

| NFPA-R = 0

| FlashPtC = 96

| AutoignitionPtC =

| LD50 = 3560 mg/kg (oral, rat){{cite journal | journal = Food and Cosmetics Toxicology | volume = 11 | pages= 95–115 | year = 1973 | doi = 10.1016/0015-6264(73)90065-5 | pmid = 4716134 | last1 = Opdyke | first1 = DL | title = Monographs on fragrance raw materials | issue = 1}}
4680 mg/kg (dermal, rabbit)}}

|Section8={{Chembox Related

| OtherFunction = 2-Nonanol

| OtherFunction_label = alcohols

| OtherCompounds =

}}

}}

1-Nonanol{{IPAc-en|ˈ|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.