1-Nonanol - Wikipedia

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• 1 Nonanols
• 2 Toxicity
• 3 References

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Appearance move to sidebar hide From Wikipedia, the free encyclopedia 1-Nonanol

Names
Preferred IUPAC name Nonan-1-ol
Other names 1-NonanolPelargonic alcoholNonyl alcoholn-Nonyl alcohol
Identifiers
CAS Number	143-08-8 Y
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:35986 Y
ChEMBL	ChEMBL24563 Y
ChemSpider	8574 Y
DrugBank	DB03143 Y
ECHA InfoCard	100.005.076
KEGG	C14696 Y
PubChem CID	8914
UNII	NGK73Q6XMC Y
CompTox Dashboard (EPA)	DTXSID6022008
InChI InChI=1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3 YKey: ZWRUINPWMLAQRD-UHFFFAOYSA-N Y InChI=1/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3Key: ZWRUINPWMLAQRD-UHFFFAOYAC
SMILES OCCCCCCCCC CCCCCCCCCO
Properties
Chemical formula	C9H20O
Molar mass	144.258 g·mol−1
Appearance	Colorless liquid
Density	0.83 g/cm3[1]
Melting point	−6 °C (21 °F; 267 K)[1]
Boiling point	214 °C (417 °F; 487 K)[1]
Solubility in water	0.13 g/L[1]
Hazards
NFPA 704 (fire diamond)	1 2 0
Flash point	96 °C (205 °F; 369 K)
Lethal dose or concentration (LD, LC):
LD50 (median dose)	3560 mg/kg (oral, rat)[2]4680 mg/kg (dermal, rabbit)[2]
Related compounds
Related alcohols	2-Nonanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Chemical compound

1-Nonanol/ˈnoʊnənɒl/ 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

[edit]

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.[3]

Toxicity

[edit]

The LD50 (oral, rats) is about 2.98 g/kg.[3]

References

[edit]

1. ^ a b c d Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
2. ^ a b Opdyke, DL (1973). "Monographs on fragrance raw materials". Food and Cosmetics Toxicology. 11 (1): 95–115. doi:10.1016/0015-6264(73)90065-5. PMID 4716134.
3. ^ a b Falbe, Jürgen; Bahrmann, Helmut; Lipps, Wolfgang; Mayer, Dieter; Frey, Guido D. (2013). "Alcohols, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a01_279.pub2. ISBN 978-3-527-30385-4.

v t e Alcohols
By consumption	Alcohols found inalcoholic drinks 1-Propanol 2-Methyl-1-butanol Ethanol Isoamyl alcohol Isobutanol Phenethyl alcohol tert-Amyl alcohol tert-Butyl alcohol Tryptophol Medical alcohol Ethchlorvynol Methylpentynol Methanol poisoning Ethanol Toxic alcohols Isopropyl alcohol Methanol
Primaryalcohols (1°)	Methanol 4-Methylcyclohexanemethanol Aminomethanol Cyclohexylmethanol Methoxymethanol Methylazoxymethanol Trifluoromethanol Ethanol 1-Aminoethanol 2,2,2-Trichloroethanol 2,2,2-Trifluoroethanol 2-(2-Ethoxyethoxy)ethanol 2-(2-Methoxyethoxy)ethanol 2-(2-Methoxyethoxy)ethanol 2-Butoxyethanol 2-Chloroethanol 2-Ethoxyethanol 2-Fluoroethanol 2-Mercaptoethanol 2-Methoxyethanol Aminoethylethanolamine Diethylethanolamine Dimethylethanolamine Ethanol Ethanolamine N,N-Diisopropylaminoethanol N-Methylethanolamine Phenoxyethanol Tribromoethanol Butanol 2-Methyl-1-butanol Isobutanol n-Butanol Straight-chainsaturatedC1 — C9 Methanol Ethanol 1-Propanol 1-Butanol 1-Pentanol 1-Hexanol 1-Heptanol 1-Octanol (capryl) 1-Nonanol (pelargonic) Straight-chainsaturatedC10 — C19 1-Decanol (capric) 1-Undecanol (hendecyl) 1-Dodecanol (lauryl) 1-Tridecanol 1-Tetradecanol (myristyl) 1-Pentadecanol 1-Hexadecanol (cetyl / palmityl) 1-Heptadecanol 1-Octadecanol (stearyl) 1-Nonadecanol Straight-chainsaturatedC20 — C29 1-Icosanol (arachidyl) 1-Heneicosanol 1-Docosanol (behenyl) 1-Tricosanol 1-Tetracosanol (lignoceryl) 1-Pentacosanol 1-Hexacosanol (ceryl) 1-Heptacosanol 1-Octacosanol (cluytyl / montanyl) 1-Nonacosanol Straight-chainsaturatedC30 — C39 1-Triacontanol (melissyl / myricyl) 1-Hentriacontanol 1-Dotriacontanol (lacceryl) 1-Tritriacontanol 1-Tetratriacontanol (geddyl) 1-Pentatriacontanol 1-Hexatriacontanol 1-Heptatriacontanol 1-Octatriacontanol 1-Nonatriacontanol Straight-chainsaturatedC40 — C49 1-Tetracontanol 1-Hentetracontanol 1-Dotetracontanol 1-Tritetracontanol 1-Tetratetracontanol 1-Pentatetracontanol 1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl alcohol Furfuryl alcohol Isoamyl alcohol Neopentyl alcohol Nicotinyl alcohol Perillyl alcohol Phenethyl alcohol Prenol Propargyl alcohol Salicyl alcohol Tryptophol Vanillyl alcohol Veratrole alcohol
Secondary alcohols (2°)	1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol Cyclohexanol Cyclopentanol Cyclopropanol Diphenylmethanol Isopropanol Pinacolyl alcohol Pirkle's alcohol Propylene glycol methyl ether
Tertiary alcohols (3°)	2-Methyl-2-pentanol 2-Methylheptan-2-ol 2-Methylhexan-2-ol 3-Methyl-3-pentanol 3-Methyloctan-3-ol Diacetone alcohol Ethchlorvynol Methylpentynol Nonafluoro-tert-butyl alcohol tert-Amyl alcohol tert-Butyl alcohol Triphenylethanol Triphenylmethanol
Hydric alcohols	Monohydric alcohols Methanol (C1) Ethanol (C2) Isopropanol (C3) 1-Butanol (C4) 1-Pentanol (C5) Cetyl alcohol (C16) Dihydric alcohols Ethylene glycol Propylene glycol Trihydric alcohols Glycerol Polyhydric alcohols (sugar alcohols) Pentaerythritol Ethylene glycol (C2) Glycerol, Propylene glycol (C3) Erythritol, Threitol (C4) Xylitol (C5) Mannitol, Sorbitol (C6) Volemitol (C7)
Amyl alcohols	2,2-Dimethylpropan-1-ol 2-Methylbutan-1-ol 2-Methylbutan-2-ol 3-Methylbutan-1-ol 3-Methylbutan-2-ol Pentan-1-ol Pentan-2-ol Pentan-3-ol
Aromatic alcohols	Benzyl alcohol 2,4-Dichlorobenzyl alcohol 3-Nitrobenzyl alcohol
Saturatedfatty alcohols	Cetostearyl alcohol Decanol Lauryl alcohol Myristyl alcohol Nonanol Octanol Tridecanol Undecanol
Branched andunsaturatedfatty alcohols	3-Methyl-3-pentanol Erucyl alcohol Linolenyl alcohol Linoleyl alcohol Oleyl alcohol Palmitoleyl alcohol tert-Amyl alcohol tert-Butyl alcohol
Sugar alcohols	C1 — C7 Methylene glycol (C1) Ethylene glycol (C2) Glycerol (C3) Erythritol (C4) Threitol (C4) Arabitol (C5) Ribitol (C5) Xylitol (C5) Mannitol (C6) Sorbitol (C6) Galactitol (C6) Iditol (C6) Volemitol (C7) Deoxy sugar alcohols Fucitol Cyclic sugar alcohols Inositol Glycylglycitols Maltitol Lactitol Isomalt Maltotriitol Maltotetraitol Polyglycitol
Terpene alcohols	Monoterpene alcohols Borneol Citronellol Geraniol Linalool Menthol Nerol Rhodinol Terpineol Sesquiterpene alcohols Bisabolol Farnesol Nerolidol Patchoulol Diterpene alcohols Phytol
Dialcohols	1,4-Butanediol 1,5-Pentanediol 2-Methyl-2-propyl-1,3-propanediol Diethylpropanediol Ethylene glycol
Trialcohols	Glycerol
Sterols	Cholesterol Ergosterol Lanosterol β-Sitosterol Stigmasterol
Fluoroalcohols	1,3-Difluoro-2-propanol 2,2,2-Trifluoroethanol 2-Fluoroethanol Nonafluoro-tert-butyl alcohol Trifluoromethanol
Preparations	Substitution of haloalkane Carbonyl reduction Ether cleavage Hydrolysis of epoxide Hydration of alkene Ziegler process
Reactions	Deprotonation Protonation Alcohol oxidation Glycol cleavage Nucleophilic substitution Fischer–Speier esterification Williamson ether synthesis Elimination reaction Nucleophilic substitution of carbonyl group Friedel-Crafts alkylation Nucleophilic conjugate addition Transesterification
Category

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• Primary alcohols
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