1-Nonanol

1-Nonanol
Names
	Preferred IUPAC name Nonan-1-ol
	Other names 1-Nonanol; Pelargonic alcohol; Nonyl alcohol; n-Nonyl alcohol
Identifiers
CAS Number	143-08-8 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEBI	CHEBI:35986 ;
ChEMBL	ChEMBL24563 ;
ChemSpider	8574 ;
DrugBank	DB03143 ;
ECHA InfoCard	100.005.076
KEGG	C14696 ;
PubChem CID	8914;
UNII	NGK73Q6XMC ;
CompTox Dashboard (EPA)	DTXSID6022008 ;
	InChI InChI=1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3 Key: ZWRUINPWMLAQRD-UHFFFAOYSA-N ; InChI=1/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3 Key: ZWRUINPWMLAQRD-UHFFFAOYAC;
	SMILES OCCCCCCCCC; CCCCCCCCCO;
Properties
Chemical formula	C9H20O
Molar mass	144.258 g·mol−1
Appearance	Colorless liquid
Density	0.83 g/cm3
Melting point	−6 °C (21 °F; 267 K)
Boiling point	214 °C (417 °F; 487 K)
Solubility in water	1 g/L
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); 4680 mg/kg (dermal, rabbit)
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). verify (what is ?) Infobox references

1-Nonanol/ˈnoʊnənɒl/ is a straight chain fatty alcohol with nine carbon atoms and the molecular formula CH₃(CH₂)₈OH. It is a colorless to slightly yellow liquid with a citrus odor similar to citronella oil.

Nonanol occurs naturally in the 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.

Toxicity

1-Nonanol shares similar toxicological properties to those of other primary alcohols. It is poorly absorbed through the skin and is severely irritating to the eyes. Vapors can be damaging to the lungs, causing pulmonary edema in severe cases. Oral exposure results in symptoms similar to those of ethanol intoxication, and like ethanol consumption, can cause liver damage. ^[3]

References

^ ^a ^b ^c ^d Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
^ ^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.
^ 1-NONANOL,HSDB, 2006

[GESTIS-1] Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health

[FCT-2] 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] 1-NONANOL,HSDB, 2006

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