Isononyl alcohol

Isononyl alcohol
Names
	IUPAC name 7-methyloctan-1-ol
Identifiers
CAS Number	2430-22-0 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	4-01-00-01806
ChEBI	CHEBI:188348;
ChemSpider	16158;
EC Number	248-471-3;
MeSH	alcohol isononyl alcohol
PubChem CID	17072;
UNII	KY36Z95MC2;
CompTox Dashboard (EPA)	DTXSID2058675 ;
	InChI InChI=1S/C9H20O/c1-9(2)7-5-3-4-6-8-10/h9-10H,3-8H2,1-2H3 Key: QDTDKYHPHANITQ-UHFFFAOYSA-N;
	SMILES CC(C)CCCCCCO;
Properties
Chemical formula	C9H20O
Molar mass	144.258 g·mol−1
Appearance	Clear liquid
Density	0.83 g/cm3
Boiling point	215 °C
Solubility in water	Slightly soluble
Vapor pressure	0.0198 mm Hg
Henry's law; constant (kH)	0.0000412 atm m3/mol
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H318, H319, H412
Precautionary statements	P264, P264 P265, P273, P280, P302 P352, P305 P351 P338, P305 P354 P338, P317, P321, P332 P317, P337 P317, P362 P364, P501
NFPA 704 (fire diamond)	1 2 0
Flash point	98 °C
Related compounds
Related compounds	3,5,5-Trimethyl-1-hexanol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Isononyl alcohol (INA) is a nine carbon primary alcohol. It is used in small amounts as fragrance in soap, hair spray, face creams, and shampoo. INA, along with 3,5,5-Trimethyl-1-hexanol, makes up the mixture sometimes referred to as isononanol.^[2]

Nonyl alcohols, including isononyl alcohol, 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]

References

^ "Isononyl alcohol". pubchem.ncbi.nlm.nih.gov.
^ McGinty, D.; Scognamiglio, J.; Letizia, C. S.; Api, A. M. (2010-07-01). "Fragrance material review on isononyl alcohol". Food and Chemical Toxicology. A Safety Assessment of Saturated Branched Chain Alcohols when used as Fragrance Ingredients. 48: S79–S81. doi:10.1016/j.fct.2010.05.034. ISSN 0278-6915. PMID 20659642.
^ 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.

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[1] "Isononyl alcohol". pubchem.ncbi.nlm.nih.gov.

[2] McGinty, D.; Scognamiglio, J.; Letizia, C. S.; Api, A. M. (2010-07-01). "Fragrance material review on isononyl alcohol". Food and Chemical Toxicology. A Safety Assessment of Saturated Branched Chain Alcohols when used as Fragrance Ingredients. 48: S79–S81. doi:10.1016/j.fct.2010.05.034. ISSN 0278-6915. PMID 20659642.

[3] 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.

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