Isononyl alcohol

Last updated
Isononyl alcohol
7-methyl-1-octanol.svg
Names
IUPAC name
7-methyloctan-1-ol
Identifiers
3D model (JSmol)
4-01-00-01806
ChEBI
ChemSpider
EC Number
  • 248-471-3
MeSH alcohol isononyl alcohol
PubChem CID
UNII
  • InChI=1S/C9H20O/c1-9(2)7-5-3-4-6-8-10/h9-10H,3-8H2,1-2H3
    Key: QDTDKYHPHANITQ-UHFFFAOYSA-N
  • CC(C)CCCCCCO
Properties
C9H20O
Molar mass 144.258 g·mol−1
AppearanceClear liquid
Density 0.83 g/cm3
Boiling point 215 °C
Slightly soluble
Vapor pressure 0.0198 mm Hg
0.0000412 atm m3/mol
Hazards
GHS labelling: [1]
GHS-pictogram-acid.svg GHS-pictogram-exclam.svg
Warning
H315, H318, H319, H412
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)
NFPA 704.svgHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
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).

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]

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<span class="mw-page-title-main">Ethanol</span> Organic compound (CH₃CH₂OH)

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2-Ethylhexanol is an organic compound with the chemical formula CH3CH2CH2CH2CH(CH2CH3)CH2OH. It is a branched, eight-carbon chiral alcohol. It is a colorless liquid that is poorly soluble in water but soluble in most organic solvents. It is produced on a large scale (>2,000,000,000 kg/y) for use in numerous applications such as solvents, flavors, and fragrances and especially as a precursor for production of other chemicals such as emollients and plasticizers. It is encountered in plants, fruits, and wines. The odor has been reported as "heavy, earthy, and slightly floral" for the R enantiomer and "a light, sweet floral fragrance" for the S enantiomer.

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Diisononyl phthalate (DINP) is a phthalate used as a plasticizer. DINP is typically a mixture of chemical compounds consisting of various isononyl esters of phthalic acid, and is commonly used in a large variety of plastic products.

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<span class="mw-page-title-main">4-Methylcyclohexanemethanol</span> Chemical compound

4-Methylcyclohexanemethanol (MCHM, systematic name 4-methylcyclohexylmethanol) is an organic compound with the formula CH3C6H10CH2OH. Classified as a saturated higher alicyclic primary alcohol. Both cis and trans isomers exist, depending on the relative positions of the methyl (CH3) and hydroxymethyl (CH2OH) groups on the cyclohexane ring. Commercial samples of MCHM consists of a mixture of these isomers as well as other components that vary with the supplier.

<span class="mw-page-title-main">3,5,5-Trimethyl-hexan-1-ol</span> Chemical compound

3,5,5-Trimethyl-1-hexanol is a nine carbon primary alcohol, and it makes up the mixture isononanol along with isononyl alcohol. It is used for fragrance in many toiletries and household cleaning products. Between one and ten metric tonnes are produced every year for use as a fragrance.

<span class="mw-page-title-main">2-Octanone</span> Chemical compound

2-Octanone is an organic compound with the formula CH3C(O)C6H13. It is a colorless volatile liquid that is produced commercially for use in the fragrance industry. It is produced by the condensation of acetone and pentanal followed by hydrogenation of the alkene. It can also be produced by selective oxidation of 1-octene. It is one of three octanones, the others being 3-octanone and 4-octanone. It is a common if trace component of many cooked foods.

References

  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.