Chemistry:3,5,5-Trimethyl-1-hexanol

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3,5,5-Trimethyl-1-hexanol
3,5,5-trimethyl-1-hexanol.svg
Names
IUPAC name
3,5,5-Trimethyl-1-hexanol
Other names
Nonylol
Trimethylhexanol [1]
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
EC Number
  • 222-376-7
MeSH 3,5,5-trimethyl-1-hexanol
Properties
C9H20O
Molar mass 144.258 g·mol−1
Appearance Clear liquid
Odor herbaceous, plant-like [2]
Density 0.824 g/mL
Melting point -70 °C
Boiling point 194.0 °C
0.45 g/L
Solubility Soluble in alcohol, acetone, ester
Vapor pressure 0.2 torr [1]
4.12·10−5 atm m3 / mol [1]
Hazards
GHS pictograms GHS08: Health hazard GHS07: Harmful GHS09: Environmental hazard
GHS Signal word Warning
H227, H315, H319, H373, H411
P210, P260, P264, P273, P280, P302+352, P305+351+338, P314, P332+313, P337+313, P362, P370+378, P391, P403+235, P501
Flash point 80°C
Related compounds
Related compounds
Isononyl alcohol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

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.[1]

References

  1. 1.0 1.1 1.2 1.3 McGinty, D.; Scognamiglio, J.; Letizia, C. S.; Api, A. M. (2010-07-01). "Fragrance material review on 3,5,5-trimethyl-1-hexanol" (in en). Food and Chemical Toxicology. A Safety Assessment of Saturated Branched Chain Alcohols when used as Fragrance Ingredients 48: S47–S50. doi:10.1016/j.fct.2010.05.026. ISSN 0278-6915. PMID 20659634. https://www.sciencedirect.com/science/article/pii/S0278691510003029. 
  2. Lee, G. H.; Shin, Y.; Oh, M. J. (2008). "Aroma-active components of Lycii fructus (kukija)". Journal of Food Science 73 (6): C500–505. doi:10.1111/j.1750-3841.2008.00851.x. ISSN 0022-1147. PMID 19241541. https://pubmed.ncbi.nlm.nih.gov/19241541/.