95851-08-4

Basic information

• Product Name: Cyclohexanpropanol, 2,2,3,6-tetramethyl-alpha-propyl-
• Synonyms: Cyclohexanpropanol, 2,2,3,6-tetramethyl-alpha-propyl-;2,2,3,6-tetramethyl-alpha-propyl-cyclohexanepropanol
• CAS NO: 95851-08-4
• Molecular Formula: C16H32 O
• Molecular Weight: 240.42
• Mol File: 95851-08-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Density: 0.902[at 20℃]
• Vapor Pressure: 0.034Pa at 25℃
• Water Solubility: 485μg/L at 20℃
• CAS DataBase Reference: Cyclohexanpropanol, 2,2,3,6-tetramethyl-alpha-propyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanpropanol, 2,2,3,6-tetramethyl-alpha-propyl-(95851-08-4)
• EPA Substance Registry System: Cyclohexanpropanol, 2,2,3,6-tetramethyl-alpha-propyl-(95851-08-4)

Safety Data

• Hazardous Substances Data: 95851-08-4(Hazardous Substances Data)

Usage

Flammability and Explosibility

Nonflammable

Upstream product

• 72074-86-3 (+-)-4t-(2,5t,6,6-Tetramethyl-cyclohex-2-en-r-yl)-but-3-en-2-on 
• 106201-72-3 2,2,t-3,t-6-Tetramethyl-r-1-cyclohexancarbaldehyd 
• 107-87-9 2-Pentanone 
• 72074-85-2 (+-)-4t-(2,5c,6,6-tetramethyl-cyclohex-2-en-r-yl)-but-3-en-2-one 
• 105-31-7 1-hexyn-3-ol 
• 59860-58-1 2,2,3,6-Tetramethyl-1-cyclohexanone 
• 59860-57-0 2,5,6,6-Tetramethyl-2-cyclohexen-1-one 

Relevant articles and documents

Optically active aliphatic alcohols and their use as perfuming ingredients

The optically active compounds of formula wherein R1 represents a hydrogen atom or a methyl radical, or of formula are useful as perfuming ingredients for the preparation of perfuming compositions and perfumed articles to which they impart woody-amber notes.

208. Diastereoselektivitaet der Geruchswahrnehmung von Alkoholen der Iononreihe

The characteristic odor of the diastereoisomers 1 and 2 of 1-(2,2,6-trimethylcyclohexyl)-3-hexanol is configuration dependent, the trans-alcohol 1 being identified as the sensorily active component.Structure modifications of model 1/2, for example substitution on C(2), C(13), and C(14) (ionon numbering) by CH3 groups, introduction of double bonds in the 3- or 4-position, and isosteric substitution of C(7) by an O-atom, leads to analogues revealing an unequivocal relation between stereochemistry and odor.The specific odor of alcohol 1 is generally released when all substituents are in an equatorial position; the resulting analogy with the molecular size and shape of odoriferous steroids suggests that the release of the particular scent can be correlated with a steroid-resembling receptor event.