3452-97-9 Usage
Description
3,5,5-Trimethyl-1-hexanol is an organic compound with the chemical formula C9H20O. It is a colorless liquid with a strong, floral odor and is commonly used in the fragrance and flavor industries.
Uses
Used in Fragrance Industry:
3,5,5-Trimethyl-1-hexanol is used as a fragrance material for its strong, floral scent. It is commonly used in perfumes, colognes, and other scented products to provide a pleasant aroma.
Used in Flavor Industry:
3,5,5-Trimethyl-1-hexanol is used as a flavoring agent in the food industry. It imparts a floral and fruity taste to various food products, such as beverages, confectionery, and baked goods.
Used in Synthetic Lubricants Industry:
3,5,5-Trimethyl-1-hexanol is used as an additive in synthetic lubricants to improve their performance and reduce friction.
Used in Additives to Lubricating Oils:
3,5,5-Trimethyl-1-hexanol is used as an additive to lubricating oils to enhance their viscosity and improve their lubricating properties.
Used in Wetting Agent Industry:
3,5,5-Trimethyl-1-hexanol is used as a wetting agent in various applications, such as in the manufacturing of plastics, to improve the wetting and spreading properties of the materials.
Used in Softener in Manufacture of Various Plastics:
3,5,5-Trimethyl-1-hexanol is used as a softener in the manufacture of various plastics to improve their flexibility and workability.
Used in Disinfectants and Germicides Industry:
3,5,5-Trimethyl-1-hexanol is used in disinfectants and germicides to provide a pleasant scent while effectively killing bacteria and other microorganisms.
Production Methods
3,5,5-Trimethylhexanol is prepared from diisobutene by the
oxo process. This alcohol is also a minor component of
isononyl alcohol.
Preparation
By oxo reaction of diisobutylene to the corresponding aldehyde, from which the alcohol is prepared by hydrogenation.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 3452-97-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3452-97:
(6*3)+(5*4)+(4*5)+(3*2)+(2*9)+(1*7)=89
89 % 10 = 9
So 3452-97-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-8(5-6-10)7-9(2,3)4/h8,10H,5-7H2,1-4H3/t8-/m0/s1
3452-97-9Relevant articles and documents
PROCESS FOR PREPARING AN ALCOHOL FROM HYDROCARBONS
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Paragraph 0066, (2020/12/25)
The invention provides a process for preparing an alcohol by hydrogenating an ester which is obtained by alkoxycarbonylating a C2 to C20 hydrocarbon having at least one multiple bond, preferably having at least one olefinic double bond, in which the homogeneous catalyst system used is separated from the product mixture by means of membrane separation. In a development of the present invention, the ester thus formed is converted to another ester by transesterification and then hydrogenated.
Pd-catalyzed reduction of aldehydes to alcohols using formic acid as the hydrogen donor
Wang, Anwei,Yang, Zhiyong,Liu, Jidan,Gui, Qingwen,Chen, Xiang,Tan, Ze,Shi, Ji-Cheng
supporting information, p. 280 - 288 (2013/12/04)
Facile and selective reduction of aromatic aldehydes as well as aliphatic aldehydes to alcohols was achieved using formic acid as the hydrogen donor in the presence of a catalytic amount of Pd(OAc)2 and Cy3P. It was found that both hydrogen atoms in the formic acid molecule can serve as the hydride source. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]
Isononyl benzoates and their use
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Page 5, (2008/06/13)
The invention relates to isomeric nonyl benzoates, processes for their preparation, mixtures of the same with alkyl phthalate, alkyl adipate, or alkyl cyclohexanedicarboxylate, and also to the use of these mixtures.
