3445-42-9

Basic information

• Product Name: 4-Isopropyl-α,α-dimethylbenzyl alcohol
• Synonyms: 2-(p-Cumenyl)-2-propanol;4-Isopropyl-α,α-dimethylbenzyl alcohol;benzyl alcohol,alpha-alpha-diMethyl-p-isopropyl-
• CAS NO: 3445-42-9
• Molecular Formula: C₁₂H₁₈O
• Molecular Weight: 178.2707
• Mol File: 3445-42-9.mol

Chemical Properties

• Melting Point: 42.5-43.0 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 225.2°Cat760mmHg
• Flash Point: 105.5°C
• Appearance: /
• Density: 0.952g/cm³
• Refractive Index: 1.492
• PKA: 14.61±0.29(Predicted)
• CAS DataBase Reference: 4-Isopropyl-α,α-dimethylbenzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Isopropyl-α,α-dimethylbenzyl alcohol(3445-42-9)
• EPA Substance Registry System: 4-Isopropyl-α,α-dimethylbenzyl alcohol(3445-42-9)

Safety Data

• Hazardous Substances Data: 3445-42-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-Isopropyl-α,α-dimethylbenzyl alcohol is used as a solvent for various pharmaceutical formulations, aiding in the dissolution and stability of active ingredients.
Used in Cosmetics Industry:
4-Isopropyl-α,α-dimethylbenzyl alcohol is used as a solvent in cosmetic products, helping to dissolve and stabilize active ingredients, as well as providing a pleasant aroma.
Used in Fragrance Industry:
4-Isopropyl-α,α-dimethylbenzyl alcohol is used as a solvent in fragrances, enhancing the solubility and stability of fragrance compounds.
Used as a Preservative:
4-Isopropyl-α,α-dimethylbenzyl alcohol is used as a preservative in various products due to its antimicrobial properties, which help extend the shelf life of formulations.
Used in Food and Beverage Industry:
4-Isopropyl-α,α-dimethylbenzyl alcohol is used as a flavoring agent in food and beverages, imparting a pleasant taste and aroma.
Used in Perfume and Cologne Industry:
4-Isopropyl-α,α-dimethylbenzyl alcohol is used as a fragrance ingredient in perfumes and colognes, contributing to the overall scent profile and longevity of the fragrance.

InChI:InChI=1/C16H26O3/c1-14(2,3)18-19-16(6,7)13-11-9-8-10-12(13)15(4,5)17/h8-11,17H,1-7H3

Upstream product

• 100-18-5 1,4-bis(1-methylethyl)benzene 
• 645-13-6 4-isopropylacetophenone 
• 98-49-7 1-(4-isopropyl-phenyl)-1-methyl-ethyl hydroperoxide 
• 3159-98-6 p-diisopropylbenzene dihydroperoxide 

Downstream Products

• 2948-45-0 hydroxyhydroperoxide of p-diisopropylbenzene 
• 33398-01-5 2,3-di-p-cumyl-2,3-dimethylbutane 
• 5650-08-8 1-(α-chloro-isopropyl)-4-isopropyl-benzene 
• 2388-14-9 para-isopropenyl cumene 
• 81194-52-7 4-(p-isopropylphenyl)-4-methyl-1-pentene 
• 100-18-5 1,4-bis(1-methylethyl)benzene 
• 77344-62-8 1-(2,5-diisopropyl-phenyl)-ethanone 
• 77344-61-7 1-(2,4-diisopropylphenyl)ethan-1-one 
• 204695-04-5 S-[(α,α-Dimethyl-4-isopropyl)benzyl]-L-cysteine hydrochloride 
• 752966-78-2 C₁₅H₂₃NO₂S 

Relevant articles and documents

Method for selectively oxidizing cumene compounds

The invention relates to a method for selectively oxidizing cumene compounds, and the method comprises the following steps: placing cumene compounds shown in a formula (I), an iron porphyrin catalyst,an oxidant and a dispersant into a ball milling tank, sealing the ball milling tank, performing ball milling for 3 to 24 hours at a rotating speed of 100 to 800 rpm at room temperature, stopping ballmilling once every 1 to 3 hours in the ball milling process, discharging gases in the ball milling tank, finishing the reaction, and performing post-treatment on a reaction mixture to obtain product2-phenyl-2-propanol compound shown in a formula (II); according to the invention, the oxidation conversion of the cumene and derivatives thereof is realized through solid-phase ball milling, the reaction mode is novel, the operation is convenient, and the energy consumption is low; the method needs no organic solvent, thus effectively avoiding the use of toxic and harmful organic solvents and being green and environment-friendly; has low peroxide content and high safety factor, and high 2-phenyl-2-propanol and derivative selectivity and meets the social requirements of the current green chemical process, environmental compatibility chemical process and biological compatibility chemical process.