36294-23-2

Basic information

• Product Name: gamma-propanol
• Synonyms: gamma-propanol;3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)-1-PROPANOL;2,6-Di-tert-butyl-4-(3-hydroxypropyl)phenol
• CAS NO: 36294-23-2
• Molecular Formula: C₁₇H₂₈O₂
• Molecular Weight: 264.4
• Mol File: 36294-23-2.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 342.2°Cat760mmHg
• Flash Point: 146.1°C
• Appearance: /
• Density: 0.986g/cm³
• Vapor Pressure: 2.94E-05mmHg at 25°C
• Refractive Index: 1.513
• CAS DataBase Reference: gamma-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: gamma-propanol(36294-23-2)
• EPA Substance Registry System: gamma-propanol(36294-23-2)

Safety Data

• Hazardous Substances Data: 36294-23-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H28O2/c1-16(2,3)13-10-12(8-7-9-18)11-14(15(13)19)17(4,5)6/h10-11,18-19H,7-9H2,1-6H3

Upstream product

• 6386-38-5 methyl 3-(4-hydroxy-3,5-di-tert-butyl)phenylpropanoate 
• 128-39-2 2,6-di-tert-butylphenol 
• 107-18-6 allyl alcohol 
• 504-63-2 trimethyleneglycol 
• 95602-92-9 3,5-di-tert-butyl-4-hydroxycinnamic acid 
• 20170-32-5 4-hydroxy-3,5-di-tert-butylphenylpropionic acid 

Downstream Products

• 119294-38-1 C₄₇H₇₅N₃O₄ 
• 719-22-2 2,6-Di-tert-butyl-1,4-benzoquinone 
• 138345-00-3 7,9-di-tert-butyl-1-oxaspiro<4.5>deca-6,9-dien-8-one 
• 125489-20-5 β-hydroxyethyl-2,6-di-tert-butylmethylenequinone 
• 95970-34-6 2-tert-butyl-4-(3-hydroxypropyl)phenol 
• 119321-16-3 2-<3-(4-hydroxy-3,5-di-tert-butylphenyl)propoxy>-4-pentyl-6-trichloromethyl-sym-triazine 
• 119294-37-0 C₄₂H₆₅N₃O₄ 
• 83191-50-8 2,6-Di-tert-butyl-4-hydroxy-4-(3-hydroxy-propyl)-cyclohexa-2,5-dienone 
• 137376-55-7 bis-3-(3',5'-di-t-butyl-4'-hydroxyphenyl)propyl dithiodipropionate 
• 52273-55-9 4-(3-bromopropyl)phenol 
• 10210-17-0 3-(4-hydroxyphenyl)propan-1-ol 

Relevant articles and documents

γ-hydroxypropylation of 2,6-dialkyl(aryl)phenols with allyl alcohol and its derivatives

The composition of the products of the reaction of 2,6-disubstituted phenols with allyl alcohol and its derivatives in an alkaline medium was investigated, the conditions for carrying out the reaction with the predominant formation of 4-(3-hydroxypropyl)-2,6-dialkyl(aryl)phenols were found, and its mechanism was suggested. The reaction was examined on an industrial scale. An important result is the practical demonstration of alkaline catalysis performed under homogeneous conditions with participation of phenols, when the used alkaline catalyst is recovered in the process without the formation of waste waters. Pleiades Publishing, Ltd., 2010.

Synthesis of benzotriazole monomer

The synthesis of benzotriazole monomers and the use of the benzotriazole monomers and one or more other monomers to prepare ultraviolet (UV) light absorbing polymer compositions. The synthetic methods described in this application provide a significant improvement over the previous methods used to prepare benzotriazole monomers.

New series of aryloxypropanolamines with both human β3-adrenoceptor agonistic activity and free radical scavenging properties

A series of 13 novel hybrid molecules designed to possess both free radical scavenging activity and to stimulate the β3-adrenoceptors in order to improve antidiabetic effect and to restore insulin sensitivity was synthesized and evaluated. Compounds were of quinolyl-, isoquinolyl-, pyridoindolyl- or carbazolyloxypropanolamine structure with a terminal amino group of benzopyranolyl-, di-tert-butylphenolyl- or methoxyindolyl-type. Some of the products possessed both the expected activities.