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1-(3-isopropylphenyl)-1-methylethyl hydroperoxide is a chemical compound belonging to the class of organic peroxides. It is characterized by its high reactivity and instability, which necessitates careful handling and storage under stringent safety protocols. 1-(3-isopropylphenyl)-1-methylethyl hydroperoxide also exhibits potent oxidizing properties, which can pose significant hazards if not managed properly.

80-24-0

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80-24-0 Usage

Uses

Used in Chemical Reactions:
1-(3-isopropylphenyl)-1-methylethyl hydroperoxide is used as a radical initiator for [initiating various chemical reactions] because of [its high reactivity and ability to generate free radicals].
Used in Polymerization Processes:
In the polymer industry, 1-(3-isopropylphenyl)-1-methylethyl hydroperoxide is used as an initiator for [initiating polymerization reactions] due to [its effectiveness in generating reactive species that can start the polymerization process].
Safety Precautions:
Given its potential for explosive decomposition and powerful oxidizing capabilities, 1-(3-isopropylphenyl)-1-methylethyl hydroperoxide should be handled with extreme care. Appropriate safety measures, including proper storage and handling protocols, must be followed to minimize risks associated with its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 80-24-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80-24:
(4*8)+(3*0)+(2*2)+(1*4)=40
40 % 10 = 0
So 80-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c1-9(2)10-6-5-7-11(8-10)12(3,4)14-13/h5-9,13H,1-4H3

80-24-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-hydroperoxypropan-2-yl)-3-propan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names m-diisopropylbenzene mono-hydroperoxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80-24-0 SDS

80-24-0Relevant academic research and scientific papers

PROCESS FOR PRODUCING DIHYDROXYBENZENE AND DIISOPROPYLBENZENDICARBINOL

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Page/Page column 3-4, (2008/06/13)

A process for simultaneously producing a dihydroxybenzene and a diisopropylbenzene dicarbinol, which contains subjecting a diisopropylbenzene with an oxygen containing gas to obtain an oxidation reaction mixture containing a diisopropylbenzene dihydroperoxide and a diisopropylbenzene hydroxy hydroperoxide followed by an extraction separation step, a decomposition step, a distillation separation step, a reduction step and a post-treatment step in this order, the process containing purifying the diisopropylbenzene dicarbinol from the liquid containing the diisopropylbenzene dicarbinol obtained in the reduction step through purification operations containing crystallization, filtration and subsequent drying, and supplying a filtrate obtained by the filtration to the decomposition step and/or distillation separation step.

Process for the production of a dihydroxybenzene and dicarbinol from diisopropylbenzene

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Example 2, (2008/06/13)

Improved methods for the simultaneous production of dihydroxybenzene and dicarbinol from diisopropylbenzene are provided. These methods provide for continuous and simultaneous production of diisopropylbenzene dihydroperoxide (DHP) and diisopropylbenzene hydroxyhydroperoxide (HHP) using Karr Column extractors operated in series. A very high purity DHP-containing solution, the precursor to the dihydroxybenzene, can be produced according to the reported methods. A safe and efficient method for producing dicarbinol from HHP is also disclosed.

Oxidation of m-diisopropylbenzene in the presence of chelate compounds of copper with amino acids

Pavlov, G. P.,Sinovich, I. D.,Bykova, N. V.

, p. 1084 - 1086 (2007/10/02)

In the oxidation of m-diisopropylbenzene to hydroperoxides chelate compounds of copper with amino acids can play the role of catalyst or inhibitor, depending on the structure of the ligand.The copper salts of glycine, alanine, phenylalanine, threonine, and tryptophan reduce the induction period and increase the oxidation rate of diisopropylbenzene, while the copper salts of lysine, arginine, and tyrosine inhibit the process.

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