2372-21-6 Usage
Uses
Used in Chemical Synthesis:
TERT-BUTYLPEROXY ISOPROPYL CARBONATE is used as a reagent for [application reason] in the chemical synthesis industry. Its peroxide nature allows it to act as a catalyst or initiator in various chemical reactions, facilitating the production of desired compounds.
Used in Polymer Industry:
In the polymer industry, TERT-BUTYLPEROXY ISOPROPYL CARBONATE is used as an initiator for [application reason]. Its ability to decompose and generate free radicals makes it an effective initiator for the polymerization of various monomers, leading to the formation of polymers with specific properties.
Used in Pharmaceutical Industry:
TERT-BUTYLPEROXY ISOPROPYL CARBONATE is used as a pharmaceutical intermediate for [application reason]. Its unique chemical structure can be utilized in the synthesis of various drugs, particularly those targeting specific biological pathways or receptors.
Used in Cosmetics Industry:
In the cosmetics industry, TERT-BUTYLPEROXY ISOPROPYL CARBONATE is used as a component in the formulation of [application type] for [application reason]. Its properties may contribute to the stability, texture, or other desired characteristics of cosmetic products.
Used in Food Industry:
TERT-BUTYLPEROXY ISOPROPYL CARBONATE is used as an additive in the food industry for [application reason]. It may be employed to improve the shelf life, texture, or other qualities of certain food products, although its use must be carefully regulated due to its sensitivity to heat and potential reactivity.
Reactivity Profile
TERT-BUTYLPEROXY ISOPROPYL CARBONATE is a oxidizing agent. Decomposes violently or explosively at temperatures 0-10°C owing to self- accelerating exothermic decomposition; Several explosions were due to shock, heat or friction. Amines and certain metals can accelerate decomposition [Bretherick 1979 p. 151].
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 2372-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2372-21:
(6*2)+(5*3)+(4*7)+(3*2)+(2*2)+(1*1)=66
66 % 10 = 6
So 2372-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O4/c1-6(2)10-7(9)11-12-8(3,4)5/h6H,1-5H3
2372-21-6Relevant articles and documents
METHOD FOR THE PRODUCTION OF ORGANIC PEROXIDES BY MEANS OF A MICROREACTION TECHNIQUE
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Page/Page column 7-8, (2009/03/07)
The invention provides a process for efficient and reliable preparation of organic peroxides, preferably dialkyl peroxides, peroxycarboxylic acids, peroxycarboxylic esters, diacyl peroxides, peroxycarbonate esters, peroxydicarbonates, ketone peroxides and perketals with the aid of at least one static micromixer and an apparatus for performing the process.
Thermolyse en solution de percarbonates de O-alkyle et O,O-t-butyle
Bourgeois, Marie-Josephe,Campagnole, Monique,Filliatre, Claude,Maillard, Bernard,Villenave, Jean-Jaques
, p. 111 - 115 (2007/10/02)
In the framework of our study of the synthesis and use of free radical initiators, we have prepared several O,O-tert-butyl peroxycarbonates corresponding to primary (methyl and ethyl), secondary (isopropyl) and tertiary (tert-butyl) alcohols.The simple one-pot procedure, which we have perfected, uses N,N'-cabonyldiimidazole as the starting reagent and either O,O-tert-butylimidazolyl percarboxylate or O-alkylimidazolyl carboxylate (in the case of the tertiary alcohol) as an intermediate.The yields of the preparation reactions are fairly good (65-70 percent).The chemical study, i.e. the analysis of the products, of the thermal decomposition in triisopropylbenzene of the prepared O-alkyl and O,O-tert-butyl peroxycarbonates has performed as well as the kinetic one: as for the latter we used Differential Scanning Microcalorimetry.We have observed that the reaction proceeds essentially via the homolysis of the peroxidic bond: no induced decomposition appears even for initial concentrations up to 1 M.The major products arise from reactions of the free radicals formed in the O-O-bond cleavage.The thermal stabilities of the various peroxycarbonates are similar and close to that of tert-butyl peroxybenzoate.Therefore, they are free radical initiators able to give tert-butoxy radicals at lower temperatures than the commonly used di-tert-butyl peroxide.
