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Peroxide, butyl 1-methyl-1-phenylethyl, also known as 1-methyl-1-phenylethyl butyl peroxide, is an organic compound with the chemical formula C14H22O2. It is a colorless to pale yellow liquid with a molecular weight of 226.32 g/mol. This peroxide is commonly used as a polymerization initiator, particularly in the production of polyvinyl chloride (PVC) and other vinyl polymers. It is also employed as a curing agent for unsaturated polyester resins and as a cross-linking agent in rubber and adhesives. Due to its reactive nature, it is essential to handle Peroxide, butyl 1-methyl-1-phenylethyl with care, as it can decompose and release oxygen, posing a risk of explosion if not stored and used properly.

1080-45-1

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1080-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1080-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1080-45:
(6*1)+(5*0)+(4*8)+(3*0)+(2*4)+(1*5)=51
51 % 10 = 1
So 1080-45-1 is a valid CAS Registry Number.

1080-45-1Downstream Products

1080-45-1Relevant academic research and scientific papers

Ultrasound-assisted green synthesis of dialkyl peroxides under phase-transfer catalysis conditions

Kope?, Daniel,Baj, Stefan,Siewniak, Agnieszka

, (2020)

The dialkyl peroxides, which contain a thermally unstable oxygen-oxygen bond, are an important source of radical initiators and cross-linking agents. New efficient and green methods for their synthesis are still being sought. Herein, ultrasound-assisted s

β-Peroxyalkyl radicals and their role in the generation of epoxides during the autoxidation of alkenes. An example of the interplay of free radical, peroxide and organometallic chemistries

Courtneidge, John L.,Bush, Melanie

, p. 57 - 76 (1992)

The systematics of the γ-scission reactions of β-peroxyalkyl radicals to yield epoxides have been extended to include variations in the degree of alkylation at the α- and β-carbon atoms and in the nature of the departing alkoxyl radical.The ratios of geometrically isomeric epoxides so produced have been shown to be dependent upon the steric bulk of the Cα- and Cβ-substituents but rather independent of the nature of the departing alkoxyl radical.The relative importance of 1,5-H atom transfer in β-peroxyalkyl radicals has been considered and some evidence forits occurrence adduced.The relevance of these findings to published data for alkene autoxidation is discussed in terms of two competing pathways, in which, it is suggested, steric factors determine the outcome.

Tri-liquid system in the synthesis of dialkyl peroxides using tetraalkylammonium salts as phase-transfer catalysts

Baj, Stefan,Siewniak, Agnieszka

experimental part, p. 208 - 213 (2011/02/23)

A highly effective method to synthesise dialkyl peroxides from alkyl hydroperoxides and alkyl bromides in a liquid-liquid-liquid system using tetraalkylammonium salts as phase-transfer catalysts is reported. This process was conducted in the presence of h

Alkylation of alkali metal salts of hydroperoxides with haloalkanes in dipolar nonhydroxyl solvents

Choban,Abramyuk,Lyavinets

, p. 2096 - 2100 (2008/09/17)

The possibility of alkylation with chloroalkanes of cumyl hydroperoxide sodium salt hexahydrate in dopolar nonhydroxyl solvents with high donor numbers was examined. The kinetic featutes of the process in hexamethylphosphoric triamide were studied.

Mild conditions synthesis of mixed organic peroxides from alkyl halides and organic hydroperoxides

Baj,Krawczyk,Siewniak,Raczkowska

, p. 381 - 384 (2007/10/03)

The synthesis of mixed organic peroxides by reaction of alkyl halides with tertiary hydroperoxides under basic phase-transfer catalysis conditions was described.

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