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98-49-7

98-49-7 Structure

98-49-7 Structure
IdentificationBack Directory
[Name]

1-(4-isopropylphenyl)-1-methylethyl hydroperoxide
[CAS]

98-49-7
[Synonyms]

Phenylhdrazine-P-sulfonic acid
p-Dipropylbenzene hydroperoxide
p-Diisopropylbenzene hydroperoxide
1-(2-hydroperoxypropan-2-yl)-4-propan-2-ylbenzene
1-(4-isopropylphenyl)-1-methylethyl hydroperoxide
1-(2-hydroperoxypropan-2-yl)-4-propan-2-yl-benzene
1-(1-hydroperoxy-1-methyl-ethyl)-4-isopropyl-benzene
Hydroperoxide,1-methyl-1-[4-(1-methylethyl)phenyl]ethyl
Hydroperoxide, 1-methyl-1-[4-(1-methylethyl) phenyl]ethyl
[EINECS(EC#)]

202-673-8
[Molecular Formula]

C12H18O2
[MOL File]

98-49-7.mol
[Molecular Weight]

194.27
Chemical PropertiesBack Directory
[Boiling point ]

290.73°C (rough estimate)
[density ]

1.0010 (rough estimate)
[refractive index ]

1.5128 (estimate)
[EPA Substance Registry System]

Hydroperoxide, 1-methyl-1-[4-(1-methylethyl)phenyl]ethyl (98-49-7)
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS05
[Signal word ]

Danger
[Hazard statements ]

H242-H314
[Precautionary statements ]

P260-P264-P280-P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P305+P351+P338-P405-P501-P210-P220-P234-P280-P370+P378-P403+P235-P411-P420-P501
Raw materials And Preparation ProductsBack Directory
Hazard InformationBack Directory
[Chemical Properties]

Light yellow transparent oily liquid. Melting point 30 ℃ (purity 98.8%). It is easily decomposed by heat or contact with acid and alkali.
[Uses]

1-(4-Isopropylphenyl)-1-methylethyl hydroperoxide can be used as an initiator for styrene-butadiene rubber polymerization, its initiation speed is 30-50% faster than cumene hydrogen peroxide, but slower than tricumene hydrogen peroxide and tert-butyl cumene hydrogen peroxide. It can also be used as initiator for other polymers. This product can cause burns when it comes into contact with the skin.
[Synthesis]

The concentration of dicumene in the cumene liquid obtained by the reaction of benzene and propylene is generally about 11%. Directly oxidize the diisopropylbenzene with air, and increase the concentration under reduced pressure to obtain 1-(4-isopropylphenyl)-1-methylhydroperoxide.
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