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1561-49-5

1561-49-5 Structure

1561-49-5 Structure
IdentificationBack Directory
[Name]

Dicyclohexyl peroxydicarbonate(technically pure)
[CAS]

1561-49-5
[Synonyms]

Dicyclohexyl perdicarbonate
dicyclohexyl peroxydicarbonate
Peroxydicarbonic acid dicyclohexyl
Bis(cyclohexyloxycarbonyl) peroxide
di-n-octanoyl peroxide, technical pure
Peroxybis(formic acid cyclohexyl) ester
Di-n-octanoyl peroxide(technically pure)
Peroxydicarbonic Acid Dicyclohexyl Ester
cyclohexyl cyclohexyloxycarbonyloxy carbonate
Dicyclohexyl Peroxydicarbonate (Technical Grade)
Dicyclohexyl peroxydicarbonate(technically pure)
Dicyclohexyl peroxydicarbonate[91% < content ≤100%]
carbonic acid cyclohexoxycarbonyloxy cyclohexyl ester
Dicyclohexyl peroxydicarbonate[content of 91% or less]
Dicyclohexyl peroxydicarbonate[content ≤42%, stable dispersion in water]
[EINECS(EC#)]

216-337-3
[Molecular Formula]

C14H22O6
[MOL File]

1561-49-5.mol
[Molecular Weight]

286.32
Chemical PropertiesBack Directory
[Boiling point ]

388.69°C (rough estimate)
[density ]

1.2106 (rough estimate)
[refractive index ]

1.4795 (estimate)
[EPA Substance Registry System]

Peroxydicarbonic acid, dicyclohexyl ester (1561-49-5)
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H242-H319-H315-H412
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P273-P501-P210-P220-P234-P280-P370+P378-P403+P235-P411-P420-P501-P264-P280-P305+P351+P338-P337+P313P
[RIDADR ]

3112
[HazardClass ]

5.2
[PackingGroup ]

II
Raw materials And Preparation ProductsBack Directory
Hazard InformationBack Directory
[Uses]

Dicyclohexyl Peroxydicarbonate is a catalyst used in the frontal copolymerization in the presence of nano-particles.
[General Description]

Dicyclohexyl peroxydicarbonate(technically pure) is particularly sensitive to temperature rises. Above a given "Control Temperature" they decompose violently. They are generally stored or transported in a water slurry.
[Reactivity Profile]

DICYCLOHEXYL PEROXYDICARBONATE 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 cause accelerated decomposition [Bretherick, 1979 p. 156].
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