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Bis(4-tert-butylcyclohexyl) peroxydicarbonate

Bis(4-tert-butylcyclohexyl) peroxydicarbonate

CAS: 15520-11-3

Molecular Formula: C22H38O6

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Bis(4-tert-butylcyclohexyl) peroxydicarbonate - Names and Identifiers

Name Bis(4-tert-butylcyclohexyl) peroxydicarbonate
Synonyms Perkadox
Perkadox 16
Di-(4-tert-butylcyclohexyl)peroxydicarbonate
Bis(4-tert-butylcyclohexyl) peroxydicarbonate
Bis(5-tert-butylcyclohexyl) peroxydicarbonate
Di-(4-tert.-butylcyclohexyl)-peroxydicarbonat
1-tert-butyl-1-[(1-tert-butylcyclohexyl)-methyldioxymethyl]cyclohexane
4-TERT-BUTYLCYCLOHEXYL {[(4-TERT-BUTYLCYCLOHEXYL)OXY]CARBONYL}OXY CARBONATE
CAS 15520-11-3
EINECS 239-557-1

Bis(4-tert-butylcyclohexyl) peroxydicarbonate - Physico-chemical Properties

Molecular FormulaC22H38O6
Molar Mass398.53
Density1.06±0.1 g/cm3(Predicted)
Melting Point91-92°C
Boling Point435.1±28.0 °C(Predicted)
Water Solubility600ng/L at 20℃
Solubility Chloroform (Slightly), Methanol (Slightly)
Vapor Presure0.01Pa at 20℃
AppearanceSolid
ColorWhite to Off-White
Storage Condition2-8°C
StabilityLight Sensitive

Bis(4-tert-butylcyclohexyl) peroxydicarbonate - Risk and Safety

Hazard SymbolsO - Oxidizing agent
Oxidizing agent
Risk Codes7 - May cause fire
Safety DescriptionS3 - Keep in a cool place.
S7 - Keep container tightly closed.
S14 - Keep away from ... (a list of incompatible materials will follow).
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S17 - Keep away from combustible material.
UN IDsUN 3114 5.2
WGK Germany1
HS Code29209090

Bis(4-tert-butylcyclohexyl) peroxydicarbonate - References

LogP8.34
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Use initiator for acrylate polymerization.
production method (1) synthesis of p-tert-butylcyclohexyl chloroformate the toluene solution of p-tert-butylcyclohexanol was dropped into a reactor filled with phosgene toluene solution, and the reaction temperature was controlled at about 5 ° C., and stirring was continued for 2 hours after the dropping. Then, the temperature was raised to 60 ° C. To remove excess phosgene and hydrogen sulfide as a by-product until there was no phosgene in the discharged gas, and the reaction solution was measured to be nearly neutral by using test paper. Finally, toluene was distilled off under reduced pressure to obtain p-tert-butylcyclohexyl chloroformate. (CH3)3COH COCl2(CH3)3COCOCl HCl (2) synthesis of TBCP water, sodium hydroxide, hydrogen peroxide and emulsifier sodium dodecyl sulfate were added to the reactor, stirred at about 10 ℃ for reaction, sodium peroxide was prepared. Then, P-tert-butyl cyclohexyl chloroformate prepared as described above was added dropwise, and the reaction temperature was controlled at about 40 °c. After the Ester was added, a small amount of hydrogen peroxide was added and the reaction was continued for 1H. The product was filtered, washed with ice water until neutral, and dried to obtain a finished product.
Last Update:2024-04-09 02:00:15
Bis(4-tert-butylcyclohexyl) peroxydicarbonate
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View History
Bis(4-tert-butylcyclohexyl) peroxydicarbonate
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