Dicyclohexyl peroxydicarbonate

Base Information

• Chemical Name: Dicyclohexyl peroxydicarbonate
• CAS No.: 1561-49-5
• Deprecated CAS: 19244-48-5
• Molecular Formula: C14H22 O6
• Molecular Weight: 286.325
• Hs Code.: 2909600000
• European Community (EC) Number: 216-337-3
• UN Number: 3112
• UNII: 7UUX7891Q7
• DSSTox Substance ID: DTXSID30862693
• Nikkaji Number: J9.204E
• Wikidata: Q27268873
• Mol file: 1561-49-5.mol

Synonyms:Dicyclohexyl peroxydicarbonate;1561-49-5;Peroxydicarbonic acid dicyclohexyl ester;cyclohexyl cyclohexyloxycarbonyloxy carbonate;Peroxydicarbonic acid, dicyclohexyl ester;UNII-7UUX7891Q7;Dicyclohexyl peroxydicarbonate(technically pure);7UUX7891Q7;EINECS 216-337-3;Peroxydicarbonic acid, C,C'-dicyclohexyl ester;Dicyclohexyl peroxalate;Dicyclohexyl perdicarbonate;SCHEMBL35537;DTXSID30862693;NA2152;NA2153;UN2152;UN2153;Di-n-octanoyl peroxide(technically pure);Q27268873

Chemical Property of Dicyclohexyl peroxydicarbonate

Chemical Property:

• Vapor Pressure: 4.56E-05mmHg at 25°C
• Refractive Index: 1.489
• Boiling Point: 349.9°Cat760mmHg
• Flash Point: 150.9°C
• PSA: 82.06000
• Density: 1.18g/cm³
• LogP: 2.08190
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 286.14163842
• Heavy Atom Count: 20
• Complexity: 286
• Transport DOT Label: Organic Peroxide Explosive

Purity/Quality:

99% ^*data from raw suppliers

DicyclohexylPeroxydicarbonate(TechnicalGrade) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(CC1)OC(=O)OOC(=O)OC2CCCCC2
• Uses: Dicyclohexyl Peroxydicarbonate is a catalyst used in the frontal copolymerization in the presence of nano-particles.

Technology Process of Dicyclohexyl peroxydicarbonate

There total 2 articles about Dicyclohexyl peroxydicarbonate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

cyclohexyl chloroformate (13248-54-9) → dicyclohexyl peroxydicarbonate (1561-49-5)

Guidance literature:

With sodium hydroxide; dihydrogen peroxide; at -10 - 3 ℃;

Reference yield:

→ dicyclohexyl peroxydicarbonate (1561-49-5)

Guidance literature:

Cyclohexylchlorformiat;

Reference yield: 70.0%

dicyclohexyl peroxydicarbonate (1561-49-5) + orthoformic acid triethyl ester (122-51-0) → diethoxycyclohexyloxymethane (25604-46-0) + formic acid ethyl ester (109-94-4) + Diethyl carbonate (105-58-8,76619-83-5)

Guidance literature:

at 60 ℃; for 2h;

upstream raw materials:

cyclohexyl chloroformate

Downstream raw materials:

1,1,2-Trimethyl-2-propenylcyclohexylcarbonat

Bis(dimethylmethylencyclohexylcarbonat)

p-Tolyl-cyclohexyl-carbonat

Cyclohexyl-o-tolyl-carbonat