Methyl ethyl ketone peroxide

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Template:Use dmy dates <templatestyles src="Chembox/styles.css"/>

Template:Chembox image cellTemplate:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox SolubilityInWaterTemplate:Chembox headerbarTemplate:Chembox HazardsTemplate:Chembox Datapage checkTemplate:Yesno
Methyl ethyl ketone peroxide
Template:Longitem Template:Unbulleted list
Template:Longitem 1759757
ChEBI Template:Unbulleted list
ChemSpider Template:Unbulleted list
DrugBank Template:Unbulleted list
EC Number Template:Unbulleted list
KEGG Template:Unbulleted list
MeSH Methyl+ethyl+ketone+peroxide
Template:Longitem Template:Unbulleted list
RTECS number Template:Unbulleted list
UN number 3105
Script error: No such module "collapsible list".
Script error: No such module "collapsible list".
Template:Longitem Template:Chembox Elements/molecular formula
Molar mass Template:Chem molar mass
Appearance Colorless liquid
Density 1.170 g cm−3
Boiling point Template:Chembox CalcTemperatures
Shock sensitivity High
Detonation velocity 5200 m/s
RE factor 0.9

Template:Chembox Footer/tracking container onlyScript error: No such module "TemplatePar".Template:Short description

Methyl ethyl ketone peroxide (MEKP) is an organic peroxide with the formula [(CH3)(C2H5)C(O2H)]2O2. MEKP is a colorless oily liquid. It is widely used in vulcanization (crosslinking) of polymers.[2]

It is derived from the reaction of methyl ethyl ketone and hydrogen peroxide under acidic conditions. Several products result from this reaction including a cyclic dimer.[3] The linear dimer, the topic of this article, is the most prevalent.[4] and this is the form that is typically quoted in the commercially available material.[5]

Solutions of 30 to 40% MEKP are used in industry and by hobbyists as catalyst to initiate the crosslinking of unsaturated polyester resins used in fiberglass, and casting. For this application, MEKP often is dissolved in a phlegmatizer such as dimethyl phthalate, cyclohexane peroxide,Script error: No such module "Unsubst". or Template:Ill to reduce sensitivity to shock. Benzoyl peroxide can be used for the same purpose.Script error: No such module "Unsubst".

Safety

Whereas acetone peroxide is a white powder at STP, MEKP is slightly less sensitive to shock and temperature, and more stable in storage.

MEKP is a severe skin irritant and can cause progressive corrosive damage or blindness.

The volatile decomposition products of MEKP can contribute to the formation of vapor-phase explosions. Ensuring safe storage is important, and the maximum storage temperature should be limited to below 30 °C.[6]

Notes

<templatestyles src="Reflist/styles.css" />

  1. Cite error: Script error: No such module "Namespace detect".Script error: No such module "Namespace detect".
  2. Template:Ullmann
  3. Script error: No such module "Citation/CS1".
  4. Script error: No such module "Citation/CS1".
  5. Script error: No such module "citation/CS1".
  6. Script error: No such module "citation/CS1".

Script error: No such module "Check for unknown parameters".

External links