Di-tert-butyl peroxide

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Di-tert-butyl peroxide
Chemical structure of di-tert-butyl peroxide
Ball-and-stick model
Identifiers
110-05-4 YesY
ChemSpider 7742 YesY
Jmol 3D model Interactive image
PubChem 8033
  • InChI=1S/C8H18O2/c1-7(2,3)9-10-8(4,5)6/h1-6H3 YesY
    Key: LSXWFXONGKSEMY-UHFFFAOYSA-N YesY
  • InChI=1/C8H18O2/c1-7(2,3)9-10-8(4,5)6/h1-6H3
    Key: LSXWFXONGKSEMY-UHFFFAOYAY
  • O(OC(C)(C)C)C(C)(C)C
Properties
C8H18O2
Molar mass 146.23 g·mol−1
Density 0.796 g/cm3
Melting point −40 °C (−40 °F; 233 K)
Boiling point 109 to 111 °C (228 to 232 °F; 382 to 384 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Di-tert-butyl peroxide or DTBP is an organic compound consisting of a peroxide group flanked by two tert-butyl groups. It is amongst the most stable organic peroxides. The peroxide bond undergoes homolysis at temperatures >100 °C, and for this reason di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry.

This compound will decompose aerobically and also anaerobically, making it a very interesting fuel source.

Decomposition reaction:

(CH3)3COOC(CH3)3 (g)C2H6 (g) + 2 (CH3)2CO (g)

Two Canadian scientists, H. O. Pritchard and P. Q. E. Clothier, have demonstrated and suggested the use of DTBP in engines where oxygen is limited, since it will work whether or not oxygen is present.[1]

References

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External links

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