Names | |
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Preferred IUPAC name
2-(tert-Butylperoxy)-2-methylpropane | |
Identifiers | |
3D model (
JSmol)
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ChemSpider | |
ECHA InfoCard | 100.003.395 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
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Properties | |
C8H18O2 | |
Molar mass | 146.230 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).
|
Di-tert-butyl peroxide or DTBP is an organic compound consisting of a peroxide group bonded to two tert-butyl groups. It is one of the most stable organic peroxides, due to the tert-butyl groups being bulky. It is a colorless liquid. [1]
The peroxide bond undergoes homolysis at temperatures above 100 °C. For this reason di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry. The decomposition reaction proceeds via the generation of methyl radicals.
DTBP can in principle be used in engines where oxygen is limited, since the molecule supplies both the oxidizer and the fuel. [2]
DTBP is an irritant to the nose, eyes, and skin. It is also flammable, and can explode unpredictably at high (≈150 °C) temperatures. [3]
Names | |
---|---|
Preferred IUPAC name
2-(tert-Butylperoxy)-2-methylpropane | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.003.395 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C8H18O2 | |
Molar mass | 146.230 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).
|
Di-tert-butyl peroxide or DTBP is an organic compound consisting of a peroxide group bonded to two tert-butyl groups. It is one of the most stable organic peroxides, due to the tert-butyl groups being bulky. It is a colorless liquid. [1]
The peroxide bond undergoes homolysis at temperatures above 100 °C. For this reason di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry. The decomposition reaction proceeds via the generation of methyl radicals.
DTBP can in principle be used in engines where oxygen is limited, since the molecule supplies both the oxidizer and the fuel. [2]
DTBP is an irritant to the nose, eyes, and skin. It is also flammable, and can explode unpredictably at high (≈150 °C) temperatures. [3]