Diacetyl peroxide

Chemical compound From Wikipedia, the free encyclopedia

Diacetyl peroxide

Diacetyl peroxide is the organic peroxide with the formula (CH3CO2)2. It is a white solid or oily liquid with a sharp odor.[4] As with a number of organic peroxides, it is explosive.[5] It is often used as a solution, e.g., in dimethyl phthalate.[2]

Quick Facts Names, Identifiers ...
Diacetyl peroxide
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Names
Preferred IUPAC name
Acetic peroxyanhydride[1]
Other names
acetyl peroxide (2:1); diacetyl peroxide; Peroxide, diacetyl; ethanoyl peroxide; acetyl ethaneperoxoate; ethanoyl ethane peroxoate; peracetic acid acetyl ester
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.003.409
EC Number
  • 203-748-8
UNII
UN number 2084
  • InChI=1S/C4H6O4/c1-3(5)7-8-4(2)6/h1-2H3 Y
    Key: ZQMIGQNCOMNODD-UHFFFAOYSA-N Y
  • O=C(OOC(=O)C)C
Properties
C4H6O4
Molar mass 118.088 g·mol−1
Appearance Colorless crystals[2]
Density 1.163 g/cm3[2]
Melting point 30 °C (86 °F; 303 K)
Boiling point 121.4 °C (250.5 °F; 394.5 K) at 760 mmHg; 63 °C (145 °F; 336 K) at 21 mmHg[3]
slight in cold water [2]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Explosive, oxidizer
NFPA 704 (fire diamond)
ThumbHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 4: Readily capable of detonation or explosive decomposition at normal temperatures and pressures. E.g. nitroglycerinSpecial hazards (white): no code
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Flash point 32.2 °C (90.0 °F; 305.3 K) (45 °C [113 °F; 318 K][4])
Explosive data
Shock sensitivity Very high / moderate when wet
Friction sensitivity Very high / moderate when wet
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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History

Diacetyl peroxide was discovered in 1858 by Benjamin Collins Brodie,[6] who obtained the compound by treating glacial acetic acid with barium peroxide in anhydrous diethyl ether.[7]

Preparation

Diacetyl peroxide forms upon combining hydrogen peroxide and excess acetic anhydride. Peracetic acid is an intermediate.[8]

Safety

Consisting of both an oxidizer, the O-O bond and reducing agents, the C-C and C-H bonds, diacetyl peroxide is shock sensitive and explosive.[8][9][2]

The threshold quantity for Process Safety Management per Occupational Safety and Health Administration 1910.119 is 5,000 lb (2,300 kg) if the concentration of the diacetyl peroxide solution is greater than 70%.[10]

There have been reports of detonation of the pure material. The 25% solution also has explosive potential.[11] The crystalline peroxide is especially shock sensitive and a high explosion risk.[12][9]

Organic peroxides are all prone to exothermic decomposition, potentially leading to explosions and fire.[13]

Contact with liquid causes irritation of the exposed area. If ingested, it irritates the mouth and stomach.[14][15][16][17]

References

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