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Caproyl peroxide

Vinyl chloride Gelatine Trichlorethylene Caproyl peroxide Demineralised water... [Pg.316]

Di-n-caproyl Peroxide or Bis(n-caproyl) -peroxide (called Di-n-caproylperoxyd in Ger), CH3.CH2.CH2.CH2.CH2.CO... [Pg.95]

There has also been a trend in recent years to the use of free-radical initiators that decompose more rapidly than the traditional initiators such as caproyl and lauryl peroxides. Currently used initiators include peroxydicarbonates, t-butylperpiva-late, azobis-(2,4-dimethylvaleronitrile) and acetyl cyclohexylsulphonyl peroxide. [Pg.317]

N-Peroxycaproic or Percaproic Acid (Caproyl-hydroperoxide). C5 H, C(0).O.O.H mw 132.195 OB to CO2 —181.55% colorl Uq mp 15° bp 62—3° at 13mm. Sol in ale, eth and petr eth V si sol in w. Prepn is by reacting an absol sulfuric acid soln of n-caproic anhydride with coned (98%) hydrogen peroxide for 20 hrs at 0 to RT. The prod is purified by vac distn. The peroxy acid decomps slowly on storage and detonates on rapid heating to 240° with evoln of flame... [Pg.691]

CAPROYL ALCOHOL (111-27-3) Combustible liquid (flash point 145°F/63°C). Reacts, possibly violently, with oxidizers, alkaline earth and alkali metals, strong acids, strong caustics, aliphatic amines, isocyanates, acetaldehyde, benzoyl peroxide, chromic acid, chromium trioxide, dialkylzincs, dichlorine oxide, ethylene oxide, hypochlorous acid, isopropyl chloro-carbonate, lithium tetrahydroaluminate, nitric acid, nitrogen dioxide, pentafluoroguanidine, phosphorus pentasulfide, tangerine oil, triethylaluminum, triisobutylaluminum. [Pg.255]


See other pages where Caproyl peroxide is mentioned: [Pg.692]    [Pg.32]    [Pg.553]    [Pg.138]    [Pg.45]    [Pg.693]    [Pg.38]    [Pg.692]    [Pg.32]    [Pg.553]    [Pg.138]    [Pg.45]    [Pg.693]    [Pg.38]    [Pg.690]    [Pg.74]    [Pg.208]    [Pg.74]   
See also in sourсe #XX -- [ Pg.32 ]

See also in sourсe #XX -- [ Pg.32 ]

See also in sourсe #XX -- [ Pg.38 ]




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