General Description
A white solid with a faint soapy odor. Less dense than water and insoluble in water. Hence floats on water. Melting point 49°C. Toxic by ingestion and inhalation. Strong skin irritant. Used as bleaching agent, drying agent for fats, oils and waxes, and as a polymerization catalyst.
Reactivity Profile
LAUROYL PEROXIDE(105-74-8) is an oxidizing agent. Can ignite organic materials; hence a dangerous fire and explosion risk [Hawley]. Strongly reduced material such as sulfides, nitrides, and hydrides may react explosively. Vigorous reactions with other reducing agents. With charcoal sometimes ignites. [Bretherick, 5th ed., 1995, p. 1194].
Air & Water Reactions
Highly flammable. Insoluble in water.
Health Hazard
Contact with liquid irritates eyes and skin. Ingestion causes irritation of mouth and stomach.
Fire Hazard
Behavior in Fire: Can increase the severity of a fire. Becomes sensitive to shock when hot. Containers may explode in a fire. May ignite or explode spontaneously if mixed with flammable materials.
Chemical Properties
Dilauroyl peroxide is a tasteless, coarse, white powder .
Dilauroyl peroxide is not a deflagration hazard. However,
it has been judged an intermediate fire hazard by Noller
et al. . When all the physical tests available for this
peroxide are evaluated collectively, it actually ranks as a
low physical hazard .
Chemical Properties
white powder
Uses
Dilauroyl peroxide is produced by reaction of lauroyl chloride with sodium
peroxide. Its major use is as an initiator for vinyl chloride. It is
used as a polymerization agent in the plastics industry and as a
curing agent for rubber. It has also been used as a burnout agent
for acetate yarns. The pharmaceutical industry uses it in topical
creams in combination with antibiotics for acne treatment .
Uses
Lauroyl peroxide acts as a bleaching agent, drying agent for fats, oils and waxes. Further, it serves as a polymerization initiator as well as vulcanizing agent. In addition to this, it plays an important role for high-pressure polyethylene and food used in bleaching agent.
Uses
Lauroyl peroxide is used as an initiatorfor free-radical polymerization in makingpolyvinyl chloride. Lauroyl peroxide constitutesabout 4% of all organic peroxides consumptionin the United States.
Definition
ChEBI: Lauroyl peroxide is a dicarboxylic acid.
Preparation
Dilauroyl peroxide is the symmetrical peroxide of lauric acid. It is produced by treating lauroyl chloride with hydrogen peroxide in the presence of base:
2C11H23COCl + H2O2+ 2NaOH → (C11H23CO2)2 + 2HCl
Flammability and Explosibility
Notclassified
Carcinogenicity
The International Agency for Research on Cancer has evaluated the carcinogenicity of
lauroyl peroxide. They classified it as a Group 3 material,
which means there is limited or inadequate evidence for
animals and inadequate or absent information for
humans . The carcinogenicity of this peroxide has primarily
been studied using skin applications. After a single
topical application of 10, 20, or 40 mg of lauroyl peroxide,
the epidermal thickness increased markedly. This hyperplasia
was characterized by a sustained production of dark basal
keratinocytes. This peroxide is inactive as a tumor
initiator or as a complete carcinogen. However, it is as
effective as benzoyl peroxide as a skin tumor promoter.
storage
Store in a well-ventilated, cool area, isolatedfrom other chemicals. It is shippedin fiber drums not exceeding 100 lb. Smallamounts may be shipped in 1-lb fiberboardboxes.
Purification Methods
Crystallise it from n-hexane or *benzene and store it below 0o. Potentially EXPLOSIVE. [cf Beilstein 2 IV 1102.]
Waste Disposal
Although lauroyl peroxide is relatively lesshazardous, it is recommended that to handlespills and disposal, the same safety measuresbe followed as those for other hazardousorganic peroxides.
