Dilauroyl peroxide

Dilauroyl peroxide Basic information
Product Name:Dilauroyl peroxide
Synonyms:bis(1-oxododecyl)-peroxid;dyp-97f;lauroylperoxide,notmorethan42%,stabledispersion,inwater;laurydol;lyp97;lyp97f;peroxide,didodecanoyl;Laurox S
CAS:105-74-8
MF:C24H46O4
MW:398.62
EINECS:203-326-3
Product Categories:
Mol File:105-74-8.mol
Dilauroyl peroxide Structure
Dilauroyl peroxide Chemical Properties
Melting point 53-57 °C(lit.)
Boiling point 441.76°C (rough estimate)
density 0,91 g/cm3
vapor density 13.7 (vs air)
vapor pressure 0Pa at 20℃
refractive index 1.4460 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly, Sonicated)
form Powder
color White
Odorwh. coarse powd., faint odor, tasteless
Water Solubility Soluble in oils and organic solvents. Slightly soluble in alcohol. Insoluble in water.
BRN 1804936
InChIKeyYIVJZNGAASQVEM-UHFFFAOYSA-N
LogP10.3
CAS DataBase Reference105-74-8(CAS DataBase Reference)
IARC3 (Vol. 36, Sup 7, 71) 1999
EPA Substance Registry SystemPeroxide, bis(1-oxododecyl) (105-74-8)
Safety Information
Hazard Codes O
Risk Statements 7
Safety Statements 14-3/7-36/37/39-14A-37/39-36
RIDADR UN 3106 5.2
WGK Germany 1
RTECS OF2625000
TSCA Yes
HazardClass 5.2
PackingGroup II
HS Code 29159000
Hazardous Substances Data105-74-8(Hazardous Substances Data)
MSDS Information
ProviderLanguage
Dilauroyl peroxide English
SigmaAldrich English
ACROS English
ALFA English
Dilauroyl peroxide Usage And Synthesis
Chemical PropertiesDilauroyl 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 .
UsesDilauroyl 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 .
UsesLauroyl peroxide is used as an initiatorfor free-radical polymerization in makingpolyvinyl chloride. Lauroyl peroxide constitutesabout 4% of all organic peroxides consumptionin the United States.
UsesLauroyl 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.
PreparationDilauroyl 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
DefinitionChEBI: Lauroyl peroxide is a dicarboxylic acid.
General DescriptionDilauroyl peroxide appears as 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.
Air & Water ReactionsHighly flammable. Insoluble in water.
Reactivity ProfileDilauroyl peroxide 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].
Health HazardContact with liquid irritates eyes and skin. Ingestion causes irritation of mouth and stomach.
Health HazardLauroyl peroxide is a mild eye irritant; theirritation from 500 mg/day in rabbits’ eyeswas mild. It is nontoxic. Prolonged exposureto laboratory animals caused tumors at thesite of application. However, the evidence ofcarcinogenicity in animals is inadequate todate.
Fire HazardBehavior 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.
Flammability and ExplosibilityNotclassified
CarcinogenicityThe 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.
storageStore 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 MethodsCrystallise it from n-hexane or *benzene and store it below 0o. Potentially EXPLOSIVE. [cf Beilstein 2 IV 1102.]
Waste DisposalAlthough lauroyl peroxide is relatively lesshazardous, it is recommended that to handlespills and disposal, the same safety measuresbe followed as those for other hazardousorganic peroxides.
Dilauroyl peroxide Preparation Products And Raw materials
Raw materialsHydrogen peroxide-->Polyethylene-->Polyvinyl chloride-->Lauroyl chloride-->SYNTHETIC OPTICAL WHITNER
Preparation ProductsPOLY(ETHYLENE-CO-METHACRYLIC ACID)
Desiccant Performic Acid Lauric acid Benzoyl peroxide n-butylhydroperoxide Bismaleimide Dipropionyl peroxide(in solution,content≤27%) Bis(cyclohexanone)oxaldihydrazone Hydrogen peroxide Peroxyacetic acid ethyl hydroperoxide Dilauroyl peroxide ACETYL PEROXIDE Sodium lauroylsarcosinate Urea hydrogen peroxide Dicumyl peroxide peroxypropionic acid Dodecanamide

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