2618-77-1 Usage
Description
2,5-DIMETHYL-2,5-DI(BENZOYLPEROXY)HEXANE is an organic peroxide compound that is highly sensitive to temperature increases and contamination. It decomposes violently when exposed to temperatures above a specific "Control Temperature." To ensure safety, it is typically stored or transported as a mixture with an inert solid.
Uses
Used in Chemical Synthesis:
2,5-DIMETHYL-2,5-DI(BENZOYLPEROXY)HEXANE is used as a curing agent for [application reason] in the chemical synthesis industry. Its rapid decomposition upon temperature rise makes it suitable for initiating polymerization reactions in the production of various polymers and plastics.
Used in Rubber Industry:
In the rubber industry, 2,5-DIMETHYL-2,5-DI(BENZOYLPEROXY)HEXANE is used as a vulcanization agent for [application reason]. Its sensitivity to temperature allows for precise control over the vulcanization process, leading to improved rubber properties and performance.
Used in Plastics Industry:
2,5-DIMETHYL-2,5-DI(BENZOYLPEROXY)HEXANE is used as an initiator for [application reason] in the plastics industry. Its decomposition at elevated temperatures helps to start the polymerization process, resulting in the formation of various types of plastics with specific characteristics and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-DIMETHYL-2,5-DI(BENZOYLPEROXY)HEXANE is used as a reagent for [application reason]. Its ability to initiate reactions at specific temperatures can be utilized in the synthesis of certain pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Coatings Industry:
2,5-DIMETHYL-2,5-DI(BENZOYLPEROXY)HEXANE is used as a curing agent for [application reason] in the coatings industry. Its temperature sensitivity allows for controlled curing of coatings, resulting in improved adhesion, durability, and performance of the final product.
Reactivity Profile
Peroxides, such as 2,5-DIMETHYL-2,5-DI-(BENZOYLPEROXY)HEXANE, are good oxidizing agents. Organic compounds can ignite on contact with concentrated peroxides. Strongly reduced material such as sulfides, nitrides, and hydrides may react explosively with peroxides. There are few chemical classes that do not at least produce heat when mixed with peroxides. Many produce explosions or generate gases (toxic and nontoxic). Generally, dilute solutions of peroxides (<70%) are safe, but the presence of a catalyst (often a transition metal such as cobalt, iron, manganese, nickel, or vanadium) as an impurity may even then cause rapid decomposition, a buildup of heat, and even an explosion. Solutions of peroxides often become explosive when evaporated to dryness or near-dryness. Danger of explosion when dry. May explode from heat, shock, friction or contamination. May ignite combustibles (wood, paper, oil, clothing, etc.). May be ignited by heat, sparks or flames.
Check Digit Verification of cas no
The CAS Registry Mumber 2618-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2618-77:
(6*2)+(5*6)+(4*1)+(3*8)+(2*7)+(1*7)=91
91 % 10 = 1
So 2618-77-1 is a valid CAS Registry Number.
InChI:InChI=1/C22H26O6/c1-21(2,27-25-19(23)17-11-7-5-8-12-17)15-16-22(3,4)28-26-20(24)18-13-9-6-10-14-18/h5-14H,15-16H2,1-4H3
2618-77-1Relevant articles and documents
Batch process for manufacturing and purifying liquid organic peroxide by distillation
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, (2008/06/13)
A batch process for the manufacture of liquid organic peroxides, such as peroxy esters and diacyl peroxides, by reacting an acid chloride, a hydroperoxide and an alkali metal hydroxide uses a countercurrent, packed distillation column for recovering a purer, drier product with higher yield than previous batch drying processes.
