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13122-18-4

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13122-18-4 Usage

Description

Tert-Butyl peroxy-3,5,5-trimethylhexanoate is a heat-sensitive peroxide that exists as a clear liquid. It requires stringent temperature control measures for safe storage due to its sensitivity to heat.

Uses

Used in Chemical Synthesis:
Tert-Butyl peroxy-3,5,5-trimethylhexanoate is used as a catalyst and initiator for various chemical reactions, particularly in the polymer and pharmaceutical industries. Its heat sensitivity allows for controlled initiation of reactions at specific temperatures, facilitating the synthesis of desired products.
Used in Polymer Industry:
In the polymer industry, tert-Butyl peroxy-3,5,5-trimethylhexanoate is used as an initiator for the polymerization of various monomers. Its controlled heat sensitivity enables the production of polymers with specific properties, such as molecular weight and polydispersity, which are crucial for their end-use applications.
Used in Pharmaceutical Industry:
Tert-Butyl peroxy-3,5,5-trimethylhexanoate is utilized as a reagent in the synthesis of certain pharmaceutical compounds. Its ability to initiate reactions at specific temperatures allows for the controlled formation of complex molecular structures, which are essential for the development of new drugs and therapeutic agents.
Used in Coatings and Adhesives:
In the coatings and adhesives industry, tert-Butyl peroxy-3,5,5-trimethylhexanoate is employed as a curing agent for certain types of resins. Its heat sensitivity allows for the controlled curing of coatings and adhesives, resulting in improved adhesion and durability of the final product.
Used in Propellant Formulation:
Tert-Butyl peroxy-3,5,5-trimethylhexanoate is also used in the formulation of solid rocket propellants. Its heat sensitivity and peroxide nature contribute to the controlled combustion of the propellant, ensuring a predictable and efficient burn rate for various applications in the aerospace industry.

Air & Water Reactions

No rapid reaction with air. No rapid reaction with water.

Reactivity Profile

TERT-BUTYL PEROXY-3,5,5-TRIMETHYL HEXANOATE explodes with great violence when rapidly heated to a critical temperature; pure form is shock sensitive and detonable [Bretherick 1979 p. 602].

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 13122-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13122-18:
(7*1)+(6*3)+(5*1)+(4*2)+(3*2)+(2*1)+(1*8)=54
54 % 10 = 4
So 13122-18-4 is a valid CAS Registry Number.
InChI:InChI:1S/C13H26O3/c1-10(9-12(2,3)4)8-11(14)15-16-13(5,6)7/h10H,8-9H2,1-7H3

13122-18-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl peroxy-3,5,5-trimethylhexanoate

1.2 Other means of identification

Product number -
Other names 42s

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13122-18-4 SDS

13122-18-4Downstream Products

13122-18-4Relevant articles and documents

Method for producing acyl peroxides

-

Page/Page column 5, (2010/02/17)

The invention relates to a method for producing acyl peroxides. According to said method, an acyl compound is reacted with an organic hydroperoxide and a base, the pH of the two-phase mixture so obtained is adjusted to 6 to 13, the obtained organic phase is extracted with an aqueous solution of a base and the aqueous extract is recirculated to the reaction step. The method according to the invention allows the recirculation of unreacted hydroperoxide to the reaction step.

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