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13467-82-8

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13467-82-8 Usage

General Description

Tert-butyl octaneperoxoate is a chemical compound commonly used as a radical initiator in polymerization reactions. It is composed of a tert-butyl group attached to an octaneperoxoate group, and its molecular formula is C14H30O4. As a peroxide, it can decompose into free radicals when exposed to heat or light, making it useful for initiating the formation of polymers such as polyethylene and polystyrene. However, it is also highly reactive and must be handled with care due to its potential for explosive decomposition. Tert-butyl octaneperoxoate is commonly used in industrial and laboratory settings for polymer production and research.

Check Digit Verification of cas no

The CAS Registry Mumber 13467-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,6 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13467-82:
(7*1)+(6*3)+(5*4)+(4*6)+(3*7)+(2*8)+(1*2)=108
108 % 10 = 8
So 13467-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O3/c1-5-6-7-8-9-10-11(13)14-15-12(2,3)4/h5-10H2,1-4H3

13467-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl octaneperoxoate

1.2 Other means of identification

Product number -
Other names t-butyl oxalate

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:13467-82-8 SDS

13467-82-8Relevant articles and documents

Mass Spectral Fragmentations and Gas Phase Reactions of t-Butyl Peresters

Madhusudanan, K. P.,Misra, Dharmendra,Singh, Chandan

, p. 398 - 401 (2007/10/02)

The mass spectral behaviour of a few aliphatic and aromatic peresters has been studied under electron impact (EI) and chemical ionization (CI) conditions.Under EI, fragmentation of the molecules occurs mainly by C-C cleavage at either side of the carbonyl group.The C4H9O+ ion generated by the attack of the CI reagent on the sample molecule adds on to the molecule leading to (M + 73)+ ion in the CI (i-C4H10) spectra while with the more basic reagent, NH3, clustering of the molecule around NH4+ ion is the predominant pathway for ion formation.

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