2123-88-8 Usage
Uses
Used in Polymer Production Industry:
t-Butyl peroxylaurate is used as a free radical initiator for the production of various polymers, such as polyethylene, polypropylene, and polystyrene. It facilitates the polymerization process by generating free radicals, which initiate the formation of polymer chains.
Used in Specialty Chemicals and Pharmaceuticals Industry:
t-Butyl peroxylaurate is used as a free radical initiator in the production of specialty chemicals and pharmaceuticals. Its reactivity enables the synthesis of complex molecules and the formation of specific chemical bonds, contributing to the development of innovative products in these industries.
However, due to the potential hazards associated with t-Butyl peroxylaurate, including flammability and toxicity, it is crucial to adhere to proper safety precautions and regulatory compliance when working with t-Butyl peroxylaurate.
Check Digit Verification of cas no
The CAS Registry Mumber 2123-88-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2123-88:
(6*2)+(5*1)+(4*2)+(3*3)+(2*8)+(1*8)=58
58 % 10 = 8
So 2123-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H32O3/c1-5-6-7-8-9-10-11-12-13-14-15(17)18-19-16(2,3)4/h5-14H2,1-4H3
2123-88-8Relevant academic research and scientific papers
Decarboxylative Borylation of mCPBA-Activated Aliphatic Acids
Wei, Dian,Liu, Tu-Ming,Zhou, Bo,Han, Bing
supporting information, p. 234 - 238 (2020/01/02)
A decarboxylative borylation of aliphatic acids for the synthesis of a variety of alkylboronates has been developed by mixing m-chloroperoxybenzoic acid (mCPBA)-activated fatty acids with bis(catecholato)diboron in N,N-dimethylformamide (DMF) at room temperature. A radical chain process is involved in the reaction which initiates from the B-B bond homolysis followed by the radical transfer from the boron atom to the carbon atom with subsequent decarboxylation and borylation.
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.
