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2123-88-8

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2123-88-8 Usage

General Description

t-Butyl peroxylaurate is an organic peroxide compound used as a free radical initiator in polymerization and crosslinking reactions. It has the chemical formula C8H18O5 and a molecular weight of 194.23 g/mol. t-Butyl peroxylaurate is a clear, colorless liquid with a characteristic odor, and it is highly reactive and unstable, requiring careful handling and storage. It is primarily used in the production of various polymers, such as polyethylene, polypropylene, and polystyrene. Additionally, it is used in the production of specialty chemicals and pharmaceuticals. However, due to its potential hazards, including flammability and toxicity, proper safety precautions and regulatory compliance are essential 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

2123-88-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl dodecaneperoxoate

1.2 Other means of identification

Product number -
Other names tert-Butyl-lauroyl-peroxid

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:2123-88-8 SDS

2123-88-8Downstream Products

2123-88-8Relevant articles and documents

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.

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