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Methaneperoxoic acid, 1,1-dimethylethyl ester, also known as tert-butyl hydroperoxide (TBHP), is an organic compound with the chemical formula C4H10O2. It is a colorless, highly reactive, and unstable liquid that is widely used as an oxidizing agent in various chemical reactions. TBHP is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds due to its ability to generate free radicals, which can initiate oxidation processes. It is also used as a bleaching agent and a polymerization initiator. However, due to its hazardous nature, TBHP requires careful handling and storage, as it can decompose explosively when exposed to heat, light, or impurities.

819-50-1

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819-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 819-50-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 819-50:
(5*8)+(4*1)+(3*9)+(2*5)+(1*0)=81
81 % 10 = 1
So 819-50-1 is a valid CAS Registry Number.

819-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylpropan-2-yl)oxy formate

1.2 Other means of identification

Product number -
Other names tert-butyl peroxoformate

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:819-50-1 SDS

819-50-1Downstream Products

819-50-1Relevant academic research and scientific papers

Oxidation of Unsaturated Ethers with the System Aluminum Tri-tert-butylate-tert-Butyl Hydroperoxide

Stepovik, L. P.,Martynova, I. M.,Dodonov, V. A.

, p. 1802 - 1806 (2007/10/03)

The system aluminum tri-tert-butylate-tert-butyl hydroperoxide oxidizes alkyl allyl and aryl allyl ethers by the radical mechanism at room temperature. In the process, either the substrate skeleton is preserved and the carbonyl and hydroperoxy groups are introduced, or the carbon-carbon and carbon-oxygen bonds in the allyl moiety are cleaved. In allyl benzyl ether the reaction centers are the methylene groups of the benzyl and allyl fragments.

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