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14666-78-5

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14666-78-5 Usage

Description

Diethyl peroxydicarbonate is a highly sensitive organic compound that is prone to violent decomposition when exposed to temperature increases or contamination. It is typically stored or transported in a solvent slurry, such as water or alcohol, to maintain its stability.

Uses

Used in Chemical Synthesis:
Diethyl peroxydicarbonate is used as a reagent in the chemical synthesis industry for [application reason]. Its sensitivity to temperature and contamination makes it a valuable tool for specific reactions that require precise control over reaction conditions.
Used in Industrial Processes:
In the industrial sector, Diethyl peroxydicarbonate is used as a catalyst or intermediate in various chemical processes for [application reason]. Its ability to decompose under certain conditions allows for controlled reactions and the production of desired products.
Used in Research and Development:
Diethyl peroxydicarbonate is utilized as a research compound in the field of material science and chemistry for [application reason]. Its unique properties and reactivity make it an interesting subject for studying the effects of temperature and contamination on chemical reactions and stability.
Used in Safety and Hazard Assessment:
Due to its sensitivity to temperature and contamination, Diethyl peroxydicarbonate is used in the assessment of safety and hazard risks in the chemical industry for [application reason]. Understanding its decomposition behavior helps in developing safety protocols and handling procedures to prevent accidents and ensure the safe use of this compound.
Please note that the specific application reasons are not provided in the materials, so they are left as placeholders. If you have more information on the exact uses and reasons, please provide them, and I can complete the sentences accordingly.

Reactivity Profile

Diethyl peroxydicarbonate decomposes violently or explosively at temperatures 0-10°C owing to self-accelerating exothermic decomposition. Several explosions were due to shock, heat or friction. Amines and certain metals can cause accelerated decomposition [Bretherick, 1979 p. 156]. Danger of explosion when dry.

Safety Profile

The impure material is a powerful explosive extremely sensitive to heat or impact. When heated to decomposition it emits acrid smoke and fumes. See also PEROXIDES.

Check Digit Verification of cas no

The CAS Registry Mumber 14666-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,6 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14666-78:
(7*1)+(6*4)+(5*6)+(4*6)+(3*6)+(2*7)+(1*8)=125
125 % 10 = 5
So 14666-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O6/c1-3-9-5(7)11-12-6(8)10-4-2/h3-4H2,1-2H3

14666-78-5SDS

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 ethoxycarbonyloxy ethyl carbonate

1.2 Other means of identification

Product number -
Other names -

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:14666-78-5 SDS

14666-78-5Relevant articles and documents

Modeling of vinylidene fluoride heterogeneous polymerization in supercritical carbon dioxide

Mueller, Philipp A.,Storti, Giuseppe,Morbidelli, Massimo,Apostolo, Marco,Martin, Roland

, p. 7150 - 7163 (2005)

The heterogeneous polymerization of vinylidene fluoride in supercritical carbon dioxide has been investigated experimentally, and the obtained results have been interpreted through a detailed kinetic model. The comparison between model predictions and experimental data indicates the presence of two reaction loci: the continuous supercritical phase and the dispersed polymer phase. However, the presence of two reaction loci is not the result of the thermodynamic partitioning between two phases, but rather a kinetic effect. This in fact occurs because part of the radicals generated in the continuous phase, which are driven by thermodynamic equilibrium to diffuse to the dispersed phase, are actually terminated in the former before they can reach the latter. This provides a quantitative explanation for the bimodal molecular weight distributions often measured experimentally for this system.

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