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2-phenoxyethyl carbonate(2:1) is a chemical compound that consists of two molecules of 2-phenoxyethyl carbonate combined with one molecule of another substance. It is characterized by its low volatility and good solvating power, which makes it an effective additive in a variety of products. Known for its low toxicity and minimal environmental impact, it is a favorable choice for many manufacturing processes.

22855-36-3

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22855-36-3 Usage

Uses

Used in Polymer Production:
2-phenoxyethyl carbonate(2:1) is used as a plasticizer and solvent for enhancing the flexibility and workability of polymers. Its low volatility contributes to the stability of the final product, while its good solvating power aids in the processing of polymers.
Used in Resin Manufacturing:
In the resin industry, 2-phenoxyethyl carbonate(2:1) serves as a crucial component that improves the flow and handling properties of resins. Its effectiveness in this application is attributed to its solubility characteristics and low toxicity, which are desirable for creating safe and high-quality resins.
Used in Coating Formulation:
2-phenoxyethyl carbonate(2:1) is utilized as a solvent in coating formulations to improve the solubility of other components and to facilitate the application process. Its low volatility ensures that the coatings dry with minimal environmental emissions, and its good solvency helps in achieving a uniform and smooth finish.
Used in Industrial Applications:
2-phenoxyethyl carbonate(2:1) is used as a versatile solvent and plasticizer across various industries for its ability to dissolve a wide range of substances and to modify the properties of materials. Its low toxicity and eco-friendly nature make it a preferred choice for applications where environmental and health concerns are paramount.

Check Digit Verification of cas no

The CAS Registry Mumber 22855-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,5 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22855-36:
(7*2)+(6*2)+(5*8)+(4*5)+(3*5)+(2*3)+(1*6)=113
113 % 10 = 3
So 22855-36-3 is a valid CAS Registry Number.

22855-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-phenoxyethyl) carbonate

1.2 Other means of identification

Product number -
Other names carbonic acid bis-(2-phenoxy-ethyl ester)

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:22855-36-3 SDS

22855-36-3Downstream Products

22855-36-3Relevant academic research and scientific papers

Carbonates as reactants for the production of fine chemicals: The synthesis of 2-phenoxyethanol

Ziosi,Tabanelli,Fornasari,Cocchi,Cavani,Righi

, p. 4386 - 4395 (2015/01/09)

The solventless and heterogeneously catalysed synthesis of 2-phenoxyethanol (ethylene glycol monophenyl ether) via the reaction between phenol and ethylene carbonate was investigated using Na-mordenite catalysts as an alternative to the industrial process using ethylene oxide and homogeneous basic conditions. Under specific reaction conditions, it was possible to obtain total selectivity to phenoxyethanol at up to 75% phenol conversion and 82% selectivity at total phenol conversion in 5-7 hours of reaction time and using a moderate excess of ethylene carbonate. The main by-product was the linear carbonate of phenoxyethanol, bis(2-phenoxyethyl)carbonate (selectivity 15%), which could then be converted to phenoxyethanol by reacting with phenol in basic medium with 100% yield; so overall, the phenoxyethanol yield was as high as 97%. With a stoichiometric feed of phenol and ethylene carbonate, the maximum conversion of phenol was just 60%, still with 100% selectivity to phenoxyethanol. An autocatalytic phenomenon was also observed due to the higher basicity of 2-phenoxyethanol compared to phenol, which overlapped the Na-catalyzed activation of phenol. Starting from a commercial Na-mordenite, which showed significant deactivation, and by applying a post-treatment aimed at the reduction of microporosity, it was possible to minimize both the deactivation and Na leaching while keeping the selectivity enhancement effect shown by the mordenite structure.

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