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10441-87-9

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10441-87-9 Usage

Description

2-Ethyl-2-(acetoxymethyl)-1,3-propanediol diacetate is a versatile chemical compound that serves as a plasticizer, solvent, and coupling agent in various industrial applications. It is recognized for its capacity to enhance the flexibility and durability of materials, making it an essential additive in the production of polymers, resins, adhesives, sealants, coatings, and paints.

Uses

Used in Plastics and Resins Industry:
2-Ethyl-2-(acetoxymethyl)-1,3-propanediol diacetate is used as a plasticizer to improve the flexibility and durability of various polymers and resins. Its incorporation into these materials results in products with enhanced physical properties, such as increased toughness and resistance to environmental stress.
Used in Adhesives and Sealants:
In the adhesives and sealants industry, 2-Ethyl-2-(acetoxymethyl)-1,3-propanediol diacetate is used as a key component to enhance the bonding strength and durability of these products. Its presence in adhesive formulations contributes to better adhesion and resistance to wear and tear, making it suitable for a wide range of applications, from construction to automotive manufacturing.
Used in Coatings and Paints:
2-Ethyl-2-(acetoxymethyl)-1,3-propanediol diacetate is employed as a plasticizer in the production of coatings and paints, where it helps to improve the flow and application properties of these materials. Its use in this industry results in coatings with better adhesion, flexibility, and resistance to cracking, making it a valuable additive in the formulation of various types of paint and protective coatings.
Used as a Solvent:
In various industrial processes, 2-Ethyl-2-(acetoxymethyl)-1,3-propanediol diacetate is used as a solvent due to its ability to dissolve a wide range of substances. Its solubility properties make it a useful component in the formulation of cleaning agents, degreasers, and other solutions where the ability to dissolve various compounds is required.
Used as a Coupling Agent:
2-Ethyl-2-(acetoxymethyl)-1,3-propanediol diacetate also serves as a coupling agent in certain industrial applications, where it helps to improve the compatibility and interaction between different materials. Its use in this capacity can lead to the development of new materials with enhanced properties, such as improved adhesion, stability, or reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 10441-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10441-87:
(7*1)+(6*0)+(5*4)+(4*4)+(3*1)+(2*8)+(1*7)=69
69 % 10 = 9
So 10441-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O6/c1-5-12(6-16-9(2)13,7-17-10(3)14)8-18-11(4)15/h5-8H2,1-4H3

10441-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-bis(acetyloxymethyl)butyl acetate

1.2 Other means of identification

Product number -
Other names 1,3-Propanediol,2-((acetyloxy)methyl)-2-ethyl-,diacetate

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:10441-87-9 SDS

10441-87-9Downstream Products

10441-87-9Relevant articles and documents

Characteristics of retention and enthalpies of sorption from the gas phase of esters of trimethylolpropane and С2–С5 acids on DB-1 stationary phase

Krasnykh,Aleksandrov, A. Yu.,Sokolova,Levanova

, p. 398 - 402 (2017/02/26)

Characteristics of retention and their temperature dependences, along with the thermodynamic characteristics of sorption on DB-1 nonpolar phase, are determined in the temperature range of 220–280°C for 21 mono-, di-, and trisubstituted esters of trimethylolpropane and monobasic acids with a variety of structures containing from 2 to 6 carbon atoms.

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