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Triethylene Glycol Diacetate is an odorless, clear, colorless liquid that serves as a versatile chemical compound with various applications across different industries.

111-21-7

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111-21-7 Usage

Uses

Used in Plasticizer Industry:
Triethylene Glycol Diacetate is used as a plasticizer to enhance the flexibility, workability, and durability of various materials, particularly in the production of plastics and resins.
Used in Solar Cell Industry:
In the solar cell industry, Triethylene Glycol Diacetate is used in the preparation method of solar cell grid line slurry, which is essential for the manufacturing process of solar cells. This application helps improve the efficiency and performance of solar cells by ensuring proper electrical conductivity and grid line formation.
General Description:
Triethylene Glycol Diacetate is an odorless clear colorless liquid, making it suitable for use in various applications without affecting the color or odor of the final product. (NTP, 1992)

Air & Water Reactions

Water soluble. Ca(C12H23C6H4SO3)2 dissolved in C4H9OH

Reactivity Profile

TRIETHYLENE GLYCOL DIACETATE can undergo polymerization upon exposure to extreme heat or light. TRIETHYLENE GLYCOL DIACETATE is incompatible with acetic acid. TRIETHYLENE GLYCOL DIACETATE is also incompatible with peroxides, strong oxidants, oxygen scavengers and heavy metal compounds. .

Fire Hazard

TRIETHYLENE GLYCOL DIACETATE is combustible.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 111-21-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111-21:
(5*1)+(4*1)+(3*1)+(2*2)+(1*1)=17
17 % 10 = 7
So 111-21-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O6/c1-9(11)15-7-5-13-3-4-14-6-8-16-10(2)12/h3-8H2,1-2H3

111-21-7 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (L12789)  Triethylene glycol diacetate, 98%   

  • 111-21-7

  • 250g

  • 505.0CNY

  • Detail
  • Alfa Aesar

  • (L12789)  Triethylene glycol diacetate, 98%   

  • 111-21-7

  • 1000g

  • 1588.0CNY

  • Detail

111-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name TRIETHYLENE GLYCOL DIACETATE

1.2 Other means of identification

Product number -
Other names Ethanol, 2,2‘-[1,2-ethanediylbis(oxy)]bis-, 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:111-21-7 SDS

111-21-7Synthetic route

acetic anhydride
108-24-7

acetic anhydride

2,2'-[1,2-ethanediylbis(oxy)]bisethanol
112-27-6

2,2'-[1,2-ethanediylbis(oxy)]bisethanol

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate
111-21-7

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate

Conditions
ConditionsYield
With phosphorus pentoxide; silica gel at 20℃;93%
anion exchange resin Vionit CS3 at 90 - 95℃; for 2h; Acetylation;86%
oxirane
75-21-8

oxirane

acetic acid
64-19-7

acetic acid

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate
111-21-7

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate

acetic acid
64-19-7

acetic acid

2,2'-[1,2-ethanediylbis(oxy)]bisethanol
112-27-6

2,2'-[1,2-ethanediylbis(oxy)]bisethanol

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate
111-21-7

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate

Conditions
ConditionsYield
With sulfuric acid; benzene
Ketene
463-51-4

Ketene

2,2'-[1,2-ethanediylbis(oxy)]bisethanol
112-27-6

2,2'-[1,2-ethanediylbis(oxy)]bisethanol

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate
111-21-7

(ethane-1,2-diylbisoxy)bis(ethane-2,1-diyl) diacetate

Conditions
ConditionsYield
With sulfuric acid

111-21-7Downstream Products

111-21-7Related news

Tailoring novel fibrillar morphologies in poly(vinylidene fluoride) membranes using a low toxic TRIETHYLENE GLYCOL DIACETATE (cas 111-21-7) (TEGDA) diluent08/20/2019

Thermally induced phase separation (TIPS) process is an important method to prepare high performance poly(vinylidene fluoride) (PVDF) membranes, but the toxic diluent for membrane formation poses environmental problems. In the present paper, triethylene glycol diacetate (TEGDA) was introduced as...detailed

111-21-7Relevant academic research and scientific papers

P2O5 / SiO2 as a mild and efficient reagent for acylation of alcohols, phenols and amines under solvent-free conditions

Eshghi, Hossein,Shafieyoon, Parvaneh

, p. 802 - 805 (2007/10/03)

P2O5 / SiO2 is a highly efficient reagent for the acetylations of a variety of alcohols, phenols and amines with acetic anhydride under solvent-free conditions. Primary, secondary, allylic and benzylic alcohols, diols and phenols with electron-donating or withdrawing substituents can be easily acetylated in good to excellent yield.

Process for preventing consolidation of p-dichlorobenzene

-

, (2008/06/13)

A triethylene glycol derivative is added to p-dichlorobenzene so as to prevent consolidation and improve flowability of p-dichlorobenzene.

THE SOLUBILITY OF CARBON DIOXIDE IN SOME ACETIC ACID ESTERS

Vilcu, Rodica,Gainar, Ion,Maior, Ovidiu,Anitescu, Gheorghe

, p. 875 - 878 (2007/10/03)

The absorption of carbon dioxide in organic solvents containing acetyl groups (ethylene glycol diacetate, diethylene glycol diacetate, triethylene glycol diacetate, propylene glycol diacetate, ethyl cellosolve acetate, 1,4-butanediol diacetate, glycerol triacetate and β-phenyl acetate) is studied. Bunsen absorption coefficients in the range of 5 to 50 atm and at 25 deg C are obtained. Some considerations about the correlation between absorptive capacity and the molecular structure of these organic compounds are presented.

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