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9004-93-7

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9004-93-7 Usage

Uses

PEG-EH can form a blend with polyvinylidene fluoride (PVDF) which can be used in the preparation of electrolytes for lithium batteries. It is also used as an additive for the development of ionization methods for mass spectroscopy.

General Description

Poly(ethylene glycol) bis(2-ethylhexanoate) (PEG-EH) is an ethylene acrylic elastomer that can be used as a low volatile plasticizer.

Check Digit Verification of cas no

The CAS Registry Mumber 9004-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,0 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 9004-93:
(6*9)+(5*0)+(4*0)+(3*4)+(2*9)+(1*3)=87
87 % 10 = 7
So 9004-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O4/c1-5-9-11-15(7-3)17(19)21-13-14-22-18(20)16(8-4)12-10-6-2/h15-16H,5-14H2,1-4H3

9004-93-7 Well-known Company Product Price

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  • Aldrich

  • (450596)  Poly(ethyleneglycol)bis(2-ethylhexanoate)  average Mn ~650

  • 9004-93-7

  • 450596-250ML

  • 519.48CNY

  • Detail

9004-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Poly(ethylene glycol) bis(2-ethylhexanoate)

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:9004-93-7 SDS

9004-93-7Downstream Products

9004-93-7Relevant articles and documents

SYNTHESIS OF TRIETHYLENE GLYCOL BIS(2-ETHYLHEXANOATE)

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Paragraph 0037, (2020/06/05)

A process for the transesterification of methyl-2- ethylhexanoate with triethylene glycol to produce triethylene glycol di-2-ethylhexanoate is provided. In the process, methyl-2- ethylhexanoate is combined with triethylene glycol to form a first mixture. The first mixture is heated in the presence of a catalyst to form a second mixture comprising methanol and triethylene glycol di-2-ethylhexanoate. Methanol is separated from the second mixture to yield triethylene glycol di-2-ethylhexanoate. Na2CO3, CS2CO3, K2CO3, Rb2CO3, sodium methoxide or titanium isopropoxide are suitable catalysts.

METHOD FOR PRODUCING AN ESTER

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Page/Page column 4, (2017/12/13)

Disclosed is a method for production of an ester obtained from a reaction between at least one alcohol having at least one hydroxyl group, such as a diol, and at least one linear of branched C3-C20 monocarboxylic acid, said reaction being performed in presence of at least one azeotropic solvent and optionally at least one antioxidant. Said method comprises the steps of (a) charging said alcohol, said monocarboxylic acid, and said azeotropic solvent and optionally said antioxidant to a reactor, (b) subjecting said alcohol and said carboxylic acid to esterification under reflux, (c) removing azeotropic solvent and unreacted carboxylic acid from yielded reaction mixture, (d) steam stripping off residual unreacted carboxylic acid, (e) neutralising yielded reaction product with an aqueous base, (f) separating water and organic phases, (g) recovering said organic phase and evaporating residual water, and (h) filtering off said antioxidant and possible remaining salts in yielded reaction product. The method is preferably performed in at least one reactor equipped with reflux, at least one vacuum pump, evaporation/distillation, steam stripping and decantation, and at least one filtration unit and optionally at least one coalescer filtre.

Method for Producing Polyol Esters

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Paragraph 0062-0063, (2016/01/09)

A process for preparing polyol esters by reacting polyols with linear or branched aliphatic monocarboxylic acids having 3 to 20 carbon atoms, is characterized in that a mixture of the starting compounds is allowed to react in the presence of a Lewis acid containing at least one element of groups 4 to 14 of the periodic table of the elements as a catalyst and in the presence of an adsorbent with removal of the water formed, and then the crude ester obtained is aftertreated by adding a further adsorbent which is an acidic activated carbon having a pH of 1 to 6.5.

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