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Ethylene glycol diglycidyl ether is a chemical compound that is commonly used as an absorbent due to its high carbon dioxide absorbing capacity.

2224-15-9

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2224-15-9 Usage

Uses

Used in Absorbent Applications:
Ethylene glycol diglycidyl ether is used as an absorbent for its high carbon dioxide absorbing capacity, making it suitable for various industrial applications where carbon dioxide removal is necessary.

Check Digit Verification of cas no

The CAS Registry Mumber 2224-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2224-15:
(6*2)+(5*2)+(4*2)+(3*4)+(2*1)+(1*5)=49
49 % 10 = 9
So 2224-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3.C2H4/c1(5-3-8-5)7-2-6-4-9-6;1-2/h5-6H,1-4H2;1-2H2

2224-15-9 Well-known Company Product Price

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  • TCI America

  • (E0342)  Ethylene Glycol Diglycidyl Ether (so called)  

  • 2224-15-9

  • 25g

  • 260.00CNY

  • Detail
  • TCI America

  • (E0342)  Ethylene Glycol Diglycidyl Ether (so called)  

  • 2224-15-9

  • 500g

  • 925.00CNY

  • Detail

2224-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethylene glycol diglycidyl ether

1.2 Other means of identification

Product number -
Other names 1,2-bis-oxiranylmethoxy-ethane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adsorbents and absorbents
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:2224-15-9 SDS

2224-15-9Synthetic route

ethylene glycol
107-21-1

ethylene glycol

epichlorohydrin
106-89-8

epichlorohydrin

ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

Conditions
ConditionsYield
With tetrabutyl-ammonium chloride; water; sodium hydroxide at 40℃; for 0.75h;89%
With fluoroboric acid; trifluorormethanesulfonic acid; boron trifluoride at 40 - 65℃; for 5h; Temperature; Reagent/catalyst; Sonication; Inert atmosphere; Molecular sieve; Large scale;55.7%
With potassium hydroxide; benzyltrioctylammonium chloride at 40℃; for 0.75h;54%
1,10-Dichloro-4,7-dioxa-2,9-decanediol
13078-45-0

1,10-Dichloro-4,7-dioxa-2,9-decanediol

ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

Conditions
ConditionsYield
With sodium hydroxide Dehydrochlorination;40 g
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

tert-butyl glycidyl ether
7580-85-0

tert-butyl glycidyl ether

C14H28O6

C14H28O6

Conditions
ConditionsYield
With boron trifluoride diethyl etherate at 80℃; for 3h;99.3%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

Ethyl 1H,1H-perfluorooctanoxyacetate
134918-67-5

Ethyl 1H,1H-perfluorooctanoxyacetate

1,1-dimethylhydrazine
57-14-7

1,1-dimethylhydrazine

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(1H,1H-perfluorooctanoxyacetyl)imide>

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(1H,1H-perfluorooctanoxyacetyl)imide>

Conditions
ConditionsYield
In methanol Heating;99%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

methyl 2,4,4,5,7,7,8,8,9,9,9-undecafluoro-2,5-bis(trifluoromethyl)-3,6-dioxanonanoate
26131-32-8

methyl 2,4,4,5,7,7,8,8,9,9,9-undecafluoro-2,5-bis(trifluoromethyl)-3,6-dioxanonanoate

1,1-dimethylhydrazine
57-14-7

1,1-dimethylhydrazine

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2,5-dimethyl-3,6-dioxanonanoyl)imide>

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2,5-dimethyl-3,6-dioxanonanoyl)imide>

Conditions
ConditionsYield
In methanol Heating;96%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

Methyl perfluoro-2,5,8,11-tetramethyl-3,6,9,12-tetraoxapentadecanoate
133609-46-8

Methyl perfluoro-2,5,8,11-tetramethyl-3,6,9,12-tetraoxapentadecanoate

1,1-dimethylhydrazine
57-14-7

1,1-dimethylhydrazine

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2,5,8,11-tetramethyl-3,6,9,12-tetraoxapentadecanoyl)imide>

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2,5,8,11-tetramethyl-3,6,9,12-tetraoxapentadecanoyl)imide>

Conditions
ConditionsYield
In methanol Heating;96%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

carbon dioxide
124-38-9

carbon dioxide

4-((2-((2-oxo-1,3-dioxolan-4-yl)methoxy)ethoxy)methyl)-1,3-dioxolan-2-one

4-((2-((2-oxo-1,3-dioxolan-4-yl)methoxy)ethoxy)methyl)-1,3-dioxolan-2-one

Conditions
ConditionsYield
With tetrabutylammomium bromide at 110℃; under 7500.75 Torr; for 3h;94%
With C42H44N8O6Zn(2+)*2Cl(1-) In neat (no solvent) at 100℃; under 750.075 Torr; for 24h; Kinetics; Pressure; Temperature; Autoclave;94.5%
With C44H20AlCl9N4; bis(triphenylphosphine)iminium chloride In neat (no solvent) at 120℃; under 22502.3 Torr; for 1h; Autoclave;
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

Methyl perfluoro-2,5,8-trimethyl-3,6,9-trioxadodecanoate
39187-47-8

Methyl perfluoro-2,5,8-trimethyl-3,6,9-trioxadodecanoate

1,1-dimethylhydrazine
57-14-7

1,1-dimethylhydrazine

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2,5,8-trimethyl-3,6,9-trioxadodecanoyl)imide>

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2,5,8-trimethyl-3,6,9-trioxadodecanoyl)imide>

Conditions
ConditionsYield
In methanol Heating;94%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

diethylene glycol mono(tert-butyl)ether
110-09-8

diethylene glycol mono(tert-butyl)ether

C16H32O7

C16H32O7

Conditions
ConditionsYield
With Amberlyst-15 resin at 70℃; for 5h;93.2%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

methyl undecafluoro-2-methyl-3-oxahexanoate
13140-34-6

methyl undecafluoro-2-methyl-3-oxahexanoate

1,1-dimethylhydrazine
57-14-7

1,1-dimethylhydrazine

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2-methyl-3-oxahexanoyl)imide>

N,N,N',N'-Tetramethyl-4,7-dioxa-2,9-dihydroxy-1,10-decanediamine-N,N'-bis<(perfluoro-2-methyl-3-oxahexanoyl)imide>

Conditions
ConditionsYield
In methanol Heating;92%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1-t-Butoxycarbonylpiperazine
57260-71-6

1-t-Butoxycarbonylpiperazine

ethylene glycol di<2-hydroxy-3-(N'-tert-butoxycarbonylpiperazinyl)>propyl ether
158328-41-7

ethylene glycol di<2-hydroxy-3-(N'-tert-butoxycarbonylpiperazinyl)>propyl ether

Conditions
ConditionsYield
In chloroform for 24h; Heating;91%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

ethane-1,2-dithiol
540-63-6

ethane-1,2-dithiol

C10H20O4S2
1273318-54-9

C10H20O4S2

Conditions
ConditionsYield
With N-benzyl-trimethylammonium hydroxide at 0℃; for 0.5h; Neat (no solvent); regiospecific reaction;90%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

(3-chloropropyl)triethoxysilane
5089-70-3

(3-chloropropyl)triethoxysilane

2,5-Dimercapto-1,3,4-thiadiazole
1072-71-5

2,5-Dimercapto-1,3,4-thiadiazole

C19H36N2O7S3Si

C19H36N2O7S3Si

Conditions
ConditionsYield
Stage #1: ethylene glycol diglycidyl ether; 2,5-Dimercapto-1,3,4-thiadiazole In methanol at 60℃; for 18h;
Stage #2: With sodium methylate In methanol at 20℃; for 0.5h;
Stage #3: (3-chloropropyl)triethoxysilane In methanol at 70℃; for 12h;
90%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

hexan-1-amine
111-26-2

hexan-1-amine

Bistriethylene glycol
92237-82-6

Bistriethylene glycol

Conditions
ConditionsYield
at 120℃; for 4h;82%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

Trimethylenediamine
109-76-2

Trimethylenediamine

1,4-dioxa-8,12-diaza-cyclopentadecane-6,14-diol

1,4-dioxa-8,12-diaza-cyclopentadecane-6,14-diol

Conditions
ConditionsYield
With sodium hydride In water Cycloaddition; Heating;82%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

N,N'-dibenzyl-1,3-diaminopropane
10239-34-6

N,N'-dibenzyl-1,3-diaminopropane

8,11-dibenzyl-1,4-dioxa-8,11-diaza-cyclotetradecane-6,13-diol

8,11-dibenzyl-1,4-dioxa-8,11-diaza-cyclotetradecane-6,13-diol

Conditions
ConditionsYield
With sodium hydride In water Cycloaddition; Heating;80%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

C8H16N6O4

C8H16N6O4

Conditions
ConditionsYield
With sodium azide; ammonium chloride In methanol; water at 80℃; for 24h;80%
With sodium azide In methanol; water at 80℃;
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

phenyl isocyanate
103-71-9

phenyl isocyanate

1,6-bis(3-phenyloxazolidin-2-on-5-yl)-2,5-dioxahexane

1,6-bis(3-phenyloxazolidin-2-on-5-yl)-2,5-dioxahexane

Conditions
ConditionsYield
Stage #1: ethylene glycol diglycidyl ether With Tributylphosphine oxide; lithium bromide In toluene for 2h; Heating;
Stage #2: phenyl isocyanate In toluene for 12h; Heating; Further stages.;
78%
carbon disulfide
75-15-0

carbon disulfide

ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1,6-bis(oxathiolane-2-thione-5-yl)-2,5-dioxahexane

1,6-bis(oxathiolane-2-thione-5-yl)-2,5-dioxahexane

Conditions
ConditionsYield
Stage #1: ethylene glycol diglycidyl ether With lithium bromide In dichloromethane for 2h; Heating;
Stage #2: carbon disulfide In dichloromethane for 10h; Heating; Further stages.;
76%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1,4,10,13-tetraoxa-7,16-diazacyclooctadecane
23978-55-4

1,4,10,13-tetraoxa-7,16-diazacyclooctadecane

A

3,10,23,29-tetrahydroxy-5,8,15,18,25,28,35,38,43,46,51,54-dodecaoxa-1,12,21,32-tetraazatricyclo<30.30.8.812,21>hexapentacontane
119017-33-3

3,10,23,29-tetrahydroxy-5,8,15,18,25,28,35,38,43,46,51,54-dodecaoxa-1,12,21,32-tetraazatricyclo<30.30.8.812,21>hexapentacontane

B

3,10-dihydroxy-5,8,15,18,23,26-hexaoxa-1,12-diazabicyclo<10.8.8>octacosane
117536-17-1

3,10-dihydroxy-5,8,15,18,23,26-hexaoxa-1,12-diazabicyclo<10.8.8>octacosane

Conditions
ConditionsYield
In tetrahydrofuran; ethanol for 10h; Heating;A 1%
B 69%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1,4,10,13-tetraoxa-7,16-diazacyclooctadecane
23978-55-4

1,4,10,13-tetraoxa-7,16-diazacyclooctadecane

3,10-dihydroxy-5,8,15,18,23,26-hexaoxa-1,12-diazabicyclo<10.8.8>octacosane

3,10-dihydroxy-5,8,15,18,23,26-hexaoxa-1,12-diazabicyclo<10.8.8>octacosane

Conditions
ConditionsYield
In tetrahydrofuran; ethanol Heating;69%
carbon disulfide
75-15-0

carbon disulfide

ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

phenyl isocyanate
103-71-9

phenyl isocyanate

5-(6-oxathiolan-2-thione-2,5-dioxahexan-5-yl)-3-phenyloxazolidin-2-one

5-(6-oxathiolan-2-thione-2,5-dioxahexan-5-yl)-3-phenyloxazolidin-2-one

Conditions
ConditionsYield
Stage #1: ethylene glycol diglycidyl ether With lithium bromide In tetrahydrofuran for 0.5h; Inert atmosphere; Reflux;
Stage #2: phenyl isocyanate In tetrahydrofuran Inert atmosphere; Reflux;
Stage #3: carbon disulfide In tetrahydrofuran at 20℃; for 7h; Inert atmosphere;
67%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

ethylamine
75-04-7

ethylamine

1-Ethylamino-3-[2-(3-ethylamino-2-hydroxy-propoxy)-ethoxy]-propan-2-ol
92237-85-9

1-Ethylamino-3-[2-(3-ethylamino-2-hydroxy-propoxy)-ethoxy]-propan-2-ol

Conditions
ConditionsYield
In water for 50h; Ambient temperature;64%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1,10-diamino-4,7-dioxadecan-2,9-diol
4454-09-5

1,10-diamino-4,7-dioxadecan-2,9-diol

Conditions
ConditionsYield
With ammonia for 50h; Ambient temperature;63%
carbon disulfide
75-15-0

carbon disulfide

ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

5-[6-oxiran-2,5-dioxahexan]-1,3-oxathiolane-2-thione

5-[6-oxiran-2,5-dioxahexan]-1,3-oxathiolane-2-thione

Conditions
ConditionsYield
With lithium bromide In dichloromethane for 5h; Inert atmosphere; Reflux; regioselective reaction;58%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1,10-Dichloro-4,7-dioxa-2,9-decanediol
13078-45-0

1,10-Dichloro-4,7-dioxa-2,9-decanediol

Conditions
ConditionsYield
With hydrogenchloride56%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

phenyl isocyanate
103-71-9

phenyl isocyanate

5-(6-oxiran-2,5-dioxahexan-5-yl)-3-phenyloxazolidin-2-one

5-(6-oxiran-2,5-dioxahexan-5-yl)-3-phenyloxazolidin-2-one

Conditions
ConditionsYield
Stage #1: ethylene glycol diglycidyl ether With lithium bromide In tetrahydrofuran for 0.5h; Inert atmosphere; Reflux;
Stage #2: phenyl isocyanate In tetrahydrofuran for 6h; Inert atmosphere; Reflux;
54%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1,4,7-tris(tert-butyloxycarbonyl)-1,4,7,10-tetraazacyclododecane
175854-39-4

1,4,7-tris(tert-butyloxycarbonyl)-1,4,7,10-tetraazacyclododecane

C54H102N8O16

C54H102N8O16

Conditions
ConditionsYield
In ethanol for 120h; Heating;53.2%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

Kryptofix 21
31249-95-3

Kryptofix 21

3,10-dihydroxy-5,8,13,18,23-pentaoxa-1,12-diazabicyclo<10.8.5>pentacosane
129940-62-1

3,10-dihydroxy-5,8,13,18,23-pentaoxa-1,12-diazabicyclo<10.8.5>pentacosane

Conditions
ConditionsYield
In tetrahydrofuran; ethanol for 10h; Heating;51%
2,3-dichlorotetrahydrofuran
3511-19-1

2,3-dichlorotetrahydrofuran

ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

1,12-di(3-chloro-2-tetrahydrofuryl)-3,10-dichloro-1,5,8,12-tetraoxadodecane
137675-79-7

1,12-di(3-chloro-2-tetrahydrofuryl)-3,10-dichloro-1,5,8,12-tetraoxadodecane

Conditions
ConditionsYield
With zinc(II) chloride In tetrachloromethane at 40℃; for 1h;50.7%
ethylene glycol diglycidyl ether
2224-15-9

ethylene glycol diglycidyl ether

diaza[12]crown-4
294-92-8

diaza[12]crown-4

A

3,10,20,27-tetrahydroxy-5,8,15,22,25,32,37,42-octaoxa-1,12,18,29-tetraazatricyclo<27.27.5.51,29>tetratetracontane
113769-01-0

3,10,20,27-tetrahydroxy-5,8,15,22,25,32,37,42-octaoxa-1,12,18,29-tetraazatricyclo<27.27.5.51,29>tetratetracontane

B

meso-3,10-dihydroxy-5,8,15,20-tetraoxa-1,12-diazabicyclo<10.5.5>docosane
113769-00-9

meso-3,10-dihydroxy-5,8,15,20-tetraoxa-1,12-diazabicyclo<10.5.5>docosane

Conditions
ConditionsYield
In tetrahydrofuran; ethanol for 10h; Heating;A 14%
B 46%
In tetrahydrofuran; ethanol for 5h; Heating;A 37.5%
B 22.5%
In tetrahydrofuran; ethanol for 10h; Heating;

2224-15-9Relevant academic research and scientific papers

Study of imidazole performance as pseudo-affinity ligand in the purification of IgG from bovine milk

Abbasi, Hassan,Pourrostam-Ravadanaq, Pariya,Safa, Kazem D.

, (2020)

The spherical sepharose CL-6B beads were activated by epichlorohydrin in different epoxy contents (80, 120 and 160 μmolepoxide/mLgel) and, L-histidine and imidazole as pseudo-affinity ligands were covalently immobilized to them. Some linkers with different length, (1,2-ethanediol diglycidyl ether and 1,4-butanediol diglycidyl ether) were synthesized for activation of sepharose and the activated sepharose beads modified with imidazole and the performance of these adsorbents in the purification of immunoglobulin G from bovine milk were evaluated. Among the L-histidine bearing adsorbents, higher adsorption of IgG (0.28 mg/mL) was obtained by adsorbent with the lower concentration of L-histidine. The highest amount of IgG adsorption (0.53 mg/mL) was obtained by imidazole bearing adsorbent with the highest amount of imidazole and Among the adsorbents with synthesized linkers, the adsorbent with 1,2-ethanediol diglycidyl ether showed better performance and was able to purify 0.25 mg/mL IgG with high purity. The synthesized pseudo-affinity adsorbents represented the abbility to purify immunoglobulin G in one-step process with high purity and efficiency.

Quaternary ammonium salt polymer and preparation method and application thereof

-

Paragraph 0061-0062, (2020/05/29)

The invention provides a quaternary ammonium salt polymer and a preparation method and application thereof. The structure of the quaternary ammonium salt polymer contains a hydrophilic group and adjustable hydrophilic/hydrophobic groups such as PPG and PAG. With high surface tension, the quaternary ammonium salt polymer can effectively separate miscellaneous oil wrapping metal cuttings and enablesthe miscellaneous oil to float above a metal processing aqueous solution, so demulsification can be effectively realized, the surface tension of the solution is increased, and the oil floats to a liquid level; and compared with an existing sedimentation additive for a metal working fluid, the quaternary ammonium salt polymer can effectively settle particles in the metal working fluid, and has good application prospects.

Polyoxyethylene ether carboxylic acid dimeric surfactant type drag reducer as well as preparation method and application thereof

-

Paragraph 0087; 0090-0091; 0096; 0099-0100; 0105; 0108-0109, (2019/09/13)

The invention discloses a polyoxyethylene ether carboxylic acid dimeric surfactant type drag reducer as well as a preparation method and application thereof. The polyoxyethylene ether carboxylic aciddimeric surfactant type drag reducer has a structure formula m=2, 3, 4, and n=1, 2, 3. The drag reducer disclosed by the invention is a dimeric surfactant type drag reducer which has a head group of carboxylic acid, and the head group has the advantages of being very good in temperature resistance, salt resistance, environment protection and the like, and is capable of overcoming influence of a high-salt environment upon drag reduction performance, so that the drag reducer disclosed by the invention is high in drag reduction efficiency, good in shearing resistance, long-lasting and stable in drag reduction rate and good in salt resistance; and polyoxyethylene ether carboxylic acid dimeric surfactants of different mass concentrations are dissolved into water, a drag reduction solution whichis high in drag reduction efficiency, good in shearing resistance, long-lasting and stable in drag reduction rate and good in salt resistance can be prepared without any other compounded chemical reagent, solution blending steps are simple, the drag reducer is very convenient to use, and meanwhile, the salt resistance is greatly improved.

Synthesis method of ethylene glycol diglycidyl ether

-

Paragraph 0014; 0015; 0016; 0017; 0018; 0019, (2017/07/21)

The invention relates to a synthesis method of ethylene glycol diglycidyl ether. According to the method, ethylene glycol and epoxy chloropropane are used as raw materials; argon gas is continuously introduced; ring-opening reaction is performed under the combined action of ultrasonic waves and a ternary composite catalyst. A 5A molecular sieve and the ternary composite catalyst are combined, so that the catalyst dosage is greatly reduced; the reaction progress is accelerated; the method is suitable for industrial large-scale production. After the reaction is completed, the temperature is lowered; the mixture and liquid alkaline take ring-closure reaction under the effects of solvent methylbenzene and a 3A molecular sieve supported phase transfer catalyst; the 3A molecular sieve supported phase transfer catalyst has high reaction activity; after the reaction is completed, water washing is very smooth; after methylbenzene and water are removed from a crude product, the ethylene glycol diglycidyl ether with high epoxide value is obtained, wherein the epoxide value can reach 0.78. Compared with the prior art, the synthesis method has the advantages that the selectivity is high; side reactions are few; the reaction effect is good; the yield is high; the product quality is the best; the cost performance is high.

One-pot Three Component Synthesis of ω-(oxathiolan-2-thion-5-yl)-α-oxazolidin-2-ones

Ghrab, Saad,Aroua, Lotfi,Beji, Mohamed

, p. 2397 - 2404 (2017/07/25)

We report a practical and one-pot synthesis of novel series of ω-(oxathiolan-2-thione-5-yl)-α- oxazolidin-2-ones (3a-h). The obtained compounds have been designed, synthesized via reaction of oligoethylene glycols diglycidyl ethers, isocyanate and carbon disulfide in the presence of catalytic amount of lithium bromide. A variety of important oxazolidinone derivatives can be obtained from simple starting materials in good yields and the biological activity of these new products will be investigated in complementary study.

Solvent-free synthesis of dihydroxy dithiacrown ethers

Zoghlami, Houcine,Romdhani-Younes, Moufida,Chaabouni, Mohamed Moncef,Baklouti, Ahmed

scheme or table, p. 881 - 883 (2011/03/20)

The solvent-free reaction of oligoethylene glycol diglycidyl ethers with dimercaptoethane in the presence of benzyltrimethylammonium hydroxide (Triton B) gave, via regiospecific epoxide opening reactions, dihydroxy dithiacrown ethers in excellent yields and in short reaction times.

Diol glycidyl ether-bridged cyclens: Preparation and their applications in gene delivery

Yi, Wen-Jing,Feng, Zhi-Hua,Zhang, Qin-Fang,Zhang, Ji,Li, Ling-Dong,Zhu, Wen,Yu, Xiao-Qi

experimental part, p. 2413 - 2421 (2011/05/14)

Polymeric 1,4,7,10-tetraazacyclododecanes (cyclens) using diol glycidyl ether with different chain length as bridges (5a-e) were designed and synthesized from various diols, 1,7-diprotected cyclen and epichlorohydrin. The molecular weights of the title polymers were measured by GPC with good polydispersity. Agarose gel retardation and fluorescent titration using ethidium bromide showed good DNA-binding ability of 5. They could retard plasmid DNA (pDNA) at an N/P ratio of 4-6 and form polyplexes with sizes around 100-250 nm from an N/P ratio of 10 to 60 and relatively low zeta-potential values (5-22 mV). The cytotoxicity of 5 assayed by MTT is much lower than that of 20 kDa PEI. In vitro transfection against A549 and 293 cells showed that the transfection efficiency (TE) of 5c/DNA polyplexes is close to that of 20 kDa PEI at an N/P ratio of 5. Structure-activity relationship (SAR) of 5 was discussed in their DNA-binding, cytotoxicity, and transfection studies. The TE of 5c/DNA polyplexes could be improved by the introduction of 50 μM of chloroquine, the endosomolytic agents, to pretreated cells. These studies may extend the application areas of macrocyclic polyamines, especially for cyclen.

Dinuclear macrocyclic polyamine zinc(II) complexes linked with flexible spacers: Synthesis, characterization, and DNA cleavage

Peng, Wei,Liu, Pei-Yan,Jiang, Ning,Lin, Hong-Hui,Zhang, Guo-Lin,Liu, Yi,Yu, Xiao-Qi

, p. 374 - 385 (2008/02/01)

Dinuclear macrocyclic polyamine zinc(II) complexes, which have two cyclen groups linked by flexible spacers, have been synthesized as DNA cleavage agents. The structures of these new dinuclear complexes are consistent with the data obtained from elemental analysis, MS and 1H NMR spectroscopy. The catalytic activity of these dinuclear complexes on DNA cleavage was studied. The results showed that the dinuclear zinc(II) complexes can catalyze the cleavage of supercoiled DNA (pUC 19 plasmid DNA) (Form I) under physiological conditions to produce selectively nicked DNA (Form II).

Structure and hardening activity of oxirane gelatin hardeners based on ethylene glycol and ethylenediamine

Serdyuk,Davydova,Chezlov,D'yakonov

, p. 1844 - 1845 (2007/10/03)

Ethylene glycol diglycidyl ether and N,N′-diglycidyl-N,N′-dibutylethylenediamine were prepared, and their cross-linking effect on gelatin was studied, judging from the melting point and mechanical strength of model gelatin layers.

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