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2602-34-8

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2602-34-8 Usage

Chemical Properties

Colorless clear liquid.

Uses

(3-Glycidyloxypropyl)triethoxysilane (GPTES) can be used as a reagent in the synthesis of: ???????? Polymer nanocomposite membranes for direct methanol fuel cells (DMFCs).??????? Azido terminated poly(ethylene glycol) silane that can be self-assembled on a metal-oxide surface to facilitate the orthogonal biofunctionalization.?????? Epoxy functionalized silsesquioxane nanoparticles (SQ-NPs). Epoxy-functionalized mesoporous cellular foams (G-MCFs) as the support for the immobilization of penicillin G acylase (PGA). GPTES can also be used as a precursor to prepare water-repellent, self-cleaning coatings.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 2602-34-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2602-34:
(6*2)+(5*6)+(4*0)+(3*2)+(2*3)+(1*4)=58
58 % 10 = 8
So 2602-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H26O5Si/c1-4-15-18(16-5-2,17-6-3)9-7-8-13-10-12-11-14-12/h12H,4-11H2,1-3H3

2602-34-8 Well-known Company Product Price

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  • Sigma-Aldrich

  • (50059)  (3-Glycidyloxypropyl)triethoxysilane  ≥97.0% (GC)

  • 2602-34-8

  • 50059-50ML

  • 3,696.03CNY

  • Detail

2602-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Triethoxy(3-glycidyloxypropyl)silane

1.2 Other means of identification

Product number -
Other names triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals
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:2602-34-8 SDS

2602-34-8Synthetic route

Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

Triethoxysilane
998-30-1

Triethoxysilane

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

Conditions
ConditionsYield
[siloxideRh(cod)](SBA-15) at 100℃;96%
With silica supported poly-3-(2-aminoethylamino)propylsiloxane platinum complex at 110℃; for 2h;94.8%
With (TFAPDI)Co(2-ethylhexanoate)2 at 0 - 20℃; for 1.08333h; Temperature; Inert atmosphere; Sealed tube;94%
Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

Triethoxysilane
998-30-1

Triethoxysilane

A

triethoxy(2-glycidoxy-1-methylethyl)silane

triethoxy(2-glycidoxy-1-methylethyl)silane

B

glycidyl 1-propenyl ether
1607-23-4

glycidyl 1-propenyl ether

C

tetraethoxy orthosilicate
78-10-4

tetraethoxy orthosilicate

D

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

Conditions
ConditionsYield
Speier's catalyst at 70 - 90℃; for 1.5h; Further byproducts.;A n/a
B n/a
C n/a
D 78.9%
Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

triethyl hydrogen silicate
27491-84-5

triethyl hydrogen silicate

A

C12H24O5Si

C12H24O5Si

B

3-Propoxy-1,2-epoxypropan
3126-95-2

3-Propoxy-1,2-epoxypropan

C

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

Conditions
ConditionsYield
[rhodium(I)(1,5-cyclooctadien)(trimethylsiloxide)(P(cyclohexyl)3)] at 25℃; for 0.25h; Product distribution; Further Variations:; Reagents; Temperatures;
Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

Triethoxysilane
998-30-1

Triethoxysilane

A

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

B

C12H24O5Si

C12H24O5Si

Conditions
ConditionsYield
With (MeAPDI)Co(OAc)2 at 20℃; for 1h; Reagent/catalyst; Inert atmosphere; Sealed tube; Overall yield = 87 %; Overall yield = 217 mg;
Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

Triethoxysilane
998-30-1

Triethoxysilane

A

glycidyl 1-propenyl ether
1607-23-4

glycidyl 1-propenyl ether

B

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

Conditions
ConditionsYield
With cobalt(II) 2-ethylhexanoate at 20℃; for 1.5h; Reagent/catalyst; Temperature; Inert atmosphere; Sealed tube; Overall yield = 326 mg;
Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

Triethoxysilane
998-30-1

Triethoxysilane

A

glycidyl 1-propenyl ether
1607-23-4

glycidyl 1-propenyl ether

B

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

C

C12H24O5Si

C12H24O5Si

Conditions
ConditionsYield
With (PyBox)Co(2-ethylhexanoate)2 at 20℃; for 1h; Reagent/catalyst; Inert atmosphere; Sealed tube; Overall yield = 68 %; Overall yield = 168 mg;
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

2-hydroxyethanethiol
60-24-2

2-hydroxyethanethiol

C14H32O6SSi

C14H32O6SSi

Conditions
ConditionsYield
With potassium carbonate at 20℃; for 3h;100%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

1,3-Di(2-tolyl)guanidine
97-39-2

1,3-Di(2-tolyl)guanidine

1,3-bis(2-methylphenyl)-1,2,3-tris(2-hydroxy-3-(3-(triethoxysilyl)propoxy)propyl)guanidine

1,3-bis(2-methylphenyl)-1,2,3-tris(2-hydroxy-3-(3-(triethoxysilyl)propoxy)propyl)guanidine

Conditions
ConditionsYield
at 85℃; for 2h;98.4%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

2-mercapto-5-methylbenzimidazole
27231-36-3

2-mercapto-5-methylbenzimidazole

1-((1-(2-hydroxy-3-(3-(triethoxysilyl)propoxy)propyl)-6-methyl-1H-benzimidazol-2-yl)thio)-3-(3-(triethoxysilyl)propoxy)propan-2-ol

1-((1-(2-hydroxy-3-(3-(triethoxysilyl)propoxy)propyl)-6-methyl-1H-benzimidazol-2-yl)thio)-3-(3-(triethoxysilyl)propoxy)propan-2-ol

Conditions
ConditionsYield
at 80 - 120℃; for 4h; Inert atmosphere;98.4%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

1,1,3-trimethylthiourea
2489-77-2

1,1,3-trimethylthiourea

N,N,N'-trimethyl-N'-(2-hydroxy-3-(3-(triethoxysilyl)propyloxy)propyl)thiourea

N,N,N'-trimethyl-N'-(2-hydroxy-3-(3-(triethoxysilyl)propyloxy)propyl)thiourea

Conditions
ConditionsYield
at 85℃; for 2h;98.2%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

N,N',N''-triphenylguanidine
101-01-9

N,N',N''-triphenylguanidine

1,2,3-triphenyl-1,3-bis(2-hydroxy-3-(3-(triethoxysilyl)propoxy)propyl)guanidine

1,2,3-triphenyl-1,3-bis(2-hydroxy-3-(3-(triethoxysilyl)propoxy)propyl)guanidine

Conditions
ConditionsYield
In toluene at 85 - 90℃; for 1h;98.1%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

1,3-dibutylthiourea
109-46-6

1,3-dibutylthiourea

N,N'-di-n-butyl-N,N'-bis({2-hydroxy-3-[3-(triethoxysilyl)propyloxy]propyl})thiourea

N,N'-di-n-butyl-N,N'-bis({2-hydroxy-3-[3-(triethoxysilyl)propyloxy]propyl})thiourea

Conditions
ConditionsYield
at 85 - 90℃; for 2.5h;97.2%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

carbon dioxide
124-38-9

carbon dioxide

C13H26O7Si

C13H26O7Si

Conditions
ConditionsYield
With tetrabutylammomium bromide In neat (no solvent) at 100℃; under 3750.38 Torr; for 2h;96%
With (2-hydroxyphenyl)diphenyl(propyl)phosphonium iodide In neat (no solvent) at 90℃; under 7500.75 Torr; for 4h; Temperature; Autoclave;93%
1,4,8,11-Tetraazacyclotetradecane
295-37-4

1,4,8,11-Tetraazacyclotetradecane

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

1-(1,4,8,11-tetraazacyclotetradecan-1-yl)-3-(3-(triethoxysilyl)-propoxy)propan-2-ol

1-(1,4,8,11-tetraazacyclotetradecan-1-yl)-3-(3-(triethoxysilyl)-propoxy)propan-2-ol

Conditions
ConditionsYield
In toluene for 24h; Reflux; Inert atmosphere;93%
In toluene for 24h; Inert atmosphere; Reflux;
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

18-crown-6 ether
17455-13-9

18-crown-6 ether

benzene-1,2-diol
120-80-9

benzene-1,2-diol

potassium[18-crown-6]bis(catecholato)(3-glycidyloxypropyl)silicate

potassium[18-crown-6]bis(catecholato)(3-glycidyloxypropyl)silicate

Conditions
ConditionsYield
With potassium methanolate In methanol at 20℃; for 3h; Inert atmosphere;92%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

C6H11F4O2Si(1-)*H3N*H(1+)

C6H11F4O2Si(1-)*H3N*H(1+)

Conditions
ConditionsYield
With ammonium hydrogen difluoride In water at 20℃;91%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

C60H110O35Si10

C60H110O35Si10

Conditions
ConditionsYield
With tetramethyl ammoniumhydroxide In water; isopropyl alcohol at 40℃; for 4h; Solvent; Reagent/catalyst; Temperature;90%
(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

1,4,7,10-tetraazacyclododecan
294-90-6

1,4,7,10-tetraazacyclododecan

1-(1,4,7,10-tetraazacyclododecan-1-yl)-3-(3-(triethoxysilyl)-propoxy)propan-2-ol

1-(1,4,7,10-tetraazacyclododecan-1-yl)-3-(3-(triethoxysilyl)-propoxy)propan-2-ol

Conditions
ConditionsYield
In toluene for 24h; Reflux; Inert atmosphere;79%
1-methyl-piperazine
109-01-3

1-methyl-piperazine

(3-glycidyloxypropyl)triethoxysilane
2602-34-8

(3-glycidyloxypropyl)triethoxysilane

A

2,2-diethoxy-8-(4-methylpiperazinyl)methyl-1,6-dioxa-2-silacyclooctane
1222257-47-7

2,2-diethoxy-8-(4-methylpiperazinyl)methyl-1,6-dioxa-2-silacyclooctane

B

C30H64N4O8Si2
1222257-50-2

C30H64N4O8Si2

C

C32H70N4O9Si2
1222257-49-9

C32H70N4O9Si2

Conditions
ConditionsYield
With sodium ethanolate In ethanol; toluene at 116 - 145℃;A 78%
B n/a
C n/a

2602-34-8Downstream Products

2602-34-8Relevant articles and documents

Preparation method of epoxy silane coupling agent

-

Paragraph 0078-0079, (2021/05/05)

The invention provides a preparation method of an epoxy silane coupling agent. The preparation method comprises the following steps: (1) synthesizing diallyl ether from chloropropene and allyl alcohol under the action of a catalyst and an alkali; (2) carrying out a hydrosilylation reaction on the diallyl ether and hydrogen-containing chlorosilane under the action of a platinum catalyst to obtain allyloxopropyl chlorosilane; (3) carrying out esterification reaction on the allyloxopropyl chlorosilane and saturated alcohol to obtain allyloxoalkoxy silane; and (4) carrying out epoxidation on the allyloxyalkoxy silane by using an oxidizing agent, so as to obtain gamma-(2, 3-epoxypropoxypropyl)alkoxy silane. The preparation method provided by the invention can be suitable for all gamma-(2, 3-epoxypropoxypropyl) epoxy silane, the used catalyst and raw materials are easy to obtain, the yield is high, and the industrial feasibility is high.

Platinum(II) complexes bearing bulky Schiff base ligands anchored onto mesoporous SBA-15 supports as efficient catalysts for hydrosilylation

Huo, Yingpeng,Hu, Jiwen,Lin, Shudong,Ju, Xingming,Wei, Yanlong,Huang, Zhenzhu,Hu, Yangfei,Tu, Yuanyuan

, (2019/04/26)

Reported herein is an easy-to-prepare novel heterogeneous catalyst of platinum complexes bearing binary ligands of bidentate naphthalenolimine and cyclo-1,5-octadiene that are anchored onto mesoporous silica SBA-15. The presence of the binary ligands not only stabilized the platinum, but also enabled the platinum atoms to form nanoclusters with diameters of ca 1?nm, and led to high platinum loading (8.69?wt%). Moreover, the platinum catalyst exhibited high catalytic activity towards hydrosilylation of terminal alkenes and styrene with silanes under mild and solvent-free conditions, with excellent regioselectivity.

Nano-dispersed platinum(0) in organically modified silicate matrices as sustainable catalysts for a regioselective hydrosilylation of alkenes and alkynes

Duke, Brett J.,Akeroyd, Evan N.,Bhatt, Shreeja V.,Onyeagusi, Chibueze I.,Bhatt, Shreya V.,Adolph, Brandy R.,Fotie, Jean

, p. 11782 - 11795 (2018/07/25)

Nano-dispersed platinum(0) particles stabilized in a range of organically modified silicate (ORMOSIL) matrices are investigated as sustainable catalysts for the hydrosilylation of alkenes and alkynes. In this study, five different siloxane matrices including triethoxysilane (HTEOS), methyltriethoxysilane (MTES), ethyltriethoxysilane (ETES), triethoxyvinylsilane (TEVS) and propyltriethoxysilane (PTES) are investigated, and the distribution of the metal particles in these materials analyzed by transition electron microscopy (TEM). The particles appeared to be generally of a small size, with a diameter of ca. 2-5 nm in each of these catalysts, however the distribution is not equally uniform from one matrix to the other. HTEOS, MTES and ETES that respectively carry a hydrogen, a methyl and an ethyl group on the triethoxysilane moiety, displayed a more uniform distribution, while particles appeared to be more scattered in the remaining matrices. Catalysts with a uniform particles distribution produced higher and consistent yields, while those with poor particles distribution produced lower and almost random yields, suggesting that the uniformity in particle distribution, and by extension the nature of the siloxane matrix, are important for the catalytic properties of these materials. The scope of the reaction was broadened to a range of olefins, with a goal of investigating the tolerability of the reaction toward a number of reactive functional groups, resulting in the preparation of 28 compounds. This catalytic system also enabled the hydrosilylation of a limited number of alkynes under the optimized reaction conditions.

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