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BIS(2-HYDROXYETHYL)-3-AMINOPROPYLTRIETHOXYSILANE, also known as 3-[Bis(2-hydroxyethyl)amino]propyl-triethoxysilane, is an organosilane compound with a unique structure that features two hydroxyethyl groups and an aminopropyl group attached to a central silicon atom, which is further connected to three ethoxy groups. BIS(2-HYDROXYETHYL)-3-AMINOPROPYLTRIETHOXYSILANE is known for its ability to form stable bonds with various surfaces, particularly inorganic materials, and is widely utilized in surface modification and functionalization processes.

7538-44-5

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7538-44-5 Usage

Uses

Used in Surface Modification Industry:
BIS(2-HYDROXYETHYL)-3-AMINOPROPYLTRIETHOXYSILANE is used as a coupling agent for promoting strong adhesion between organic and inorganic materials. Its application reason is due to its ability to form covalent bonds with inorganic surfaces and hydrogen bonds with organic materials, thus improving the compatibility and interfacial properties of the materials.
Used in Nanoporous Silica Functionalization:
BIS(2-HYDROXYETHYL)-3-AMINOPROPYLTRIETHOXYSILANE is used as a functionalizing agent for nanoporous silica (SBA-15). The application reason is to introduce hydroxyethyl and aminopropyl groups onto the silica surface, which can enhance the material's properties, such as hydrophilicity, and enable further chemical modifications or the attachment of specific functional groups for various applications, including catalysis, drug delivery, and sensing.

Check Digit Verification of cas no

The CAS Registry Mumber 7538-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7538-44:
(6*7)+(5*5)+(4*3)+(3*8)+(2*4)+(1*4)=115
115 % 10 = 5
So 7538-44-5 is a valid CAS Registry Number.

7538-44-5 Well-known Company Product Price

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  • Aldrich

  • (14865)  3-[Bis(2-hydroxyethyl)amino]propyl-triethoxysilanesolution  technical, ~65% in ethanol

  • 7538-44-5

  • 14865-50ML

  • 6,677.19CNY

  • Detail

7538-44-5SDS

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 BIS(2-HYDROXYETHYL)-3-AMINOPROPYLTRIETHOXYSILANE

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:7538-44-5 SDS

7538-44-5Synthetic route

(3-chloropropyl)triethoxysilane
5089-70-3

(3-chloropropyl)triethoxysilane

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

Conditions
ConditionsYield
With potassium iodide In dimethyl sulfoxide at 120℃; Inert atmosphere;
3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

ethanol
64-17-5

ethanol

trimethylaluminum
75-24-1

trimethylaluminum

C15H34AlNO6Si

C15H34AlNO6Si

Conditions
ConditionsYield
In toluene at 0℃; for 4h; Inert atmosphere; Schlenk technique;95%
3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

ethanol
64-17-5

ethanol

dibutylmagnesium
1191-47-5

dibutylmagnesium

C14H33MgNO6Si

C14H33MgNO6Si

Conditions
ConditionsYield
In n-heptan1ol at 0 - 20℃; for 4h; Inert atmosphere; Schlenk technique;91%
3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

ethanol
64-17-5

ethanol

aluminum isopropoxide
555-31-7

aluminum isopropoxide

C15H34AlNO6Si

C15H34AlNO6Si

Conditions
ConditionsYield
In toluene at 0℃; for 4h; Inert atmosphere; Schlenk technique;88%
titanium(IV) isopropylate
546-68-9

titanium(IV) isopropylate

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

C19H43NO7SiTi

C19H43NO7SiTi

Conditions
ConditionsYield
In ethanol; dichloromethane at 20℃; for 4h; Inert atmosphere; Schlenk technique;
3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

C23H43N5O9Si

C23H43N5O9Si

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: 35 h / 80 °C / Inert atmosphere
1.2: 0.75 h / 150 °C / Inert atmosphere
2.1: water / 2 h / 85 °C
View Scheme
3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

C35H65N5O9Si2

C35H65N5O9Si2

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: 35 h / 80 °C / Inert atmosphere
1.2: 0.75 h / 150 °C / Inert atmosphere
2.1: water / 2 h / 85 °C
3.1: ethanol / 3 h / 40 °C
View Scheme
1,6-dicyanatohexane

1,6-dicyanatohexane

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane
7538-44-5

3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane

C29H55N5O9Si

C29H55N5O9Si

Conditions
ConditionsYield
Stage #1: 1,6-dicyanatohexane; 3-[bis(2-hydroxyethyl)amino]propyltriethoxysilane at 80℃; for 35h; Inert atmosphere;
Stage #2: With tin(IV) chloride at 150℃; for 0.75h; Inert atmosphere;

7538-44-5Downstream Products

7538-44-5Relevant academic research and scientific papers

Preparation method of organic silicon toughened isocyanate resin based on chemical bonding (by machine translation)

-

Paragraph 0024-0027, (2020/07/21)

Under the catalysis of potassium iodide, hydroxyl is introduced, hydroxyl is introduced, hydroxyl is introduced, hydroxyl is introduced into an ethanol solution of 3 - dodecyl triethoxysilane, hydroxyl is introduced, hydroxyl is introduced, and finally silanol cyanate is immersed in a dodecyl trimethyl diisocyanate ethanol solution to obtain the modified hexamethylene diisocyanate. M1, and finally, the silicon alcohol M1 cyanate ester is immersed in an aqueous solution to obtain the modified hexamethylene diisocyanate resin, and finally, the hydroxyl is introduced into an ethanol solution of M3 the dodecyl trimethyl diisocyanate to obtain the modified hexamethylenediisocyanate resin. (by machine translation)

SILANE COMPOSITIONS FOR POLYESTER NANOCOMPOSITES

-

Page/Page column 6, (2012/02/06)

Novel silane compositions have been prepared by reacting a 3-isocyanatopropyl trialkoxysilane with an alcohol or diol having a divalent alkylene or alkylene-ether group. The alcohol or diol has a formula weight less than about 5000. The compositions can be used to modify the surfaces of inorganic oxygen-containing materials, including but not limited to silica, silicates, borosilicates, aluminosilicates, days, and metal oxides. Surface treatment of silica nanoparticles with these compositions improves their improved dispersion in polyester nanocomposites.

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