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Tris[2-(2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethyl]amine is a complex organic compound with the molecular formula C12H33N3O6Si3. It is a cyclic structure containing three ethylamine groups attached to a central silicon atom, with each ethylamine group featuring a 2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecane ring. tris[2-(2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethyl]amine is known for its unique properties, such as its ability to act as a chelating agent, which allows it to form stable complexes with metal ions. It is often used in various applications, including as a stabilizer in polymers, a component in catalysts, and in the synthesis of other organosilicon compounds. Due to its specific structure and reactivity, it is a subject of interest in the field of organosilicon chemistry and materials science.

29167-65-5

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29167-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29167-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29167-65:
(7*2)+(6*9)+(5*1)+(4*6)+(3*7)+(2*6)+(1*5)=135
135 % 10 = 5
So 29167-65-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H48N4O12Si3/c1-13-29-41(30-14-2-25(1)3-15-31-41)38-22-10-28(11-23-39-42-32-16-4-26(5-17-33-42)6-18-34-42)12-24-40-43-35-19-7-27(8-20-36-43)9-21-37-43/h1-24H2

29167-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecan-5-yloxy)-N,N-bis[2-(4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecan-5-yloxy)ethyl]ethanamine

1.2 Other means of identification

Product number -
Other names EINECS 249-476-3

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

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More Details:29167-65-5 SDS

29167-65-5Relevant academic research and scientific papers

A new route to silicon alkoxides from silica

Kemmitt, Tim,Henderson, William

, p. 1031 - 1035 (2007/10/03)

A novel route to tetraethoxysilane and other silicon alkoxides is described, from amorphous silica (SiO2·H2O) as the raw material. The reaction of amorphous silica with triethanolamine is enhanced by using an alkali metal hydroxide catalyst, to form a range of triethanolamine-substituted silatrane species. These can undergo alkoxide exchange in acidic alcohols to form alkoxysilatranes, tetraalkoxysilanes, hexaalkoxydisiloxanes and higher siloxanes. Reaction of triethanolamine-substituted silatranes with acetic anhydride produces acetoxysilatrane. Products were identified by multinuclear (1H, 13C and 29Si) magnetic resonance spectroscopy, electrospray mass spectrometry or high-resolution gas chromatography electron impact mass spectrometry.

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