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17877-23-5

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17877-23-5 Usage

General Description

TRIISOPROPYLSILANOL 98 is a chemical compound with the molecular formula C9H22OSi. It is a colorless, clear liquid with a high boiling point and low vapor pressure. TRIISOPROPYLSILANOL 98 is primarily used as a reagent in the synthesis of organosilicon compounds. It is also utilized as a crosslinking agent in silicone rubber and as a surface modifier in various industrial applications. The compound is known for its hydrophobic and hydrophilic properties, making it suitable for use in coatings, adhesives, and sealants. Additionally, TRIISOPROPYLSILANOL 98 can be employed as a coupling and dispersing agent in the formulation of paints and coatings, providing improved adhesion and dispersion properties. Overall, TRIISOPROPYLSILANOL 98 is a versatile chemical with a range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17877-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,7 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17877-23:
(7*1)+(6*7)+(5*8)+(4*7)+(3*7)+(2*2)+(1*3)=145
145 % 10 = 5
So 17877-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H22OSi/c1-7(2)11(10,8(3)4)9(5)6/h7-10H,1-6H3

17877-23-5 Well-known Company Product Price

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  • Aldrich

  • (495565)  Triisopropylsilanol  98%

  • 17877-23-5

  • 495565-1G

  • 562.77CNY

  • Detail
  • Aldrich

  • (495565)  Triisopropylsilanol  98%

  • 17877-23-5

  • 495565-10G

  • 2,861.82CNY

  • Detail

17877-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name hydroxy-tri(propan-2-yl)silane

1.2 Other means of identification

Product number -
Other names Triisopropylsilanol

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:17877-23-5 SDS

17877-23-5Relevant articles and documents

Novel Si(II)+and Ge(II)+Compounds as Efficient Catalysts in Organosilicon Chemistry: Siloxane Coupling Reaction ?

Fritz-Langhals, Elke,Kneissl, Sotirios,Piroutek, Phillip,Werge, Sven

, (2020/09/02)

Novel catalytically active cationic Si(II) and Ge(II) compounds were synthesized and isolated in pure form. The Ge(II)+-based compounds proved to be stable against air and moisture and therefore can be handled very easily. All compounds efficiently catalyze the oxidative coupling of hydrosil(ox)anes with aldehydes and ketones as oxidation reagents and simultaneously the reductive ether coupling at very low amounts of 0.01 mol %. Because the catalysts also catalyze the reversible cyclotrimerization of aldehydes, paraldehyde can be used as a convenient source for acetaldehyde in siloxane coupling. It is shown that the reaction is especially suitable to make siloxane copolymers. Moreover, a new fluorine-free weakly coordinating boronate anion, B(SiCl3)4-, was successfully combined with the Si(II) and Ge(II) cations to give the stable catalytically active ion pairs Cp*Si:+B(SiCl3)4-, Cp*Ge:+B(SiCl3)4-, and [Cp(SiMe3)3Ge:+]B(SiCl3)4-.

An efficient catalytic approach for the synthesis of unsymmetrical siloxanes

Hreczycho, Grzegorz

, p. 67 - 72 (2015/01/30)

The potential for expanding the variety of catalytic methods for siloxane bond formation is explored. Alkoxysilanes react with methylallylsilanes in the presence of scandium(III) trifluoromethanesulfonate to yield disiloxanes and isobutene. The reaction p

Catalytic hydrogen evolution from hydrolytic oxidation of organosilanes with silver nitrate catalyst

Teo, Alan Kay Liang,Fan, Wai Yip

, p. 37645 - 37648 (2014/11/27)

In the light of uncertainty over the amount of recoverable fossil fuel reserves, hydrogen is touted to be a promising energy carrier in the future. Nevertheless, hydrogen storage remains a daunting challenge but a potential reaction for the generation of hydrogen on demand is the hydrolytic oxidation of organosilanes. Here, we demonstrate that silver nitrate, a readily available ionic salt, can catalyze the hydrolysis of organosilanes to produce hydrogen and organosilanols. In particular, turnover numbers and turnover frequencies in excess of 5 × 103 and 102 min-1 respectively are obtainable for the hydrolysis of triethylsilane at room temperature. This proposed silver nitrate mediated system is, by far, the simplest and cheapest catalytic hydrolysis of organosilanes. Results from the kinetic studies suggested a mechanistic scenario in which the hydrolysis of organosilanes is third order overall and first order in organosilane, water, and catalyst. The high hydrogen yield observed makes the silver nitrate catalyst an attractive material for hydrogen evolution. the Partner Organisations 2014.

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