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Dipropan-2-ylsilanediol, with the molecular formula C6H16O2Si, is a silanol derivative that features a silicon atom bonded to a hydroxyl group. This chemical compound is known for its versatile applications in various industries due to its unique properties.

18173-88-1

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18173-88-1 Usage

Uses

Used in Adhesives, Coatings, and Sealants Industry:
Dipropan-2-ylsilanediol is used as a silane coupling agent for surface treatment, enhancing the adhesion, durability, and performance of adhesives, coatings, and sealants.
Used in Organosilicon Compounds Synthesis:
It serves as a basic building block in the synthesis of other organosilicon compounds, contributing to the development of new materials with specific properties and applications.
Used in Silicone Polymers and Resins Production:
Dipropan-2-ylsilanediol is utilized in the production of silicone polymers and resins, imparting characteristics such as water repellency, thermal stability, and flexibility, which are valuable in a wide range of applications.
Used in Organic Synthesis Reactions:
It functions as a reagent in organic synthesis reactions, facilitating the creation of various organic compounds for different uses across multiple industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18173-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,7 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18173-88:
(7*1)+(6*8)+(5*1)+(4*7)+(3*3)+(2*8)+(1*8)=121
121 % 10 = 1
So 18173-88-1 is a valid CAS Registry Number.

18173-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dihydroxy-di(propan-2-yl)silane

1.2 Other means of identification

Product number -
Other names diisopropylsilanediol

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:18173-88-1 SDS

18173-88-1Downstream Products

18173-88-1Relevant academic research and scientific papers

Supramolecular aggregates of silanols and solid-state synthesis of siloxanes

Unno, Masafumi,Takada, Keisuke,Kawaguchi, Yasuaki,Matsumoto, Hideyuki

, p. 259 - 264 (2005)

Cocrystallization of all-cis-tetraisopropylcyclotetrasiloxanetetraol and diisopropylsilanediol gave single crystals, which were proved to have a nano-size tube-like aggregate structure. Six molecules of the cyclic tetraol and four molecules of the dial form an asymmetric unit by means of hydrogen bonding. The structure and properties of the aggregates are discussed in detail, and also the possibility of solid-state synthesis of siloxanes is described.

Oxidation of Triorganosilanes and Related Compounds by Chlorine Dioxide

Grabovskiy,Kabal’nova

, p. 2391 - 2402 (2022/01/22)

Abstract: Oxidation of triethylsilane, tert-butyldimethylsilane, dimethylphenylsilane, triphenylsilane, 1,1,1,2tetramethyl-2-phenyldisilane, tris(trimethylsilyl)silane, hexamethyldisilane, tetrakis(trimethylsilyl)silane, 1,1,3,3tetraisopropyldisiloxane with chlorine dioxide was carried out. The reaction products of studied triorganosilanes with chlorine dioxide in an acetonitrile solution were the corresponding silanols and siloxanes. A mechanism explaining the formation of products and the observed regularities of the oxidation of silanes with chlorine dioxide has been proposed. A thermochemical analysis of some possible pathways in the gas phase using methods G4, G3, M05, and in an acetonitrile solution by the SMD-M05 method was carried out. The oxidation process can occur both with the participation of ionic and radical intermediates, depending on the structure of the oxidized substrate and medium.

Silane-based Resins That Can Be Photochemically And/or Thermally Structured, Single-step Method for Their Production, Parent Compounds and Production Methods That Can Be Used for Said Resins

-

Page/Page column 5, (2008/12/07)

A silane resin that can be structured photochemically and/or thermally is obtained by at least partial condensation of a mixture of a) at least one silane compound RaR2bSiX4-a-b wherein R is a group polymerizabl

Stepwise Synthesis of Chain and Ring Siloxanes - Crystal Structures

Graalmann, Onno,Klingebiel, Uwe,Clegg, William,Haase, Martin,Sheldrick, George M.

, p. 2988 - 2997 (2007/10/02)

Disilanols of the type R2Si(OH)2 (1, 2: R = CHMe2, CMe3) and the fluorosilanol (Me3C)2Si(OH)F (3) serve as starting materials in the reaction with halosilanes for the stepwise construction of chain siloxanes (4 - 15, 16 - 20).Even siloxanes with bulky tert-butyl or silylamino groups are easily prepared (10, 16, 17, 20).Crystalline silanediols (2, 14, 19) are connected in chains (19) or dimeric rings (2, 14) by hydrogen bonding.The 1,3-difluoro- (18), 1,3-dihydroxy- (19), and 1-fluoro-3-hydroxydisiloxane 6 as well as the cyclotrisiloxane 21 were isolated from the reaction of F2Si(CHMe2)2 with potassium hydroxide.Directed synthesis of Si-O six-membered rings (21 - 24) is possible via reaction of 1,3-dihydroxydisiloxanes 19, 20 with di- and trihalosilanes.The crystal structures of 2, 14, and 24 are discussed.

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