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80399-29-7

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80399-29-7 Usage

Description

Trimethylsiloxyvinyldimethyl carbinol, with the molecular formula C7H16O2Si, is a clear, colorless liquid that is a common silicon-based chemical. It is known for its reactive vinyl functionality, which allows it to participate in crosslinking reactions essential for the formation of silicone-based materials.

Uses

Used in Silicone Polymer and Resin Production:
Trimethylsiloxyvinyldimethyl carbinol is used as a coupling agent in the production of silicone polymers and resins. Its reactive vinyl group enables it to effectively bond with other components, enhancing the overall properties and performance of the resulting materials.
Used in Coatings and Adhesives Industry:
In the coatings and adhesives industry, trimethylsiloxyvinyldimethyl carbinol is utilized as a surface modifier. Its ability to participate in crosslinking reactions contributes to the improvement of adhesion, durability, and overall performance of the coatings and adhesives.
Used in Specialty Chemical Product Manufacturing:
Trimethylsiloxyvinyldimethyl carbinol is a key ingredient in the production of specialty chemical products such as siloxane resins and silane coupling agents. Its presence in these products is crucial for achieving desired properties and performance characteristics in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 80399-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,9 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80399-29:
(7*8)+(6*0)+(5*3)+(4*9)+(3*9)+(2*2)+(1*9)=147
147 % 10 = 7
So 80399-29-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O2Si/c1-8(2,9)6-7-10-11(3,4)5/h6-7,9H,1-5H3/b7-6+

80399-29-7SDS

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 Trimethylsiloxyvinyldimethyl carbinol

1.2 Other means of identification

Product number -
Other names 3-methyl-1-trimethylsilanyl-but-3-en-2-ol

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:80399-29-7 SDS

80399-29-7Relevant articles and documents

Efficient construction of the clerodane decalin core by an asymmetric Morita-Baylis-Hillman reaction/Lewis acid promoted annulation strategy

Rodgen, Stacy A.,Schaus, Scott E.

, p. 4929 - 4932 (2007/10/03)

(Chemical Equation Presented) Linking rings: A general route toward the clerodane diterpene core using an asymmetric Morita-Baylis-Hillman (MBH)/ Lewis acid mediated ring-annulation process has been developed. The scope of the asymmetric Bronsted acid cat

ENE-REACTIVITE D'ALLYLSILANES: FONCTIONNALISATION ET REGIOCHIMIE

Dubac, J.,Laporterie, A.,Iloughmane, H.,Pillot, J. P.,Deleris, G.,Dunogues, J.

, p. 149 - 162 (2007/10/02)

The hydroperoxidation of various allylsilanes by singlet oxygen has been studied.The regioselectivity of this reaction compared to those of ethyl azodicarboxylate and 4-phenyl-1,2,4-triazoline-3,5-dione, is discussed.Mechanisms are considered in the general field of the ene reaction applied to allylic organometallic Group IVB compounds.The structures of the new products (alcohols, urazoles, hydrazines) have been determined, directly or after transformations, by NMR spectroscopy.

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