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18182-14-4

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18182-14-4 Usage

General Description

Dimethylmethoxy-N-propylsilane is a chemical compound with the formula C6H16OSi. It is a clear, colorless liquid with a characteristic odor. DIMETHYLMETHOXY-N-PROPYLSILANE is widely used as a coupling agent in various applications, including adhesives, sealants, and surface modifying agents. It is also utilized as a raw material in the production of silane-modified polymers, which have many industrial and commercial uses. Dimethylmethoxy-N-propylsilane is considered to be a versatile and effective silane coupling agent, known for its ability to improve adhesion and compatibility between different materials. It should be handled and used with caution due to its flammability and potential for skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 18182-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,8 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18182-14:
(7*1)+(6*8)+(5*1)+(4*8)+(3*2)+(2*1)+(1*4)=104
104 % 10 = 4
So 18182-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H16OSi/c1-5-6-8(3,4)7-2/h5-6H2,1-4H3

18182-14-4SDS

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 DIMETHYLMETHOXY-N-PROPYLSILANE

1.2 Other means of identification

Product number -
Other names n-PROPYLDIMETHYLMETHOXYSILANE

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:18182-14-4 SDS

18182-14-4Downstream Products

18182-14-4Relevant articles and documents

Silicon α-effect: A systematic experimental and computational study of the hydrolysis of Cα- and Cγ-functionalized alkoxytriorganylsilanes of the formula type ROSiMe2(CH 2)nX (R = Me, Et; N = 1, 3; X = functional group)

Berkefeld, Andre,Guerra, Celia Fonseca,Bertermann, Ruediger,Troegel, Dennis,Daiss, Juergen O.,Stohrer, Juergen,Bickelhaupt, F. Matthias,Tacke, Reinhold

, p. 2721 - 2737 (2014/06/24)

To understand the silicon α-effect in terms of an enhanced reactivity of the Si-OC bond of α-silanes of the formula type ROSiMe 2CH2X compared to analogous γ-silanes ROSiMe 2(CH2)3X (R = Me, Et; X = functional group), a systematic experimental and computational study of the kinetics and mechanisms of hydrolysis of such compounds was performed. For this purpose, a series of suitable model compounds was synthesized and studied for their hydrolysis kinetics in CD3CN/D2O under basic and acidic conditions, using 1H NMR spectroscopy as the analytical tool. To get more information about the reaction mechanisms, the experimental investigations were complemented by computational studies. These investigations demonstrated that the silicon α-effect cannot be rationalized in terms of a special single effect. The reactivities observed rather result from a summation of different components, such as electronic and steric effects, pD dependence, and hydrogen bonds between the functional group (or even protonated functional group) and the alkoxy leaving group. Therefore, the term silicon α-effect should not be used furthermore to explain the hydrolysis reactivity at the silicon atom of alkoxyorganylsilanes with functional groups in α- or γ-position of the organyl groups (so-called α- or γ-silanes).

SILICENIUM IONS: A GAS-PHASE RADIOLYTIC APPROACH

Angelini, Giancarlo,Keheyan, Yeghis,Laguzzi, Giuseppe,Lilla, Gaetano

, p. 4159 - 4162 (2007/10/02)

The gas-phase protonation of vinyltrimethylsilane was carried out, using γ-radiolysis of methane.The ionic species, involved in the process, were trapped by nucleophilic attack of methanol.

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