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1,3-DI-N-OCTYLTETRAMETHYLDISILOXANE is an organosilicon compound characterized by a silicon atom bonded to two methyl groups and two octyl groups. It is recognized for its high thermal stability, low surface tension, and hydrophobic properties, which contribute to its diverse applications across various industries.

18642-94-9

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18642-94-9 Usage

Uses

Used in Industrial Applications:
1,3-DI-N-OCTYLTETRAMETHYLDISILOXANE is used as a surfactant, lubricant, and component in silicone-based polymers for its water-repelling and high thermal stability properties, making it suitable for waterproofing agents, mold release agents, and as a coating for various surfaces.
Used in Personal Care Products:
In the personal care industry, 1,3-DI-N-OCTYLTETRAMETHYLDISILOXANE is used as an ingredient in formulations due to its ability to improve product performance and provide a smooth texture.
Used in Adhesives:
1,3-DI-N-OCTYLTETRAMETHYLDISILOXANE is used as a component in adhesive formulations to enhance their bonding properties and durability.
Used in Pharmaceutical Industry:
1,3-DI-N-OCTYLTETRAMETHYLDISILOXANE is used in drug delivery systems to improve the efficacy and targeted delivery of pharmaceutical compounds.
While generally considered to have low toxicity, it is important to note that prolonged exposure to high concentrations of 1,3-DI-N-OCTYLTETRAMETHYLDISILOXANE can potentially cause respiratory irritation and skin sensitization, necessitating proper handling and safety measures in occupational settings.

Check Digit Verification of cas no

The CAS Registry Mumber 18642-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,4 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18642-94:
(7*1)+(6*8)+(5*6)+(4*4)+(3*2)+(2*9)+(1*4)=129
129 % 10 = 9
So 18642-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H46OSi2/c1-7-9-11-13-15-17-19-22(3,4)21-23(5,6)20-18-16-14-12-10-8-2/h7-20H2,1-6H3

18642-94-9SDS

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 1,3-DI-N-OCTYLTETRAMETHYLDISILOXANE

1.2 Other means of identification

Product number -
Other names 1,1,3,3-Tetramethyl-1,3-dioctyl-disiloxan

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:18642-94-9 SDS

18642-94-9Relevant academic research and scientific papers

An efficient method for synthesizing monofunctionalized derivatives of 1,1,3,3-tetramethyldisiloxane in ionic liquids as recoverable solvents for rhodium catalyst

Kukawka,Januszewski,Kownacki,Smiglak,Maciejewski

, p. 59 - 63 (2018/02/09)

Functionalized siloxanes, as one of the most important classes of organosilicon compounds, are widely applied in industry. In our studies, we have investigated, the reaction between 1,1,3,3-tetramethyldisiloxane (TMDSO) and 1-octene, using the rhodium cat

An efficient catalytic and solvent-free method for the synthesis of mono-organofunctionalized 1,1,3,3-tetramethyldisiloxane derivatives

Januszewski, Rafa?,Kownacki, Ireneusz,Maciejewski, Hieronim,Marciniec, Bogdan

, p. 263 - 268 (2017/07/06)

Selective mono-functionalization of 1,1,3,3-tetramethyldisiloxane (TMDSO) with olefins via hydrosilylation reaction is reported. On the basis of a study of platinum- and rhodium complexes in the reactions between TMDSO and selected olefins containing C=C bond, it was possible to choose the most efficient catalyst whose application in the solvent-free system led to selective mono-functionalization of the disiloxane reagent and simultaneous formation of only β-regioisomeric products, bearing in their structure functional groups of unique reactivity or physicochemical properties.

Hydrosilylation of alkenes catalyzed by rhodium with polyethylene glycol-based ionic liquids as ligands

Xu, Yisong,Bai, Ying,Peng, Jiajian,Li, Jiayun,Xiao, Wenjun,Lai, Guoqiao

, p. 59 - 63 (2014/06/09)

A series of polyethylene glycol-functionalized imidazolium ionic liquids has been prepared and characterized. These ionic liquids have been successfully applied in the hydrosilylation of alkenes catalyzed by rhodium complexes. The effects of the length of the polyether chain, the amount of ionic liquid, and the reaction temperature on the catalytic performance of hydrosilylation have been investigated. Furthermore, the catalytic system has been tested for the hydrosilylation of different alkenes with triethoxysilane. The new catalytic system exhibits both excellent catalytic activity and selectivity under low-temperature conditions. The catalyst system could be recycled five times with slightly deactivation.

Fixed-Bed Hydrosilylation Catalyst Complexes and Related Methods

-

Page/Page column 3, (2010/12/29)

The invention includes a fixed-bed catalyst complex that includes (i) a metal carbene catalyst, wherein the metal is platinum, and (ii) a catalyst support that includes one or more of silica, alumina and/or glass. The invention provides a fixed-bed catalyst complex that includes a catalyst complex including a carbene chosen from those represented by at least one of Formulae (I), (II), (III), and (IV): Where the vales of X and R1 to R7 are specifically defined. The complex also includes a catalyst support that comprises silica, related reaction products, and related reaction systems.

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