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[(1-Ethyloctyl)oxy](trimethyl)silane, also known as EOTS, is a versatile and widely used silicone-based chemical compound. It is characterized by its unique molecular structure, featuring an ethyloctyl group attached to a silicon atom, with three methyl groups also bonded to the same silicon atom. This structure endows EOTS with excellent hydrophobic and oleophobic properties, making it a valuable ingredient in formulations that require water and oil repellency. EOTS is primarily used as a silane coupling agent and adhesion promoter, enhancing the performance of sealants, adhesives, and coatings.

61180-95-8

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61180-95-8 Usage

Uses

Used in Sealants and Adhesives:
EOTS is used as a silane coupling agent and adhesion promoter in the formulation of sealants and adhesives. Its hydrophobic and oleophobic properties contribute to the improved performance and durability of these products by enhancing their resistance to water and oil.
Used in Coatings:
In the coatings industry, EOTS is utilized to improve the adhesion of silicones to various substrates, such as glass, metal, and plastics. Its unique molecular structure allows for better bonding and increased durability of the coatings.
Used as a Crosslinker in Silicone Rubber:
EOTS acts as a crosslinker in silicone rubber, improving the material's mechanical properties and overall performance.
Used as a Surface Modifier:
EOTS is employed as a surface modifier in various applications, enhancing the hydrophobic and oleophobic characteristics of materials, which can be beneficial in a range of industries, from textiles to construction.
Used as an Anti-Foaming Agent:
In industrial processes, EOTS is used as an anti-foaming agent to control and prevent the formation of foam, which can be detrimental to the efficiency and quality of certain manufacturing processes.
Used as a Release Agent:
EOTS is also used as a release agent in various industrial processes, where it helps to facilitate the separation of materials, reducing the need for additional mechanical force and improving overall process efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 61180-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61180-95:
(7*6)+(6*1)+(5*1)+(4*8)+(3*0)+(2*9)+(1*5)=108
108 % 10 = 8
So 61180-95-8 is a valid CAS Registry Number.

61180-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1-Ethyloctyl)oxy](trimethyl)silane

1.2 Other means of identification

Product number -
Other names -

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:61180-95-8 SDS

61180-95-8Downstream Products

61180-95-8Relevant academic research and scientific papers

CYP505E3: A Novel Self-Sufficient ω-7 In-Chain Hydroxylase

Maseme, Mpeyake Jacob,Opperman, Diederik Johannes,Pennec, Alizé,Smit, Martha Sophia,van Marwijk, Jacqueline

supporting information, p. 10359 - 10362 (2020/04/23)

The self-sufficient cytochrome P450 monooxygenase CYP505E3 from Aspergillus terreus catalyzes the regioselective in-chain hydroxylation of alkanes, fatty alcohols, and fatty acids at the ω-7 position. It is the first reported P450 to give regioselective in-chain ω-7 hydroxylation of C10–C16 n-alkanes, thereby enabling the one step biocatalytic synthesis of rare alcohols such as 5-dodecanol and 7-tetradecanol. It shows more than 70 percent regioselectivity for the eighth carbon from one methyl terminus, and displays remarkably high activity towards decane (TTN≈8000) and dodecane (TTN≈2000). CYP505E3 can be used to synthesize the high-value flavour compound δ-dodecalactone via two routes: 1) conversion of dodecanoic acid into 5-hydroxydodecanoic acid (24 percent regioselectivity), which at low pH lactonises to δ-dodecalactone, and 2) conversion of 1-dodecanol into 1,5-dodecanediol (55 percent regioselectivity), which can be converted into δ-dodecalactone by horse liver alcohol dehydrogenase.

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