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2,4,6-Trimethylcyclotrisiloxane 99, also known as trimethylsiloxy-terminated trimethylsiloxane, is a colorless, odorless organosilicon compound with a molecular formula of C9H24O3Si3. It is a versatile chemical used in various industrial applications due to its high purity level of 99%.

13269-39-1

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13269-39-1 Usage

Uses

Used in Silicone Industry:
2,4,6-Trimethylcyclotrisiloxane 99 is used as a key component in the production of silicone rubber, which is known for its excellent elasticity, thermal stability, and resistance to weathering. It contributes to the manufacturing of high-quality silicone products used in various applications, such as automotive, aerospace, and electronics industries.
Used in Adhesives and Sealants Industry:
This organosilicon compound is used as a raw material for the formulation of adhesives and sealants. Its properties, such as high purity and compatibility with other materials, make it suitable for creating strong bonds and seals in construction, automotive, and aerospace applications.
Used in Coatings Industry:
2,4,6-Trimethylcyclotrisiloxane 99 is used as a component in the formulation of coatings, providing excellent adhesion, durability, and resistance to environmental factors. It enhances the performance of coatings used in various industries, including automotive, marine, and architectural applications.
Used as a Lubricant:
Due to its low friction coefficient and chemical stability, 2,4,6-trimethylcyclotrisiloxane 99 is used as a lubricant in various industrial applications. It helps reduce wear and tear on machinery, improving the efficiency and longevity of equipment.
Used as an Anti-Foaming Agent:
This organosilicon compound is used as an anti-foaming agent in various industrial processes, such as chemical manufacturing, fermentation, and food processing. It helps control foam formation, ensuring smooth and efficient operation of processes and preventing product contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 13269-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,6 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13269-39:
(7*1)+(6*3)+(5*2)+(4*6)+(3*9)+(2*3)+(1*9)=101
101 % 10 = 1
So 13269-39-1 is a valid CAS Registry Number.

13269-39-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-trimethyl-1,3,5,2λ<sup>3</sup>,4λ<sup>3</sup>,6λ<sup>3</sup>-trioxatrisilinane

1.2 Other means of identification

Product number -
Other names Cyclosiloxanes,Me hydrogen

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:13269-39-1 SDS

13269-39-1Upstream product

13269-39-1Relevant academic research and scientific papers

Hydrocarbyl the cyclosiloxane preparation method (by machine translation)

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Paragraph 0019; 0026; 0027; 0031, (2017/09/20)

The invention discloses a preparation method of alkyl cyclosiloxane. The preparation method is characterized by comprising the following steps: taking alkyl halogenosilane as a raw material, taking crown ether as a solvent and dropping the alkyl halogenosilane in a mixed solution formed by water and the crown ether while continuously stirring the alkyl halogenosilane; carrying out hydrolysis at a certain temperature to carry out condensation polymerization; standing after the reaction to carry out layering; and directly carrying out decompressed rectification on the obtained hydrolyzed oil to separate trialkylcyclotrisiloxane, tetraalkylcyclotetrasiloxane, pentaalkylcyclopentasiloxane and hexaalkylcyclohexasiloxane. The preparation method has the advantages that alcohols and low-boiling point hydrocarbons are not used as solvents, the crown ether is used as solvent and direct rectification is carried out on the prepared hydrolyzed oil to obtain the alkyl cyclosiloxane, so that the processes of washing, neutralization, drying and filtering are saved; and the solvent which undergoes standing and layering after the hydrolysis can be reused or can be cooled to a certain temperature to separate out the crown ether for recovery, so that the production cost is saved.

Preparation of cyclic oligosiloxane

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Page/Page column 9, (2008/06/13)

Cyclic oligosiloxane is prepared through disproportionation reaction of organopolysiloxane in the presence of a catalyst. Cyclic oligpsiloxane of high purity can be produced in high yields by using a catalyst having formula (4): wherein M is Al, Ti, Zr, Sn or Zn, p is the valence of M, and R4 is a monovalent hydrocarbon group or the like.

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