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15901-49-2

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15901-49-2 Usage

Chemical composition

1,3,5-TRIETHYL-1,3,5-TRIMETHYLCYCLOTRISILOXANE is composed of three silicon atoms, five methyl groups, and three ethyl groups arranged in a cyclic structure.

Classification

It is classified as a cyclic siloxane, which is a type of organosilicon compound.

Usage

This chemical is often used as a precursor for the synthesis of other silicon-based materials and in the production of silicone polymers.

Industrial applications

It is utilized in various industrial and commercial applications, such as in the manufacturing of adhesives, sealants, and coatings.

Sectors

It is also used in the electronics and automotive industries.

Thermal stability

It can withstand high temperatures without breaking down or decomposing.

Chemical inertness

It does not react easily with other chemicals, making it a stable compound for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 15901-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,0 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15901-49:
(7*1)+(6*5)+(5*9)+(4*0)+(3*1)+(2*4)+(1*9)=102
102 % 10 = 2
So 15901-49-2 is a valid CAS Registry Number.

15901-49-2 Well-known Company Product Price

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  • Aldrich

  • (540196)  2,4,6-Triethyl-2,4,6-trimethylcyclotrisiloxane  97%

  • 15901-49-2

  • 540196-1ML

  • 668.07CNY

  • Detail

15901-49-2SDS

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-triethyl-2,4,6-trimethyl-1,3,5,2,4,6-trioxatrisilinane

1.2 Other means of identification

Product number -
Other names 1,3,5-Triethyl-1,3,5-trimethylcyclotrisiloxane

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:15901-49-2 SDS

15901-49-2Downstream Products

15901-49-2Relevant articles and documents

A methyl ethyl the cyclosiloxane preparation method

-

Paragraph 0056-0058, (2017/05/18)

The invention discloses a preparation method of methyl ethyl cyclosiloxane. The method comprises the following steps of: placing methyldichlorosilae into an autoclave for hydrosilylation with ethylene under the action of platinum catalyst, and then rectifying the reactant to obtain methyl ethyl dichlorosilane; dripping the methyl ethyl dichlorosilane into dilute acid solution for hydrolyzation and obtaining hydrolysate; performing pyrolysis to the hydrolysate under the action of high boiling point solvents and base catalysts, and finally rectifying the pyrolysis product to obtain trimethyl triethyl cyclotrisiloxane and tetramethyl tetraethyl cyclotetrasiloxane. The methyl ethyl cyclosiloxane is prepared by hydrosilylation of the methyldichlorosilae and the ethylene so as to greatly improve the product yield, reduce the production cost and enlarge the reaction device based on the demands to improve the capacity; the solvent is used in the pyrolysis process so as to reduce material crosslinking, improve the pyrolysis speed, reduce the pyrolysis temperature and decrease the usage amounts of the base catalysts; the method has the advantages of high efficiency and low energy consumption, etc.

THE SILICON-OXYGEN DOUBLE-BONDED INTERMEDIATES. A NEW METHOD FOR THE FORMATION OF ORGANOSILANONES

Tomadze, A. V.,Yablokova, N. V.,Yablokov, V. A.,Razuvaev, G. A.

, p. 43 - 50 (2007/10/02)

The kinetics and mechanism of thermal decomposition of R1R2(H)SiOOR3 silylperoxides have been studied.It has been shown that peroxides generated diorganosilanones, R1R2Si=O, with a high yield in the temperature range 130-180 deg C.A mechanism is suggested for the silanone formation.The interaction of silanones with cyclosiloxanes, triethylsilane, α-methylstyrene has been investigated as well as the cyclisation of silanones.

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