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2,4,6,8,10,12-HEXAMETHYLCYCLOHEXASILOXANE, 96 is a siloxane compound characterized by its low viscosity, high molecular weight, and excellent thermal stability. It is widely used in the production of personal care products and industrial goods, providing a smooth and silky texture to various formulations.

6166-87-6

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6166-87-6 Usage

Uses

Used in Personal Care Products:
2,4,6,8,10,12-HEXAMETHYLCYCLOHEXASILOXANE, 96 is used as a texture enhancer in skin and hair care items for its ability to provide a smooth and silky feel to the products.
Used in Industrial and Household Goods:
This chemical is utilized in the manufacturing of various industrial and household goods due to its high molecular weight and excellent thermal stability, making it suitable for heat-resistant applications.
It is crucial to handle 2,4,6,8,10,12-HEXAMETHYLCYCLOHEXASILOXANE, 96 with care and adhere to safety guidelines to prevent potential health hazards during its use in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6166-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6166-87:
(6*6)+(5*1)+(4*6)+(3*6)+(2*8)+(1*7)=106
106 % 10 = 6
So 6166-87-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H24O6Si6/c1-13-7-14(2)9-16(4)11-18(6)12-17(5)10-15(3)8-13/h13-18H,1-6H3

6166-87-6Downstream Products

6166-87-6Relevant academic research and scientific papers

Preparation of cyclic oligosiloxane

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Page/Page column 7-8, (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.

PROCESS FOR PREPARING CYCLIC ORGANOHYDROGENSILOXANES

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Page/Page column 6; 7, (2008/06/13)

A process for preparing cyclic organohydrogensiloxanes comprises: (A) contacting a silane of the formula RHSiCl2, where R is selected from alkyl radicals having 1 to 12 carbon atoms and aryl radicals, with water to form a hydrolyzate comprising cyclic organohydrogensiloxanes and linear organohydrogensiloxanes, and (B) contacting the hydrolyzate with an acidic rearrangement catalyst in the presence of an inert liquid diluent to increase the ratio of the cyclic organohydrogensiloxanes to linear organohydrogensiloxanes in the hydrolyzate. The acidic rearrangement catalyst is an organic compound containing a strong acid group, for example a sulphonic acid, which is dissolved in the inert diluent present.

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