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Cyclohexasiloxane, also known as D6 or hexamethylcyclotrisiloxane, is a cyclic organic silicon compound with the chemical formula (CH3)3SiO)3Si(CH3)3. It is a colorless, odorless, and non-toxic liquid that is widely used in various industries, including personal care products, textiles, and coatings. Cyclohexasiloxane is known for its excellent volatility, low surface tension, and high thermal stability, which make it an ideal component in defoamers, hair care products, and as a carrier for other ingredients. However, due to concerns about its potential environmental and health impacts, its use has been restricted or banned in some regions.

295-01-2

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295-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 295-01-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,9 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 295-01:
(5*2)+(4*9)+(3*5)+(2*0)+(1*1)=62
62 % 10 = 2
So 295-01-2 is a valid CAS Registry Number.

295-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3,5,5,7,7,9,9,11,11-dodecahydro-cyclohexasiloxane

1.2 Other means of identification

Product number -
Other names cyclohexsiloxane

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:295-01-2 SDS

295-01-2Downstream Products

295-01-2Relevant academic research and scientific papers

Process for the manufacture of hydrogen-rich cyclosiloxane

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Page/Page column 6, (2010/02/17)

The present invention relates to a for controlled synthesis of hydrogen-rich cyclosiloxanes of the (H2SiO)n type. where n is an integer equal to or greater than 3, by reacting: a.) a halosilane of the H2SiX2 type where X=halogen withb.) a lithium salt, copper(II) salt or a salt of a metal from main group 2 or transition group 2 of the periodic table of the elements, or a mixture of these salts. The ring size is advantageously adjustable to n=3, 4, 5, 6 (especially n=4 to 6), such that larger rings are not formed. In a particularly advantageous embodiment of the process, for the selective preparation of cyclohexasiloxane (H2SiO)6, after the reaction, the solvent is at least partly removed and then solvent is added again.

Linear polysiloxanes from dichlorosilane

Seyferth, Dietmar,Prud'homme, Christian C.

, p. 4412 - 4417 (2008/10/08)

Polysiloxanes of type RR′R″SiO(SiH2O)nSiRR′R″ (R, R′, R″ = Me, Me, Me; Me, H, H; Et, Et, Et; Me, Me, H) have been prepared by three different methods: (1) reactions of ClSiH2O(SiH2O)nSiH2Cl with CH3MgBr, Me3SiOH, and Et3SiOH; (2) H2SO4-catalyzed equilibration of cyclic [H2SiO]n oligomers with Me3SiOSiMe3; (3) cohydrolysis of H2SiCl2 with Me3SiCl and Me2HSiCl using NaH2PO4/Na2HPO4-buffered media. Lower species, Me2RSiO(SiH2O)nSiMe2R (n = 1-3), were isolated and characterized (R = Me, H).

Cyclic polysiloxanes from the hydrolysis of dichlorosilane

Seyferth, Dietmar,Prud'homme, Christian,Wiseman, Gary H.

, p. 2163 - 2167 (2008/10/08)

The hydrolysis of H2SiCl2 in dichloromethane solution, either with a stoichiometric amount of water at -30 to -20°C or by slow, controlled addition of a slight excess of water at 0°C, results in the formation of siloxanes of type [H2SiO]n. In the volatile fraction oligomers with n from 4 up to 23 were found. Those with n = 4-6 were isolated by GC and characterized (1H and 29Si NMR, IR, n25D, mass spectroscopy). A brief study was made of the hydrolysis of MeSiHCl2 and Me2SiCl2 under comparable conditions.

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