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18297-88-6

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18297-88-6 Usage

Description

Cyclotetrasiloxane, chloroheptamethylis an intermediate compound in the synthesis of Heptamethylcyclotetrasiloxan-2-ol (H281305). It is derived from Octamethylcyclotetrasiloxane (O237145), an organometallic reagent that plays a significant role in the preparation of siloxane polymers. Cyclotetrasiloxane, chloroheptamethylis characterized by its high surface-hydrophobicity restoration property, making it a valuable component in various applications.

Uses

Used in Chemical Synthesis:
Cyclotetrasiloxane, chloroheptamethylis used as an intermediate in the synthesis of Heptamethylcyclotetrasiloxan-2-ol (H281305) for its role in creating a derivative of Octamethylcyclotetrasiloxane (O237145). This derivative is essential in the development of organometallic reagents.
Used in Polymer Industry:
Cyclotetrasiloxane, chloroheptamethylis used as a component in the preparation of siloxane polymers for its high surface-hydrophobicity restoration property. This property is crucial in enhancing the performance and durability of the polymers, making them suitable for various applications, such as coatings, adhesives, and sealants.
Used in Surface Coating Applications:
Cyclotetrasiloxane, chloroheptamethylis used as an additive in surface coatings to improve their hydrophobic properties. The high surface-hydrophobicity restoration capability of this compound makes it an ideal choice for creating water-repellent and stain-resistant coatings for various surfaces, including automotive, architectural, and industrial applications.
Used in Adhesive and Sealant Formulations:
Cyclotetrasiloxane, chloroheptamethylis used as a component in adhesive and sealant formulations to enhance their hydrophobic and bonding properties. The high surface-hydrophobicity restoration property of this compound contributes to the improved performance and durability of adhesives and sealants, making them suitable for various applications, such as construction, automotive, and electronics industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18297-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,9 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18297-88:
(7*1)+(6*8)+(5*2)+(4*9)+(3*7)+(2*8)+(1*8)=146
146 % 10 = 6
So 18297-88-6 is a valid CAS Registry Number.

18297-88-6SDS

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-chloro-2,4,4,6,6,8,8-heptamethyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane

1.2 Other means of identification

Product number -
Other names Chlor-heptamethyl-cyclotetrasiloxan

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:18297-88-6 SDS

18297-88-6Relevant articles and documents

Synthesis of high-purity heptamethylchlorocyclotetrasiloxane

Martynova,Voronkov

, p. 921 - 922 (2007/10/03)

The procedures of preparation of heptamethylcyclotetrasiloxane (CH3)7Si4O4H in a 60% yield, its exhaustive purification, and its chlorination to form (CH3)7Si4O4Cl in a quantitative yield were developed. The composition of heptamethylchlorocyclotetrasiloxane and the content of alkali and heavy metal impurities in this compound, permissible for materials used in electronics, were determined by elemental analysis, gas-liquid chromatography, flame photometry, and atomic absorption analysis.

SYNTHESIS OF STEREOREGULAR CYCLOLINEAR METHYLSILOXANE COPOLYMERS WITH VARYING RING SIZE IN THE MACROMOLECULAR CHAIN

Makarova, N. N.,Petrova, I. M.,Godovskii, Yu. K.,Lavryukhin, B. D.,Zhdanov, A. A.

, p. 137 - 143 (2007/10/02)

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