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17928-31-3

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17928-31-3 Usage

Description

1,7-Dimethoxy octamethyltetrasiloxane is a colorless liquid chemical compound with the formula C12H36O2Si4. It has a mild odor and is commonly used as a lubricant and ingredient in personal care products, as well as in the manufacturing of silicone rubbers, resins, and adhesives. 1,7-DIMETHOXY OCTAMETHYLTETRASILOXANE is considered to have low toxicity and is generally regarded as safe for use in consumer products when used in accordance with safety guidelines.

Uses

Used in Personal Care Products:
1,7-Dimethoxy octamethyltetrasiloxane is used as an ingredient in personal care products such as shampoos, conditioners, and moisturizers for its lubricating properties, which help improve the texture and feel of these products.
Used in Lubricants:
1,7-Dimethoxy octamethyltetrasiloxane is used as a lubricant in various applications due to its ability to reduce friction and wear between moving parts.
Used as a Surfactant:
1,7-Dimethoxy octamethyltetrasiloxane is used as a surfactant in various industrial processes to help lower the surface tension of liquids, allowing for better spreading and wetting of surfaces.
Used as an Antifoaming Agent:
1,7-Dimethoxy octamethyltetrasiloxane is used as an antifoaming agent in various industrial processes to help control and prevent the formation of foam, which can interfere with the efficiency of these processes.
Used in Manufacturing of Silicone Rubbers, Resins, and Adhesives:
1,7-Dimethoxy octamethyltetrasiloxane is used in the manufacturing of silicone rubbers, resins, and adhesives due to its ability to improve the properties of these materials, such as their flexibility, durability, and adhesion.
Used in Pharmaceutical Industry:
1,7-Dimethoxy octamethyltetrasiloxane is used as a carrier for drug delivery systems, aiming to improve the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical compounds.
Used in Cosmetic Industry:
1,7-Dimethoxy octamethyltetrasiloxane is used as a carrier for cosmetic ingredients, aiming to improve the delivery, stability, and effectiveness of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 17928-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,2 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17928-31:
(7*1)+(6*7)+(5*9)+(4*2)+(3*8)+(2*3)+(1*1)=133
133 % 10 = 3
So 17928-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO5S/c1-14-5-2-3-7(15(8,12)13)6(4-5)9(10)11/h2-4H,1H3

17928-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methoxy-[[[methoxy(dimethyl)silyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilane

1.2 Other means of identification

Product number -
Other names 1,7-dimethoxy-1,1,3,3,5,5,7,7-octamethyl-tetrasiloxane

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:17928-31-3 SDS

17928-31-3Downstream Products

17928-31-3Relevant articles and documents

Rate studies of the acid-catalyzed solvolysis of eight-membered cyclosilazoxanes

Lasocki, Zygmunt,Witekowa, Malgorzata

, p. 27 - 33 (2007/10/02)

The solvolysis of N-phenyl-1,1,3,3,5,5,7,7-octamethyl-1,3,5,7-tetrasila-2-aza-4,6,8-trioxacyclooctane (1) and N,N'-diphenyl-1,1,3,3,5,5,7,7-octamethyl-1,3,5,7-tetrasila-2,6-diaza-4,8-dioxacyclooctane (II) in methanol/water in the presence of an acetate buffer is a pseudo-first-order process, subject to general acid-catalysis.The catalytic rate constants have been determined spectrophotometrically for the solvolysis of I.The ring cleavage is slower than that of analogous six-membered cyclosilazoxanes, but the catalytic mode and the solvent isotope effect indicate a close mechanistic similarity between the solvolyses of six- and eight-membered rings.

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