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OCTADECAMETHYLCYCLONONASILOXANE is a chemical compound known for its unique properties and potential applications across various industries. It is characterized by its cyclic structure and nonasiloxane functional group, which contributes to its stability and reactivity.

556-71-8

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556-71-8 Usage

Uses

Used in Antimicrobial Applications:
OCTADECAMETHYLCYCLONONASILOXANE is used as an antibacterial agent, particularly effective against marine Bacillus cereus. Its ability to target and eliminate harmful bacteria makes it a valuable component in various antimicrobial formulations.
Used in Marine Industry:
In the marine industry, OCTADECAMETHYLCYCLONONASILOXANE is used as a biocidal agent for protecting marine equipment and structures from bacterial colonization and biofouling. Its effectiveness against marine Bacillus cereus ensures the longevity and performance of submerged assets.
Used in Personal Care Industry:
OCTADECAMETHYLCYCLONONASILOXANE can also be utilized in the personal care industry as an ingredient in antibacterial soaps, lotions, and other hygiene products. Its ability to combat bacteria on the skin contributes to improved personal hygiene and reduced risk of infection.
Used in Medical Applications:
In the medical field, OCTADECAMETHYLCYCLONONASILOXANE may be employed as a component in disinfectants and sterilants for medical equipment. Its antibacterial properties help to ensure a sterile environment and reduce the risk of hospital-acquired infections.
Used in Water Treatment:
OCTADECAMETHYLCYCLONONASILOXANE can be applied in water treatment processes to control bacterial growth and maintain water quality. Its effectiveness against marine Bacillus cereus makes it suitable for use in both freshwater and marine environments.
Overall, OCTADECAMETHYLCYCLONONASILOXANE is a versatile compound with a wide range of applications, particularly in industries where antibacterial properties are crucial for maintaining cleanliness, safety, and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 556-71-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 556-71:
(5*5)+(4*5)+(3*6)+(2*7)+(1*1)=78
78 % 10 = 8
So 556-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H54O9Si9/c1-28(2)19-29(3,4)21-31(7,8)23-33(11,12)25-35(15,16)27-36(17,18)26-34(13,14)24-32(9,10)22-30(5,6)20-28/h1-18H3

556-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4,6,6,8,8,10,10,12,12,14,14,16,16,18,18-octadecamethyl-1,3,5,7,9,11,13,15,17-nonaoxa-2,4,6,8,10,12,14,16,18-nonasilacyclooctadecane

1.2 Other means of identification

Product number -
Other names OCTADECAMETHYLCYCLONONASILOXANE

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:556-71-8 SDS

556-71-8Downstream Products

556-71-8Relevant academic research and scientific papers

Hydrogenolysis of Polysilanes Catalyzed by Low-Valent Nickel Complexes

Comas-Vives, Aleix,Eiler, Frederik,Grützmacher, Hansj?rg,Pribanic, Bruno,Trincado, Monica,Vogt, Matthias

supporting information, p. 15603 - 15609 (2020/04/29)

The dehydrogenation of organosilanes (RxSiH4?x) under the formation of Si?Si bonds is an intensively investigated process leading to oligo- or polysilanes. The reverse reaction is little studied. To date, the hydrogenolysis of Si?Si bonds requires very harsh conditions and is very unselective, leading to multiple side products. Herein, we describe a new catalytic hydrogenation of oligo- and polysilanes that is highly selective and proceeds under mild conditions. New low-valent nickel hydride complexes are used as catalysts and secondary silanes, RR′SiH2, are obtained as products in high purity.

High-efficiency macrocyclic dimethyl siloxane compound preparation method

-

Paragraph 0008; 0023, (2017/10/13)

The invention discloses a high-efficiency macrocyclic dimethyl siloxane compound preparation method which comprises the following steps: (1) utilizing tetramethyl disiloxane and octamethyl cyclotetrasiloxane as raw materials, performing ring-openingopen cycle in a sodium hydroxide or potassium hydroxide water solution and then inserting again to obtain dimethyl hydrogen silicone end capped direct-linked siloxane; (2) chlorinating the dimethyl hydrogen silicone end capped direct-linked siloxane with acetyl chloride under a catalytic effect of aluminum trichloride to obtain dimethyl chlorosilane end capped direct-linked siloxane; (3) hydrolyzing the direct-linked siloxane under the alkali condition to obtain varieties of macrocyclic diemthyl silicon ring bodies. The preparation method has simple steps and economical and safe technology and can be used for obtaining varieties of high-purity macrocyclic diemthyl silicon ring body products from simple raw materials; thus, high-difficulty distillation is avoided, and the preparation method is very suitable for industrial production.

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