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Eicosamethylcyclopentasiloxane, a cyclic siloxane compound with the molecular formula C26H54O6Si6, is a silicone-based ingredient widely utilized in cosmetic and personal care products. Known for its smooth and silky feel, it serves as an emollient and conditioning agent, enhancing the texture and appearance of skin and hair. Its low viscosity and quick evaporation properties contribute to a non-greasy, easily spreadable texture, making it a popular alternative to traditional hydrocarbon-based oils and emollients.

18772-36-6

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18772-36-6 Usage

Uses

Used in Cosmetic and Personal Care Industry:
Eicosamethylcyclopentasiloxane is used as an emollient and conditioning agent for its ability to provide a smooth and silky feel to the skin and hair. It is incorporated into various beauty products such as lotions, creams, and hair care products to improve their texture and performance.
Used in Skin Care Products:
Eicosamethylcyclopentasiloxane is used as a skin conditioning agent to enhance the smoothness and softness of the skin. Its non-greasy texture and quick absorption make it an ideal ingredient for skin care formulations, providing a pleasant sensory experience for users.
Used in Hair Care Products:
In hair care products, Eicosamethylcyclopentasiloxane is used as a conditioning agent to improve the manageability, shine, and overall health of the hair. Its ability to provide a smooth texture without weighing the hair down makes it a preferred ingredient in hair care formulations.
Used as an Alternative to Traditional Hydrocarbon-based Oils and Emollients:
Eicosamethylcyclopentasiloxane is used as a substitute for traditional hydrocarbon-based oils and emollients due to its unique properties, such as low viscosity, quick evaporation, and non-greasy texture. This makes it a preferred choice for formulations that require a lightweight, smooth, and silky feel.

Check Digit Verification of cas no

The CAS Registry Mumber 18772-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,7 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18772-36:
(7*1)+(6*8)+(5*7)+(4*7)+(3*2)+(2*3)+(1*6)=136
136 % 10 = 6
So 18772-36-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H60O10Si10/c1-31(2)21-32(3,4)23-34(7,8)25-36(11,12)27-38(15,16)29-40(19,20)30-39(17,18)28-37(13,14)26-35(9,10)24-33(5,6)22-31/h1-20H3

18772-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4,6,6,8,8,10,10,12,12,14,14,16,16,18,18,20,20-icosamethyl-1,3,5,7,9,11,13,15,17,19-decaoxa-2,4,6,8,10,12,14,16,18,20-decasilacycloicosane

1.2 Other means of identification

Product number -
Other names Cyclodeiloxane,eicosamethyl

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:18772-36-6 SDS

18772-36-6Downstream Products

18772-36-6Relevant 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; 0026, (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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