Dodecyltrimethoxysilane Basic Product Information

Product Name	Dodecyltrimethoxysilane	CAS	3069-21-4
Synonyms	1-(Trimethoxysilyl)dodecane;n-Dodecyltrimethoxysilane;Trimethoxydodecylsilane;	Molecular Formula	C15H34O3Si
EINECS Number	221-332-4	Molecular Structure
Appearance	Light Yellow Powder
Purity	AR 98%
Supply Ability

Dodecyltrimethoxysilane Quality documents

Dodecyltrimethoxysilane Appearance/Package/Shipping/Storage

package

storage condition

Store in cool & dry place,Keep away from strong light and heat

Dodecyltrimethoxysilane Application

Dodecyltrimethoxysilane literature

TWO-COMPONENT SYSTEM FOR SMOOTHING AND CARE OF HAIR

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, (2022/01/23)

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COSMETIC PRODUCT FOR TREATING A KERATIN MATERIAL, COMPRISING A FILM-FORMING AND/OR SETTING CONSTITUENT

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, (2022/01/21)

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METHOD OF PRODUCING A HYDROLYZABLE SILICON-CONTAINING COMPOUND

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Page/Page column 17; 20, (2012/07/14)

The present invention provides a safe, inexpensive, and high yield means of producing a hydrolyzable silicon-containing compound, e.g., an organooxysilane and the like. A compound (A) represented by the general formula R¹-O-R² wherein R¹ represents a C_4-30, substituted or unsubstituted, tertiary alkyl group or aralkyl group and R² represents a C_1-30, substituted or unsubstituted, monovalent hydrocarbyl group or acyl group, is reacted in the presence of a Lewis acid catalyst with a halosilane (B) represented by the general formula R³_mSiX_4-m wherein R³ represents the hydrogen atom or a C_1-30 substituted or unsubstituted monovalent hydrocarbyl group, X is independently bromine or chlorine, and m represents an integer from 0 to 3.

Practical conversion of chlorosilanes into alkoxysilanes without generating HCl

Wakabayashi, Ryutaro,Sugiura, Yasushi,Shibue, Toshimichi,Kuroda, Kazuyuki

supporting information; experimental part, p. 10708 - 10711 (2011/12/05)

Alcohol-free: A versatile, efficient, and practical synthesis of alkoxysilanes without generation of HCl involves the reaction of chlorosilanes with unsymmetrical ethers in the presence of a Lewis acid (see scheme). The reaction proceeds through selective cleavage of C-O bonds and is superior to conventional processes. Industrially feasible reagents are used and only one by-product results. Copyright

Dodecyltrimethoxysilane Upstream and downstream

3069-21-4 Upstream product

• 67-56-1

  methanol 

• 15890-72-9

  laurylmagnesium bromide 

• 865-33-8

  potassium methanolate 

• 113823-65-7

  Trihydroxydodecylsilan 

• 4484-72-4

  n-dodecyltrichlorosilane 

• 1634-04-4

  tert-butyl methyl ether 

3069-21-4 Downstream Products

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