3-Glycidoxypropyltrimethoxysilane Basic Product Information

Product Name	3-Glycidoxypropyltrimethoxysilane	CAS	2530-83-8
Synonyms	((3-(Trimethoxysilyl)propoxy)methyl)oxirane;(3-(Glycidyloxy)propyl)trimethoxysilane;(3-Glycidoxypropyl)trimethoxysilane;1-(Glycidyloxy)-3-(trimethoxysilyl)propane;3-(2,3-Epoxypropoxy)propyltrimethoxysilane;Glycidyl 3-(trimethoxysilyl)propyl ether;Glycidyloxypropyltrimethoxysilane;	Molecular Formula	C9H20O5Si
EINECS Number	219-784-2	Molecular Structure
Appearance	Light Yellow Powder
Purity	AR 98%
Supply Ability

3-Glycidoxypropyltrimethoxysilane Quality documents

3-Glycidoxypropyltrimethoxysilane Appearance/Package/Shipping/Storage

package

storage condition

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

3-Glycidoxypropyltrimethoxysilane Application

3-Glycidoxypropyltrimethoxysilane literature

Process for preparing 3-glycidyloxypropyltrialkoxysilanes

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Paragraph 0139-0142; 0144-0153, (2019/02/24)

A process can prepare a 3-glycidyloxypropylalkoxysilane of formula (I), (R′)O—(CH₂)₃—Si(OR)₃ (I), where R groups are independently a methyl or ethyl group and R′ represents an H₂C(O)CHCH₂— group. The process includes reacting (i) a functionalized alkene of formula (II), (R′)O—C₃H₅ (II), where R′ represents an H₂C(O)CHCH₂— group, with (ii) at least one hydroalkoxysilane of formula (III), HSi(OR)₃ (III), where R groups are independently a methyl or ethyl group. The reacting takes place in the presence of (iii) a Karstedt catalyst or a catalyst having hexachloroplatinic acid as a homogeneous catalyst, and (iv) 2-ethylhexanoic acid, isononanoic acid, or both. The process further includes obtaining a product of the reacting.

An Easily Accessed Nickel Nanoparticle Catalyst for Alkene Hydrosilylation with Tertiary Silanes

Buslov, Ivan,Song, Fang,Hu, Xile

supporting information, p. 12295 - 12299 (2016/10/13)

The first efficient and non-precious nanoparticle catalyst for alkene hydrosilylation with commercially relevant tertiary silanes has been developed. The nickel nanoparticle catalyst was prepared in situ from a simple nickel alkoxide precatalyst Ni(O^tBu)₂?x KCl. The catalyst exhibits high activity for anti-Markovnikov hydrosilylation of unactivated terminal alkenes and isomerizing hydrosilylation of internal alkenes. The catalyst can be applied to synthesize a single terminal alkyl silane from a mixture of internal and terminal alkene isomers, and to remotely functionalize an internal alkene derived from a fatty acid.

Method for preparing organic silicon by passage reaction device

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Paragraph 0049, (2016/10/17)

The invention provides a method for preparing organic silicon by a passage reaction device. Under the condition of main catalysts Z, hydrogen-containing silane X and an unsaturated compound Y are introduced into the passage reaction device; hydrosilylation reaction is performed to prepare the organic silicon, wherein the hydrogen-containing silane X has the structure being HSiRR'Cl, in the formula, R and R' are independently C1 to C16 alkyl or alkoxy; a=1, 2 or 3; b, c and d are respectively and independently 0, 1, 2 or 3; the unsaturated compound Y is a monoene compound or single-alkyne compound; the main catalysts Z are one or several mixed ones of single-component complexes or multi-component complexes of Pt, Pd, Rh, Ru, Cu, Ag, Au or Ir; the passage surface in which reaction flow contacts is subjected to inactivation treatment by an activating agent Z. The problems of long reaction period, poor stability and the like of large-sized reaction equipment are solved; the problem that mixing, pre-reaction and afterreaction are separated and are performed in multi-unit equipment is solved.