Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1067-25-0

Post Buying Request

1067-25-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1067-25-0 Usage

Description

Trimethoxypropylsilane, also known as Propyltrimethoxysilane, is an alkylalkoxysilane that exists as a colorless, low viscosity liquid. It consists of an n-propyl organic group and a trimethoxysilyl inorganic group, which together provide a hydrophobic surface treatment. This versatile compound is widely utilized in various industries due to its unique properties and applications.

Uses

Trimethoxypropylsilane is used as a key material in sol-gel production, where it adds moderate organic properties to the silicone mesh, similar to the propyl group in the product. The presence of propyl groups also enhances the organic properties of the product.
Used in Sol-Gel Production:
Trimethoxypropylsilane is used as an important material in sol-gel production for providing a hydrophobic surface treatment to inorganic powders or filler materials. This application is crucial in creating materials with tailored properties for various industries.
Used in Polyolefin Production:
Trimethoxypropylsilane serves as one of the catalyst components for polyolefin production using Ziegler-Natta catalysts. Its role in this process is essential for the efficient and effective production of polyolefins.
Used in Silicone Sealant Formulations:
Trimethoxypropylsilane is used as a neutral curing agent in silicone sealant formulations. It is primarily utilized for crosslinking α,ω-silanol polydimethylsiloxanes in the presence of atmospheric moisture. This silane is often the main crosslinker of choice for oxime silicone sealants and can be used alone or in combination with other oxime silanes to achieve targeted properties, such as desired cure rate and adhesion.
Chemical Properties:
Trimethoxypropylsilane is a colorless or yellowish clear liquid with unique chemical properties that make it suitable for a wide range of applications. Its ability to react faster with water than other similar compounds allows customers to regulate the rate of hydrolysis according to their specific application needs.

Flammability and Explosibility

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 1067-25-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1067-25:
(6*1)+(5*0)+(4*6)+(3*7)+(2*2)+(1*5)=60
60 % 10 = 0
So 1067-25-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H16O3Si/c1-5-6-10(7-2,8-3)9-4/h5-6H2,1-4H3

1067-25-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B21033)  n-Propyltrimethoxysilane, 98+%   

  • 1067-25-0

  • 25g

  • 303.0CNY

  • Detail
  • Alfa Aesar

  • (B21033)  n-Propyltrimethoxysilane, 98+%   

  • 1067-25-0

  • 100g

  • 663.0CNY

  • Detail
  • Alfa Aesar

  • (B21033)  n-Propyltrimethoxysilane, 98+%   

  • 1067-25-0

  • 500g

  • 2412.0CNY

  • Detail
  • Aldrich

  • (662275)  Trimethoxy(propyl)silane  97%

  • 1067-25-0

  • 662275-100ML

  • 370.89CNY

  • Detail
  • Aldrich

  • (662275)  Trimethoxy(propyl)silane  97%

  • 1067-25-0

  • 662275-1L

  • 975.78CNY

  • Detail

1067-25-0SDS

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 Trimethoxy(propyl)silane

1.2 Other means of identification

Product number -
Other names trimethoxy(propyl)silane

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:1067-25-0 SDS

1067-25-0Synthetic route

2-methylene-1,3-diglycidoxypropane
3775-28-8

2-methylene-1,3-diglycidoxypropane

trimethoxysilane
2487-90-3

trimethoxysilane

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

Conditions
ConditionsYield
chloroplatinic acid In isopropyl alcohol85%
trimethoxysilane
2487-90-3

trimethoxysilane

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

A

bis(trimethoxysilyl)propane

bis(trimethoxysilyl)propane

B

3-chloropropyltrichlorosilane
253586-30-0

3-chloropropyltrichlorosilane

C

chlorotrimethoxysilane
4668-00-2

chlorotrimethoxysilane

D

tetramethylorthosilicate
681-84-5

tetramethylorthosilicate

E

1-Chloropropane
540-54-5

1-Chloropropane

F

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

G

3-Chloropropyltrimethoxysilan
2530-87-2

3-Chloropropyltrimethoxysilan

Conditions
ConditionsYield
With toluene; ruthenium trichloride In methanol at 20 - 83℃; for 2h; Product distribution / selectivity;
[ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In dichloromethane at 20 - 83℃; for 2h; Product distribution / selectivity;
ruthenium trichloride In methanol at 75 - 169℃; for 18h; Product distribution / selectivity; Continuous operation;
trimethoxysilane
2487-90-3

trimethoxysilane

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

A

3-chloropropyltrichlorosilane
253586-30-0

3-chloropropyltrichlorosilane

B

chlorotrimethoxysilane
4668-00-2

chlorotrimethoxysilane

C

tetramethylorthosilicate
681-84-5

tetramethylorthosilicate

D

1-Chloropropane
540-54-5

1-Chloropropane

E

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

F

3-Chloropropyltrimethoxysilan
2530-87-2

3-Chloropropyltrimethoxysilan

Conditions
ConditionsYield
With toluene; ruthenium trichloride In methanol at 20 - 83℃; for 2h; Product distribution / selectivity;
Stage #1: trimethoxysilane; ruthenium trichloride In methanol; toluene at 20 - 80℃; Heating / reflux;
Stage #2: 3-chloroprop-1-ene at 78 - 83℃; for 2h;
1,1,1,3,3-pentamethyl-1,3-disiloxane
1438-82-0

1,1,1,3,3-pentamethyl-1,3-disiloxane

C13H22OSi

C13H22OSi

A

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

B

C11H30O5Si3
1254985-33-5

C11H30O5Si3

C

C12H22O2Si2

C12H22O2Si2

Conditions
ConditionsYield
With tris(pentafluorophenyl)borate In hexane; toluene at 20℃;
1,1,1,3,3-pentamethyl-1,3-disiloxane
1438-82-0

1,1,1,3,3-pentamethyl-1,3-disiloxane

C9H24O4Si2

C9H24O4Si2

A

1,1,1,5,5,5-hexamethyl-3-propyl-3-[(trimethylsilyl)oxy]trisiloxane

1,1,1,5,5,5-hexamethyl-3-propyl-3-[(trimethylsilyl)oxy]trisiloxane

B

Octamethyltrisiloxane
107-51-7

Octamethyltrisiloxane

C

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

D

C11H30O5Si3
1254985-33-5

C11H30O5Si3

Conditions
ConditionsYield
With tris(pentafluorophenyl)borate In hexane; toluene at 20℃; for 0.0833333h;
methanol
67-56-1

methanol

n-propyltrichlorosilane
141-57-1

n-propyltrichlorosilane

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

Conditions
ConditionsYield
at 20℃; pH=5.6; pH-value;
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

potassium propyl silicate

potassium propyl silicate

Conditions
ConditionsYield
With hydrogenchloride; methanol; potassium chloride In water at 32 - 35℃; for 3.03h;95.1%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

1-oxo-1-methyl-4-ethyl-4-hydroxymethyl-2,6-dioxa-1-phosphacyclohexane
1365801-87-1

1-oxo-1-methyl-4-ethyl-4-hydroxymethyl-2,6-dioxa-1-phosphacyclohexane

C12H27O6PSi

C12H27O6PSi

Conditions
ConditionsYield
In 1,4-dioxane at 90℃; for 11h; Solvent; Temperature; Inert atmosphere;94.7%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

2,3-naphthalenediol
92-44-4

2,3-naphthalenediol

Potassium; 3-(2-propyl-1,3-dioxa-2-sila-cyclopenta[b]naphthalen-2-yloxy)-naphthalen-2-olate

Potassium; 3-(2-propyl-1,3-dioxa-2-sila-cyclopenta[b]naphthalen-2-yloxy)-naphthalen-2-olate

Conditions
ConditionsYield
With potassium ethoxide In ethanol Heating;94%
Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

A

1,1,1,5,5,5-hexamethyl-3-propyl-3-[(trimethylsilyl)oxy]trisiloxane

1,1,1,5,5,5-hexamethyl-3-propyl-3-[(trimethylsilyl)oxy]trisiloxane

B

n-PrSi(OMe)(OSiMe3)2

n-PrSi(OMe)(OSiMe3)2

C

n-PrSi(OH)(OSiMe3)2

n-PrSi(OH)(OSiMe3)2

Conditions
ConditionsYield
Stage #1: Hexamethyldisiloxane With methanol; sulfuric acid at 5 - 10℃; for 1h;
Stage #2: n-propyltrimethoxysilane at 5 - 10℃; for 1.75h;
Stage #3: With sulfuric acid; water more than 3 stages;
A 93.8%
B n/a
C n/a
18-crown-6 ether
17455-13-9

18-crown-6 ether

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

benzene-1,2-diol
120-80-9

benzene-1,2-diol

C15H15O4Si(1-)*C12H24KO6(1+)

C15H15O4Si(1-)*C12H24KO6(1+)

Conditions
ConditionsYield
With potassium methanolate In methanol at 20℃; for 3h; Schlenk technique; Inert atmosphere;91%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

ethriol phosphite
824-11-3

ethriol phosphite

C24H49O12P3Si

C24H49O12P3Si

Conditions
ConditionsYield
With dimethyl sulfate at 140 - 160℃; for 16h; Concentration; Temperature; Reagent/catalyst; Solvent; Inert atmosphere;90.4%
Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

1,1,1,5,5,5-hexamethyl-3-propyl-3-[(trimethylsilyl)oxy]trisiloxane

1,1,1,5,5,5-hexamethyl-3-propyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
Stage #1: Hexamethyldisiloxane With sulfonic acid In methanol at 5 - 10℃;
Stage #2: n-propyltrimethoxysilane In methanol at 5 - 10℃; for 1.75h;
Stage #3: With water In methanol at 5 - 25℃; for 5h;
90%
Stage #1: Hexamethyldisiloxane With methanol; sulfuric acid at -10 - 10℃; for 1h;
Stage #2: n-propyltrimethoxysilane at 5 - 10℃; for 1.75h;
Stage #3: With water at 5 - 25℃; for 4h;
88.2%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

C3H7F4Si(1-)*K(1+)

C3H7F4Si(1-)*K(1+)

Conditions
ConditionsYield
With potassium hydrogen bifluoride In water; acetone at 20℃; for 0.166667h;89%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

C3H9KO2Si

C3H9KO2Si

Conditions
ConditionsYield
With water; potassium hydroxide In methanol at 40 - 110℃; for 1.5h;78%
1,2,3-trimethoxybenzene
621-23-8

1,2,3-trimethoxybenzene

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

dimethoxy(2,4,6-trimethoxyphenyl)propylsilane

dimethoxy(2,4,6-trimethoxyphenyl)propylsilane

Conditions
ConditionsYield
Stage #1: 1,2,3-trimethoxybenzene With n-butyllithium; N,N,N,N,-tetramethylethylenediamine In hexane; pentane at 20℃; for 17h;
Stage #2: n-propyltrimethoxysilane In diethyl ether; hexane; pentane at 20℃; for 17h;
72%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

trisodium tri-n-propylcyclotrisiloxanolate

trisodium tri-n-propylcyclotrisiloxanolate

Conditions
ConditionsYield
With sodium hydroxide In ethanol; water for 0.5h; Reflux;71%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

4-methoxyphenyl magnesium bromide
13139-86-1

4-methoxyphenyl magnesium bromide

dimethoxy(4-methoxyphenyl)propylsilane

dimethoxy(4-methoxyphenyl)propylsilane

Conditions
ConditionsYield
In tetrahydrofuran; diethyl ether at 20℃; for 19h;67%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

C3H7F4Si(1-)*H3N*H(1+)

C3H7F4Si(1-)*H3N*H(1+)

Conditions
ConditionsYield
With ammonium hydrogen difluoride In water; acetone at 20℃; Solvent;67%
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

1,3-Dimethoxybenzene
151-10-0

1,3-Dimethoxybenzene

dimethoxy(2,6-dimethoxyphenyl)propylsilane

dimethoxy(2,6-dimethoxyphenyl)propylsilane

Conditions
ConditionsYield
Stage #1: 1,3-Dimethoxybenzene With n-butyllithium; N,N,N,N,-tetramethylethylenediamine In hexane; pentane at 20℃; for 17h;
Stage #2: n-propyltrimethoxysilane In diethyl ether; hexane; pentane at 20℃; for 17h;
58%
1,3,5,7,9,11,14-heptaisobutyltricyclo[7.3.3.15,11]heptasiloxane-endo-3,7,14-triol
307531-92-6

1,3,5,7,9,11,14-heptaisobutyltricyclo[7.3.3.15,11]heptasiloxane-endo-3,7,14-triol

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

C31H70O12Si8

C31H70O12Si8

Conditions
ConditionsYield
In hexane48%
N,N-bis-(2-hydroxyethyl)glycine
150-25-4

N,N-bis-(2-hydroxyethyl)glycine

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

1-propyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecan-3-one
85462-12-0

1-propyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecan-3-one

Conditions
ConditionsYield
In N,N-dimethyl-formamide; benzene
3-(trimethoxysilyl)-1-propanethiol
4420-74-0

3-(trimethoxysilyl)-1-propanethiol

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

A

octa-n-propylsilsesquioxane
18971-71-6

octa-n-propylsilsesquioxane

B

Si8O12(CH2CH2CH3)6((CH2)3SH)2
161678-45-1

Si8O12(CH2CH2CH3)6((CH2)3SH)2

C

C24H56O12S2Si8

C24H56O12S2Si8

D

Si8O12(CH2CH2CH3)7(CH2)3SH
161678-44-0

Si8O12(CH2CH2CH3)7(CH2)3SH

Conditions
ConditionsYield
With hydrogenchloride In methanol at 20℃; for 504h; Yield given. Further byproducts given. Yields of byproduct given;
3-(trimethoxysilyl)-1-propanethiol
4420-74-0

3-(trimethoxysilyl)-1-propanethiol

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

A

octa-n-propylsilsesquioxane
18971-71-6

octa-n-propylsilsesquioxane

B

C24H56O12S2Si8

C24H56O12S2Si8

C

C24H56O12S2Si8

C24H56O12S2Si8

D

Si8O12(CH2CH2CH3)7(CH2)3SH
161678-44-0

Si8O12(CH2CH2CH3)7(CH2)3SH

Conditions
ConditionsYield
With hydrogenchloride In methanol at 20℃; for 504h; Yield given. Further byproducts given. Yields of byproduct given;
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

A

octa-n-propylsilsesquioxane
18971-71-6

octa-n-propylsilsesquioxane

B

Si8O12(CH2CH2CH3)6((CH2)3SH)2
161678-45-1

Si8O12(CH2CH2CH3)6((CH2)3SH)2

C

C24H56O12S2Si8

C24H56O12S2Si8

D

Si8O12(CH2CH2CH3)7(CH2)3SH
161678-44-0

Si8O12(CH2CH2CH3)7(CH2)3SH

Conditions
ConditionsYield
With hydrogenchloride; 3-(trimethoxysilyl)-1-propanethiol In methanol at 20℃; for 504h; Yield given. Further byproducts given. Yields of byproduct given;
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

propyl silanetriol

propyl silanetriol

Conditions
ConditionsYield
With acetic acid In isopropyl alcohol pH=3.5-5.5;
With water
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

methyl hypophosphite
14684-31-2

methyl hypophosphite

Conditions
ConditionsYield
With anilinium hypophosphorous salt In acetonitrile for 3h; Heating;100 % Spectr.
With hypophosphorous acid In water; acetonitrile for 3h; Reflux; Inert atmosphere;
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

C5H14O3Si

C5H14O3Si

Conditions
ConditionsYield
With hydrogenchloride In acetone at 29.85℃; pH=4; Kinetics; Further Variations:; pH-values; Reagents;
n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

phenylmagnesium bromide
100-58-3

phenylmagnesium bromide

(phenyl)-propyl-dimethoxysilane

(phenyl)-propyl-dimethoxysilane

1-Bromo-2,4-dimethoxybenzene
17715-69-4

1-Bromo-2,4-dimethoxybenzene

n-propyltrimethoxysilane
1067-25-0

n-propyltrimethoxysilane

(2,4-dimethoxyphenyl)-propyl-dimethoxysilane
344927-18-0

(2,4-dimethoxyphenyl)-propyl-dimethoxysilane

Conditions
ConditionsYield
With n-butyllithium In ethanol; hexane

1067-25-0Relevant articles and documents

Jones,P.R.,Lim,T.F.O.

, p. 27 - 33 (1976)

Synthetic method of linear dihydric alcohol

-

Paragraph 0104-0106; 0125-0130, (2021/09/01)

The invention discloses a synthetic method of linear dihydric alcohol. The synthetic method comprises the following steps: (1) carrying out hydrosilylation reaction on alpha-olefin and siloxane to obtain alkyl siloxane; (2) carrying out hydroxymethylation reaction on alkyl siloxane, organic metal alkali and a hydrogen acceptor to obtain silyl alcohol; and (3) carrying out oxidation reaction on the silyl alcohol, fluorine-containing metal salt and peroxide to obtain the linear dihydric alcohol. The method has the advantages of mild process, easily available raw material sources, no need of post-treatment after the reaction is completed, capability of being directly used for the next reaction, simplification of the process flow, high conversion rate, high selectivity, low cost and suitability for large-scale production.

COSMETIC TREATMENT METHOD COMPRISING THE APPLICATION OF A COATING BASED ON AN AEROGEL COMPOSITION OF LOW BULK DENSITY

-

Paragraph 0067, (2014/02/15)

The present invention relates to a cosmetic treatment method comprising the formation of a coating on keratin fibres characterized in that it comprises: 1) the preparation of an aerogel precursor composition comprising:—at least one organic solvent chosen from acetone, C1-C4 alcohols, C1-C6 alkanes, C1-C4 ethers, which may or may not be perfluorinated, and mixtures thereof and at least one precursor compound that contains:—at least one atom chosen from silicon, titanium, aluminium and zirconium,—at least one hydroxyl or alkoxy function directly attached to the atom chosen from silicon, titanium, aluminium and zirconium by an oxygen atom, and,—optionally an organic group directly attached to the atom chosen from silicon, titanium, aluminium and zirconium by a carbon atom, 2) the removal of the solvent or solvents resulting in the formation of an aerogel composition having a bulk density less than or equal to 0.35 g/cm3, 3) the application to the keratin fibres of the aerogel composition resulting from step 2) or of the aerogel precursor composition resulting from step 1). Advantageously, the molar ratio between the precursor compounds and the solvent is at most 1/20.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1067-25-0