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CAS

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3-Aminopropyltriethoxysilane, also known as gamma-Aminopropyltriethoxysilane, is a versatile amino-functional coupling agent that provides superior bonds between inorganic substrates and organic polymers. The silicon-containing portion of the molecule offers strong bonding to substrates, while the primary amine function reacts with a wide array of thermoset, thermoplastic, and elastomeric materials.

919-30-2

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  • Top purity KH550 3-Aminopropyltriethoxysilane,KH-550 Union Carbide A-1100 Dow Corning Z-6011 KBM-903 3-Aminopropyltriethoxysilane with high quality and best price cas:919-30-2

    Cas No: 919-30-2

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919-30-2 Usage

Uses

Used in Plastic Products Industry:
3-Aminopropyltriethoxysilane is used as a coupling agent for enhancing the physical and electrical properties of mineral-filled phenolics, epoxies, polyamides, polybutylene terephthalate, and other thermoset and thermoplastic composites. It improves filler wetting and dispersibility in the polymer matrix.
Used in Rubber Products Industry:
3-Aminopropyltriethoxysilane is used as a coupling agent to improve adhesion between magnetic powder and organic resins, as well as the dispersion of magnetic powder in inorganic resins. This results in magnetic appliances with higher magnetic orientation, excellent magnetic properties, higher mechanical strength, good processability, and excellent weathering resistance.
Used in Adhesives and Coatings Industry:
3-Aminopropyltriethoxysilane is used as a coupling agent to improve pigment dispersion and maximize adhesion to glass, aluminum, and steel in nitrile, polysulfide, epoxy, urethane, and adhesives and sealants.
Used in Glass-Reinforced Thermoset Plastics Industry:
3-Aminopropyltriethoxysilane is used as a coupling agent to enhance the flexural, compressive, and interlaminar shear strengths before and after exposure to humidity, as well as to greatly improve wet electrical properties.
Used in Glass Fiber and Mineral Wool Insulation Industry:
3-Aminopropyltriethoxysilane is used as a phenolics resin binder additive to impart moisture resistance and allow recovery after compression.
Used in Shell Molding Foundry Applications:
3-Aminopropyltriethoxysilane is used as a coupling agent to strengthen the bond between the phenolics binder and foundry sand.
Used in Grinding Wheels Industry:
3-Aminopropyltriethoxysilane is used as a coupling agent to promote an improved, water-resistant bond between the abrasive grit and phenolics resin binder.
Used in Glass-Reinforced Thermoplastics Industry:
3-Aminopropyltriethoxysilane is used as a coupling agent to increase flexural and tensile strengths before and after wet exposure in polyamides, polyesters, and polycarbonates.
Used in Urethane, Epoxy, and Acrylic Latex Coatings, Adhesives, and Sealants Industry:
3-Aminopropyltriethoxysilane is used as an adhesion promoter to enhance the performance of these materials.
Used in Laboratory Applications:
3-Aminopropyltriethoxysilane is used to form aminopropyl derivatives of glass, acting as an adsorbent for affinity chromatography. It is also used to prepare positively charged slides suitable for various immunohistochemical and in situ hybridization procedures.
Used in Silylation Applications:
3-Aminopropyltriethoxysilane is used as a silylation reagent for coating glass and silica surfaces and to crosslink and immobilize proteins and other molecules.

Silane coupling agent KH-550

3-Aminopropyltriethoxysilane is the earliest widely used coupling agent, so far has been more than 40 years of history. One end of the structure is provided with an active group, such as amino and vinyl, which can react with synthetic resin molecules such as epoxy, phenolic, polyester. The other end is alkoxy (such as methoxy, ethoxy etc.) or chlorine atoms which connected with silicon, and these groups. These groups can react with the hydroxyl groups on the surface of glass, minerals, inorganic fillers and generate reactive silicon alcohol in the presence of water in the aqueous solution or air. Therefore, silane coupling agent is often used in silicate-filled epoxy, phenolic, polyester resin and so on. In addition, it can also be used in the production of glass fiber reinforced plastic, in order to improve its mechanical strength and resistance to wet environment. The organic group of the silane coupling agent has selectivity to the reaction of the synthetic resin. Generally, these organic groups are insufficiently reactive with synthetic resins such as polyethylene, polypropylene, polystyrene and so on, so that the coupling effect is poor. In recent years, new types of silane coupling agents have been developed which have a good coupling effect on polyolefins, but it is not widely used in cost and other properties. Silane coupling agent, also known as silane treatment agent, primer. The general formula is Y (CH2) nSiX3, it is an organic silicon monomer with two or more different reactive groups in the molecule, which can be chemically bonded (coupled) with organic and inorganic materials, and increase the bonding property of the two materials. In the general formula, N is an integer of 0 to 3; X is a hydrolyzable group, such as chlorine, methoxy, ethoxy, acetoxy and the like, and is easily hydrolyzed to form a silanol which can be combined with an inorganic substance; Y is an organic functional group, such as a vinyl group, an amino group, an epoxy group, a methacryloyloxy group, a mercapto group and the like, which can react with organic compounds and combine. The performance of typical silane coupling agent is as follows: For glass fiber, inorganic filler surface treatment. Used as a sealant, adhesive and paint thickener. It also can be used to the immobilized enzyme attached to the surface of glass substrate, to sand control in oil well drilling, to prevent sand from drilling, to brick surface with hydrophobic, to make the fluorescent lamp coating have high surface resistance, and to improve the moisture absorption properties of organic matter on the surface of glass in the medium of liquid chromatography. It is catalyst in the platinum by the chloroform and alkene with the active group? and then obtained by alcoholysis. The molecular structure and application information of silane coupling agent 3-aminopropyltriethoxysilane are edited and edited by chemcialbook andy.

Flammability and Explosibility

Notclassified

Biochem/physiol Actions

(3-Aminopropyl)triethoxysilane forms aminopropyl derivative of glass, an adsorbent for affinity chromatography. It is used to prepare positively charged slides suitable for use with various immunohistochemical and in situ hybridization procedures.

Safety Profile

Poison by intraperitoneal route.Moderately toxic by ingestion and skin contact. A skin andeye irritant. When heated to decomposition it emits toxicfumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 919-30-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,1 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 919-30:
(5*9)+(4*1)+(3*9)+(2*3)+(1*0)=82
82 % 10 = 2
So 919-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H23NO3Si/c1-4-11-14(12-5-2,13-6-3)9-7-8-10/h4-10H2,1-3H3

919-30-2 Well-known Company Product Price

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  • Alfa Aesar

  • (A10668)  (3-Aminopropyl)triethoxysilane, 98%   

  • 919-30-2

  • 100g

  • 335.0CNY

  • Detail
  • Alfa Aesar

  • (A10668)  (3-Aminopropyl)triethoxysilane, 98%   

  • 919-30-2

  • 500g

  • 943.0CNY

  • Detail
  • Alfa Aesar

  • (A10668)  (3-Aminopropyl)triethoxysilane, 98%   

  • 919-30-2

  • 2500g

  • 3943.0CNY

  • Detail
  • Sigma-Aldrich

  • (A3648)  (3-Aminopropyl)triethoxysilane  ≥98%

  • 919-30-2

  • A3648-100ML

  • 655.20CNY

  • Detail
  • Sigma-Aldrich

  • (A3648)  (3-Aminopropyl)triethoxysilane  ≥98%

  • 919-30-2

  • A3648-500ML

  • 2,289.69CNY

  • Detail
  • Aldrich

  • (440140)  (3-Aminopropyl)triethoxysilane  99%

  • 919-30-2

  • 440140-100ML

  • 833.04CNY

  • Detail
  • Aldrich

  • (440140)  (3-Aminopropyl)triethoxysilane  99%

  • 919-30-2

  • 440140-500ML

  • 2,861.82CNY

  • Detail
  • Aldrich

  • (706493)  (3-Aminopropyl)triethoxysilane  packaged for use in deposition systems, ≥98%

  • 919-30-2

  • 706493-20ML

  • 13,700.70CNY

  • Detail
  • Aldrich

  • (741442)  (3-Aminopropyl)triethoxysilane  ≥98.0%

  • 919-30-2

  • 741442-100ML

  • 732.42CNY

  • Detail
  • Aldrich

  • (741442)  (3-Aminopropyl)triethoxysilane  ≥98.0%

  • 919-30-2

  • 741442-500ML

  • 2,529.54CNY

  • Detail

919-30-2SDS

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 (3-Aminopropyl)triethoxysilane

1.2 Other means of identification

Product number -
Other names 1-Propanamine, 3-(triethoxysilyl)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,CBI,Intermediates,Paint additives and coating additives not described by other categories,Processing aids, specific to petroleum production
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:919-30-2 SDS

919-30-2Synthetic route

C12H27NO3Si

C12H27NO3Si

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
In water at 65 - 75℃; for 3h; Concentration; Temperature;98%
sodium hydroxide
1310-73-2

sodium hydroxide

rhodium(III) chloride trihydrate

rhodium(III) chloride trihydrate

Triethoxysilane
998-30-1

Triethoxysilane

1-amino-2-propene
107-11-9

1-amino-2-propene

A

beta-aminopropyl triethoxy silane
53218-21-6

beta-aminopropyl triethoxy silane

B

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
In 5,5-dimethyl-1,3-cyclohexadieneA 90%
B n/a
(3-chloropropyl)triethoxysilane
5089-70-3

(3-chloropropyl)triethoxysilane

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
With ammonia81%
With ammonia
With ammonia
Triethoxysilane
998-30-1

Triethoxysilane

1-amino-2-propene
107-11-9

1-amino-2-propene

A

beta-aminopropyl triethoxy silane
53218-21-6

beta-aminopropyl triethoxy silane

B

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
In para-xyleneA 81%
B n/a
In tolueneA 78%
B n/a
In tolueneA 78%
B n/a
Triethoxysilane
998-30-1

Triethoxysilane

1-amino-2-propene
107-11-9

1-amino-2-propene

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
75%
rhodium hydride carbonyl-tris(triphenylphosphine)34%
rhodium hydride carbonyl-tris(triphenylphosphine)34%
With rhodium(III) trichloride hydrate; triphenylphosphine at 95℃;
1,5-cis,cis-cyclooctadiene
1552-12-1, 111-78-4

1,5-cis,cis-cyclooctadiene

Triethoxysilane
998-30-1

Triethoxysilane

1-amino-2-propene
107-11-9

1-amino-2-propene

A

beta-aminopropyl triethoxy silane
53218-21-6

beta-aminopropyl triethoxy silane

B

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
In 5,5-dimethyl-1,3-cyclohexadieneA 75%
B n/a
In 5,5-dimethyl-1,3-cyclohexadieneA 75%
B n/a
Triethoxysilane
998-30-1

Triethoxysilane

1-amino-2-propene
107-11-9

1-amino-2-propene

A

tetraethoxy orthosilicate
78-10-4

tetraethoxy orthosilicate

B

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
With dihydrogen hexachloroplatinate; 7,8-dicarba-nido-undecaborate(1-) for 10h; Product distribution; Heating; other reaction time, various catalyst composition, other catalysts;A 11.1%
B 69.9%
With dihydrogen hexachloroplatinate; 7,8-dicarba-nido-undecarborate(1-) for 10h;A 11.1%
B 69.9%
allylamino-trimethyl-silane
10519-97-8

allylamino-trimethyl-silane

Triethoxysilane
998-30-1

Triethoxysilane

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
With dihydrogen hexachloroplatinate; ethanol
2-cyanoethyltriethoxysilane
919-31-3

2-cyanoethyltriethoxysilane

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
With nickel Hydrogenation;
Triethoxysilane
998-30-1

Triethoxysilane

1-amino-2-propene
107-11-9

1-amino-2-propene

A

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

B

(2-amino-1-methylethyl)triethoxysilane
36957-84-3

(2-amino-1-methylethyl)triethoxysilane

Conditions
ConditionsYield
With Allyl glycidyl ether; dihydrogen hexachloroplatinate; isopropyl alcohol for 13h; Product distribution; Mechanism; influence unsaturated Si-comp. on rate of hydrosilylation; effect of other additives;A 74.8 % Chromat.
B n/a
With (dicyclopentadiene)platinum(II) dichloride at 85℃; for 20h; Inert atmosphere; Schlenk technique; Overall yield = 84 %Spectr.;
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 80℃; for 20h; Schlenk technique; Inert atmosphere; Overall yield = 94.2 %Spectr.; regioselective reaction;
(3-chloropropyl)triethoxysilane
5089-70-3

(3-chloropropyl)triethoxysilane

A

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

B

bis-<3-triethoxysilanyl-propyl>-amine and tris-<3-triethoxysilanyl-propyl>-amine

bis-<3-triethoxysilanyl-propyl>-amine and tris-<3-triethoxysilanyl-propyl>-amine

Conditions
ConditionsYield
With ammonia
ethanol
64-17-5

ethanol

C11H27NO4Si

C11H27NO4Si

A

2-ethoxy-ethanol
110-80-5

2-ethoxy-ethanol

B

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
at 20℃; Kinetics; Equilibrium constant;
2,2-diethoxy-1,2-azasilolidine

2,2-diethoxy-1,2-azasilolidine

ethanol
64-17-5

ethanol

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

3-(triethoxysilyl)propylammonium 3-(triethoxysilyl)propylcarbamate
140236-87-9

3-(triethoxysilyl)propylammonium 3-(triethoxysilyl)propylcarbamate

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
at 120℃; for 2h;
at 69℃;
ethanol
64-17-5

ethanol

C3H11NSi*TiO2

C3H11NSi*TiO2

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Conditions
ConditionsYield
With hydrogenchloride In water for 1h;
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

<3-(2-Pyridyl)-1-pyrazolyl>essigsaeure-ethylester
162435-10-1

<3-(2-Pyridyl)-1-pyrazolyl>essigsaeure-ethylester

N-(3-triethoxysilylpropyl)-[3-(2-pyridyl)-1-pyrazolyl]acetamide

N-(3-triethoxysilylpropyl)-[3-(2-pyridyl)-1-pyrazolyl]acetamide

Conditions
ConditionsYield
at 150℃; for 2h;100%
In tetrahydrofuran at 150℃; for 2h;
maleic anhydride
108-31-6

maleic anhydride

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

(E)-butenedioic acid 3-(triethoxysilyl)propylamide

(E)-butenedioic acid 3-(triethoxysilyl)propylamide

Conditions
ConditionsYield
100%
at 50 - 60℃;99%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

acrylonitrile
107-13-1

acrylonitrile

N-(3-triethoxysilylpropyl)-3-aminopropanenitrile
13497-26-2

N-(3-triethoxysilylpropyl)-3-aminopropanenitrile

Conditions
ConditionsYield
In tetrahydrofuran at 40℃; for 4h;100%
at 120℃; for 6h;65%
4-Octyne
1942-45-6

4-Octyne

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

(1-propylpent-1-enyl)phosphinic acid ethyl ester
853411-25-3

(1-propylpent-1-enyl)phosphinic acid ethyl ester

Conditions
ConditionsYield
With hypophosphorous acid; trifluoroacetic acid; nickel dichloride In acetonitrile for 13h; Heating;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

oxiranyl-methanol
556-52-5

oxiranyl-methanol

Gly-APTES

Gly-APTES

Conditions
ConditionsYield
at 0 - 50℃; for 1h;100%
8-hydroxyquinoline-5-carbaldehyde
2598-30-3

8-hydroxyquinoline-5-carbaldehyde

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

5-(CHN(CH2)3Si(OC2H5)3)-8-hydroxyquinoline

5-(CHN(CH2)3Si(OC2H5)3)-8-hydroxyquinoline

Conditions
ConditionsYield
In ethanol for 12h; Heating;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

octadecyl isocyanate
112-96-9

octadecyl isocyanate

N-octadecyl-N'-(3-triethoxysilyl)propyl urea
106868-86-4

N-octadecyl-N'-(3-triethoxysilyl)propyl urea

Conditions
ConditionsYield
100%
In chloroform for 12h; Reflux;82%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

3,6-epoxy-N-phenyl-1,2,3,6-tetrahydrophthalimide
27742-33-2

3,6-epoxy-N-phenyl-1,2,3,6-tetrahydrophthalimide

N-(propyltriethoxysilane)maleimide-furan adduct

N-(propyltriethoxysilane)maleimide-furan adduct

Conditions
ConditionsYield
Stage #1: 3-aminopropyltriethoxysilane; 3,6-epoxy-N-phenyl-1,2,3,6-tetrahydrophthalimide In toluene at 20℃; for 12h;
Stage #2: With 1,2-dichloro-benzene at 140℃; for 5h;
100%
2,7,12,17-tetra-n-propylporphycene-3-sulfonyl chloride

2,7,12,17-tetra-n-propylporphycene-3-sulfonyl chloride

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

C41H59N5O5SSi

C41H59N5O5SSi

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h;100%
succinic acid anhydride
108-30-5

succinic acid anhydride

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

4-oxo-4-((3-(triethoxysilyl)propyl)amino)butanoic acid
32267-20-2

4-oxo-4-((3-(triethoxysilyl)propyl)amino)butanoic acid

Conditions
ConditionsYield
In tetrahydrofuran100%
In tetrahydrofuran at -5 - 5℃; for 6h; Inert atmosphere;99%
In 1,4-dioxane at 20℃; for 1h; Inert atmosphere;94%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-propenoate
17527-29-6

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-propenoate

C31H37F26NO7Si
497841-73-3

C31H37F26NO7Si

Conditions
ConditionsYield
In ethanol at 60℃; for 5h;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

acrylic acid 3,3,5,5,6,6,7,7,8,8,8-undecafluoro-octyl ester
56281-05-1

acrylic acid 3,3,5,5,6,6,7,7,8,8,8-undecafluoro-octyl ester

C31H41F22NO7Si
1159854-22-4

C31H41F22NO7Si

Conditions
ConditionsYield
In ethanol at 60℃; for 5h;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester
1030617-61-8

acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester

C29H37F22NO9Si
1159854-27-9

C29H37F22NO9Si

Conditions
ConditionsYield
In ethanol at 60℃; for 5h; Michael Addition;100%
acrylic acid 3,3,5,5,6,6,7,7,8,8,9,9,10,10,10-pentadecafluoro-decyl ester
49676-59-7

acrylic acid 3,3,5,5,6,6,7,7,8,8,9,9,10,10,10-pentadecafluoro-decyl ester

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

C35H41F30NO7Si
1159854-25-7

C35H41F30NO7Si

Conditions
ConditionsYield
In ethanol at 60℃; for 5h;100%
acrylic acid 3,3,5,5,7,7,8,8,9,9,10,10,10-tridecafluoro-decyl ester
932747-91-6

acrylic acid 3,3,5,5,7,7,8,8,9,9,10,10,10-tridecafluoro-decyl ester

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

C35H45F26NO7Si
1159854-26-8

C35H45F26NO7Si

Conditions
ConditionsYield
In ethanol at 60℃; for 5h; Michael Addition;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

D,L-valine
516-06-3

D,L-valine

C14H32N2O4Si

C14H32N2O4Si

Conditions
ConditionsYield
at 170℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W);100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

rac-Ala-OH
302-72-7

rac-Ala-OH

C12H28N2O4Si

C12H28N2O4Si

Conditions
ConditionsYield
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W);100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

glycine
56-40-6

glycine

C11H26N2O4Si
76444-79-6

C11H26N2O4Si

Conditions
ConditionsYield
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W);100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

C15H35N3O4Si

C15H35N3O4Si

Conditions
ConditionsYield
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W);100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Phenylalanine
150-30-1

Phenylalanine

C18H32N2O4Si

C18H32N2O4Si

Conditions
ConditionsYield
at 160℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W);100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

rac-Pro-OH
609-36-9

rac-Pro-OH

C14H30N2O4Si

C14H30N2O4Si

Conditions
ConditionsYield
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W);100%
Conditions
ConditionsYield
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W);100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

Cyclopropylacetylene
6746-94-7

Cyclopropylacetylene

ethyl (1-cyclopropyl-vinyl) phosphinate
1262853-89-3

ethyl (1-cyclopropyl-vinyl) phosphinate

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); hypophosphorous acid; trifluoroacetic acid In toluene for 12h; Reflux; regioselective reaction;100%
2-bromoisobutyric acid bromide
20769-85-1

2-bromoisobutyric acid bromide

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

2-bromo-2-methyl-(N-3-(triethoxysilyl)propyl)propanamide
908595-77-7

2-bromo-2-methyl-(N-3-(triethoxysilyl)propyl)propanamide

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 0 - 20℃; for 3h;100%
With triethylamine In toluene at 0 - 20℃; for 26h;78%
With triethylamine In toluene at 0 - 20℃; Inert atmosphere;7.1 g
With triethylamine In toluene at 0 - 20℃; for 26h; Inert atmosphere;
With triethylamine In toluene at 0 - 20℃; for 26h; Inert atmosphere;
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

C46H32F4N4O8P2
1430737-67-9

C46H32F4N4O8P2

C82H120N8O20P2Si4
1610459-21-6

C82H120N8O20P2Si4

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; Inert atmosphere; Schlenk technique;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

ethyl ester of perfluoropelargonic acid
41430-70-0

ethyl ester of perfluoropelargonic acid

N-[3-(triethoxysilyl)propyl]perfluoroheptanamide

N-[3-(triethoxysilyl)propyl]perfluoroheptanamide

Conditions
ConditionsYield
In ethanol at 60℃; for 2h;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

2-((4-azidomethyl)phenyl )-4,4-dimethyloxazol-5(4H)-one

2-((4-azidomethyl)phenyl )-4,4-dimethyloxazol-5(4H)-one

N-(2-(3-(triethoxysilyl)propylcarbamoyl)propan-2-yl)-4-(azidomethyl)benzamide

N-(2-(3-(triethoxysilyl)propylcarbamoyl)propan-2-yl)-4-(azidomethyl)benzamide

Conditions
ConditionsYield
In toluene at 20℃; for 12h;100%
2-chloroethyl isothiocyanate
1943-83-5

2-chloroethyl isothiocyanate

3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

(EtO)3Si-CH2CH2CH2-NH-CO-NH-CH2CH2-Cl

(EtO)3Si-CH2CH2CH2-NH-CO-NH-CH2CH2-Cl

Conditions
ConditionsYield
In pentane Solvent;100%
In pentane at -78 - 20℃; for 4.5h;100%
In ethanol at -78 - 50℃; for 2.5h;90.8%
In ethanol at -78 - -68℃; for 1.75h;
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

3-(diethylamino)phenyl 4-formylbenzoate

3-(diethylamino)phenyl 4-formylbenzoate

3-(diethylamino)phenyl 4-((3-(triethoxysilyl)propylimino)methyl)benzoate

3-(diethylamino)phenyl 4-((3-(triethoxysilyl)propylimino)methyl)benzoate

Conditions
ConditionsYield
With magnesium sulfate In chloroform at 20℃; for 24h; Inert atmosphere;100%
3-aminopropyltriethoxysilane
919-30-2

3-aminopropyltriethoxysilane

3-(dimethylamino)phenyl 4-formylbenzoate

3-(dimethylamino)phenyl 4-formylbenzoate

3-(dimethylamino)phenyl 4-((3-(triethoxysilyl)propylimino)methyl)benzoate

3-(dimethylamino)phenyl 4-((3-(triethoxysilyl)propylimino)methyl)benzoate

Conditions
ConditionsYield
With magnesium sulfate In chloroform at 20℃; for 24h; Inert atmosphere;100%

919-30-2Related news

Optimization of graphene-MoS2 barristor by 3-Aminopropyltriethoxysilane (cas 919-30-2) (APTES)07/19/2019

We theoretically and experimentally investigated the influence of the Fermi level position of graphene relative to the Dirac point on the performance of a graphene/MoS2 heterojunction barristor. A large Fermi level modulation (ΔEF?=?0.28?eV) of graphene, when the VGS is changed between??20?V an...detailed

Functionalization of 4-aminothiophenol and 3-Aminopropyltriethoxysilane (cas 919-30-2) with graphene oxide for potential dye and copper removal07/18/2019

In this work, 4-aminothiophenol and 3-aminopropyltriethoxysilane were firstly used to functionalize graphene oxide (GO) in order to promote the sorption efficiencies of methylene blue (MB) and copper (Cu2+). Characterization experiments illustrated that sulfydryl group (SH) and amino group (NH2)...detailed

The effect of electro-migrating 3-Aminopropyltriethoxysilane (cas 919-30-2) on the improvement of the reinforced concrete durability07/11/2019

In this study, 3-Aminopropyltriethoxysilane (APS) was selected as a new corrosion inhibitor used in electro-migration treatment for repairing reinforced concrete buildings and its corrosion inhibitive effectiveness was evaluated. The results indicated that the corrosion current density decreased...detailed

919-30-2Relevant articles and documents

THE PROCESS FOR THE PREPARATION AND USE OF HAIR TREATMENT COMPOSITIONS CONTAINING ORGANIC C1-C6 ALKOXY SILANES

-

, (2022/01/12)

The subject of the present application is a method for the preparation and use of an agent for the treatment of keratinous material, in particular human hair, comprising the following steps: (1) Mixing one or more organic C1-C6 alkoxy silanes with water,(2) optionally, partial, or complete removal from the reaction mixture of the C1-C6 alcohols liberated by the reaction in step (1),(3) if necessary, addition of one or more cosmetic ingredients,(4) Filling of the preparation into a packaging unit,(5) Storage of the preparation in the packaging unit for a period of at least about 5 days; and(6) Application of the preparation on the keratinous material.

Structure-Property Relationships of Silylamine-Type Reversible Ionic Liquids for Use as a Switchable Electrolyte

Jung, Sungyup,Podder, Showmik,Chen, Josephine,Biddinger, Elizabeth J.

, (2021/04/23)

Switchable electrolytes, whose properties (i.e., conductivity and polarity) can be switched dramatically are very useful. They can address problems associated with multiple electrochemical systems: (1) the need to separate products from the electrolyte after electro-organic syntheses, and; (2) the desire to stop the acceleration of electrochemical reactions in energy storage devices during thermal excursions. Silylamine-type reversible ionic liquids (RevILs) in co-solvents were used as switchable electrolytes in this work. The silylamine RevILs in co-solvents can have a dramatic change in conductivity when switching from a RevIL state to a molecular liquid (state) when heat is applied. The silylamines also have significant changes in polarity with switching. The fundamental silylamine structure-property relationships that can be tuned to control relevant properties such as conductivity, viscosity, thermal switch temperature, and solubility were investigated. In addition, these silylamine RevILs were tested with the addition of metal salts, which were found to increase the conductivity in both the RevIL and ML states. By tailoring the silylamine RevIL structures, the thermo-physical properties for the electrochemical application can be met.

AGENT FOR DYEING HAIR, CONTAINING AT LEAST ONE ORGANIC SILICON COMPOUND, A COLORING COMPOUND AND A FILM-FORMING, HYDROPHILIC POLYMER

-

, (2021/11/26)

The subject of the present disclosure is a composition for coloring keratinous material, in particular human hair, containing in a cosmetic carrier (a) at least one organic silicon compound selected from silanes having one, two or three silicon atoms, said organic silicon compound further comprising one or more basic chemical functions and one or more hydroxyl groups or hydrolysable groups per molecule,(b) at least one colorant compound from the group of pigments and/or direct dyes, and(c) at least one film-forming hydrophilic polymer.

METHOD FOR TREATING HAIR, COMPRISING THE APPLICATION OF AN ORGANIC SILICON COMPOUND, AN ALKALISING AGENT AND A FILM-FORMING POLYMER

-

, (2022/01/08)

It is an object of the present disclosure to provide a method for treating keratinous material, in particular human hair, comprising the following steps: Application of a water-containing agent (a) to the keratinous material, wherein the agent (a) has and contains a pH of at least 9.6:(a1) at least one organic silicon compound selected from the group including silanes having one, two or three silicon atoms, and(a2) at least one alkalizing agent selected from the group including ammonia, alkanolamines and basic amino acids, andApplication of an agent (b) to the keratinous material, wherein the agent (b) includes:(b1) at least one film-forming polymer.

PROCESS FOR DYEING HAIR

-

, (2021/01/22)

The subject of the present disclosure is a process for dyeing human hair, in which a pretreatment agent (A) which contains at least one organic silicon compound of the formula (I) and/or (II) and contains no direct dyes and no pigments, anda colorant (B) which contains at least one organic silicon compound of the formula (I) and/or (II) and further contains at least one colorant compound from the group of direct dyes and/or pigments, can be applied to the hair, wherein the organic silicon compounds of formulae (I) and (II) are defined as follows [in-line-formulae]R1R2N-L-Si(OR3)a(R4)b??(I),[/in-line-formulae] [in-line-formulae](R5O)c(R6)dSi-(A)e-[NR7-(A′)]f—[O-(A″)]g-[NR8-(A′″)]h—Si(R6′)d′(OR5′)c′??(II).[/in-line-formulae]

(Dicyclopentadiene) platinum(II) dichloride: An efficient catalyst for the hydrosilylation reaction between alkenes and triethoxysilane

Wu, Huarui,Zheng, Chaoyue,Chen, Naiwu,Zhu, Jie,Gao, Deqing

supporting information, p. 1576 - 1578 (2017/04/03)

(Dicyclopentadiene) platinum(II) dichloride was found to be an efficient hydrosilylation catalyst (homogeneous) upon a wide variety of functionalized alkenes and alkenes terminated with chemical moieties (diphenyl amino-, N-carbazol- and N-isoindoline-1,3-dione-). It is noteworthy that the hydrosilylation of aminated alkenes with triethoxysilane exhibited the yield of over 70% and the selectivity (γ-isomer/β-isomer) of more than 3/1. Due to steric hindrance lowering Markovnikov probability, the alkenes with big terminal moieties (diphenyl amino-, N-carbazol- and N-isoindoline-1,3-dione-) presented the high ratio of anti-Markovnikov isomers. The strategy of the hydrosilylation of the protected diamino chelating alkene was developed.

Study of Karstedt's Catalyst for Hydrosilylation of a Wide Variety of Functionalized Alkenes with Triethoxysilane and Trimethoxysilane

Pan, Zhenhuan,Liu, Minglun,Zheng, Chaoyue,Gao, Deqing,Huang, Wei

supporting information, p. 1227 - 1230 (2017/09/02)

The hydrosilylation is one of the most important methods for the synthesis of organosilicon compounds. Karstedt's catalyst [Ptn(H2C=CHSiMe2OSiMe2CH=CH2)m] is a kind of platinum catalyst which is widely used in the hydrosilylation. In this paper, we studied the catalytic activity of Karstedt's catalyst for the hydrogenation of olefins and especially aminated alkenes with trimethoxysilane and triethoxysilane, and demonstrated the excellent performance in terms of the yield and selectivity.

Synthesis method of aminopropyl triethoxysilane

-

Paragraph 0017; 0020, (2017/01/02)

The invention relates to a synthesis method of aminopropyl triethoxysilane and belongs to the technical field of fine chemical engineering.According to the method, acetone and allyl amine are put into a reactor according to a proportion, a water absorbing agent is added, after a stirring and temperature-raising reaction, reactants are distilled and filtered, filter residues are reused after being regenerated, filter liquor and triethoxysilane are subjected to an addition reaction through a Custer catalyst, purified products obtained after being distilled react with deionized water, and after low-boiling-point acetone is obtained through distillation, an aminopropyl triethoxysilane product is obtained.The yield of the aminopropyl triethoxysilane product is high, energy consumption is low, production cost is low, side products and raw materials can be recycled, and environmental pollution is avoided.

Method for preparing organic silicon by passage reaction device

-

Paragraph 0051, (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.

Process for manufacturing polysiloxane microcapsules that are functionalized and are not very porous

-

Page/Page column 4, (2016/09/26)

A method is provided for encapsulating products that can have lipophilic or hydrophilic, including volatile, properties in a polysiloxane membrane that is particularly impervious. A method is also provided for evaluating the imperviousness of capsules. The present method includes the following steps: a) formation of droplets by an emulsion between an oily phase containing the product to be encapsulated and an acidic aqueous phase heated to around 50° C. and in the presence of surfactants; b) addition and hydrolysis of at least one silane in order to obtain a silanol; c) increasing the pH in order to start condensation of the silanol to form a first membrane around the droplets of the product to be encapsulated; d) lowering the pH; e) increasing the pH, optionally preceded by adding a silane, in order to obtain a new condensation of silanol around the droplets of the product to be encapsulated.

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