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2530-83-8 Usage

Silane Coupling Agents KH-560

KH-560 is the first widely used coupling agent and has been used for 40 years. One end of its structure with reactive groups such as amino and vinyl, can react with epoxy, phenolic, polyester and other synthetic resin molecules. The other end is alkoxy (such as methoxy, ethoxy etc.) or chlorine atoms which is connected with silicon. These groups can be transformed into silanol in the hydrolysis in water solution or damp air. And the formed silanol is able to react with surface hydroxyl of glass, minerals and inorganic filler. Therefore, silane coupling agent is commonly used in silicate-filled epoxy, phenolic, polyester resin and other systems. In addition, it can also be used for FRP production, in order to improve its mechanical strength and resistance to wet environment. The organic groups of the silane coupling agent are selective about the reaction of the synthetic resin. Generally, these organic groups lack sufficient reactivity with synthetic resins such as polyethylene, polypropylene and polystyrene, and thus the coupling effect for them is poor. In recent years, new varieties of silane coupling agents with better coupling for polyolefins have been developed, but are limited in cost and other properties and are not yet widely used. Silane coupling agent is also known as silane treatment agent. Its general formula is Y (CH2) nSiX3. Wherein n is an integer of 0 to 3; X is a hydrolyzable group such as chlorine, methoxy, ethoxy and acetoxy; Y is an organic functional group such as a vinyl, an amino, an epoxy group, a methacryloyloxy group and sulfydryl.

Physicochemical Properties

Colorless transparent liquid; Soluble in a variety of organic solvents; Easy to hydrolysis; Able for condensation to form polysiloxanes; Easy to polymerize in the presence of overheating, light and peroxide.

Molecular Structure

Fig: Molecular structure

Uses

Different sources of media describe the Uses of 2530-83-8 differently. You can refer to the following data:
1. 3-Glycidoxypropyltrimethoxysilane is an epoxy-functional silane, it is a clear, light straw liquid. 3-Glycidoxypropyltrimethoxysilane may be used as a coupling agent in polysulfide and polyurethane caulks and sealants, in mineral-filled or glass-reinforced thermosets and thermoplastics, and in glass roving size-binders. It is particularly employed as an adhesion-promoting additive in waterborne systems, e.g. improving the adhesion of acrylic latex sealants. Applications: 3-Glycidoxypropyltrimethoxysilane may improve dry and wet strength in cured composites reinforced with glass fiber rovings Enhance wet electrical properties of epoxy-based encapsulate and packaging materials. Eliminate the need for a separate primer in polysulfide and urethane sealants. Improve adhesion in waterborne acrylic sealants and in urethane and epoxy coatings.
2. Pre-treatment of carbon steel with 3-(Glycidoxypropyl)trimet?hoxysilane enhances the dry and wet adhesion while reducing the cathotic disbondment rate of an epoxy coating
3. (3-Glycidoxypropyl)trimethoxysilane is used in the production of carbon steel and its pre treatment favors the dry and wet adhesion of epoxy coating. It is also used to prepare epoxy-functionalized silica nanoparticles, which gives a reactive surface for one-step and high-density protein immobilization. It serves as a coupling agent and adhesion promoter.

Application

It is mainly used in unsaturated polyester composites to improve the mechanical properties, electrical properties and light transmission properties of the composites, especially to improve their performance in wet environment. In wire and cable industry, when used to treat EPDM system stuffed by pottery clay and crosslinked by peroxide, it can improve consumption factor and specific inductance captance. Used for its copolymerization with monomers like vinyl acetate and acrylic acid or methacrylic, to form the polymers widely used in coatings, adhesives and sealants, providing excellent adhesion and durability.

Handling and Storage

Handling Normal measures for preventive fire protection. Storage Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature is 2-8 °C.

Fire-fighting measures

Flammable properties Flash point: 135 °C (275 °F)-closed cup Ignition temperature: 400 °C (752 °F) Suitable extinguishing media Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Special protective equipment for fire-fighters Wear self-contained breathing apparatus for fire-fighting if necessary.

Toxicological Information

Acute toxicity: LD50 Oral-rat-8,030 mg/kg ???????????????????????? LD50 Dermal-rabbit-4,248 mg/kg Irritation and corrosion: Eyes-rabbit-Mild eye irritation

Chemical Properties

Colorless transparent liquid

General Description

(3-Glycidyloxypropyl)trimethoxysilane (GPTMS) is a bifunctional organosilane with three methoxy groups on one side and an epoxy ring on the other. The methoxy groups bind well with glass substrates creating a 3D matrix. The epoxy group is reactive with amides, alcohols, thiols and acids. GPTMS is highly reactive in water and can be used as a linking agent between the surface of the silica and the polymeric matrix.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 2530-83-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2530-83:
(6*2)+(5*5)+(4*3)+(3*0)+(2*8)+(1*3)=68
68 % 10 = 8
So 2530-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O5Si/c1-10-15(11-2,12-3)6-4-5-13-7-9-8-14-9/h9H,4-8H2,1-3H3/t9-/m0/s1

2530-83-8 Well-known Company Product Price

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

  • (A18431)  (3-Glycidoxypropyl)trimethoxysilane, 97%   

  • 2530-83-8

  • 25g

  • 280.0CNY

  • Detail
  • Alfa Aesar

  • (A18431)  (3-Glycidoxypropyl)trimethoxysilane, 97%   

  • 2530-83-8

  • 100g

  • 375.0CNY

  • Detail
  • Alfa Aesar

  • (A18431)  (3-Glycidoxypropyl)trimethoxysilane, 97%   

  • 2530-83-8

  • 500g

  • 1272.0CNY

  • Detail
  • Aldrich

  • (440167)  (3-Glycidyloxypropyl)trimethoxysilane  ≥98%

  • 2530-83-8

  • 440167-100ML

  • 531.18CNY

  • Detail
  • Aldrich

  • (440167)  (3-Glycidyloxypropyl)trimethoxysilane  ≥98%

  • 2530-83-8

  • 440167-500ML

  • 1,763.19CNY

  • Detail
  • Aldrich

  • (440167)  (3-Glycidyloxypropyl)trimethoxysilane  ≥98%

  • 2530-83-8

  • 440167-1L

  • 2,943.72CNY

  • Detail
  • Aldrich

  • (440167)  (3-Glycidyloxypropyl)trimethoxysilane  ≥98%

  • 2530-83-8

  • 440167-2.5L

  • 7,211.88CNY

  • Detail

2530-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Glycidoxypropyltrimethoxysilane

1.2 Other means of identification

Product number -
Other names Z 6040

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:2530-83-8 SDS

2530-83-8Synthetic route

Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

trimethoxysilane
2487-90-3

trimethoxysilane

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

Conditions
ConditionsYield
Stage #1: trimethoxysilane; C13H28N2OPtSi2 In xylene for 0.0833333h; Inert atmosphere; Reflux;
Stage #2: Allyl glycidyl ether In xylene for 2h; Product distribution / selectivity; Reflux;
82%
80%
With 2C4H9O(1-)*Ni(2+)*(x)KCl In tetrahydrofuran at 20℃; for 12h; Glovebox; Inert atmosphere;61%
Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

trimethoxysilane
2487-90-3

trimethoxysilane

A

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

B

(Z)-1-propenyl glycidyl ether

(Z)-1-propenyl glycidyl ether

Conditions
ConditionsYield
With acetic acid; platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 160℃; Product distribution / selectivity; tube reactor;
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; 2-Ethylhexanoic acid at 100℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature;
Allyl glycidyl ether
106-92-3

Allyl glycidyl ether

trimethoxysilane
2487-90-3

trimethoxysilane

A

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

B

(Z)-1-propenyl glycidyl ether

(Z)-1-propenyl glycidyl ether

C

(E)-1-propenyl glycidyl ether

(E)-1-propenyl glycidyl ether

Conditions
ConditionsYield
platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 160℃; Product distribution / selectivity; tube reactor;
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 160℃; Temperature;
phenyl(2,4,6-trimethylbenzoyl)phosphinic acid

phenyl(2,4,6-trimethylbenzoyl)phosphinic acid

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

(2,4,6-trimethylbenzoyl)phenylphosphinic acid 2-hydroxy-[3-(3-trimethoxysilyl)propyloxy] propyl ester

(2,4,6-trimethylbenzoyl)phenylphosphinic acid 2-hydroxy-[3-(3-trimethoxysilyl)propyloxy] propyl ester

Conditions
ConditionsYield
In n-heptane at 20℃; for 12h; Inert atmosphere;100%
phenyl(2,4,6-trimethylbenzoyl)phosphinic acid

phenyl(2,4,6-trimethylbenzoyl)phosphinic acid

2-Isocyanatoethyl methacrylate
30674-80-7

2-Isocyanatoethyl methacrylate

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C32H46NO11PSi

C32H46NO11PSi

Conditions
ConditionsYield
With triethylamine In n-heptane at 20℃; Inert atmosphere;100%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

2-Amino-5-mercapto-1,3,4-thiadiazole
2349-67-9

2-Amino-5-mercapto-1,3,4-thiadiazole

C11H23N3O5S2Si

C11H23N3O5S2Si

Conditions
ConditionsYield
Stage #1: 2-Amino-5-mercapto-1,3,4-thiadiazole In methanol
Stage #2: 3-glycidoxypropyltrimethoxysilane In methanol at 65℃; for 18h;
100%
In methanol at 65℃; for 18h;
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

5-amino-3-mercapto-4H-[1,2,4]triazole
16691-43-3

5-amino-3-mercapto-4H-[1,2,4]triazole

C11H24N4O5SSi

C11H24N4O5SSi

Conditions
ConditionsYield
Stage #1: 5-amino-3-mercapto-4H-[1,2,4]triazole In methanol
Stage #2: 3-glycidoxypropyltrimethoxysilane In methanol at 65℃; for 18h; Solvent; Temperature;
100%
In methanol at 65℃; for 18h; Solvent;
3-(1H-imidazol-1-yl)propan-1-amine
5036-48-6

3-(1H-imidazol-1-yl)propan-1-amine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C15H31N3O5Si
1204776-56-6

C15H31N3O5Si

Conditions
ConditionsYield
In tetrahydrofuran at 95℃; for 6h; Inert atmosphere;98%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C104H203N9O35Si8

C104H203N9O35Si8

C110H211N9O37Si9

C110H211N9O37Si9

Conditions
ConditionsYield
With titanium(IV) isopropylate In methanol; toluene Heating;97%
C14H18O5S
1254067-29-2

C14H18O5S

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C23H38O10SSi
1254067-30-5

C23H38O10SSi

Conditions
ConditionsYield
With triethylamine In dichloromethane at 40℃; Inert atmosphere;97%
phosgene
75-44-5

phosgene

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

[1-(chloromethyl)-2-(3-trimethoxysilylpropoxy)ethyl]carbonochloridate

[1-(chloromethyl)-2-(3-trimethoxysilylpropoxy)ethyl]carbonochloridate

Conditions
ConditionsYield
With tetrabutyl-ammonium chloride at 15 - 20℃; for 10h; Inert atmosphere;96%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

1,3-propane diol monoglycidyl ether

1,3-propane diol monoglycidyl ether

Conditions
ConditionsYield
Stage #1: 3-glycidoxypropyltrimethoxysilane With ammonium hydrogen difluoride In water at 20℃; for 1h;
Stage #2: With dihydrogen peroxide In water at 20℃; for 4h; Fleming-Tamao Oxidation;
95%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

allyl bromide
106-95-6

allyl bromide

3-[2-hydroxy-4-oxa-7-(trimethoxysilanyl)heptylamino]-5-(2-propenylthio)-4H-1,2,4-triazole

3-[2-hydroxy-4-oxa-7-(trimethoxysilanyl)heptylamino]-5-(2-propenylthio)-4H-1,2,4-triazole

Conditions
ConditionsYield
Stage #1: allyl bromide; 3-amino-1H-1,2,4-triazole-5-thiol With triethylamine In N,N-dimethyl-formamide at 70℃; for 24h;
Stage #2: 3-glycidoxypropyltrimethoxysilane In N,N-dimethyl-formamide at 70℃; for 18h;
93%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C60H110O35Si10

C60H110O35Si10

Conditions
ConditionsYield
With tetraethylammonium hydroxide In propan-1-ol; water at 50℃; for 8h; Reagent/catalyst; Solvent; Temperature;92%
carbon dioxide
124-38-9

carbon dioxide

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

4-((3-(trimethoxysilyl)propoxy)methyl)-1,3-dioxolan-2-one

4-((3-(trimethoxysilyl)propoxy)methyl)-1,3-dioxolan-2-one

Conditions
ConditionsYield
With N,N-dimethyl-formamide at 160℃; under 37503 Torr; for 15h;86%
With bis(2-hydroxyethyl) bis-(quaternary ammonium)iodide salt immobilized on ordered mesoporous organosilica at 100℃; under 7500.75 Torr; for 24h; Pressure; Temperature; Autoclave;85.1%
With tetra-(n-butyl)ammonium iodide at 105℃; under 775.252 Torr; for 20h; Schlenk technique;
With tetra-(n-butyl)ammonium iodide In neat (no solvent) at 105℃; under 775.252 Torr; for 20h; Schlenk technique; Sealed tube; Green chemistry;
triisopropanolamine
122-20-3

triisopropanolamine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

3,7,10-trimethyl-1-(3-(oxiran-2-ylmethoxy)propyl)-2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecane
1026852-18-5

3,7,10-trimethyl-1-(3-(oxiran-2-ylmethoxy)propyl)-2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecane

Conditions
ConditionsYield
With titanium(IV) isopropylate In methanol; toluene for 18h; Heating;85%
1-methyl-piperazine
109-01-3

1-methyl-piperazine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

A

2,2-dimethoxy-8-(4-methylpiperazinyl)methyl-1,6-dioxa-2-silacyclooctane
1222257-17-1

2,2-dimethoxy-8-(4-methylpiperazinyl)methyl-1,6-dioxa-2-silacyclooctane

B

C26H56N4O8Si2
1222257-23-9

C26H56N4O8Si2

C

C27H60N4O9Si2
1222257-21-7

C27H60N4O9Si2

Conditions
ConditionsYield
With sodium methylate In methanol; toluene Product distribution / selectivity; Reflux;A 84%
B n/a
C n/a
C6H6F9N3O6S3(2-)*2Li(1+)

C6H6F9N3O6S3(2-)*2Li(1+)

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C15H26F9N3O11S3Si(2-)*2Li(1+)

C15H26F9N3O11S3Si(2-)*2Li(1+)

Conditions
ConditionsYield
In tetrahydrofuran at 60℃; for 2h; Inert atmosphere;81%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C78H153N7O27Si6

C78H153N7O27Si6

C84H161N7O29Si7

C84H161N7O29Si7

Conditions
ConditionsYield
With titanium(IV) isopropylate In methanol; toluene Heating;80.9%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

chloroacetic acid ethyl ester
105-39-5

chloroacetic acid ethyl ester

3-[2-hydroxy-4-oxa-7-(trimethoxysilanyl)heptylamino]-5-(ethoxycarbonylmethylthio)-4H-1,2,4-triazole

3-[2-hydroxy-4-oxa-7-(trimethoxysilanyl)heptylamino]-5-(ethoxycarbonylmethylthio)-4H-1,2,4-triazole

Conditions
ConditionsYield
Stage #1: chloroacetic acid ethyl ester; 3-amino-1H-1,2,4-triazole-5-thiol With triethylamine In N,N-dimethyl-formamide at 75℃; for 24h;
Stage #2: 3-glycidoxypropyltrimethoxysilane In N,N-dimethyl-formamide at 70℃; for 18h;
79%
triethanolamine
102-71-6

triethanolamine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

1-(3-Oxiranylmethoxy-propyl)-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane

1-(3-Oxiranylmethoxy-propyl)-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane

Conditions
ConditionsYield
In methanol; toluene for 16h; Heating;78%
C33H62O4

C33H62O4

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C50H96O12Si2

C50H96O12Si2

Conditions
ConditionsYield
With trifluoroacetic acid In toluene at 120 - 140℃; for 4h; Inert atmosphere;78%
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

1-((2-Hydroxy-ethyl)-{2-hydroxy-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propyl}-amino)-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propan-2-ol

1-((2-Hydroxy-ethyl)-{2-hydroxy-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propyl}-amino)-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propan-2-ol

C38H73N3O13Si3

C38H73N3O13Si3

Conditions
ConditionsYield
With titanium(IV) isopropylate In methanol; toluene Heating;75%
1-methyl-piperazine
109-01-3

1-methyl-piperazine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

A

2,2-dimethoxy-8-(4-methylpiperazinyl)methyl-1,6-dioxa-2-silacyclooctane
1222257-17-1

2,2-dimethoxy-8-(4-methylpiperazinyl)methyl-1,6-dioxa-2-silacyclooctane

B

C14H32N2O5Si
1222257-19-3

C14H32N2O5Si

C

C26H56N4O8Si2
1222257-23-9

C26H56N4O8Si2

Conditions
ConditionsYield
at 140 - 149℃; Product distribution / selectivity;A 75%
B n/a
C n/a
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

1-(Bis-{2-hydroxy-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propyl}-amino)-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propan-2-ol

1-(Bis-{2-hydroxy-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propyl}-amino)-3-[3-(3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-yl)-propoxy]-propan-2-ol

C51H98N4O17Si4
1026552-21-5

C51H98N4O17Si4

Conditions
ConditionsYield
With titanium(IV) isopropylate In methanol; toluene Heating;54%
morpholine
110-91-8

morpholine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

A

1,1-dimethoxy-3-morpholinomethyl-2,5-dioxa-1-silacyclooctane
1222257-39-7

1,1-dimethoxy-3-morpholinomethyl-2,5-dioxa-1-silacyclooctane

B

1-morpholino-3-(3-trimethoxysilylpropoxy)propan-2-ol
1222257-40-0

1-morpholino-3-(3-trimethoxysilylpropoxy)propan-2-ol

C

C24H50N2O10Si2
1222257-42-2

C24H50N2O10Si2

D

C25H54N2O11Si2

C25H54N2O11Si2

Conditions
ConditionsYield
With sodium methylate In methanol; toluene at 116 - 140℃;A 53%
B n/a
C n/a
D n/a
phenyl(2,4,6-trimethylbenzoyl)phosphinic acid

phenyl(2,4,6-trimethylbenzoyl)phosphinic acid

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

A

(2,4,6-trimethylbenzoyl)phenylphosphinic acid 2-hydroxy-[3-(3-trimethoxysilyl)propyloxy] propyl ester

(2,4,6-trimethylbenzoyl)phenylphosphinic acid 2-hydroxy-[3-(3-trimethoxysilyl)propyloxy] propyl ester

B

1,1-dimethoxy-3-[methyl(2,4,6-trimethylbenzoyl)phenylphosphinate]-2,5-dioxa-1-silacyclooctane

1,1-dimethoxy-3-[methyl(2,4,6-trimethylbenzoyl)phenylphosphinate]-2,5-dioxa-1-silacyclooctane

Conditions
ConditionsYield
In toluene at 60℃; for 6h;A 5%
B 35%
propan-1-ol
71-23-8

propan-1-ol

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

A

C13H28O5Si

C13H28O5Si

B

C11H24O5Si

C11H24O5Si

Conditions
ConditionsYield
With boron trifluoride diethyl etherate In dichloromethane at 20℃; for 1.5h; Inert atmosphere;A 10%
B 18.5%
di(pyridin-2-yl)amine
1202-34-2

di(pyridin-2-yl)amine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C19H29N3O5Si

C19H29N3O5Si

Conditions
ConditionsYield
In methanol for 65h; Heating;
bis[2-(2-pyridyl)ethyl]amine
15496-36-3

bis[2-(2-pyridyl)ethyl]amine

3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

C23H37N3O5Si

C23H37N3O5Si

Conditions
ConditionsYield
In methanol for 65h; Heating;
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

bis[(2-pyridyl)methyl]amine
1539-42-0

bis[(2-pyridyl)methyl]amine

C21H33N3O5Si

C21H33N3O5Si

Conditions
ConditionsYield
In methanol for 65h; Heating;
3-glycidoxypropyltrimethoxysilane
2530-83-8

3-glycidoxypropyltrimethoxysilane

(2-pyridin-2-yl-ethyl)-pyridin-2-ylmethyl-amine
15395-61-6

(2-pyridin-2-yl-ethyl)-pyridin-2-ylmethyl-amine

C22H35N3O5Si

C22H35N3O5Si

Conditions
ConditionsYield
In methanol for 65h; Heating;

2530-83-8Relevant articles and documents

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.

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.

SILICA PARTICLES COATED WITH BETA-CYCLODEXTRIN FOR THE REMOVAL OF EMERGING CONTAMINANTS FROM WASTEWATER

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, (2014/09/03)

Provided is a silica particle coated with β-cyclodextrin, wherein said cyclodextrin is attached to said silica particle via at least one crosslinking agent and/or at least one copolymer. Also provided are methods of removing contaminants from a flowing or stationary liquid phase comprising the step of contacting said liquid phase with the silica particle coated with β-cyclodextrin.

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