3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
In water at 65 - 75℃; for 3h; Concentration; Temperature; | 98% |
sodium hydroxide
Triethoxysilane
1-amino-2-propene
A
beta-aminopropyl triethoxy silane
B
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
In 5,5-dimethyl-1,3-cyclohexadiene | A 90% B n/a |
Conditions | Yield |
---|---|
With ammonia | 81% |
With ammonia | |
With ammonia |
Triethoxysilane
1-amino-2-propene
A
beta-aminopropyl triethoxy silane
B
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
In para-xylene | A 81% B n/a |
In toluene | A 78% B n/a |
In toluene | A 78% B n/a |
Conditions | Yield |
---|---|
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
Triethoxysilane
1-amino-2-propene
A
beta-aminopropyl triethoxy silane
B
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
In 5,5-dimethyl-1,3-cyclohexadiene | A 75% B n/a |
In 5,5-dimethyl-1,3-cyclohexadiene | A 75% B n/a |
Triethoxysilane
1-amino-2-propene
A
tetraethoxy orthosilicate
B
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
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
Triethoxysilane
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; ethanol |
Conditions | Yield |
---|---|
With nickel Hydrogenation; |
Triethoxysilane
1-amino-2-propene
A
3-aminopropyltriethoxysilane
B
(2-amino-1-methylethyl)triethoxysilane
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
With ammonia |
Conditions | Yield |
---|---|
at 20℃; Kinetics; Equilibrium constant; |
3-(triethoxysilyl)propylammonium 3-(triethoxysilyl)propylcarbamate
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
at 120℃; for 2h; | |
at 69℃; |
Conditions | Yield |
---|---|
With hydrogenchloride In water for 1h; |
3-aminopropyltriethoxysilane
<3-(2-Pyridyl)-1-pyrazolyl>essigsaeure-ethylester
Conditions | Yield |
---|---|
at 150℃; for 2h; | 100% |
In tetrahydrofuran at 150℃; for 2h; |
Conditions | Yield |
---|---|
100% | |
at 50 - 60℃; | 99% |
3-aminopropyltriethoxysilane
acrylonitrile
N-(3-triethoxysilylpropyl)-3-aminopropanenitrile
Conditions | Yield |
---|---|
In tetrahydrofuran at 40℃; for 4h; | 100% |
at 120℃; for 6h; | 65% |
4-Octyne
3-aminopropyltriethoxysilane
(1-propylpent-1-enyl)phosphinic acid ethyl ester
Conditions | Yield |
---|---|
With hypophosphorous acid; trifluoroacetic acid; nickel dichloride In acetonitrile for 13h; Heating; | 100% |
Conditions | Yield |
---|---|
at 0 - 50℃; for 1h; | 100% |
Conditions | Yield |
---|---|
In ethanol for 12h; Heating; | 100% |
3-aminopropyltriethoxysilane
octadecyl isocyanate
N-octadecyl-N'-(3-triethoxysilyl)propyl urea
Conditions | Yield |
---|---|
100% | |
In chloroform for 12h; Reflux; | 82% |
3-aminopropyltriethoxysilane
3,6-epoxy-N-phenyl-1,2,3,6-tetrahydrophthalimide
Conditions | Yield |
---|---|
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% |
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; | 100% |
succinic acid anhydride
3-aminopropyltriethoxysilane
4-oxo-4-((3-(triethoxysilyl)propyl)amino)butanoic acid
Conditions | Yield |
---|---|
In tetrahydrofuran | 100% |
In tetrahydrofuran at -5 - 5℃; for 6h; Inert atmosphere; | 99% |
In 1,4-dioxane at 20℃; for 1h; Inert atmosphere; | 94% |
3-aminopropyltriethoxysilane
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-propenoate
C31H37F26NO7Si
Conditions | Yield |
---|---|
In ethanol at 60℃; for 5h; | 100% |
3-aminopropyltriethoxysilane
acrylic acid 3,3,5,5,6,6,7,7,8,8,8-undecafluoro-octyl ester
C31H41F22NO7Si
Conditions | Yield |
---|---|
In ethanol at 60℃; for 5h; | 100% |
3-aminopropyltriethoxysilane
acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester
C29H37F22NO9Si
Conditions | Yield |
---|---|
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
3-aminopropyltriethoxysilane
C35H41F30NO7Si
Conditions | Yield |
---|---|
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
3-aminopropyltriethoxysilane
C35H45F26NO7Si
Conditions | Yield |
---|---|
In ethanol at 60℃; for 5h; Michael Addition; | 100% |
Conditions | Yield |
---|---|
at 170℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W); | 100% |
Conditions | Yield |
---|---|
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W); | 100% |
Conditions | Yield |
---|---|
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W); | 100% |
2,6-diaminocaproic acid
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W); | 100% |
Conditions | Yield |
---|---|
at 160℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W); | 100% |
Conditions | Yield |
---|---|
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W); | 100% |
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
at 200℃; for 0.05h; Product distribution / selectivity; Microwave irradiation (300 W); | 100% |
3-aminopropyltriethoxysilane
Cyclopropylacetylene
ethyl (1-cyclopropyl-vinyl) phosphinate
Conditions | Yield |
---|---|
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
3-aminopropyltriethoxysilane
2-bromo-2-methyl-(N-3-(triethoxysilyl)propyl)propanamide
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; | 100% |
3-aminopropyltriethoxysilane
ethyl ester of perfluoropelargonic acid
Conditions | Yield |
---|---|
In ethanol at 60℃; for 2h; | 100% |
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
In toluene at 20℃; for 12h; | 100% |
Conditions | Yield |
---|---|
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
Conditions | Yield |
---|---|
With magnesium sulfate In chloroform at 20℃; for 24h; Inert atmosphere; | 100% |
3-aminopropyltriethoxysilane
Conditions | Yield |
---|---|
With magnesium sulfate In chloroform at 20℃; for 24h; Inert atmosphere; | 100% |
The 3-Aminopropyltriethoxysilane, with the CAS registry number 919-30-2, is also known as Trimethoxy[3-(2-oxiranylmethoxy)propyl]silane.It belongs to the product organic raw material. Its EINECS number is 213-048-4. This chemical's molecular formula is C9H23NO3Si and molecular weight is 221.37. What's more,Its systematic name is 3-Aminopropyltriethoxysilane.
Physical properties about 3-Aminopropyltriethoxysilane are:(1)ACD/LogP: 2.604; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -0.49; (4)ACD/LogD (pH 7.4): -0.13; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4): 1.16; (9)#H bond acceptors: 4; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 10; (12)Index of Refraction: 1.433; (13)Molar Refractivity: 61.233 cm3; (14)Molar Volume: 235.598 cm3; (15)Surface Tension: 27.0729999542236 dyne/cm; (16)Density: 0.94 g/cm3; (17)Flash Point: 104.444 °C; (18)Enthalpy of Vaporization: 45.853 kJ/mol; (19)Boiling Point: 222.079 °C at 760 mmHg; (20)Vapour Pressure: 0.104000002145767 mmHg at 25°C.
3-Glycidoxypropyltrimethoxysilane may cause damage to health.When you are using Sulphur, please be cautious about it as the following: (1)Harmful if swallowed; (2)Causes burns; (3)In case of contact with eyes, rinse immediately with plenty of water and seek medical advice; (4)In case of accident or if you feel unwell, seek medical advice immediately (show label where possible); (5)Wear suitable protective clothing, gloves and eye/face protection.The Safety Information of 3-Aminopropyltriethoxysilane as follows:(1)RIDADR:UN 2735 8/PG 2; (2)WGK Germany:1; (3)RTECS:TX2100000; (4)F:10-34; (5)TSCA:Yes; (6)HazardClass:8; (7)PackingGroup:III; (8)HS Code:29310095; (9)Transport Information:UN 3267.
You can still convert the following datas into molecular structure:
(1)SMILES:CCO[Si](CCCN)(OCC)OCC;
(2)Std. InChI:InChI=1S/C9H23NO3Si/c1-4-11-14(12-5-2,13-6-3)9-7-8-10/h4-10H2,1-3H3;
(3)Std. InChIKey:WYTZZXDRDKSJID-UHFFFAOYSA-N.
The toxicity data of 3-Aminopropyltriethoxysilane as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mammal (species unspecified) | LD50 | oral | 4gm/kg (4000mg/kg) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 39(4), Pg. 86, 1974. | |
mammal (species unspecified) | LD50 | unreported | > 4gm/kg (4000mg/kg) | Chemical Abstracts. Vol. 70, Pg. 36149, 1969. | |
mouse | LD50 | intraperitoneal | 260mg/kg (260mg/kg) | Russian Chemical Reviws Vol. 38, Pg. 975, 1969. | |
mouse | LD50 | oral | 4gm/kg (4000mg/kg) | LUNGS, THORAX, OR RESPIRATION: EMPHYSEMA BEHAVIORAL: EXCITEMENT BLOOD: CHANGES IN LEUCOCYTE (WBC) COUNT | Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 11, Pg. 118, 1969. |
rabbit | LD50 | skin | 4mL/kg (4mL/kg) | Union Carbide Data Sheet. Vol. 1/19/1972, | |
rat | LD50 | oral | 1780mg/kg (1780mg/kg) | American Industrial Hygiene Association Journal. Vol. 23, Pg. 95, 1962 |
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