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Triphenylsilanol
Base Information
• Chemical Name: Triphenylsilanol
• CAS No.: 791-31-1
• Molecular Formula:C18H16OSi
• Molecular Weight:276.41
• EINECS No.:212-339-3
• Hs Code.:29310095
• Mol file:791-31-1.mol
Synonyms: Silanol,triphenyl- (8CI,9CI);Hydroxytriphenylsilane;LS 6400;NSC 12564;Triphenylhydroxysilane;Triphenylsilyl hydroxide; Z 6800;
Chemical Property of Triphenylsilanol
Chemical Property:
• Appearance/Colour: White crystal solid or powder
• Vapor Pressure:9.79E-07mmHg at 25deg;C
• Melting Point:150-153 deg;C(lit.)
• Refractive Index:1.628
• Boiling Point:388.6 deg;C at 760 mmHg
• PKA:13.39plusmn;0.58(Predicted)
• Flash Point:188.8 deg;C
• PSA:20.23000
• Density:1.13 g/cm3
• LogP:1.64580
• Storage Temp.: Store below +30deg;C.
• Sensitive: Air Sensitive
• Water Solubility: reacts
Purity/Quality: 98% Triphenylsilanol
Safety Information:
• Pictogram(s):Xi
• Hazard Codes: Xi
• Statements:36/37/38
• Safety Statements:26-36
Useful:
• Chemical Properties White crystal solid or powder
• Uses Triphenylsilanol is used as a water surrogate for regioselective Pd catalyzed allylations. A thick on germanium substrates have been produced by the electron bombardment of an evaporated thin film of triphenylsilanol.
• Definition ChEBI: An organosilanol in which silicon is bonded to a single hydroxy function and to three phenyl groups.
• Purification Methods It is purified by dissolving in pet ether, passing through an Al2O3 column, eluting thoroughly with CCl4 to remove impurities and then eluting the silanol with MeOH. Evaporation gives crystals with m 153-155o. It can be recrystallised from pet ether, CCl4 or from *benzene or Et2O/pet ether (1:1). It has also been recrystallised by partial freezing from the melt to constant melting point. [George & Gilman J Am Chem Soc 81 3288 1959, IR: Tatlock & Rochow J Org Chem 17 1555 1952 and Richards & Thompson J Chem Soc 124 1949, Beilstein 16 IV 1480.]
• InChI:InChI=1/C18H16OSi/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,19H
For example, the phenyl silicone resin is synthesized with triphenylsilanol as a raw material and can be used in high-temperature resistant coatings within the range of 400 - 650 degrees Celsius. After curing, the pencil hardness is ≥ 2H, the viscosity is 20 - 50 seconds (measured by Ford cup No. 4), and the acid value is ≤ 4mgKOH/g.
When triphenylsilanol is added to an acrylate coating, after QUV accelerated aging tests, the gloss retention rate of the coating with the additive can still reach more than 70% after 1000 hours of aging, while the gloss retention rate of the coating without the additive is less than 50%, effectively reducing phenomena such as powdering and cracking.
•
Triphenylsilanol
Base Information
• Chemical Name: Triphenylsilanol
• CAS No.: 791-31-1
• Molecular Formula:C18H16OSi
• Molecular Weight:276.41
• EINECS No.:212-339-3
• Hs Code.:29310095
• Mol file:791-31-1.mol
Synonyms: Silanol,triphenyl- (8CI,9CI);Hydroxytriphenylsilane;LS 6400;NSC 12564;Triphenylhydroxysilane;Triphenylsilyl hydroxide; Z 6800;
Chemical Property of Triphenylsilanol
Chemical Property:
• Appearance/Colour: White crystal solid or powder
• Vapor Pressure:9.79E-07mmHg at 25deg;C
• Melting Point:150-153 deg;C(lit.)
• Refractive Index:1.628
• Boiling Point:388.6 deg;C at 760 mmHg
• PKA:13.39plusmn;0.58(Predicted)
• Flash Point:188.8 deg;C
• PSA:20.23000
• Density:1.13 g/cm3
• LogP:1.64580
• Storage Temp.: Store below +30deg;C.
• Sensitive: Air Sensitive
• Water Solubility: reacts
Purity/Quality: 98% Triphenylsilanol
Safety Information:
• Pictogram(s):Xi
• Hazard Codes: Xi
• Statements:36/37/38
• Safety Statements:26-36
Useful:
• Chemical Properties White crystal solid or powder
• Uses Triphenylsilanol is used as a water surrogate for regioselective Pd catalyzed allylations. A thick on germanium substrates have been produced by the electron bombardment of an evaporated thin film of triphenylsilanol.
• Definition ChEBI: An organosilanol in which silicon is bonded to a single hydroxy function and to three phenyl groups.
• Purification Methods It is purified by dissolving in pet ether, passing through an Al2O3 column, eluting thoroughly with CCl4 to remove impurities and then eluting the silanol with MeOH. Evaporation gives crystals with m 153-155o. It can be recrystallised from pet ether, CCl4 or from *benzene or Et2O/pet ether (1:1). It has also been recrystallised by partial freezing from the melt to constant melting point. [George & Gilman J Am Chem Soc 81 3288 1959, IR: Tatlock & Rochow J Org Chem 17 1555 1952 and Richards & Thompson J Chem Soc 124 1949, Beilstein 16 IV 1480.]
• InChI:InChI=1/C18H16OSi/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,19H
For example, the phenyl silicone resin is synthesized with triphenylsilanol as a raw material and can be used in high-temperature resistant coatings within the range of 400 - 650 degrees Celsius. After curing, the pencil hardness is ≥ 2H, the viscosity is 20 - 50 seconds (measured by Ford cup No. 4), and the acid value is ≤ 4mgKOH/g.
When triphenylsilanol is added to an acrylate coating, after QUV accelerated aging tests, the gloss retention rate of the coating with the additive can still reach more than 70% after 1000 hours of aging, while the gloss retention rate of the coating without the additive is less than 50%, effectively reducing phenomena such as powdering and cracking.
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