31024-56-3

Basic information

• Product Name: N-(3-(Trimethoxysilyl)propyl)butylamine
• Synonyms: n-[3-(trimethoxysilyl)propyl]-1-butanamin;N-[3-(trimethoxysilyl)propyl]-1-Butanamine;N-BUTYLAMINOPROPYLTRIMETHOXYSILANE;N-(3-Trimethoxysilylpropyl)butan-1-amine;n-(3-(trimethoxysilyl)propyl)butylamine;N-(n-Butyl)-3-aminopropyltrimethoxysilane;N-(n-butyl)-3-aminopropyltrime;1-Butanamine,N-[3-(trimethoxysilyl)propyl]-
• CAS NO: 31024-56-3
• Molecular Formula: C₁₀H₂₅NO₃Si
• Molecular Weight: 235.4
• EINECS: 250-437-8
• Product Categories: Amino Silanes
• Mol File: 31024-56-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: <-38°C
• Boiling Point: 238°C
• Flash Point: 110°C
• Appearance: Colorless or yellowish clear liquid
• Density: 0,947 g/cm3
• Vapor Pressure: 0.0971mmHg at 25°C
• Refractive Index: 1.4246
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 10.94±0.19(Predicted)
• Water Solubility: 13-1000g/L at 20℃
• CAS DataBase Reference: N-(3-(Trimethoxysilyl)propyl)butylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-(Trimethoxysilyl)propyl)butylamine(31024-56-3)
• EPA Substance Registry System: N-(3-(Trimethoxysilyl)propyl)butylamine(31024-56-3)

Safety Data

• TSCA: Yes
• Hazardous Substances Data: 31024-56-3(Hazardous Substances Data)

Usage

Chemical Properties

Colorless or yellowish clear liquid

Uses

n-Butylaminopropyltrimethoxysilane is a silane coupling agent. n-Butylaminopropyltrimethoxysilane is a hydrophobic polysiloxane barrier coating corrosion resistance material.

Flammability and Explosibility

Notclassified

InChI:InChI=1/C10H25NO3Si/c1-6-8-9-11-10(7-2)15(12-3,13-4)14-5/h10-11H,6-9H2,1-5H3

Upstream product

• 109-73-9 N-butylamine 
• 2530-87-2 3-Chloropropyltrimethoxysilan 

Downstream Products

• 618914-44-6 2,2-dimethoxy-1-butyl-1-aza-2-silacyclopentane 

Relevant articles and documents

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

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.

METHOD FOR THE AQUEOUS TREATMENT OF AN AMINO-FUNCTIONAL ORGANOSILANE CONTAINING AMMONIUM HALIDES AND/OR ORGANIC AMINE HYDROHALIDES

The invention relates to a method for the treatment of an amino functional organosilane containing ammonium halides and/or organic amine hydrohalides, wherein at least one non-polar organic solvent is optionally added to the amino functional organosilane containing the ammonium halides and/or organic amine hydrohalides, an aqueous lye is added. The mixture is reacted and subsequently the aqueous phase is separated from the organic phase, the solvent contained in the organic phase is removed from said phase and the residual organic phase is recovered.

Phosphazenium chloride catalysts immobilized on SBA-15 mesoporous material and silica gel: New exceptionally active catalysts for the chlorination of organic acids

Novel reusable phosphazenium chloride catalysts immobilized on SBA-15 mesoporous material and silica gel show exceptional activities and selectivities even in the continuous chlorination reaction of organic acids with thionyl chloride or phosgene.