CAS 151613-25-1
:n-Octyldiisopropyl(dimethylamino)silane
Description:
n-Octyldiisopropyl(dimethylamino)silane, with the CAS number 151613-25-1, is an organosilicon compound characterized by its unique structure that includes a silicon atom bonded to an octyl group and two isopropyl groups, along with a dimethylamino group. This compound is typically a colorless to pale yellow liquid, exhibiting low volatility and moderate viscosity. It is known for its applications in surface modification, particularly in enhancing the hydrophobicity of materials and improving adhesion properties. The presence of the dimethylamino group imparts basic characteristics, which can facilitate interactions with various substrates. Additionally, the long octyl chain contributes to its lipophilicity, making it suitable for use in formulations requiring compatibility with organic solvents. n-Octyldiisopropyl(dimethylamino)silane is also of interest in the field of materials science and nanotechnology, where it can be utilized in the synthesis of functionalized silanes for coatings and composites. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C16H37NSi
InChI:InChI=1S/C16H37NSi/c1-8-9-10-11-12-13-14-18(15(2)3,16(4)5)17(6)7/h15-16H,8-14H2,1-7H3
InChI key:InChIKey=KWIDFNSKSFZDPV-UHFFFAOYSA-N
SMILES:[Si](CCCCCCCC)(C(C)C)(C(C)C)N(C)C
Synonyms:- (Dimethylamino)diisopropyl(octyl)silane
- 1,1-Diisopropyl-N,N-dimethyl-1-octylsilanamine
- Diisopropyldimethylaminooctylsilane
- N,N-dimethyl-1,1-bis(1-methylethyl)-1-octylsilanamine
- Silanamine, N,N-dimethyl-1,1-bis(1-methylethyl)-1-octyl-
- diisopropyldimethylaminooctasilane
- N-OCTYLDIISOPROPYL DIMETHYL AMINO SILANE
- Diisopropyl(dimethylamino)octylsilane, N,N-Dimethyl-diisopropyloctylsilylamine
- N,N-Dimethyl-diisopropyloctylsilylamine
- Octyldiisopropyl(dimethylamino)silane
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Found 2 products.
n-OCTYLDIISOPROPYL(DIMETHYLAMINO)SILANE
CAS:<p>Alkyl Silane - Conventional Surface Bonding<br>Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure.<br>n-Octyldiisopropyl(dimethylamino)silane; N,N-Dimethyl-1,1-bis(1-methylethyl)-1-octyl silanamine<br>Reagent for HPLC bonded phases without acidic byproducts<br></p>Formula:C16H37NSiPurity:97%Color and Shape:Straw LiquidMolecular weight:271.57

