CAS 181231-67-4

1-butil-N,N,1,1-tetrametilsilanamina

Descripción:

1-butil-N,N,1,1-tetrametilsilanamina es un compuesto organosilícico caracterizado por su estructura única, que incluye un grupo butilo y una porción de tetrametilsilanamina. Este compuesto típicamente exhibe propiedades asociadas tanto con materiales orgánicos como inorgánicos, como volatilidad moderada y solubilidad en disolventes orgánicos. A menudo se utiliza como reactivo o intermedio en diversas síntesis químicas, particularmente en el campo de la química organosilícica. La presencia del grupo silano confiere cierta reactividad, permitiéndole participar en reacciones de condensación o servir como precursor de polímeros que contienen silicio. Además, el compuesto puede exhibir baja toxicidad y estabilidad en condiciones estándar, lo que lo hace adecuado para diversas aplicaciones en ciencia de materiales y fabricación química. Sus propiedades físicas y químicas específicas, como el punto de ebullición, el punto de fusión y la reactividad, pueden variar según las condiciones ambientales y la presencia de otras sustancias. En general, 1-butil-N,N,1,1-tetrametilsilanamina es un compuesto versátil con aplicaciones tanto en investigación como en entornos industriales.

Fórmula: C₈H₂₁NSi

InChI: InChI=1S/C8H21NSi/c1-6-7-8-10(4,5)9(2)3/h6-8H2,1-5H3

Clave InChI: InChIKey=AKWXSZZKOUAVJY-UHFFFAOYSA-N

SMILES: [Si](N(C)C)(CCCC)(C)C

Sinónimos:

• (Butyldimethylsilyl)dimethylamine
• 1-butyl-N,N,1,1-tetramethylsilanamine
• Butyldimethyl(dimethylamino)silane
• Silanamine, 1-butyl-N,N,1,1-tetramethyl-

Silanamine, 1-butyl-N,N,1,1-tetramethyl-

CAS: 181231-67-4

Fórmula: C₈H₂₁NSi

Pureza: 96%

Forma y color: Liquid

Peso molecular: 159.3445

Ref: IN-DA0022QU

1-Butyl-N,N,1,1-tetramethylsilanamine

CAS: 181231-67-4

1-Butyl-N,N,1,1-tetramethylsilanamine

Pureza: 96%

Ref: 54-OR1077027

n-BUTYLDIMETHYL(DIMETHYLAMINO)SILANE

CAS: 181231-67-4

Trialkylsilyl Blocking Agent
Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.
Alkyl Silane - Conventional Surface Bonding
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.
n-Butyldimethyl(dimethylamino)silane; Trimethylsilyldimethylamine
Reactive aminofunctional organosilaneHighly reactive reagent for bonded phases without acidic byproductSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure

Fórmula: C₈H₂₁NSi

Pureza: 97%

Forma y color: Straw Liquid

Peso molecular: 159.35

Ref: 3H-SIB1937.0