CAS 181231-67-4

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

Descrizione:

1-butil-N,N,1,1-tetrametilsilanamina è un composto organosiliconico caratterizzato dalla sua struttura unica, che include un gruppo butile e una porzione di tetrametilsilanamina. Questo composto tipicamente mostra proprietà associate sia a materiali organici che inorganici, come volatilità moderata e solubilità in solventi organici. È spesso utilizzato come reagente o intermedio in varie sintesi chimiche, in particolare nel campo della chimica organosiliconica. La presenza del gruppo silano conferisce una certa reattività, permettendogli di partecipare a reazioni di condensazione o di fungere da precursore per polimeri contenenti silicio. Inoltre, il composto può mostrare bassa tossicità e stabilità in condizioni standard, rendendolo adatto per varie applicazioni nella scienza dei materiali e nella produzione chimica. Le sue specifiche proprietà fisiche e chimiche, come il punto di ebollizione, il punto di fusione e la reattività, possono variare in base alle condizioni ambientali e alla presenza di altre sostanze. In generale, 1-butil-N,N,1,1-tetrametilsilanamina è un composto versatile con applicazioni sia nella ricerca che in contesti industriali.

Formula: C₈H₂₁NSi

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

InChI key: InChIKey=AKWXSZZKOUAVJY-UHFFFAOYSA-N

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

Sinonimi:

• (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

Formula: C₈H₂₁NSi

Purezza: 96%

Colore e forma: Liquid

Peso molecolare: 159.3445

Ref: IN-DA0022QU

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

CAS: 181231-67-4

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

Purezza: 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

Formula: C₈H₂₁NSi

Purezza: 97%

Colore e forma: Straw Liquid

Peso molecolare: 159.35

Ref: 3H-SIB1937.0