CAS 181231-67-4

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

Description:

1-Butyl-N,N,1,1-tetramethylsilanamine is an organosilicon compound characterized by its unique structure, which includes a butyl group and a tetramethylsilanamine moiety. This compound typically exhibits properties associated with both organic and inorganic materials, such as moderate volatility and solubility in organic solvents. It is often used as a reagent or intermediate in various chemical syntheses, particularly in the field of organosilicon chemistry. The presence of the silane group imparts certain reactivity, allowing it to participate in condensation reactions or serve as a precursor for silicon-containing polymers. Additionally, the compound may exhibit low toxicity and stability under standard conditions, making it suitable for various applications in materials science and chemical manufacturing. Its specific physical and chemical properties, such as boiling point, melting point, and reactivity, can vary based on environmental conditions and the presence of other substances. Overall, 1-Butyl-N,N,1,1-tetramethylsilanamine is a versatile compound with applications in both research and industrial settings.

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

Synonyms:

• (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

Purity: 96%

Color and Shape: Liquid

Molecular weight: 159.3445

Ref: IN-DA0022QU

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

CAS: 181231-67-4

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

Purity: 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

Purity: 97%

Color and Shape: Straw Liquid

Molecular weight: 159.35

Ref: 3H-SIB1937.0