CAS 1009-93-4

2,2,4,4,6,6-hexametilciclotrisilazano

Descripción:

2,2,4,4,6,6-hexametilciclotrisilazano, con número CAS 1009-93-4, es un compuesto de silazano cíclico caracterizado por su estructura única, que consiste en un anillo de silazano de tres miembros con seis grupos metilo unidos a los átomos de silicio. Este compuesto es conocido por su estabilidad térmica y resistencia a la humedad, lo que lo hace útil en diversas aplicaciones, particularmente en el campo de la química de silicona. Su estructura molecular otorga propiedades como baja volatilidad y alta viscosidad, que son ventajosas en formulaciones para selladores, adhesivos y recubrimientos. Además, 2,2,4,4,6,6-hexametilciclotrisilazano exhibe buena compatibilidad con disolventes orgánicos y puede mejorar las propiedades mecánicas de las matrices poliméricas cuando se utiliza como aditivo. La presencia de nitrógeno en su estructura contribuye a su reactividad única, permitiéndole participar en reacciones químicas adicionales, como la polimerización. En general, este compuesto es significativo en la ciencia de materiales y aplicaciones industriales debido a sus propiedades distintivas y versatilidad.

Fórmula: C₆H₂₄N₃Si₃

InChI: InChI=1/C6H21N3Si3/c1-8-10-7-11(3,4)9(2)12(8,5)6/h7H,10H2,1-6H3

Clave InChI: InChIKey=WGGNJZRNHUJNEM-UHFFFAOYSA-N

SMILES: C[Si]1(C)N[Si](C)(C)N[Si](C)(C)N1

Sinónimos:

• 1,1,3,3,5,5-Hexamethylcyclotrisilazane
• 1,2,2,3,4,4-Hexamethyl-1,3,5,2,4,6-Triazatrisilinane
• 2,2,4,4,6,6-Hexamethyl-1,3,5,2,4,6-triazatrisilinane
• 213-773-6
• Cyclotrisilazane, 2,2,4,4,6,6-hexamethyl-
• Hmcts
• NSC 139842
• 2,2,4,4,6,6-Hexamethylcyclotrisilazane
• Dimethylsilazane trimer
• HEXAMETHYLCYCLOTRISILAZANE
• LABOTEST-BB LT00454897
• 2,2,4,4,6,6-Hexamethyl-1,3,5-triaza-2,4,6-trisilacyclohexane
• CH7250
• DIMETHYLSILAZANE CYCLIC TRIMER
• dimethylsilazanetrimer
• 2,2,4,4,6,6-Hexamethylcyclohexanetrisilazane
• nsc139842
• 2,2,4,4,6,6-hexamethyl-cyclotrisilazan
• Cyclotrisilazane, hexamethyl-

2,2,4,4,6,6-Hexamethylcyclotrisilazane, 97%

CAS: 1009-93-4

2,2,4,4,6,6-Hexamethylcyclotrisilazane, 97%

Fórmula: C₆H₂₁N₃Si₃

Pureza: 97%

Forma y color: colorless liq.

Peso molecular: 219.51

Ref: 08-14-1510

Cyclotrisilazane, 2,2,4,4,6,6-hexamethyl-

CAS: 1009-93-4

Fórmula: C₆H₂₁N₃Si₃

Pureza: 95%

Forma y color: Liquid

Peso molecular: 219.5075

Ref: IN-DA00035O

2,2,4,4,6,6-Hexamethylcyclotrisilazane

CAS: 1009-93-4

2,2,4,4,6,6-Hexamethylcyclotrisilazane

Pureza: 95%

Peso molecular: 219.51g/mol

Ref: 54-OR1009876

2,2,4,4,6,6-Hexamethylcyclotrisilazane

CAS: 1009-93-4

Fórmula: C₆H₂₁N₃Si₃

Pureza: >97.0%(GC)(T)

Forma y color: Colorless to Almost colorless clear liquid

Peso molecular: 219.51

Ref: 3B-H0909

1,1,3,3,5,5 -Hexamethylcyclotrisilazane

CAS: 1009-93-4

S09525 - 1,1,3,3,5,5 -Hexamethylcyclotrisilazane

Fórmula: C₆H₂₁N₃Si₃

Pureza: 97.0%(GC)(T)

Forma y color: Liquid

Peso molecular: 219.51

Ref: 10-S09525

1,1,3,3,5,5-HEXAMETHYLCYCLOTRISILAZANE

CAS: 1009-93-4

Bridging Silicon-Based 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.
Hexamethylcyclotrisilazane; Hexamethylcyclotrisilazane; 2,2,4,4,6,6-Hexamethylcyclotrisilazane
Viscosity, 20 °C: 1.7 cStΔHform: 553 kJ/molDielectric constant: 1000Hz: 2.57Dipole moment: 0.92 debyePolymerizes to polydimethylsilazane oligomer in presence of Ru/H2Modifies positive resists for O2 plasma resistanceSilylates diols with loss of ammoniaSimilar in reactivity to HMDS, SIH6110.0Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure

Fórmula: C₆H₂₁N₃Si₃

Pureza: 97%

Forma y color: Liquid

Peso molecular: 219.51

Ref: 3H-SIH6102.0