Gelest, Inc. DIETHYLDICHLOROSILANE SID3402.0

Description
Additional Properties Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents Surface Tension (mN/m) 30.3 Safety Hazard Info oral rat, LD20: 1,000 mg/kg Packaging Under Nitrogen 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. Diethyldichlorosilan e; Dichlorodiethylsilan e; DES ΔHvap: 41.9 kJ/mol Dipole moment: 2.4 debye Surface tension: 30.3 mN/m Vapor pressure, 21 °C: 10 mm Thermal conductivity: 0.134 W/m°C Similar to, but more stable derivatives than dimethylsilylenes Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure
Datasheet
Description
Additional Properties Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents Surface Tension (mN/m) 30.3 Safety Hazard Info oral rat, LD20: 1,000 mg/kg Packaging Under Nitrogen 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. Diethyldichlorosilan e; Dichlorodiethylsilan e; DES ΔHvap: 41.9 kJ/mol Dipole moment: 2.4 debye Surface tension: 30.3 mN/m Vapor pressure, 21 °C: 10 mm Thermal conductivity: 0.134 W/m°C Similar to, but more stable derivatives than dimethylsilylenes Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure
Datasheet

Suppliers

Company
Product
Description
Supplier Links
DIETHYLDICHLOROSILANE - SID3402.0 - Gelest, Inc.
Morrisville, PA, United States
DIETHYLDICHLOROSILANE
SID3402.0
DIETHYLDICHLOROSILANE SID3402.0
Additional Properties Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents Surface Tension (mN/m) 30.3 Safety Hazard Info oral rat, LD20: 1,000 mg/kg Packaging Under Nitrogen 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. Diethyldichlorosilan e; Dichlorodiethylsilan e; DES ΔHvap: 41.9 kJ/mol Dipole moment: 2.4 debye Surface tension: 30.3 mN/m Vapor pressure, 21 °C: 10 mm Thermal conductivity: 0.134 W/m°C Similar to, but more stable derivatives than dimethylsilylenes Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure

Additional Properties


  • Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents
  • Surface Tension (mN/m) 30.3
    Safety
  • Hazard Info oral rat, LD20: 1,000 mg/kg
  • Packaging Under Nitrogen
    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.
    Diethyldichlorosilane; Dichlorodiethylsilane; DES
  • ΔHvap: 41.9 kJ/mol
  • Dipole moment: 2.4 debye
  • Surface tension: 30.3 mN/m
  • Vapor pressure, 21 °C: 10 mm
  • Thermal conductivity: 0.134 W/m°C
  • Similar to, but more stable derivatives than dimethylsilylenes
  • Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure
Supplier's Site Datasheet

Technical Specifications

  Gelest, Inc.
Product Category Organic Chemicals
Product Number SID3402.0
Product Name DIETHYLDICHLOROSILANE
Chemical Formula C 4 H 1 0 Cl 2 Si
CAS Number 1719-53-5
Boiling Point 266 F (130 C)
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