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N,N-Bis(3-trimethoxysilylpropyl)urea

Base Information
  • Chemical Name:N,N-Bis(3-trimethoxysilylpropyl)urea
  • CAS No.:18418-53-6
  • Molecular Formula:C13H32N2O7Si2
  • Molecular Weight:382.60100
  • Hs Code.:
  • European Community (EC) Number:805-212-4
  • Nikkaji Number:J2.511.559G
  • Mol file:18418-53-6.mol
N,N-Bis(3-trimethoxysilylpropyl)urea

Synonyms:18418-53-6;N,N-BIS(3-TRIMETHOXYSILYLPROPYL)UREA;N,N'-Bis(3-Trimethoxysilylpropyl)urea;Urea, N,N'-bis[3-(trimethoxysilyl)propyl]-;1,3-bis(3-trimethoxysilylpropyl)urea;bis(trimethoxysilylpropyl)urea;SCHEMBL254189;HSDGFGSXXVWDET-UHFFFAOYSA-N;MFCD26792606;AKOS030529971;FS-3990

Suppliers and Price of N,N-Bis(3-trimethoxysilylpropyl)urea
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • BIS(TRIMETHOXYSILYLPROPYL)UREA 95.00%
  • 5MG
  • $ 497.64
Total 26 raw suppliers
Chemical Property of N,N-Bis(3-trimethoxysilylpropyl)urea
Chemical Property:
  • Vapor Pressure:4.44E-07mmHg at 25°C 
  • Refractive Index:1.4488 
  • Boiling Point:414.5oC at 760 mmHg 
  • PKA:14.29±0.46(Predicted) 
  • Flash Point:204.5oC 
  • PSA:87.28000 
  • Density:1.046g/cm3 
  • LogP:2.48060 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:14
  • Exact Mass:384.17480443
  • Heavy Atom Count:24
  • Complexity:296
Purity/Quality:

98% *data from raw suppliers

BIS(TRIMETHOXYSILYLPROPYL)UREA 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CO[Si](CCCNC(=O)NCCC[Si](OC)(OC)OC)(OC)OC
  • Description Dipodal silanes are a series of adhesion promoters that have intrinsic hydrolytic stabilities up to ~10,000 times greater than conventional silanes and are used in applications such as plastic optics, multilayer printed circuit boards and as adhesive primers for ferrous and nonferrous metals. They have the ability to form up to six bonds to a substrate compared to conventional silanes with the ability to form only three bonds to a substrate. Many conventional coupling agents are frequently used in combination with 10-40% of a non-functional dipodal silane, where the conventional coupling agent provides the appropriate functionality for the application, and the non-functional dipodal silane provides increased durability. Also known as bis-silanes additives enhance hydrolytic stability, which impacts on increased product shelf life, ensures better substrate bonding and also leads to improved mechanical properties in coatings as well as composite applications.
  • Uses Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials.
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