104275-58-3 Usage
Description
N-(3-Triethoxysilylpropyl)gluconamide is a versatile organosilicon compound and a gluconamide derivative characterized by the presence of three triethoxysilylpropyl groups attached to the nitrogen atom. This unique structure allows it to effectively bond with both organic and inorganic materials, making it a valuable coupling agent in the synthesis of hybrid organic-inorganic materials.
Uses
Used in the Synthesis of Hybrid Organic-Inorganic Materials:
N-(3-Triethoxysilylpropyl)gluconamide is used as a coupling agent for the synthesis of hybrid organic-inorganic materials, such as silica-reinforced composites. Its triethoxysilylpropyl groups facilitate strong bonding between organic and inorganic components, enhancing the mechanical, thermal, and chemical properties of the resulting materials.
Used in Adhesives:
N-(3-Triethoxysilylpropyl)gluconamide is used as a coupling agent in adhesive formulations to improve adhesion between different substrates, including metals, plastics, and ceramics. Its ability to bond with both organic and inorganic materials enhances the adhesive's performance and durability.
Used in Sealants:
In the sealant industry, N-(3-Triethoxysilylpropyl)gluconamide is used as a coupling agent to enhance the compatibility and bonding between the sealant and various substrates. This results in improved sealing performance, resistance to environmental factors, and longer service life.
Used in Coatings:
N-(3-Triethoxysilylpropyl)gluconamide is used as a coupling agent in coatings to improve their adhesion to various surfaces and enhance their overall performance. Its presence in the coating formulation contributes to better durability, corrosion resistance, and resistance to environmental degradation.
Used in Plastics:
In the plastics industry, N-(3-Triethoxysilylpropyl)gluconamide is used as a coupling agent to improve the compatibility and bonding between different polymers and fillers. This results in enhanced mechanical properties, thermal stability, and overall performance of the plastic materials.
Check Digit Verification of cas no
The CAS Registry Mumber 104275-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,7 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104275-58:
(8*1)+(7*0)+(6*4)+(5*2)+(4*7)+(3*5)+(2*5)+(1*8)=103
103 % 10 = 3
So 104275-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H33NO9Si/c1-4-23-26(24-5-2,25-6-3)9-7-8-16-15(22)14(21)13(20)12(19)11(18)10-17/h11-14,17-21H,4-10H2,1-3H3,(H,16,22)/t11-,12-,13-,14-/m0/s1
104275-58-3Relevant articles and documents
Reduced shrinkage of sol-gel derived silicas using sugar-based silsesquioxane precursors
Chen, Yang,Zhang, Zheng,Sui, Xihua,Brennan, John D.,Brook, Michael A.
, p. 3132 - 3141 (2005)
Monolithic siliceous materials were prepared, using sol-gel based methods, from mixtures of trifunctional silanes based on sugar lactones, including silyl-modified gluconamide GLS and maltonamide MLS, and a tetrafunctional silane derived from glycerol. The tri- and tetrafunctional compounds cured at different rates, which led to an enhanced presence of sugar moieties at the external surface of the pores in the monoliths. The resulting silicas exhibited dramatically reduced degrees of shrinkage (10%) when compared to silica monoliths prepared in the absence of trifunctional silanes (up to 85%). The sugars also alter the morphology of the material, with significant reductions in both micropore volume and surface area for materials containing GLS. The reduced shrinkage, presence of sugars on the silica surface, and altered morphology are likely to be important factors in providing such materials with the ability to stabilize entrained proteins. The Royal Society of Chemistry 2005.
