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104275-58-3

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104275-58-3 Usage

General Description

N-(3-Triethoxysilylpropyl)gluconamide is a chemical compound that belongs to the class of organosilicon compounds. It is a gluconamide derivative with three triethoxysilylpropyl groups attached to the nitrogen atom. This chemical is commonly used as a coupling agent in various industrial applications, particularly in the synthesis of hybrid organic-inorganic materials, such as silica-reinforced composites. Its three triethoxysilylpropyl groups enable it to readily bond with both organic and inorganic materials, making it a versatile component in a wide range of products, including adhesives, sealants, coatings, and plastics.

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

104275-58-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxy-N-(3-triethoxysilylpropyl)hexanamide

1.2 Other means of identification

Product number -
Other names (2R,3S,4R,5R)-2,3,4,5,6-Pentahydroxy-N-(3-(triethoxysilyl)propyl)hexanamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:104275-58-3 SDS

104275-58-3Downstream Products

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.

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