10489-99-3 Usage
Uses
Used in Organic Synthesis:
2-(dimethylnitroryl)ethanol is used as a reagent in organic synthesis for the preparation of other chemicals and pharmaceuticals. Its unique chemical properties make it a valuable intermediate in the synthesis of a wide range of compounds.
Used in Adhesives Production:
In the adhesives industry, 2-(dimethylnitroryl)ethanol is used as a building block for the development of high-performance adhesives. Its incorporation enhances the adhesive's bonding strength and durability.
Used in Coatings Production:
2-(dimethylnitroryl)ethanol is utilized in the coatings industry to improve the performance of various types of coatings. Its addition contributes to enhanced durability, resistance to environmental factors, and overall coating quality.
Used in Surfactants Production:
In the production of surfactants, 2-(dimethylnitroryl)ethanol is employed as a key component. It helps in creating surfactants with improved solubility, emulsification, and stabilization properties.
Safety Precautions:
It is crucial to handle 2-(dimethylnitroryl)ethanol with care due to its potential hazards. Inhalation, ingestion, or skin absorption can cause harm, and it may lead to respiratory system and skin irritation. Additionally, being flammable, it requires proper storage and handling to prevent accidents.
Check Digit Verification of cas no
The CAS Registry Mumber 10489-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10489-99:
(7*1)+(6*0)+(5*4)+(4*8)+(3*9)+(2*9)+(1*9)=113
113 % 10 = 3
So 10489-99-3 is a valid CAS Registry Number.
10489-99-3Relevant academic research and scientific papers
Aksamentova, Tamara N.,Chipanina, Nina N.,Oznobikhina, Larisa P.,Adamovich, Sergei N.,Smirnov, Vladimir I.
, p. 142 - 151 (2018)
Tris- 1, bis- 2, and mono- 3 (2-hydroxyethyl)amine-N-oxides isomers, their protonated forms, and H-complexes with acids have been studied in gas phase and DMSO solution by the quantum chemical calculations using DFT and MP2 methods. It is found that the proton affinity of the endo isomers 1a–3a, exo isomers 1b–3b and epi isomer 1c depends on the number of the hydroxyethyl groups, steric factors and strengths of the intramolecular H-bonds OH???ON in 1a–3a and OH???OH in 1b–3b. The peculiarities of formation of the hydrogen bonded and proton transfer complexes of tris(2-hydroxyethyl)amine-N-oxide with trifluoroacetic and 2-methylphenyloxyacetic acids are defined by 1 configuration, acid strength and solvent polarity. The structure of 1 and its complexes upon transition to solution was determined using FTIR spectroscopy.
