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25066-20-0

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25066-20-0 Usage

General Description

N-[3-(dimethylamino)propyl]stearamide N-oxide is a chemical compound that belongs to the class of amides and oxides. It is formed by the reaction of stearic acid with N-[3-(dimethylamino)propyl]amine, resulting in the formation of a tertiary amine oxide. This chemical is commonly used as a surfactant in a variety of industrial and household products, including detergents, fabric softeners, and shampoo. It acts as a wetting agent and helps to reduce the surface tension of liquids, allowing them to spread more easily and penetrate surfaces. N-[3-(dimethylamino)propyl]stearamide N-oxide is also a key ingredient in many personal care products for its ability to provide conditioning and anti-static properties to hair and skin.

Check Digit Verification of cas no

The CAS Registry Mumber 25066-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,6 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25066-20:
(7*2)+(6*5)+(5*0)+(4*6)+(3*6)+(2*2)+(1*0)=90
90 % 10 = 0
So 25066-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C23H48N2O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-23(26)25(27)22-19-21-24(2)3/h25H,4-22H2,1-3H3

25066-20-0Downstream Products

25066-20-0Relevant articles and documents

The surface properties of amine oxides with a fluoroether chain

Chen, Qing-Yun,Dai, Longhao,Guo, Yong,Huang, Meiwei,Shen, Qing,Su, Qin,Su, Zhaoben,Wu, Chengying,Zhao, Zhi-Gang

, (2021)

Persistent organic pollutants (POPs) includes long-chained fluorosurfactants, for instance, perfluorooctanonate (PFOA) and perfluorooctanesulfonate (PFOS). In order to find out alternative fluorosurfactants, we synthesized eight amine oxides with a fluoroether chain. Their surface properties were evaluated and compared with perfluoroalkyl and hydrocarbon analogues. The surface tensions at critical micelle concentration (γcmc) for the eight amine oxides with a fluoroether chain were at a range from 15.5 to 23.0 mN/m, and γcmc of four fluoroether amine oxides were below 17 mN/m comparable to perfluorooctyl analogues (16.4 mN/m) and much lower than perfluorohexyl (20.5 mN/m) and hydrocarbon analogues (24.2 and 24.7 mN/m). The critical micelle concentration (cmc) for the eight amine oxides with a fluoroether chain were 3 to 535 × 10?4 mol/L. The cmc of four fluoroether amine oxides were 3 to 21 × 10?4 mol/L (0.2 to 1.0 g/L) comparable to perfluorooctyl (0.4 g/L) and hydrocarbon analogues (4 and 10 × 10?4 mol/L) and much lower than perfluorohexyl analogue (36.9 g/L). The surface excesses, the limiting molecule areas and the free energies of micellization of amine oxides were calculated. Fluoroether surfactants are promising alternatives for PFOA and PFOS.

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