14206-60-1 Usage
Amphiphilic molecule
2-(undecylamino)ethanol has both hydrophilic (water-loving) and hydrophobic (water-repelling) parts, which allows it to interact with both water and oil.
Long alkyl chain
The undecyl group in the molecule has a long alkyl chain of 11 carbon atoms, which contributes to its surfactant and emulsifying properties.
Non-ionic surfactant
2-(undecylamino)ethanol is a non-ionic surfactant, meaning it does not contain charged ions, which makes it less likely to cause irritation or react with other chemicals.
Reduces surface tension
The surfactant properties of 2-(undecylamino)ethanol allow it to reduce the surface tension of water, making it easier for other substances to mix with water.
Increases solubility
2-(undecylamino)ethanol can increase the solubility of oils and other non-polar substances in water, making it useful in products like shampoos and detergents.
Effective emulsifier
The unique structure of 2-(undecylamino)ethanol allows it to act as an effective emulsifier, stabilizing mixtures of oil and water.
Mild detergent properties
2-(undecylamino)ethanol exhibits mild detergent properties, making it suitable for use in personal care products as a mild cleanser.
Widely used in various industries
2-(undecylamino)ethanol is commonly used in personal care, cleaning, and pharmaceuticals industries due to its surfactant and emulsifying properties.
Check Digit Verification of cas no
The CAS Registry Mumber 14206-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14206-60:
(7*1)+(6*4)+(5*2)+(4*0)+(3*6)+(2*6)+(1*0)=71
71 % 10 = 1
So 14206-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H29NO/c1-2-3-4-5-6-7-8-9-10-11-14-12-13-15/h14-15H,2-13H2,1H3
14206-60-1Relevant articles and documents
Diamine derivative anti-Trichomonas vaginalis and anti-Tritrichomonas foetus activities by effect on polyamine metabolism
Rigo, Graziela Vargas,Trein, Márcia Rodrigues,da Silva Trentin, Danielle,Macedo, Alexandre José,de Oliveira, Bruno Assis,de Almeida, Angelina Maria,Giordani, Raquel Brandt,de Almeida, Mauro Vieira,Tasca, Tiana
, p. 847 - 855 (2017/09/13)
Human and bovine trichomoniasis are sexually transmitted diseases (STD) caused by Trichomonas vaginalis and Tritrichomonas foetus, respectively. Human trichomoniasis is the most common non-viral STD in the world and bovine trichomoniasis causes significant economic losses to breeders. Considering the significant impact of the infections caused by these protozoa and the treatment failures, the search for new therapeutic alternatives becomes crucial. In this study the effect of diamines and amino alcohols in the in vitro viability of trichomonads was evaluated. Screening demonstrated the high activity of diamine 4 against these protozoa. Although cytotoxicity against HMVII cell line and slight hemolysis were observed in vitro, the compound showed no toxic effect on the Galleria mellonella in vivo model. Importantly, diamine 4 was active against both trichomonads species at 6 h and 24 h of incubation, and these effects was reverted by putrescine, a polyamine, suggesting competition for the same metabolic pathway. These findings indicate that the mechanism of action of diamine 4 is through the polyamine metabolism, a pathway distinct from that presented by metronidazole, the drug usually used to treat trichomoniasis and to which resistance is widely reported. These data demonstrate the importance of diamines as potential novel candidates as anti-T. vaginalis and anti-T. foetus agents.
