25054-76-6 Usage
Uses
Given the complexity of the compound and the lack of specific information on its uses, potential applications can be hypothesized based on its functional groups and chemical properties. However, without concrete data, the following uses are speculative and would require further research and validation:
Used in Pharmaceutical Industry:
(Z)-(carboxymethyl)dimethyl-3-[(1-oxo-9-octadecenyl)amino]propylammonium hydroxide could be used as a pharmaceutical agent for [specific medical condition or treatment] due to its unique structure and functional groups that may interact with biological systems.
Used in Chemical Research:
In the field of chemical research, (Z)-(carboxymethyl)dimethyl-3-[(1-oxo-9-octadecenyl)amino]propylammonium hydroxide may serve as a subject for studying the effects of complex molecular structures on chemical behavior and reactivity.
Used in Material Science:
(Z)-(carboxymethyl)dimethyl-3-[(1-oxo-9-octadecenyl)amino]propylammonium hydroxide might be utilized in material science for the development of new materials with specific properties, such as improved conductivity or stability, based on its chemical composition.
Check Digit Verification of cas no
The CAS Registry Mumber 25054-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,5 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25054-76:
(7*2)+(6*5)+(5*0)+(4*5)+(3*4)+(2*7)+(1*6)=96
96 % 10 = 6
So 25054-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C25H48N2O3/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-24(28)26-21-19-22-27(2,3)23-25(29)30/h11-12H,4-10,13-23H2,1-3H3,(H-,26,28,29,30)/b12-11-
25054-76-6Relevant articles and documents
Synthesis and surface activities of amidobetaine surfactants with ultra-long unsaturated hydrophobic chains
Feng, Dan,Zhang, Yongmin,Chen, Quansheng,Wang, Jiyu,Li, Bin,Feng, Yujun
, p. 657 - 661 (2012/11/07)
Recent studies have shown that the surfactants bearing an ultra-long hydrophobic chain (>C18) exhibit unique self-assembly properties. However, their synthesis and surface activities have been less documented. In this work, monounsaturated alkyl dimethyl amidopropyl betaines, UCnDAB (n = 18, 22, and 24), were prepared by the reaction of the corresponding fatty acids with N,N-dimethyl-1,3-propanediamine, followed by quaternization with sodium choloroacetate of the obtained intermediates. The intermediates and final surfactants were characterized by 1H NMR and ESI-HRMS, respectively. Krafft temperature (TK) and surface activities of the surfactants were also examined. It was found that TK of all these surfactants is lower than 0°C, and their critical micellar concentration (CMC) is within the range of 10-3 mmol/L. In addition, the linear relationship between lg CMC and n is still in evidence.
