16263-51-7 Usage
Uses
Used in Personal Care Products:
2,4,4-trimethyl-2-pentyl-1,3-oxazolidin-3-ol is used as an antimicrobial agent in personal care products for its ability to inhibit the growth of bacteria and fungi, thereby promoting cleanliness and reducing the risk of infections.
Used in Healthcare Settings:
In healthcare settings, 2,4,4-trimethyl-2-pentyl-1,3-oxazolidin-3-ol is used as a disinfectant for surfaces and medical equipment to prevent the spread of infections and maintain a hygienic environment.
However, the use of 2,4,4-trimethyl-2-pentyl-1,3-oxazolidin-3-ol has been a subject of controversy due to concerns about potential health and environmental risks. Some research suggests that it may contribute to the development of antibiotic-resistant bacteria and disrupt hormone regulation in animals. As a result, its use has been banned from certain products, and regulations are being implemented in various countries to mitigate these risks.
Check Digit Verification of cas no
The CAS Registry Mumber 16263-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,6 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16263-51:
(7*1)+(6*6)+(5*2)+(4*6)+(3*3)+(2*5)+(1*1)=97
97 % 10 = 7
So 16263-51-7 is a valid CAS Registry Number.
16263-51-7Relevant academic research and scientific papers
Selective formation of aminoxyls or oxaziridines by oxidation of 2,2,4,4-tetrasubstituted oxazolidines
Hamdani, Mourad,Scholler, Denise,Bouquant, James,Feigenbaum, Alexandre
, p. 605 - 616 (2007/10/03)
The reactivity of 2,2,4,4-tetrasubstituted-1,3-oxazolidines 1 with m-chloroperbenzoic acid was reinvestigated. Aminoxyls 5 are isolated in good yields in ether at -15°C, or in anhydrous dichloromethane at 0°C. Oxaziridines 4 are promoted at room temperature, or in the presence of an acid. In any case, short reaction times prevented the degradation of aminoxyls and oxaziridines. The competition between oxaziridines 4 and aminoxyls 5 is ruled by the oxazolidine imine equilibrium.
