24448-04-2 Usage
Uses
Used in Industrial Applications:
4-Ethyl-2-heptadecyl-2-oxazoline-4-methanol is used as a surfactant or emulsifier for its ability to lower surface tension between substances, aiding in their mixing and improving the efficiency of various industrial processes.
Used in Agricultural Applications:
In agriculture, 4-Ethyl-2-heptadecyl-2-oxazoline-4-methanol is used as a formulation aid to enhance the solubility and stability of agrochemicals, ensuring their effective application and reducing environmental impact.
Used in Pharmaceutical Applications:
4-Ethyl-2-heptadecyl-2-oxazoline-4-methanol is used as a solubility enhancer in pharmaceutical formulations, improving the bioavailability of drugs and facilitating their delivery to target sites within the body.
Used in Cosmetic Applications:
In the cosmetics industry, 4-Ethyl-2-heptadecyl-2-oxazoline-4-methanol is used as an emulsifier to create stable mixtures of oil and water, ensuring the longevity and effectiveness of cosmetic products.
Check Digit Verification of cas no
The CAS Registry Mumber 24448-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,4 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24448-04:
(7*2)+(6*4)+(5*4)+(4*4)+(3*8)+(2*0)+(1*4)=102
102 % 10 = 2
So 24448-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C23H45NO2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-24-23(4-2,20-25)21-26-22/h25H,3-21H2,1-2H3
24448-04-2Relevant academic research and scientific papers
Compositions and method comprising heterocyclic compounds containing two heteroatoms
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, (2008/06/13)
A method and compositions for topically administering physiologically active agents through the skin and mucous membranes of humans and animals in a transdermal device or formulation for systemic use or to the skin of humans and animals for localized use comprising applying to such skin or membrane a mixture of said physiologically active agent and a non-toxic, effective penetrating amount of penetration enhancing compound having the structural formula I: STR1 wherein: R is a saturated or unsaturated hydrocarbon group with from 5 to 19 carbon atoms; R' and R" are hydrogen, lower alkyl, trifluoromethyl, lower hydroxyalkyl or lower alkyl ester of lower hydroxyalkyl, with the proviso that both R' and R" are not lower hydroxyalkyl; X is O or NR1 ; R1 being hydrogen, lower alkyl, lower alkenyl, lower hydroxyalkyl or lower alkyl ester of lower hydroxyalkyl are disclosed.
