1466552-36-2 Usage
Uses
Used in Fragrance Industry:
[D18]nonanal is used as a fragrance ingredient for its strong fruity odor, which can be utilized in the creation of various scent profiles for perfumes, cosmetics, and other fragrance products.
Used in Pharmaceutical Industry:
[D18]nonanal is used as an active pharmaceutical ingredient for its antibacterial properties, which can be applied in the development of new drugs to combat bacterial infections.
Used in Nutraceutical Industry:
[D18]nonanal is used as a nutraceutical ingredient for its hypolipidemic activity, which can help in the development of supplements and functional foods aimed at promoting heart health and reducing cholesterol levels.
Used in Research and Development:
[D18]nonanal is used as a research tool in the study of essential oils and their various applications, as well as in the development of new products and formulations in the fragrance, pharmaceutical, and nutraceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1466552-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,6,6,5,5 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1466552-36:
(9*1)+(8*4)+(7*6)+(6*6)+(5*5)+(4*5)+(3*2)+(2*3)+(1*6)=182
182 % 10 = 2
So 1466552-36-2 is a valid CAS Registry Number.
1466552-36-2Relevant academic research and scientific papers
Darwish, Tamim A.,Luks, Emily,Moraes, Greta,Yepuri, Nageshwar R.,Holden, Peter J.,Jamesa, Michael
, p. 520 - 529 (2013)
Oleic acid and its phospholipid derivatives are fundamental to the structure and function of cellular membranes. As a result, there has been increasing interest in the availability of their deuterated forms for many nuclear magnetic resonance, infrared, mass spectroscopy and neutron scattering studies. Here, we present for the first time a straightforward, large-scale (gram quantities) synthesis of highly deuterated [D32]oleic acid by using multiple, yet simple and high yielding reactions. The precursors for the synthesis of [D32]oleic acid are [D14]azelaic acid and [D17]nonanoic acid, which were obtained by complete deuteration (>98% D) of their 1H forms by using metal catalysed hydrothermal H/D exchange reactions. The oleic acid was producedwith ca. 94% D isotopic purity and with no contamination by the trans-isomer (elaidic acid). The subsequent synthesis of [D64]dioleoyl-sn-glycero-3-phosphocholine from [D32]oleic acid is also described. Copyright
