7617-82-5 Usage
General Description
3-Myristyloxy propylamine, also known as 3-MYRISTYLOXY PROPYLAMINE, is a chemical compound that belongs to the class of alkylamines. It is a long-chain alkylamine, specifically a myristylamine, and is used in various industrial applications. 3-MYRISTYLOXY PROPYLAMINE is commonly used as a surfactant and emulsifier in cosmetic and personal care products, as well as in the production of pharmaceuticals and agricultural chemicals. It is also used as a corrosion inhibitor and as an intermediate in the synthesis of other chemical compounds. 3-Myristyloxy propylamine is known for its ability to reduce the surface tension of liquids and improve the dispersion and stability of emulsions. However, it is important to handle this chemical with caution as it can cause irritation to the skin, eyes, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 7617-82-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,1 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7617-82:
(6*7)+(5*6)+(4*1)+(3*7)+(2*8)+(1*2)=115
115 % 10 = 5
So 7617-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H37NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-19-17-14-15-18/h2-18H2,1H3
7617-82-5Relevant articles and documents
Lipophilic amines as potent inhibitors of N-acylethanolamine-hydrolyzing acid amidase
Yamano, Yumiko,Tsuboi, Kazuhito,Hozaki, Yuki,Takahashi, Kiyohiro,Jin, Xing-Hua,Ueda, Natsuo,Wada, Akimori
, p. 3658 - 3665 (2012/07/28)
N-Acylethanolamines (NAEs) including N-arachidonoylethanolamine (anandamide) and N-palmitoylethanolamine are endogenous lipid mediators. These molecules are degraded to the corresponding fatty acids and ethanolamine by fatty acid amide hydrolase (FAAH) or NAE-hydrolyzing acid amidase (NAAA). Lipophilic amines, especially pentadecylamine (2c) and tridecyl 2-aminoacetate (11b), were found to exhibit potent NAAA inhibitory activities (IC50 = 5.7 and 11.8 μM), with much weaker effects on FAAH. These simple structures would provide a scaffold for further improvement in NAAA inhibitory activity.
