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N-ethylhexadecan-1-amine is an organic compound with the chemical formula C18H39N. It is a primary amine, characterized by the presence of an amino group (-NH2) attached to a long-chain alkane (hexadecane) with 16 carbon atoms. The ethyl group (-CH2CH3) is attached to the nitrogen atom, making it a branched-chain amine. N-ethylhexadecan-1-amine is used in various applications, such as a chemical intermediate in the synthesis of surfactants, emulsifiers, and other specialty chemicals. It is also known for its potential use in the production of cationic surfactants, which have applications in the textile, paper, and leather industries. Due to its chemical structure, N-ethylhexadecan-1-amine is a colorless to pale yellow liquid with a characteristic amine odor. It is soluble in organic solvents and has a relatively high boiling point, reflecting its non-polar nature.

5877-76-9

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5877-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5877-76-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5877-76:
(6*5)+(5*8)+(4*7)+(3*7)+(2*7)+(1*6)=139
139 % 10 = 9
So 5877-76-9 is a valid CAS Registry Number.

5877-76-9Downstream Products

5877-76-9Relevant academic research and scientific papers

Bis(dialkylaminethiocarbonyl)disulfides as potent and selective monoglyceride lipase inhibitors

Kapanda, Coco N.,Muccioli, Giulio G.,Labar, Geoffray,Poupaert, Jacques H.,Lambert, Didier M.

supporting information; experimental part, p. 7310 - 7314 (2010/07/14)

Monoglyceride lipase (MGL) inhibition may offer an approach in treating diseases in which higher 2-arachidonoyglycerol activity would be beneficial. We report here the synthesis and pharmacological evaluation of bis(dialkylaminethiocarbonyl)disulfide derivatives as irreversible MGL inhibitors. Inhibition occurs through interactions with MGL C208 and C242 residues, and these derivatives exhibit high inhibition selectivity over fatty acid amide hydrolase, another endocannabinoid-hydrolyzing enzyme. 2009 American Chemical Society.

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