36341-65-8 Usage
Uses
Used in Surfactant Synthesis:
3-(hexadecylamino)propiononitrile is used as a key component in the synthesis of surfactants for its ability to lower the surface tension between substances, which is crucial in various industrial processes and formulations.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3-(hexadecylamino)propiononitrile is used as an intermediate in the production of various chemicals, contributing to the development of new drugs and medicinal compounds.
Used in Agricultural Product Manufacturing:
3-(hexadecylamino)propiononitrile is utilized as an intermediate in the creation of agricultural products, potentially enhancing the effectiveness of pesticides, fertilizers, or other agrochemicals.
Used in Chemical Intermediates:
3-(hexadecylamino)propiononitrile is used as a chemical intermediate for the production of a wide range of other chemicals, highlighting its versatility and importance in chemical synthesis processes.
Check Digit Verification of cas no
The CAS Registry Mumber 36341-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,4 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36341-65:
(7*3)+(6*6)+(5*3)+(4*4)+(3*1)+(2*6)+(1*5)=108
108 % 10 = 8
So 36341-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H38N2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18-21-19-16-17-20/h21H,2-16,18-19H2,1H3
36341-65-8Relevant academic research and scientific papers
Structure-activity relationships of lipopolysaccharide sequestration in N-alkylpolyamines
Shrestha, Anurupa,Sil, Diptesh,Malladi, Subbalakshmi S.,Warshakoon, Hemamali J.,David, Sunil A.
supporting information; experimental part, p. 2478 - 2481 (2009/12/25)
We have previously shown that simple N-acyl or N-alkyl polyamines bind to and sequester Gram-negative bacterial lipopolysaccharide, affording protection against lethality in animal models of endotoxicosis. Several iterative design-and-test cycles of SAR studies, including high-throughput screens, had converged on compounds with polyamine scaffolds which have been investigated extensively with reference to the number, position, and length of acyl or alkyl appendages. However, the polyamine backbone itself had not been explored sufficiently, and it was not known if incremental variations on the polymethylene spacing would affect LPS-binding and neutralization properties. We have now systematically explored the relationship between variously elongated spermidine [NH2-(CH2)3-NH-(CH2) 4-NH2] and norspermidine [NH2-(CH2)3-NH-(CH2) 3-NH2] backbones, with the N-alkyl group being held constant at C16 in order to examine if changing the spacing between the inner secondary amines may yield additional SAR information. We find that the norspermine-type compounds consistently showed higher activity compared to corresponding spermine homologues.
