775242-37-0 Usage
Uses
Used in Biochemistry:
N-Dodecanoyl-L-alanine is used as a building block for the manufacture of polymers and surfactants due to its unique hydrophobic nature and structural properties.
Used in Pharmaceutical Industry:
N-Dodecanoyl-L-alanine is used as a precursor in the synthesis of various pharmaceutical compounds, leveraging its chemical reactivity and functional groups.
Used in Cosmetics Industry:
N-Dodecanoyl-L-alanine is used as an ingredient in cosmetic formulations for its emulsifying and stabilizing properties, which can improve the texture and performance of products.
Used in Research and Development:
N-Dodecanoyl-L-alanine is utilized in research settings to study the properties and interactions of hydrophobic amino acid derivatives, contributing to the understanding of biochemical processes and the development of new materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 775242-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,5,2,4 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 775242-37:
(8*7)+(7*7)+(6*5)+(5*2)+(4*4)+(3*2)+(2*3)+(1*7)=180
180 % 10 = 0
So 775242-37-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H29NO3/c1-3-4-5-6-7-8-9-10-11-12-14(17)16-13(2)15(18)19/h13H,3-12H2,1-2H3,(H,16,17)(H,18,19)/t13-/m0/s1
775242-37-0Relevant academic research and scientific papers
Investigation into the Mechanism for Generation of the Helical Axis in Cholesteric Lyotropic Liquid Crystals
Tracey, Alan S.,Zhang, Xin
, p. 3889 - 3894 (2007/10/02)
The molecular based process responsible for the generation of the helical axis in the cholesteric mesophase of potassium N-dodecanoyl-L-alaninate, decanol, electrolyte, and water has been investigated.The headgroup dipolar couplings have been correlated with deuterium quadrupole splittings from the aliphatic chain as a function of amphiphile concentration.The results show that the change in the pitch of the helical axis with concentration is reflected by a change in preferred conformation of the amphiphile.This change in conformation is centered about the amide bonds where the aliphatic chain is joined to the alaninate headgroups.The effect presumably results from destabilization of the normally preferred rotamer in favor to others and will have its source in selective interactions between the chiral centers of adjacent amphiphiles.Studies similar to those discussed show that the variation in pitch caused by temperature changes is not correlated with similar selective changes in headgroup orientation.
