157-07-3 Usage
Uses
Used in Pharmaceutical Industry:
L-Argininic Acid is used as a therapeutic agent for the treatment of various medical conditions. Its application reason lies in its ability to improve the immune system, promote wound healing, and enhance the body's overall health.
Used in Sports Nutrition:
In the sports nutrition industry, L-Argininic Acid is used as a dietary supplement to enhance athletic performance. It is valued for its role in increasing nitric oxide production, which can improve blood flow, muscle pump, and exercise endurance.
Used in Cosmetics:
L-Argininic Acid is utilized in the cosmetics industry as an ingredient in skincare products. It serves as an anti-aging agent, helping to reduce the appearance of fine lines and wrinkles by promoting collagen synthesis and improving skin elasticity.
Used in Research:
In the field of scientific research, L-Argininic Acid is employed as a valuable tool for studying various biological processes and mechanisms. Its application reason is based on its ability to serve as a substrate for enzymes and its involvement in the urea cycle, making it an essential component in understanding cellular metabolism and nitrogen balance.
Check Digit Verification of cas no
The CAS Registry Mumber 157-07-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 157-07:
(5*1)+(4*5)+(3*7)+(2*0)+(1*7)=53
53 % 10 = 3
So 157-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N3O3/c7-6(8)9-3-1-2-4(10)5(11)12/h4,10H,1-3H2,(H,11,12)(H4,7,8,9)/t4-/m0/s1
157-07-3Relevant academic research and scientific papers
Reactivite du nitrite de sodium. V. Action sur les amino-acides, peptides et proteines
Gouesnard, Jean-Paul
, p. 88 - 94 (2007/10/02)
The action of sodium nitrite on various amino-acids was re-examined in conditions approximating to a biological medium. 13C-NMR provides evidence of the existence of intramolecular ring closures and the formation of 5-membered rings with ornithine, citrulline and arginine.The reaction of cystine shows the opening of the sulphur bridges, whereas cysteine leads to the formation of carboxy-thiiran and 3-sulpho-lactic acid.The hydrolysis of the amide bonds of asparagine and glutamine is complete whereas the peptides studied - carnosine and aspartam - do not undergo hydrolysis of the peptide linkage.However, the first deamination of glutathion (γ-Glu-Cys-Gly) induces the peptide link to be broken and a cyclization with the formation of lactone to occur.A second deamination takes place on the cysteinyl residue released and allows the formation of a thiiran by intramolecular cyclization with the thiol group.The formation of thiiran was also observed with oxidized glutathion which has an S-S bridge.Finally, the formation of nitrosamines was detected by 15N-NMR during the reaction of sodium nitrite with two commercial products available to the general public.
