89717-54-4 Usage
Uses
Used in Dietary Supplements:
DL-Gamma-ornithine dihydrochloride is used as a dietary supplement for its potential benefits in athletic performance and recovery. It is believed to support muscle growth and reduce muscle fatigue, making it a popular choice among athletes and fitness enthusiasts.
Used in Sports Nutrition Products:
DL-Gamma-ornithine dihydrochloride is often included in sports nutrition products due to its potential to enhance athletic performance and aid in recovery. It is commonly found in pre-workout supplements, protein powders, and other products designed to support muscle growth and overall health.
Used in Metabolic Disorders Treatment:
DL-Gamma-ornithine dihydrochloride has been studied for its potential role in treating certain metabolic disorders. Its involvement in the urea cycle and liver function makes it a promising candidate for therapeutic applications in this area.
Used in Liver Function Support:
DL-Gamma-ornithine dihydrochloride has been researched for its effects on liver function, with potential benefits for individuals with liver-related health concerns. Its role in the urea cycle and ammonia removal may contribute to improved liver health and function.
Overall, DL-Gamma-ornithine dihydrochloride is generally considered safe for consumption when used as directed, making it a popular choice for those seeking to enhance their athletic performance, support their liver function, and address certain metabolic disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 89717-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,1 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89717-54:
(7*8)+(6*9)+(5*7)+(4*1)+(3*7)+(2*5)+(1*4)=184
184 % 10 = 4
So 89717-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O2/c6-3-4(7)1-2-5(8)9/h4H,1-3,6-7H2,(H,8,9)
89717-54-4Relevant academic research and scientific papers
Bifunctional Chelating Agents. Part 2. Synthesis of 1-(2-Carboxyethyl)ethylenediaminetetra-acetic Acid by Ring Cleavage of a Substituted Imidazole
Altman, Janina,Shoef, Nurit,Wilchek, Meir,Warshawsky, Abraham
, p. 59 - 62 (2007/10/02)
The synthesis of 1-(2-carboxyethyl)ethylenediaminetetra-acetic acid, a new bifunctional analogue of ethylenediaminetetra-acetic acid (EDTA) is described.This is carried out via ring-opening benzoylation of ethyl imidazol-4-ylpropanoate, hydrogenation and hydrolysis to 4,5-diaminovaleric acid (DL-γ-ornithine) dihydrochloride, and subsequent alkylation.
