220144-84-3 Usage
General Description
2-Amino-5-guanidinopentanoic acid hydrochloride is a chemical compound that is derived from the amino acid arginine. It is commonly used as a dietary supplement and is known for its potential to improve blood flow and overall cardiovascular health. The compound functions by increasing nitric oxide production in the body, which helps to relax blood vessels and improve circulation. It is often used to support athletic performance and to aid in the treatment of conditions related to high blood pressure and poor blood flow. Additionally, 2-Amino-5-guanidinopentanoic acid hydrochloride may have potential applications in the treatment of other medical conditions, making it an area of ongoing research and interest in the pharmaceutical and nutraceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 220144-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,4 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 220144-84:
(8*2)+(7*2)+(6*0)+(5*1)+(4*4)+(3*4)+(2*8)+(1*4)=83
83 % 10 = 3
So 220144-84-3 is a valid CAS Registry Number.
220144-84-3Relevant articles and documents
Method for the Racemization of Optically Active Amino Acids
Yamada, Shigeki,Hongo, Chikara,Yoshioka, Ryuzo,Chibata, Ichiro
, p. 843 - 846 (2007/10/02)
A practical method for the racemization of optically active amino acids has been developed.A wide variety of optically active α-amino acids, including neutral amino acids, acidic amino acids, basic amino acids, and imino acids, could be racemized by heating in a medium of acetic acid at 80-100 deg C for 1 h in the presence of 0.05 molar equiv of an aliphatic or an aromatic aldehyde.The factors influencing the racemization were investigated.Phenylglycine, (p-hydroxyphenyl)glycine, and serine could be racemized without complete dissolution of the optically active isomers.Thus, isolation of the racemic modification was easily achieved by simple filtration of the racemic modification suspended in the reaction mixture.The mechanism of the racemization is discussed.
