6211-16-1

Usage

Uses

Used in Nutritional Supplements:
L-Ornithine dihydrochloride is used as a nutritional supplement for its potential benefits in promoting liver health, reducing ammonia levels in the blood, and supporting overall health.
Used in Liver Health:
L-Ornithine dihydrochloride is used as a liver health promoter for its role in the urea cycle, which aids in the removal of ammonia from the body, thus supporting liver function.
Used in Exercise Performance:
L-Ornithine dihydrochloride is used as an exercise performance enhancer due to its potential to improve physical performance and reduce fatigue.
Used in Wound Healing:
L-Ornithine dihydrochloride is used as a wound healing promoter, potentially aiding in the healing process by supporting tissue repair and regeneration.
Used in Immune Function Support:
L-Ornithine dihydrochloride is used as an immune function supporter, potentially enhancing the body's ability to fight off infections and maintain overall health.

InChI:InChI=1/C5H12N2O2.2ClH/c6-3-1-2-4(7)5(8)9;;/h4H,1-3,6-7H2,(H,8,9);2*1H/t4-;;/m0../s1

Upstream product

• 77300-45-9 2,5-Bis(methoxycarbonylamino)valeriansaeure-methylester 
• 50995-48-7 methyl 2,5-dibromovalerate 
• 26302-89-6 L-ornithine tert-butyl ester 
• 271601-29-7 5-amino-2-(benzhydryl-amino)-pentanoic acid tert-butyl ester 
• 271601-28-6 1,1-dimethylethyl 4-cyano-(2S)-[(diphenylmethylene)amino]butanoate 

Downstream Products

• 123-75-1 pyrrolidine 
• 2149-70-4 N^ω-nitro-L-arginine 
• 126581-97-3 DPAB-L-Orn (trans) 
• 126581-97-3 DPAB-L-Orn (cis) 
• 58001-44-8 clavulanic acid 
• 126581-97-3 DPAB-D-Orn (trans) 
• 126581-97-3 DPAB-D-Orn (cis) 
• 88763-76-2 (R)-(+)-3-Amino-2-piperidinon 
• 334618-23-4 3-(R)-aminopiperidine dihydrochloride 
• 1892-22-4 3-aminopiperidin-2-one 

Relevant academic research and scientific papers

Highly enantioselective synthesis of non-natural aliphatic α-amino acids via asymmetric hydrogenation

By employing a rhodium-Duanphos complex as the catalyst, β-alkyl (Z)-N-acetyldehydroamino esters were smoothly hydrogenated in a highly efficient and enantioselective way. Excellent enantioselectivities together with excellent yields were achieved for a series of substrates. An efficient approach for the synthesis of the intermediate of the orally administered anti-diabetic drugs Alogliptin and Linagliptin in the DPP-4 inhibitor class was also developed.

Highly enantioselective Michael reactions catalyzed by a chiral quaternary ammonium salt. Illustration by asymmetric syntheses of (S)-ornithine and chiral 2-cyclohexenones.

[formula: see text] The use of the chiral quaternary ammonium salts 1a and 1b makes possible enantioselective Michael reactions which have been applied to the asymmetric syntheses of (S)-ornithine (2) and the chiral 2-cyclohexenone 6.

Aminosaeuren, I. Darstellung von Aminosaeuren aus Halogencarbonsaeure-alkylestern mit Alkalimetallcyanaten

α- and ω-halo- as well as α,ω-dihalocarboxylic alkyl esters react with potassium cyanate in the presence of alcohol at 80 - 120 deg C in dipolar aprotic solvents to yield α- and ω-(alkoxycarbonylamino)- and α,ω-bis(alkoxycarbonylamino)carboxylic alkyl esters, respectively, in good yields.Hydrolytic cleavage of these mono- or diurethanes with an aqueous solution of hydrochloric acid/formic acid leads to the corresponding amino acid hydrochlorides in nearly quantitative yields.

Process for the production of aminoacid hydrochlorides/or diaminoacid dihydrochlorides

Aminoacid hydrochlorides or diaminoacid dihydrochlorides are produced by first reacting a halocarboxylic acid ester with an alkali metal cyanate in the presence of an alcohol to form the corresponding mono- or diurethane and then saponifying this to the corresponding mono- or dihydrochloride. The new process is relatively versatile in its use and above all opens up an elegant synthesis route for lysine.