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L-Ornithine (70-26-8)

Identification
Name:L-Ornithine
Synonyms:Ornithine,L- (8CI); (+)-S-Ornithine; (S)-2,5-Diaminopentanoic acid; (S)-Ornithine; (S)-a,d-Diaminovaleric acid; L-(-)-Ornithine; L-Norvaline,5-amino-; Ornithine; Pentanoic acid, 2,5-diamino-, (S)-
CAS:70-26-8
EINECS: 200-731-7
Molecular Formula: C5H12N2O2
Molecular Weight: 132.16
InChI: InChI=1/C5H12N2O2/c6-3-1-2-4(7)5(8)9/h4H,1-3,6-7H2,(H,8,9)/t4-/m0/s1
Molecular Structure: (C5H12N2O2) Ornithine,L- (8CI); (+)-S-Ornithine; (S)-2,5-Diaminopentanoic acid; (S)-Ornithine; (S)-a,d-Diaminova...
Properties
Density:1.165 g/cm3
Solubility:soluble in water and ethanol, slightly soluble in diethyl ether
Specification:

L-Ornithine (70-26-8) is one of the products of the action of the enzyme arginase on L-arginine, creating urea. Therefore, ornithine is a central part of the urea cycle, which allows for the disposal of excess nitrogen. Ornithine is recycled and in a manner is a catalyst. First, ammonia is converted into carbamoyl phosphate (phosphate-CONH2), which creates one half of urea. Ornithine is converted into a urea derivative at the δ (terminal) nitrogen by carbamoyl phosphate. Another nitrogen is added from aspartate, producing the denitrogenated fumarate, and the resulting arginine (a guanidinium compound) is hydrolysed back to ornithine, producing urea. The nitrogens of urea come from the ammonia and aspartate, and the nitrogen in ornithine remains intact.
Ornithine (70-26-8) is not an amino acid coded for by DNA, and, in that sense, is not involved in protein synthesis. However, in mammalian non-hepatic tissues, the main use of the urea cycle is in arginine biosynthesis, so as an intermediate in metabolic processes, ornithine is quite important. It is believed to not be a part of genetic code because polypeptides containing unprotected ornithines undergo spontaneous lactamization
 

Report:

Reported in EPA TSCA Inventory.

Safety Data