CAS 660-88-8
:5-Aminovaleric acid
- 5-Amino-n-valeric acid
- 5-Aminopentanoic Acid
- 5-Aminopentonoic acid
- 5-Aminovaleriansaeure
- Acide 5-Aminovalerique
- Acido 5-Aminovalerico
- Aminovaleric acid
- Aminovalericacid
- Dava
- H-5-Ava-OH
- Nsc 58383
- Nsc 73123
- Pentanoic acid, 5-amino-
- Valeric acid, 5-amino-
- δ-Amino-n-valeric acid
- δ-Aminopentanoic acid
- δ-Aminovaleric acid
- ω-Aminopentanoic acid
- ω-Aminovaleric acid
- See more synonyms
5-Aminovaleric Acid
CAS:Formula:C5H11NO2Purity:>98.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:117.155-Aminovaleric acid
CAS:5-Aminovaleric acidFormula:C5H11NO2Purity:97%Color and Shape: off white crystalline powderMolecular weight:117.15g/mol5-Aminovaleric acid
CAS:Formula:C5H11NO2Purity:96.5 - 103.5 %Color and Shape:White to off-white powderMolecular weight:117.155-Aminovaleric acid
CAS:5-Aminovalerate, a lysine metabolite, can form endogenously or from bacterial lysine catabolism; indicates bacterial overgrowth or tissue necrosis.Formula:C5H11NO2Purity:99.86%Color and Shape:SolidMolecular weight:117.155-Aminovaleric Acid
CAS:Controlled ProductApplications 5-Aminovaleric acid is used in the study of metabolic changes in male germ cells (toxins) after 24 hours of extinguishing cigarette smokes. Also used in the comprehensive characterization of the human saliva metabolome and in identification of different metabolites like sphingomyelins, phosphatidyl cholines, vitamins and trace elements in human saliva which showed diurnal variation.
References Xu, B., et al.: Sci. Rep., 5, 15512 (2015); Dame, Z. T., et al.: Metabolomics, 11, 1864 (2015)Formula:C5H11NO2Color and Shape:NeatMolecular weight:117.155-Aminopentanoic acid
CAS:Formula:C5H11NO2Purity:95%Color and Shape:Solid, White to very pale yellow powderMolecular weight:117.1485-Aminovaleric acid
CAS:5-Aminovaleric acid is a cyclic peptide that is an antagonist of the enzyme 5-aminovaleric acid hydrolase that catalyzes the conversion of 5-aminovaleric acid to succinic semialdehyde. The physiological function of 5-aminovaleric acid hydrolase is not known, but it has been implicated in a number of neurological disorders, such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. The reaction solution contains 5-aminovaleric acid (5AVA), hydrogen fluoride (HF), and l-lysine (Lys). Upon addition of HF to the solution, it reacts with Lys to form a dinucleotide phosphate intermediate. This intermediate then reacts with 5AVA to form an intramolecular hydrogen bond with the amino group of Lys and release hydrogen gas. The detection sensitivity for this reaction can be increased by using a cyclic peptide inhibitor.
Formula:C5H11NO2Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:117.15 g/molRef: 3D-FA13122
Discontinued product







