| Identification | More | [Name]
5-AMINOVALERIC ACID | [CAS]
660-88-8 | [Synonyms]
5-AMINO-N-PENTANOIC ACID
5-AMINO-N-VALERIC ACID
5-AMINOPENTANOIC ACID
5-AMINOVALERIC ACID
DELTA-AMINO-N-VALERIC ACID
DELTA-AMINOVALERIC ACID
H-5-AVA-OH
H-APE(5)-OH
HOMOPIPERIDINIC ACID
NH2-(CH2)4-COOH
RARECHEM AN KA 1519
H2N(CH2)4COOH
Pentanoic acid, 5-amino-
Valeric acid, 5-amino-
D-AMINO-N-VALERIC ACID FREE ACID
5-Aminopentonoicacid
D-AMINO-N-VALERICACID
D-AMINOVALERIC ACID
5-AMINOVALERIC ACID 98%
5-Aminopentanoic acid, Homopiperidinic acid | [EINECS(EC#)]
211-544-5 | [Molecular Formula]
C5H11NO2 | [MDL Number]
MFCD00008232 | [Molecular Weight]
117.15 | [MOL File]
660-88-8.mol |
| Chemical Properties | Back Directory | [Appearance]
white to off-white crystalline powder | [Melting point ]
158-161 °C(lit.)
| [Boiling point ]
247.5±23.0 °C(Predicted) | [density ]
1.2000 (estimate) | [refractive index ]
1.4650 (estimate) | [storage temp. ]
Store at 0-5°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly), Water (Slightly) | [form ]
Crystalline Powder | [pka]
4.27(at 25℃) | [color ]
White to off-white | [BRN ]
906833 | [InChI]
InChI=1S/C5H11NO2/c6-4-2-1-3-5(7)8/h1-4,6H2,(H,7,8) | [InChIKey]
JJMDCOVWQOJGCB-UHFFFAOYSA-N | [SMILES]
C(O)(=O)CCCCN | [CAS DataBase Reference]
660-88-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [HS Code ]
29224999 |
| Hazard Information | Back Directory | [Chemical Properties]
white to off-white crystalline powder | [Uses]
5-Aminovaleric Acid is used in the development of drugs that halts severe type of seizures.
| [Definition]
ChEBI: A delta-amino acid comprising pentanoic acid with an amino substituent at C-5; a methylene homologue of gamma-aminobutyric acid (GABA) that is a weak GABA agonist. | [reaction suitability]
reaction type: solution phase peptide synthesis | [Purification Methods]
Crystallise it from H2O/EtOH. When heated above its melting point, it is converted to 2-piperidone with m 200o. [Wood & Colver J Am Chem Soc 67 654 1945, Beilstein 4 IV 2636.] |
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