H2N(CH2)4COOH
5-Aminovaleric acid
CAS: 660-88-8
Molecular Formula: C5H11NO2
H2N(CH2)4COOH - Names and Identifiers
| Name | 5-Aminovaleric acid |
| Synonyms | 5-Ava-OH H-5-Ava-OH H2N(CH2)4COOH Aminovalericacid 5-Aminovaleric acid 5-Aminopentanoic acid Valeric acid, 5-amino- DELTA-AMINOVALERIC ACID Pentanoic acid, 5-amino- DELTA-AMINO-N-VALERIC ACID 5-Aminovaleric acid, (5-Aminopentonoic acid) |
| CAS | 660-88-8 |
| EINECS | 211-544-5 |
| InChI | InChI=1/C5H11NO2/c6-4-2-1-3-5(7)8/h1-4,6H2,(H,7,8) |
H2N(CH2)4COOH - Physico-chemical Properties
| Molecular Formula | C5H11NO2 |
| Molar Mass | 117.15 |
| Density | 1.2000 (estimate) |
| Melting Point | 158-161°C(lit.) |
| Boling Point | 247.5±23.0 °C(Predicted) |
| Solubility | Chloroform (Slightly), Methanol (Slightly), Water (Slightly) |
| Appearance | Crystalline Powder |
| Color | White to off-white |
| BRN | 906833 |
| pKa | 4.27(at 25℃) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.4650 (estimate) |
| MDL | MFCD00008232 |
| In vitro study | 5-Aminovaleric acid is a normal metabolite present in human saliva, with a tendency to elevated concentration in patients with chronic periodontitis. 5-Aminovaleric acid is also believed to act as a methylene homologue of gamma-aminobutyric acid (GABA) and functions as a weak GABA agonist. It is also known as an antifibrinolytic amino acid analog and so it functions as a weak inhibitor of the blood clotting pathway. |
H2N(CH2)4COOH - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | 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 |
H2N(CH2)4COOH - Reference Information
| biological activity | 5-aminopentanoic acid is considered to be a methylene homolog of GABA and a weak agonist of GABA. |
Last Update：2024-04-09 15:16:52
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