H-APE(5)-OH HCL
5-Aminovaleric acid hydrochloride
CAS: 627-95-2
Molecular Formula: C5H12ClNO2
H-APE(5)-OH HCL - Names and Identifiers
| Name | 5-Aminovaleric acid hydrochloride |
| Synonyms | H-APE(5)-OH HCL 5-aminopentanoic acid 5-AminopentanoicacidHCl 4-carboxybutylammonium chloride 5-AMINOVALERIC ACID HYDROCHLORIDE 5-Aminovaleric acid hydrochloride HOMOPIPERIDINIC ACID HYDROCHLORIDE 5-AMINOPENTANOIC ACID HYDROCHLORIDE 5-Aminopentanoic acid hydrochloride 5-AMINO-N-VALERIC ACID HYDROCHLORIDE DELTA-AMINO-N-VALERIC ACID HYDROCHLORIDE |
| CAS | 627-95-2 |
| EINECS | 211-021-1 |
| InChI | InChI=1/C5H11NO2.ClH/c6-4-2-1-3-5(7)8;/h1-4,6H2,(H,7,8);1H |
H-APE(5)-OH HCL - Physico-chemical Properties
| Molecular Formula | C5H12ClNO2 |
| Molar Mass | 153.61 |
| Density | 1.0962 g/cm3 |
| Melting Point | 95-97°C(lit.) |
| Boling Point | 131-132 °C(Press: 3 Torr) |
| Flash Point | 103.5°C |
| Vapor Presure | 0.00825mmHg at 25°C |
| Appearance | powder to crystal |
| Color | White to Light yellow to Light orange |
| BRN | 3683907 |
| Storage Condition | Room Temprature |
| Sensitive | Hygroscopic |
| MDL | MFCD00012919 |
H-APE(5)-OH HCL - 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 | 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 |
H-APE(5)-OH HCL - Reference Information
| Application | 5-aminopentanoic acid hydrochloride as a bio-derived chemical can be used to synthesize valerolactam of nylon 5. In addition, as a C5 platform compound, 5-aminopentanoic acid can also be used to synthesize Glutaric acid, pentanediol, 5-pentanoic acid, etc. |
| Use | 5-aminovaleric acid is a typical terminal amino acid, it can be used to produce novel odd-numbered nylons, such as nylon -5, nylon -6,5 and nylon -5,5. In addition, 5-aminopentanoic acid is also an important C5 platform compound, which can be used in the synthesis of important compounds such as Glutaric acid, 1, 5-pentanediol and 5-hydroxyvaleric acid. |
| preparation | There are three main biosynthetic pathways of 5-aminopentanoic acid: enzyme-catalyzed pathway, whole-cell catalytic pathway and fermentation pathway. The conversion solution of 5-aminopentanoic acid obtained by enzyme catalysis is NH4HCO3 solution with pH 7.8, and the conversion solution also contains a small amount of substrate lysine and product 5-aminopentanoic acid; the 5-aminopentanoic acid conversion solution obtained by whole cell catalysis contains about 14g/L phosphate buffer solution, about 2g/L sulfate, and a small amount of lysine and glucose; the fermentation broth of 5-aminopentanoic acid obtained by fermentation contains about 10g/L of phosphate, about 16g/L of sulfate, and a small amount of residual glucose and lysine, separation of 5-aminopentanoic acid by ion exchange resin, the method to filter bacteria through flocculation, macroporous adsorption resin decolorization, and finally by ion exchange resin separation of 5-aminopentanoic acid. |
Last Update：2024-04-09 21:00:56
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