4-Pyridineethanol Hydrochloride
≥98%
- Product Code: 118881
CAS:
383177-54-6
| Molecular Weight: | 159.61 g./mol | Molecular Formula: | C₇H₉NOHCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321183 | |
| Melting Point: | 149-152°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
4-Pyridineethanol Hydrochloride is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of various pharmaceutical compounds. Its structure, featuring both a pyridine ring and an ethanol group, makes it valuable in the development of drugs targeting neurological and cardiovascular diseases. It is also employed in the synthesis of ligands for metal complexes, which are used in catalysis and material science. Additionally, this compound finds application in research settings for studying biochemical pathways and receptor interactions, particularly those involving nicotinic acetylcholine receptors. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous-based reactions and formulations.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | €55.14 |
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4-Pyridineethanol Hydrochloride
4-Pyridineethanol Hydrochloride is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of various pharmaceutical compounds. Its structure, featuring both a pyridine ring and an ethanol group, makes it valuable in the development of drugs targeting neurological and cardiovascular diseases. It is also employed in the synthesis of ligands for metal complexes, which are used in catalysis and material science. Additionally, this compound finds application in research settings for studying biochemical pathways and receptor interactions, particularly those involving nicotinic acetylcholine receptors. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous-based reactions and formulations.
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