- 2-Pyridylethylamine
-
- $0.00 / 25kg
-
2024-06-06
- CAS:2706-56-1
- Min. Order: 1kg
- Purity: 99% GC
- Supply Ability: 5-10 MTs
- 2-Pyridylethylamine
-
- $1.10 / 1g
-
2024-04-17
- CAS:2706-56-1
- Min. Order: 1g
- Purity: 99.0% min
- Supply Ability: 100 tons min
- 2-Pyridylethylamine
-
- $0.00 / 1KG
-
2023-09-06
- CAS:2706-56-1
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500000kg
|
| | 2-Pyridylethylamine Basic information |
| Product Name: | 2-Pyridylethylamine | | Synonyms: | RARECHEM AL BW 0258;2-PYRIDYLETHYLAMINE;2-Pyridineethanamine;2-(PYRIDIN-2-YL)ETHANAMINE;2-PYRIDIN-2-YL-ETHYLAMINE;2-aminoethylpyridine;2-(2-AMINOETHYL)PYRIDINE;2-(2-PYRIDYL)ETHYLAMINE | | CAS: | 2706-56-1 | | MF: | C7H10N2 | | MW: | 122.17 | | EINECS: | 220-295-1 | | Product Categories: | Pyridine | | Mol File: | 2706-56-1.mol |  |
| | 2-Pyridylethylamine Chemical Properties |
| Melting point | 198-200 °C(Solv: ethanol (64-17-5)) | | Boiling point | 92-93 °C12 mm Hg(lit.) | | density | 1.021 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.536(lit.) | | Fp | 213 °F | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | form | Liquid | | pka | pK1: 4.24(+2);pK2: 9.78(+1) (25°C,μ=0.05) | | color | Clear colorless to yellow | | Specific Gravity | 1.021 | | Water Solubility | Soluble in water (partly), and most common polar solvent. Insoluble in non-polar solvents, and oils. | | Sensitive | Air Sensitive | | BRN | 111208 | | CAS DataBase Reference | 2706-56-1(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Pyridineethanamine(2706-56-1) | | EPA Substance Registry System | 2-Pyridineethanamine (2706-56-1) |
| | 2-Pyridylethylamine Usage And Synthesis |
| Chemical Properties | clear colorless to yellow liquid | | Uses | 2-(2-Aminoethyl)pyridine is used as active pharmaceutical ingredients. | | Definition | ChEBI: An aminoalkylpyridine that is pyridine substituted by a ethanamino group at position 2. | | Biological Activity |
Low doses of histamine or H1R agonist 2-pyridylethylamine (2-PEA) into the knee-joint were found to decrease formalin-induced articular nociception in rats. The pharmacological blockade and neurotoxic ablation of cells expressing neuropeptide Y1 receptor (Y1R) in the spinal cord were able to prevent the antinociceptive effect produced by the intra-articular administration of the histamine H1 receptor (H1R) agonist, 2-pyridylethilamine (2-PEA), in the formalin-induced articular incapacitation in rats[1].
| | References | [1] Eduardo Souza-Silva. “Intra-articular injection of 2-pyridylethylamine produces spinal NPY-mediated antinociception in the formalin-induced rat knee-joint pain model.” Brain Research 1735 (2020): Article 146757. |
| | 2-Pyridylethylamine Preparation Products And Raw materials |
|