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| | (4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Basic information |
| | (4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Chemical Properties |
| Boiling point | 606.6±45.0 °C(Predicted) | | density | 1.12±0.1 g/cm3(Predicted) | | solubility | DMF: 15 mg/ml; DMSO: 14 mg/ml; Ethanol: 15 mg/ml | | form | A crystalline solid | | pka | 15.17±0.10(Predicted) |
| | (4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Usage And Synthesis |
| Description | JWH 210 is a potent cannabimimetic alkylindole that has been identified in extracts from herbal blends. Structurally and functionally similar alkylindoles are rapidly metabolized by the liver and secreted in the urine, with 5-carboxypentyl metabolites detected in the urine.1,2,3 JWH 210 N-(5-hydroxypentyl) metabolite is an expected metabolite of JWH 210, detectable in the serum and urine. Its biological activities have yet to be determined. This product is intended for forensic purposes. | | Uses | JWH-210 (Indole-d5) 5-Hydroxypentyl JWH-210 5-Hydroxypentyl (J211490) which is a urinary metabolite of JWH-210, an analgesic chemical that acts as a potent cannabinoid agonist at both the CB1 and CB2 receptors. | | References | 1. Teske, J., Weller, J.P., Fieguth, A., et al. Sensitive and rapid quantification of the cannabinoid receptor agonist naphthalen-1-yl-(1-pentylindol-3-yl)methanone (JWH-018) in human serum by liquid chromatography-tandem mass spectrometry J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 878(27),2659-2663(2010). 2. Sobolevsky, T., Prasolov, I., and Rodchenkov, G. Detection of JWH-018 metabolites in smoking mixture post-administration urine Forensic Sci. Int. 200(1-3),141-147(2010). 3. Wintermeyer, A., Mller, I., Thevis, M., et al. In vitro phase I metabolism of the synthetic cannabimimetic JWH-018 Anal. Bioanal. Chem. 398(5),2141-2153(2010). |
| | (4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Preparation Products And Raw materials |
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