|
|
| | N-(1-Phenethyl-4-piperidyl)propionanilide hydrochloride Basic information |
| Product Name: | N-(1-Phenethyl-4-piperidyl)propionanilide hydrochloride | | Synonyms: | LHCBOXPPRUIAQT-UHFFFAOYSA-N;N-(1-Phenethyl-4-piperidyl)propionanilide hydrochloride;Ionsys;Propionanilide, N-(1-phenethyl-4-piperidyl)-, hydrochloride;Unii-59H156xy46;PropanaMide, N-phenyl-N-[1-(2-phenylethyl)-4-piperidinyl]-, hydrochloride (1:1);Fentanyl (hydrochloride) (CRM);Fentanyl Hydrochloride (100 μg/mL in Methanol) | | CAS: | 1443-54-5 | | MF: | C22H29ClN2O | | MW: | 372.94 | | EINECS: | | | Product Categories: | | | Mol File: | 1443-54-5.mol |  |
| | N-(1-Phenethyl-4-piperidyl)propionanilide hydrochloride Chemical Properties |
| | N-(1-Phenethyl-4-piperidyl)propionanilide hydrochloride Usage And Synthesis |
| Description | Fentanyl (hydrochloride) (CRM) (Item No. ISO60197) is a certified reference material categorized as an opioid. It is more effective than morphine at reducing pain but is also more lethal. Fentanyl is highly abused and is associated with many fatal overdoses. Fentanyl is regulated as a Schedule II compound in the United States. Fentanyl (hydrochloride) (CRM) (Item No. ISO60197) is provided as a DEA exempt preparation. This product is intended for research and forensic applications. | | Uses | Fentanyl Hydrochloride is used in the study of the fatalities associated with fentanyl and co-administered cocaine or opiates. An opiate receptor and also a controlled substance. | | References | [1] S. MALLORY BURNS Susan L M Christopher W Cunningham. DARK Classics in Chemical Neuroscience: Fentanyl[J]. ACS Chemical Neuroscience, 2018, 9 10: 2428-2437. DOI: 10.1021/acschemneuro.8b00174 [2] SEISHI KATSUMATA . Pharmacological characterization of KT-90 using cloned μ-, δ- and κ-opioid receptors[J]. European journal of pharmacology, 1996, 312 3: Pages 349-355. DOI: 10.1016/0014-2999(96)00469-4 [3] YOSHIYASU HIGASHIKAWA S S. Studies on 1-(2-phenethyl)-4-(N-propionylanilino)piperidine (fentanyl) and its related compounds. VI. Structure-analgesic activity relationship for fentanyl, methyl-substituted fentanyls and other analogues[J]. Forensic Toxicology, 2008, 26 1: 1-5. DOI: 10.1007/s11419-007-0039-1 [4] PATIL ARMENIAN . Fentanyl, fentanyl analogs and novel synthetic opioids: A comprehensive review[J]. Neuropharmacology, 2018, 134: Pages 121-132. DOI: 10.1016/j.neuropharm.2017.10.016 |
| | N-(1-Phenethyl-4-piperidyl)propionanilide hydrochloride Preparation Products And Raw materials |
|