| pipradrol Basic information |
Product Name: | pipradrol | Synonyms: | Detaril;Pipradol;di(phenyl)-(2-piperidyl)methanol;di(phenyl)-piperidin-2-ylmethanol;di(phenyl)-piperidin-2-yl-methanol;pipradrol;Azacyclononl;XSWHNYGMWWVAIE-UHFFFAOYSA-N | CAS: | 467-60-7 | MF: | C18H21NO | MW: | 267.37 | EINECS: | 207-394-5 | Product Categories: | | Mol File: | 467-60-7.mol | |
| pipradrol Chemical Properties |
Melting point | 81-82 °C(Solv: ethanol (64-17-5)) | Boiling point | 410.55°C (rough estimate) | density | 1.0449 (rough estimate) | refractive index | 1.5100 (estimate) | pka | pKa 9.71 (Uncertain) |
| pipradrol Usage And Synthesis |
Originator | Alertonic ,Adcock Ingram Ltd. | Definition | ChEBI: Pipradrol is a diarylmethane. | Manufacturing Process | A mixture of 48 g (0.167 mole) of α,α-diphenyl-2-pyridinemethanol hydrochloride (Emraert et al., Ber. 72B, 1188 (1939); 74B, 714 (1940), 160 ml of ethanol, and 3 0.5 g of Adams' platinum catalyst was shaken under an initial hydrogen pressure of 60 pounds. The theoretical amount of hydrogen was absorbed in 5 hours. The reaction mixture was refluxed, diluted with enough water to dissolve all the white solid, and filtered hot from the catalyst. The filtrate was cooled and filtered; yield of 38 g of α,α-diphenyl-alpha-(2piperidyl)methanol white product melting at 308-309°C with decomposition. A mixture of 3.5 grams (0.013 mole) of the above α,α-diphenyl-alpha-(2piperidyl)methanol, 4 g (0.05 mole) of formaldehyde (37%), and 6 grams (0.1 mole) of formic acid was refluxed for 2 days. The reaction mixture was treated with 1.3 g (0.013 mole) of conc. hydrochloric acid and vacuum distilled on the steam bath. The residue was recrystallized from butanone to give the α,αdiphenyl-alpha-(2-piperidyl)methanol hydrochloride which melted at 228229°C (dec.). | Brand name | Meratran (Marion Merrell Dow);Alertonic;Gerodryl;Leptidrol;Meratonic;Metadin;Peratran;Piridrol;Stimolag fortis. | Therapeutic Function | Central stimulant | World Health Organization (WHO) | Pipradrol, a central nervous system stimulant, was introduced in
1955 for use as an anorexic agent. Pipradrol is controlled under Schedule IV of the
1971 Convention on Psychotropic Substances.
(Reference: (UNCPS4) United Nations Convention on Psychotropic Substances (IV),
, , 1971) |
| pipradrol Preparation Products And Raw materials |
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