Proxibarbal
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| Structural formula without stereochemistry | |||||||||||||||||||
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| Non-proprietary name | Proxibarbal | ||||||||||||||||||
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| Molecular formula | C 10 H 14 N 2 O 4 | ||||||||||||||||||
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| properties | |||||||||||||||||||
| Molar mass | 226.23 g · mol -1 | ||||||||||||||||||
| Physical state |
firmly |
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| Melting point |
157-158 ° C , also 167-169 ° C |
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| pK s value |
8.31 |
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| solubility |
moderately in water |
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | |||||||||||||||||||
Proxibarbital (non-proprietary name: Proxibarbal) is a drug from the group of barbiturates . From a chemical point of view, it is a barbituric acid derivative, which occurs in two stereoisomeric forms and was used as a racemate . It was patented by Hommel AG in 1964 and was mainly used for migraines ("Axeen-Hommel"). At the moment there are no more preparations based on proxibarbital.
Legal status
Proxibarbital is a marketable and prescription narcotic drug in the Federal Republic of Germany due to its listing in Appendix 3 BtMG. Handling without permission or prescription is generally punishable. Further information can be found in the main article Narcotics Law in Germany .
Internationally, proxibarbital falls under the Convention on Psychotropic Substances .
Individual evidence
- ↑ a b c d Entry on Proxibarbital. In: Römpp Online . Georg Thieme Verlag, accessed on July 27, 2019.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.