Sulfonal
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Sulfonal | |||||||||||||||
other names |
2,2-bis (ethylsulfonyl) propane |
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Molecular formula | C 7 H 16 O 4 S 2 | |||||||||||||||
Brief description |
colorless, odorless and tasteless papers |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 228.33 g mol −1 | |||||||||||||||
Physical state |
firmly |
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Melting point |
124-126 ° C |
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boiling point |
300 ° C |
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solubility |
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safety instructions | ||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Sulfonal is a chemical compound from the group of sulfones . Sulphonal was produced by Eugen Baumann in 1888 and later introduced as a sleeping pill by Alfred Kast . Sulfonal has also been used in the treatment of the mentally ill . The sulfonals were replaced by the development of barbiturates .
Extraction and presentation
Sulfonal is produced from acetone and ethanethiol in the presence of hydrochloric acid and subsequent oxidation.
Homologues
Sulfonals | ||||
Surname | Sulfonal | Trional | Tetronal | |
Basic structure | ||||
structure | ||||
R 1 | -CH 3 | -CH 3 | -C 2 H 5 | |
R 2 | -CH 3 | -C 2 H 5 | -C 2 H 5 | |
CAS number | 115-24-2 | 76-20-0 | 2217-59-6 | |
PubChem | 8262 | 6433 | 75197 | |
Molecular formula | C 7 H 16 O 4 S 2 | C 8 H 18 O 4 S 2 | C 9 H 20 O 4 S 2 | |
Molar mass | 228.33 g mol −1 | 242.35 g mol −1 | 256.38 g mol −1 | |
Melting point | 124-126 ° C | 74-76 ° C | 85 ° C |
Individual evidence
- ↑ a b c d e f Entry on sulfonal. In: Römpp Online . Georg Thieme Verlag, accessed on March 3, 2014.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ^ "Sulfonal-Bayer": the new sleeping pill from Professors Baumann and Kast; the members and participants of the 61st Assembly of German Naturalists and Physicians in Cologne a. rh. presented by the paint factories, formerly Friedrich Bayer and Co.
- ↑ Hans Bangen: History of the drug therapy of schizophrenia , Berlin 1992, page 23, ISBN 3-927408-82-4 .
- ^ Otto Lueger: Sulfonal at Zeno.org .