Ammonium bromide
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Ammonium bromide | |||||||||||||||
other names |
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Molecular formula | NH 4 Br | |||||||||||||||
Brief description |
colorless, odorless, slightly hygroscopic solid |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 97.94 g mol −1 | |||||||||||||||
Physical state |
firmly |
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density |
2.43 g cm −3 (20 ° C) |
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Sublimation point |
452 ° C |
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solubility | ||||||||||||||||
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 . |
Ammonium bromide , NH 4 Br, forms hygroscopic cubic crystals that are readily soluble in acetone, ethanol and water. It has a sublimation point of 452 ° C, a density of 2.43 g · cm −3 and a relative molecular mass M r of 97.942.
synthesis
Ammonium bromide can be produced by the action of hydrogen bromide on ammonia :
The direct reaction of ammonia with bromine in water also gives the salt.
Another production option is the reaction of ammonia with iron (II) bromide .
properties
Ammonium bromide forms pale yellow crystals or powders that sublime at 452 ° C under normal pressure . A melting point of 542 ° C. is observed in a closed capillary . The salt is very soluble in water. The solubility increases with increasing temperature. The compound dissolves well in ethanol and acetone .
solubility in water temperature in ° C 0 20th 40 60 80 100 solubility in g / 100 g H 2 O 59.5 74.2 89.8 105 117 135
use
Ammonium bromide is used in the phototechnical industry and in medicine as a sedative . Ammonium bromide can also act as a bromide source in electrochemical bromination.
Individual evidence
- ↑ a b c d e f Entry on ammonium bromide in the GESTIS substance database of the IFA , accessed on February 1, 2016(JavaScript required) .
- ↑ a b entry on ammonium bromide. In: Römpp Online . Georg Thieme Verlag, accessed on July 15, 2014.
- ↑ a b c d e f g Yoffe, D .; Frim, R .; Ukeles, SD; Dagani, MJ; Barda, HJ; Benya, TJ; Sanders, DC: Bromine Compounds , in: Ullmanns Enzyklopädie der Technischen Chemie , Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2013; doi : 10.1002 / 14356007.a04_405.pub2 .
- ↑ Xiang Yang, Qi-Liang Yang, Xiang-Yang Wang, Hao-Han Xu, Tian-Sheng Mei: Copper-Catalyzed Electrochemical Selective Bromination of 8-Aminoquinoline Amide Using NH 4 Br as the Brominating Reagent . In: The Journal of Organic Chemistry . tape 85 , no. 5 , March 6, 2020, ISSN 0022-3263 , p. 3497-3507 , doi : 10.1021 / acs.joc.9b03223 .