Bromal hydrate

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Bromal hydrate
Bromal hydrate.png
Names
IUPAC name
2,2,2-Tribromo-1,1-ethanediol
Other names
tribromoethylidene glycol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.340 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 208-073-2
PubChem CID
UNII
  • InChI=1S/C2H3Br3O2/c3-2(4,5)1(6)7/h1,6-7H
    Key: NJHVMXFNIZTTBV-UHFFFAOYSA-N
  • C(C(Br)(Br)Br)(O)O
Properties
C2H3Br3O2
Molar mass 298.756 g·mol−1
Appearancewhite crystalline solid with bromal-like smell and taste [1]
Melting point 53.5 °C (128.3 °F; 326.6 K)
Soluble
Solubility Soluble in ethanol, Diethyl ether, chloroform and Glycerin
Hazards
GHS labelling: [2]
GHS-pictogram-exclam.svg
Warning
H302, H315, H319, H335
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Bromal hydrate is an organobromine compound with the chemical formula C2H3Br3O2. It is the bromine analogue of chloral hydrate. Bromal hydrate forms when bromal is reacted with water. It decomposes to bromal and water upon distillation. [1] It has hypnotic and analgesic properties but acts like a stimulant at lower doses. [3] Bromal hydrate is more physiologically active than its chlorine analogue, chloral hydrate. [4] Its direct effect on the heart muscles is stronger than that of chloral hydrate. [3] Its analgesic effects were attributed to the proposed metabolism to bromoform. [5]

It was also tried as a medication for epilepsy, but was found ineffective. [1]

Related Research Articles

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Archibald Magill Fauntleroy was a physician. He graduated in medicine at the University of Pennsylvania in 1856, and in 1857 entered the United States Army as assistant surgeon; but, upon the start of the Civil War, he and his brother, a lieutenant in the navy, resigned at the same time with their father, Thomas T. Fauntleroy. He became a surgeon in the Confederate army, and was president of the board for the admission of surgeons, and chief officer on the medical staff of Gen. Joseph E. Johnston, and served with him until the battle of Seven Pines. He was then ordered to build and organize the hospitals at Danville, Virginia, and afterward had charge of the military hospital at Staunton, Virginia, until the war ended. He remained and practised at Staunton after the war, and was for several years superintendent of the lunatic asylum at that place. His contributions to medical literature include papers on potassium bromide, chloral hydrate, the use of chloroform in obstetrical practice, and a “Report upon Advance in Therapeutics,” which was printed in the Transactions of the Virginia Medical Society.

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<span class="mw-page-title-main">Tribromoethanol</span> Chemical compound

2,2,2-Tribromoethanol, often called just tribromoethanol, is a chemical compound with formula Br3C−CH2OH. Its molecule can be described as that of ethanol, with the three hydrogen atoms in position 2 replaced by bromine. It is a white crystalline solid, soluble in water and other solvents, that absorbs strongly in the UV below 290 nm.

<span class="mw-page-title-main">Chloral cyanohydrin</span> Chemical compound

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References

  1. 1 2 3 BROMAL – BROMAL HYDRATE, Stillé, A., Maisch, J. M. (1884). The National Dispensatory: Containing the Natural History, Chemistry, Pharmacy, Actions, and Uses of Medicine. Including Those Recognized in the Pharmacopoeias of the United States, Great Britain, and Germany, with Numerous References to the French Codex. H.C. Lea.
  2. "Bromal hydrate". pubchem.ncbi.nlm.nih.gov.
  3. 1 2 Bromal Hydrate (page 53), Cerna, D. (1894). Notes on the newer remedies. USA: W.B. Saunders.
  4. BENNETT, J. H. (1875). Researches into the Antagonism of Medicines; being the report of the Edinburgh Committee of the British Medical Association ... Reprint from the British Medical Journal. J.&A. Churchill.
  5. Bromal Hydrate, E. Steinauer (1871)