|Name, Symbol, Number||bromine, Br, 35|
|Group, Period, Block||17, 4, p|
|Standard atomic weight||79.904(1) g·mol−1|
|Electron configuration||[Ar] 4s2 3d10 4p5|
|Electrons per shell||2, 8, 18, 7|
|Density (near r.t.)||(Br2, liquid) 3.1028 g·cm−3|
|Melting point|| 265.8 K|
(-7.2 °C, 19 °F)
|Boiling point|| 332.0 K|
(58.8 °C, 137.8 °F)
|Critical point||588 K, 10.34 MPa|
|Heat of fusion||(Br2) 10.571 kJ·mol−1|
|Heat of vaporization||(Br2) 29.96 kJ·mol−1|
|Heat capacity|| (25 °C) (Br2)|
|Oxidation states|| 5, 4, 3, 1, -1|
(strongly acidic oxide)
|Electronegativity||2.96 (scale Pauling)|
| Ionization energies
|1st: 1139.9 kJ·mol−1|
|2nd: 2103 kJ·mol−1|
|3rd: 3470 kJ·mol−1|
|Atomic radius||115 pm|
|Atomic radius (calc.)||94 pm|
|Covalent radius||114 pm|
|Van der Waals radius||185 pm|
|Electrical resistivity||(20 °C) 7.8×1010 Ω·m|
|Thermal conductivity||(300 K) 0.122 W·m−1·K−1|
|Speed of sound||(20 °C) ? 206 m/s|
|CAS registry number||7726-95-6|
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Bromine (pronounced /ˈbroʊmiːn/, /ˈbroʊmaɪn/, /ˈbroʊmɪn/, Greek: βρῶμος, brómos, meaning "stench (of he-goats)" ), is a chemical element with the symbol Br and atomic number 35. A halogen element, bromine is a red volatile liquid at standard room temperature that is intermediate in reactivity between chlorine and iodine. Bromine vapours are corrosive toxic. Approximately 730,000,000 kg were produced in 1993. The main applications for bromine are in fire retardants and fine chemicals.
Bromine was discovered by Antoine Balard at the salt marshes of Montpellier in 1826, but was not produced in quantity until 1860. The French chemist and physicist Joseph-Louis Gay-Lussac suggested the name bromine due to the characteristic smell of the vapors. Some also suggest that it may have been discovered by Bernard Courtois, the man who discovered iodine.
Bromine has 2 stable isotopes: Br-79 (50.69%) and Br-81 (49.31%). At least another 23 isotopes are known to exist. Many of the bromine isotopes are fission products. Several of the heavier bromine isotopes from fission are delayed neutron emitters. All of the radioactive bromine isotopes are relatively short lived. The longest half life is the neutron deficient Br-77 at 2.376 days. The longest half life on the neutron rich side is Br-82 at 1.471 days. A number of the bromine isotopes exhibit metastable isomers. Stable Br-79 exhibits a radioactive isomer, with a half life of 4.86 seconds. It decays by isomeric transition to the stable ground state.
Bromine is the only liquid nonmetallic element at room temperature and one of only six elements on the periodic table that are liquid at or close to room temperature. The pure chemical element has the physical form of a diatomic molecule, Br2. It is a dense, mobile, reddish-brown liquid, that evaporates easily at standard temperature and pressures to give a red vapor (its color resembles nitrogen dioxide) that has a strong disagreeable odor resembling that of chlorine. Bromine is a halogen, and is less reactive than chlorine and more reactive than iodine. Bromine is slightly soluble in water, and highly soluble in carbon disulfide, aliphatic alcohols (such as methanol), and acetic acid. It bonds easily with many elements and has a strong bleaching action.
Certain bromine-related compounds have been evaluated to have an ozone depletion potential or bioaccumulate in living organisms. As a result many industrial bromine compounds are no longer manufactured, are being restricted, or scheduled for phasing out.
Bromine has no known role in human health. Organobromine compounds do occur naturally, a famous example being Tyrian purple. Most organobromine compounds in nature arise via the action of vanadium bromoperoxidase.
Occurrence and production
- See also Halide minerals.
The diatomic compound Br2 does not occur naturally. Instead, bromine exists exclusively as bromide salts in diffuse amounts in crustal rock. Due to leaching, bromide salts have accumulated in sea water (85 ppm), but at a lower concentration than chloride. Bromine may be economically recovered from bromide-rich brine wells and from the Dead Sea waters (up to 50000 ppm).
Approximately 500,000 metric tons (worth around US$350 million) of bromine are produced per year (2001) worldwide with the United States and Israel being the primary producers. Bromine production has increased sixfold since the 1960s. The largest bromine reserve in the United States is located in Columbia and Union County, Arkansas, U.S. Israel's bromine reserves are contained in the waters of the Dead Sea. The bromide-rich brines are treated with chlorine gas, flushing through with air. In this treatment, bromide anion is oxidized to bromine by the chlorine gas.
- 2 Br− + Cl2 → 2 Cl− + Br2
Because of its commercial availability and long shelf-life, bromine is not typically prepared. Small amounts of bromine can however be generated through the reaction of solid sodium bromide with concentrated sulfuric acid (H2SO4). The first stage is formation of hydrogen bromide (HBr), which is a gas, but under the reaction conditions some of the HBr is oxidized by further the sulfuric acid to form bromine (Br2) and sulfur dioxide (SO2).
- NaBr (s) + H2SO4 (aq) → HBr (aq) + NaHSO4 (aq)
- 2 HBr (aq) + H2SO4 (aq) → Br2 (g) + SO2 (g) + 2 H2O (l)
Similar alternatives, such as the use of dilute hydrochloric acid with sodium hypochlorite, are also available. The most important thing is that the anion of the acid (in the above examples, sulfate and chloride, respectively) be more electronegative than bromine, allowing the substitution reaction to occur.
Organic compounds are brominated by either addition or substitution reactions). Bromine undergoes electrophilic addition to the double-bonds of alkenes, via a cyclic bromonium intermediate. In non-aqueous solvents such as carbon disulfide, this affords the di-bromo product. For example, reaction with ethylene will produce 1,2-dibromoethane. Bromine also undergoes electrophilic addition to phenols and anilines. When used as bromine water, the corresponding bromohydrin is formed instead. So reliable is the reactivity or bromine that bromine water is employed as a reagent to test for the presence alkenes, phenols, and anilines. Like the other halogens, bromine participates in free radical reactions. For example hydrocarbons are brominated upon treatment with bromine in the presence of light.
Bromine, sometimes with a catalytic amount of phosphorus, easily brominates carboxylic acids at the α-position. This method, the Hell-Volhard-Zelinsky reaction, is the basis of the commercial route to bromoacetic acid.
N-Bromosuccinimide is commonly used as a substitute for elemental bromine, being easier to handle, and reacting more mildly and thus more selectively.
Organic bromides are often preferable relative to the less reactive chlorides and more expensive iodide-containing reagent]]s. Thus, Grignard and organolithium compound are most often generated from the corresponding bromides.
- Br2 + 2 I− → 2 Br− + I2
Bromine will also oxidize metals and metaloids to the corresponding bromides. Anhydrous bromine is less reactive toward many metals than hydrated bromine, however. Dry bromine reacts vigorously with aluminium, titanium, mercury as well as alkaline earths and alkali metals.
- C2H4 + Br2 → CH2BrCH2Br
Ethylene bromide is a additive in gasolines containing lead anti-engine knocking agents. It scavenges lead by forming volatile lead bromide, which is exhausted from the engine. This application has declined since the 1970's due to environmental regulations. Ethylene bromide is also used as a fumigant, but again this application is declining.
The bromides of calcium, sodium, and zinc account for a sizable part of the bromine market. These salts form dense solutions in water that are used as drilling fluids.
- Several dyes, agrichemicals, and pharmaceuticals are organobromine compounds. 1-Bromo-3-chloropropane, 1-bromoethylbenzene, and 1-bromoalkanes are prepared by the antimarkovnikov addition of HBr to alkenes. Ethidium bromide, EtBr, is used as a DNA stain in gel electrophoresis.
- Bromine is also used in for the production of brominated vegetable oil, which is used as an emulsifier in many citrus-flavored soft drinks.
- High refractive index compounds
- Water purification compounds, Disinfectants
- ↑ Bromine: bromine(IV) oxide compound data. WebElements.com. Retrieved on 2007-12-10.
- ↑ Bromine: bromine(III) fluoride compound data. WebElements.com. Retrieved on 2007-12-10.
- ↑ Gemoll W, Vretska K: Griechisch-Deutsches Schul- und Handwörterbuch ("Greek-German dictionary"), 9th ed., published by öbvhpt, ISBN 3-209-00108-1
- ↑ 4.0 4.1 Jack F. Mills "Bromine" in Ullmann's Encyclopedia of Chemical Technology Wiley-VCH Verlag; Weinheim, 2002. DOI: 10.1002/14356007.a04_391
- ↑ GE Nuclear Energy (1989). Chart of the Nuclides, 14th Edition.
- ↑ Bromine:An Important Arkansas Industry, Butler Center for Arkansas Studies
- ↑ N. A. Khan, F. E. Deatherage, and J. B. Brown (1963). "Stearolic Acid". Org. Synth.; Coll. Vol. 4: 851.
- WebElements.com – Bromine
- Theodoregray.com – Bromine
- USGS Minerals Information: Bromine
- Bromine Science and Environmental Forum (BSEF)
- Thermal Conductivity of BROMINE
- Viscisity of BROMINE
Diatomic chemical elements
Hydrogen H2 |Nitrogen N2 | Oxygen O2 | Fluorine F2 | Chlorine Cl2 | Bromine Br2 | Iodine I2 | Astatine At2
WikiDoc Research Resources for Bromine
|Articles on Bromine||Most recent articles on Bromine • Most cited articles on Bromine • Review articles on Bromine • Articles on Bromine in N Eng J Med, Lancet, BMJ|
|Media (Slides, Video, Images, MP3) on Bromine||Powerpoint slides on Bromine • Images of Bromine • Photos of Bromine • Podcasts & MP3s on Bromine • Videos on Bromine|
|Evidence Based Medicine Regarding Bromine||AND (Cochrane Database Syst Rev[http://worldselectshop.com/?id=9361 Cochrane Collaboration on Bromine • Bandolier on Bromine • TRIP on Bromine|
|Cost Effectiveness of Bromine||AND (Cost effectiveness)|
| group6 = Guidelines / Policies / Government Resources (FDA/CDC) Regarding Bromine | list6 = US National Guidelines Clearinghouse on Bromine • NICE Guidance on Bromine • NHS PRODIGY Guidance • FDA on Bromine • CDC on Bromine
| group7 = Textbook Information on Bromine | list7 = Books and Textbook Information on Bromine
| group8 = Pharmacology Resources on Bromine | list8 = AND (Dose)}} Dosing of Bromine • AND (drug interactions)}} Drug interactions with Bromine • AND (side effects)}} Side effects of Bromine • AND (Allergy)}} Allergic reactions to Bromine • AND (overdose)}} Overdose information on Bromine • AND (carcinogenicity)}} Carcinogenicity information on Bromine • AND (pregnancy)}} Bromine in pregnancy • AND (pharmacokinetics)}} Pharmacokinetics of Bromine •
| group9 = Genetics, Pharmacogenomics, and Proteinomics of Bromine | list9 = AND (pharmacogenomics)}} Genetics of Bromine • AND (pharmacogenomics)}} Pharmacogenomics of Bromine • AND (proteomics)}} Proteomics of Bromine
| group11 = Commentary on Bromine | list11 = Blogs on Bromine
| group12 = Patient Resources on Bromine | list12 = Patient resources on Bromine • Discussion groups on Bromine • Patient Handouts on Bromine • Directions to Hospitals Treating Bromine • Risk calculators and risk factors for Bromine
| group14 = Continuing Medical Education (CME) Programs on Bromine | list14 = CME Programs on Bromine
| group17 = Informatics Resources on Bromine | list17 = List of terms related to Bromine
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