2008/9 Schools Wikipedia Selection. Related subjects: Chemical elements

53 telluriumiodinexenon


Periodic table (standard)">Periodic Table - Extended Periodic Table
Name, Symbol, Number iodine, I, 53
Chemical series halogens
Group, Period, Block 17, 5, p
Appearance violet-dark gray, lustrous
Standard atomic weight 126.90447 (3)  g·mol−1
Electron configuration [Kr] 4d10 5s2 5p5
Electrons per shell 2, 8, 18, 18, 7
Physical properties
Phase solid
Density (near r.t.) 4.933  g·cm−3
Melting point 386.85  K
(113.7 ° C, 236.66 ° F)
Boiling point 457.4  K
(184.3 ° C, 363.7 ° F)
Critical point 819 K, 11.7 MPa
Heat of fusion (I2) 15.52   kJ·mol−1
Heat of vaporization (I2) 41.57   kJ·mol−1
Specific heat capacity (25 °C) (I2) 54.44  J·mol−1·K−1
Vapor pressure (rhombic)
P(Pa) 1 10 100 1 k 10 k 100 k
at T(K) 260 282 309 342 381 457
Atomic properties
Crystal structure orthorhombic
Oxidation states ±1, 5, 7
(strongly acidic oxide)
Electronegativity 2.66 (Pauling scale)
Ionization energies 1st: 1008.4 kJ/mol
2nd: 1845.9 kJ/mol
3rd: 3180 kJ/mol
Atomic radius 140   pm
Atomic radius (calc.) 115  pm
Covalent radius 133  pm
Van der Waals radius 198 pm
Magnetic ordering nonmagnetic
Electrical resistivity (0 °C) 1.3×107 Ω·m
Thermal conductivity (300 K) 0.449  W·m−1·K−1
Bulk modulus 7.7  GPa
CAS registry number 7553-56-2
Selected isotopes
Main article: Isotopes of iodine
iso NA half-life DM DE ( MeV) DP
127I 100% 127I is stable with 74 neutrons
129I syn 15.7×106 y β- 0.194 129Xe
131I syn 8.02070 d β- 0.971 131Xe
CAS number [7553-56-2]
R-phrases R21 R23 R25 R34
S-phrases gas/fumes/vapour/spray (appropriate wording to be specified by the manufacturer)">S23 S25
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)
Infobox disclaimer and references

Iodine (IPA: /ˈaɪədaɪn, ˈaɪədɪn/, or /ˈaɪədiːn/; from Greek: iodes "violet"), is a chemical element that has the symbol I and atomic number 53. Naturally-occurring iodine is a single isotope with 74 neutrons.

Chemically, iodine is the least reactive of the halogens, and the most electropositive halogen after astatine. However, the element does not occur in the free state in nature. As with all other halogens (members of Group VII in the Periodic Table), when freed from its compounds iodine forms diatomic molecules (I2).

Iodine and its compounds are primarily used in medicine, photography and in dyes. Although it is rare in the solar system and Earth's crust, the iodides are very soluble in water, and the element is concentrated in seawater. This mechanism helps to explain how the element came to be required in trace amounts by all animals and some plants, being by far the heaviest element known to be necessary to living organisms.


Iodine under standard conditions is a dark-purple/dark-brown solid. It can be seen apparently subliming at standard temperatures into a violet-pink gas that has an irritating odour. This halogen forms compounds with many elements, but is less reactive than the other members of its Group VII (halogens) and has some metallic light reflectance.

Elemental iodine dissolves easily in chloroform and carbon tetrachloride. The solubility of elementary iodine in water can be vastly increased by the addition of potassium iodide. The molecular iodine reacts reversibly with the negative ion, creating the triiodide anion, I3, which dissolves well in water. This is also the formulation of some types of medicinal (antiseptic) iodine, although tincture of iodine classically disolves the element in alcohol. The deep blue colour of starch-iodine complexes is produced only by the free element.

Students who have seen the classroom demonstration in which iodine crystals are gently heated in a test tube to violet vapor, may gain the impression that liquid iodine does not exist at atmospheric pressure. This misconception arises because the small amount of vapor produced has such a deep colour that the liquid appears not to form. In fact, if iodine crystals are heated carefully to just above their melting point of 113.7 °C, the crystals melt into a liquid which is present under a dense blanket of the vapor.


Iodine was discovered by Bernard Courtois in 1811. He was born to a manufacturer of saltpeter (a vital part of gunpowder). At the time of the Napoleonic Wars, France was at war and saltpeter was in great demand. Saltpeter produced from French niter beds required sodium carbonate, which could be isolated from seaweed washed up on the coasts of Normandy and Brittany. To isolate the sodium carbonate, seaweed was burned and the ash then washed with water. The remaining waste was destroyed by adding sulfuric acid. One day Courtois added too much sulfuric acid and a cloud of purple vapor rose. Courtois noted that the vapor crystallized on cold surfaces making dark crystals. Courtois suspected that this was a new element but lacked the money to pursue his observations.

However he gave samples to his friends, Charles Bernard Desormes (1777 - 1862) and Nicolas Clément (1779 - 1841), to continue research. He also gave some of the substance to Joseph Louis Gay-Lussac (1778 - 1850), a well-known chemist at that time, and to André-Marie Ampère (1775 - 1836). On 29 November 1813, Dersormes and Clément made public Courtois’ discovery. They described the substance to a meeting of the Imperial Institute of France. On December 6, Gay-Lussac announced that the new substance was either an element or a compound of oxygen. Ampère had given some of his sample to Humphry Davy (1778 - 1829). Davy did some experiments on the substance and noted its similarity to chlorine. Davy sent a letter dated December 10 to the Royal Society of London stating that he had identified a new element. A large argument erupted between Davy and Gay-Lussac over who identified iodine first but both scientists acknowledged Courtois as the first to isolate the chemical element.


Iodine is used in pharmaceuticals, antiseptics, medicine, food supplements, dyes, catalysts, halogen lights, photography, water purifying, and starch detection.

  • Tincture of iodine (10% elemental iodine in ethanol base) is an essential component of any emergency survival kit, used both to disinfect wounds and to sanitize surface water for drinking (3 drops per litre, let stand for 30 minutes). Alcohol-free iodine solutions such as Lugol's iodine, as well as other iodophor type antiseptics, are also available as effective elemental iodine sources for this purpose.
  • Iodine compounds are important in the field of organic chemistry
  • Iodine, as a heavy element, is quite radio-opaque. Organic compounds of a certain type (typically iodine-substituted benzene derivatives) are thus used in medicine as X-ray radiocontrast agents for intravenous injection. This is often in conjunction with advanced X-ray techniques such as angiography and CT scanning
  • Silver iodide is used in photography.
  • Tungsten iodide is used to stabilize the filaments in light bulbs.

Occurrence on earth

Iodine naturally occurs in the environment chiefly as dissolved iodide in seawater, although it is also found in some minerals and soils. The element may be prepared in an ultrapure form through the reaction of potassium iodide with sulfate">copper(II) sulfate. There are also a few other methods of isolating this element in the laboratory-- for example the method used to isolate other halogens: oxygenation of the iodide in hydroiodic acid (often made in situ with an iodide and sulfuric acid) by manganese dioxide (see below in Descriptive chemistry). Although the element is actually quite rare, kelp and certain plants and algae have some ability to concentrate iodine, which helps introduce the element into the food chain.

Descriptive chemistry

Elemental iodine is poorly soluble in water, with one gram dissolving in 3450 ml at 20 °C and 1280 ml at 50 °C. By contrast with chlorine, the formation of the hypohalite ion (IO) in neutral aqueous solutions of iodine is negligible.

I2+ H2O ↔ H+ + I + HIO   (K = 2.0×10-13)

Solubility in water is greatly improved if the solution contains dissolved iodides such as hydroiodic acid, potassium iodide, or sodium iodide. Dissolved bromides also improve water solubility of iodine. Iodine is soluble in a number of organic solvents, including ethanol (20.5 g/100 ml at 15 °C, 21.43 g/100 ml at 25 °C), diethyl ether (20.6 g/100 ml at 17 °C, 25.20 g/100 ml at 25 °C), chloroform, acetic acid, glycerol, benzene (14.09 g/100 ml at 25 °C), carbon tetrachloride (2.603 g/100 ml at 35 °C), and carbon disulfide (16.47 g/100 ml at 25 °C). Aqueous and ethanol solutions are brown. Solutions in chloroform, carbon tetrachloride, and carbon disulfide are violet.

Elemental iodine can be prepared by oxidizing iodides with chlorine:

2I + Cl2 → I2 + 2Cl

or with manganese dioxide in acid solution:

2I + 4H+ + MnO2 → I2 + 2H2O + Mn2+

Iodine is reduced to hydroiodic acid by hydrogen sulfide:

I2 + H2S → 2HI + S↓

or by hydrazine:

2I2 + N2H4 → 4HI + N2

Iodine is oxidized to iodate by nitric acid:

I2 + 10HNO3 → 2HIO3 + 10NO2 + 4H2O

or by chlorates:

I2 + 2ClO3 → 2IO3 + Cl2

Iodine is converted in a two stage reaction to iodide and iodate in solutions of alkali hydroxides (such as sodium hydroxide):

I2 + 2OH → I + IO + H2O (K = 30)
3IO → 2I + IO3 (K = 1020)

Notable inorganic iodine compounds

LiI BeI2 BI3 CI4 NI3 I2O4 I2O5 I4O9 IF IF3 IF5 IF7 Ne
NaI MgI2 AlI3 SiI4 PI3 S ICl ICl3 Ar
KI CaI2 Sc TiI4 V Cr MnI2 Fe Co NiI2 CuI ZnI2 Ga2I6 GeI2 GeI4 As Se IBr Kr
RbI SrI2 Y ZrI4 Nb Mo Tc Ru Rh Pd AgI CdI2 InI3 SnI4 SnI2 SbI3 TeI4 I Xe
CsI BaI2 Hf Ta W Re Os Ir Pt AuI HgI2 TlI PbI2 Bi Po At Rn
Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Uub Uut Uuq Uup Uuh Uus Uuo
La Ce Pr Nd Pm SmI2 Eu Gd TbI3 Dy Ho Er Tm Yb Lu
Ac ThI4 Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr

Stable iodine in biology

Iodine is an essential trace element; its only known roles in biology are as constituents of the thyroid hormones, thyroxine (T4) and triiodothyronine (T3). These are made from addition condensation products of the amino acid tyrosine, and are stored prior to release in a protein-like iodine-containing molecule called thyroglobulin. T4 and T3 contain four and three atoms of iodine per molecule, respectively. The thyroid gland actively absorbs iodide from the blood to make and release these hormones into the blood, actions which are regulated by a second hormone TSH from the pituitary. Thyroid hormones are phylogenetically very old molecules which are synthesized by most multicellular organisms, and which even have some effect on unicellular organisms.

Thyroid hormones play a very basic role in biology, acting on gene transcription to regulate the basal metabolic rate. The total deficiency of thyroid hormones can reduce basal metabolic rate up to 50%, while in excessive production of thyroid hormones the basal metabolic rate can be increased by 100%. T4 acts largely as a precursor to T3, which is (with some minor exceptions) the biologically active hormone.

Human dietary intake

The United States Food and Drug Administration recommends 150 micrograms of iodine per day for both men and women. This is necessary for proper production of thyroid hormone. Natural sources of iodine include sea life, such as kelp and certain seafood, as well as plants grown on iodine-rich soil. Salt for human consumption is often fortified with iodine and is referred to as iodized salt.

Iodine deficiency

In areas where there is little iodine in the diet—typically remote inland areas and semi-arid equatorial climates where no marine foods are eaten— iodine deficiency gives rise to hypothyroidism, symptoms of which are extreme fatigue, goitre, mental slowing, depression, weight gain, and low basal body temperatures.

Iodine deficiency is also the leading cause of preventable mental retardation, an effect which happens primarily when babies and small children are made hypothyroid by lack of the element. The addition of iodine to table salt has largely eliminated this problem in the wealthier nations, but as of March 2006, iodine deficiency remained a serious public health problem in the developing world.

Radioiodine and biology

Radioiodine and the thyroid

Human exposure to radioactive iodine will cause thyroid uptake, as with all iodine, leading to elevated chances of thyroid cancer. Isotopes with shorter half-lives such as 131I present a greater risk than those with longer half-lives since they generate more radiation per unit of time. Taking large amounts of regular iodine will saturate the thyroid and prevent uptake. Iodine pills are sometimes distributed to persons living close to nuclear establishments, for use in case of accidents that could lead to releases of radioactive iodine.

  • Iodine-123 and iodine-125 are used in medicine as tracers for imaging and evaluating the function of the thyroid.
  • Uncombined (elemental) iodine is mildly toxic to all living things.

The artificial radioisotope 131I (a beta emitter), has a half-life of 8.0207 days. Also known as radioiodine, 131I has been used in treating cancer and other pathologies of the thyroid glands. 123I is the radioisotope most often used in nuclear imaging of the kidney and thyroid as well as thyroid uptake scans (used for the evaluation of Graves' Disease). The most common compounds of iodine are the iodides of sodium and potassium (KI) and the iodates (KIO3).

Potassium iodide (KI tablets, or "SSKI" = "Saturated Solution of KI" liquid drops) can be given to people in a nuclear disaster area when fission has taken place, to block the uptake of iodine-131 by the thyroid. The protective effect of KI lasts approximately 24 hours, so it should be dosed daily until a risk of significant exposure to radioiodines no longer exists. The exposure can be reduced by evacuation, sheltering, and by control of the food supply. Iodine-131 also decays rapidly, with a half-life of 8 days, so that 99.95% of the original radioiodine is gone after three months.

Iodine-129 129I ( half-life 15.7 million years) is a product of cosmic ray spallation on various isotopes of xenon in the atmosphere, in cosmic ray muon interaction with tellurium-130, and also and uranium and plutonium fission, both in subsurface rocks and nuclear reactors. Nuclear processes, in particular nuclear fuel reprocessing and atmospheric nuclear weapons tests have now swamped the natural signal for this isotope. 129I was used in rainwater studies following the Chernobyl accident. It also has been used as a ground-water tracer and as an indicator of nuclear waste dispersion into the natural environment.

Radioiodine and the kidney

In the 1970s imaging techniques were developed in California to utilize radioiodine in diagnostics for renal hypertension.


There are 37 isotopes of iodine and only one, 127I, is stable.

In many ways, 129I is similar to 36Cl. It is a soluble halogen, fairly non-reactive, exists mainly as a non-sorbing anion, and is produced by cosmogenic, thermonuclear, and in-situ reactions. In hydrologic studies, 129I concentrations are usually reported as the ratio of 129I to total I (which is virtually all 127I). As is the case with 36Cl/Cl, 129I/I ratios in nature are quite small, 10−14 to 10−10 (peak thermonuclear 129I/I during the 1960s and 1970s reached about 10−7). 129I differs from 36Cl in that its half-life is longer (15.7 vs. 0.301 million years), it is highly biophilic, and occurs in multiple ionic forms (commonly, I and IO3) which have different chemical behaviors. This makes it fairly easy for 129I to enter the biosphere as it becomes incorporated into vegetation, soil, milk, animal tissue, etc.

Excesses of stable 129Xe in meteorites have been shown to result from decay of "primordial" Iodine-129 produced newly by the supernovas which created the dust and gas from which the solar system formed. 129I was the first extinct radionuclide to be identified as present in the early solar system. Its decay is the basis of the I-Xe Iodine-xenon radiometric dating scheme, which covers the first 83 million years of solar system evolution.

Effects of various radioiodine isotopes in biology are discussed below.

Toxicity of iodine

Excess iodine has symptoms similar to those of iodine deficiency. Commonly encountered symptoms are abnormal growth of the thyroid gland and disorders in functioning and growth of the organism as a whole. Elemental iodine, I2, is a deadly poison if taken in larger amounts; if 2-3 grams of it is consumed, it is fatal to humans. Iodides are similar in toxicity to bromides.

Precautions for stable iodine

Direct contact with skin can cause lesions, so it should be handled with care. Iodine vapor is very irritating to the eye and to mucous membranes. Concentration of iodine in the air should not exceed 1 mg/ m³ (eight-hour time-weighted average). When mixed with ammonia, it can form nitrogen triiodide which is extremely sensitive and can explode unexpectedly.

Clandestine use

In the United States, the Drug Enforcement Agency (DEA) regards iodine and compounds containing iodine (ionic iodides, iodoform, ethyl iodide, and so on) as reagents useful for the clandestine manufacture of methamphetamine. Persons who attempt to purchase significant quantities of such chemicals without establishing a legitimate use are likely to find themselves the target of a DEA investigation. Persons selling such compounds without doing due diligence to establish that the materials are not being diverted to clandestine use may be subject to stiff penalties, such as expensive fines or even imprisonment.

Retrieved from ""
The 2008 Wikipedia for Schools is sponsored by SOS Children , and is mainly selected from the English Wikipedia with only minor checks and changes (see for details of authors and sources). The articles are available under the GNU Free Documentation License. See also our Disclaimer.