Basic information
- Name:
Iodine
- CAS No.:
7553-56-2
- Molecular Structure:

- Formula:
- I2
- Synonyms:
- Actomar;DentaPure DP 90;Diatomic iodine;Diiodine;Eranol;Iodel FD;Iodine (127I2);Iodine colloidal;Iodine crystals;Iodine sublimed;Iodomarin;Iosan Superdip;Jodosan;Molecular iodine;NSC 42355;Tegodyne;
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Chemistry
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IUPAC Name: Molecular iodine
Molecular Formula: I2
Molecular Weight: 253.81 g/mol
Canonical SMILES: II
InChI: InChI=1S/I2/c1-2
EINECS: 231-442-4
Classification Code: Anti-Infective Agents; Anti-infective agents, local; Anti-infective, topical; Growth Substances; Human Data; Micronutrients; Reproductive Effect; Trace Elements
Melting Point: 113 °C(lit.)
storage temperature: Store at RT.
form: particles (round)
Water Solubility: 0.3 g/L (20 °C)
Index of Refraction: 1.788
Molar Refractivity: 27.98 cm3
Molar Volume: 66.1 cm3
Surface Tension: 54.8 dyne/cm
Density: 3.834 g/cm3
Enthalpy of Vaporization: 41.57 kJ/mol
Boiling Point: 184.3 °C at 760 mmHg
Vapour Pressure of Iodine (CAS NO.7553-56-2): 0.49 mmHg at 25 °C
History
Iodine was discovered by Bernard Courtois in 1811. 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 physicist André-Marie Ampère (1775–1836). On 29 November 1813, Dersormes and Clément made public Courtois’s discovery. 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. element.
Uses
Iodine (CAS NO.7553-56-2) is used for the manufacture of organic compounds, for the manufacture of potassium iodide and sodium iodide, and for the manufacture of other inorganic compounds. Iodine is used as a catalyst in the chlorination of organic compounds and in analytical chemistry for determination of the iodine numbers of oils. Iodine for medicinal, photographic, and pharmaceutical purposes is usually in the form of alkali iodides, prepared through the agency of ferrous iodide. It is also used for the manufacture of dyes and as a germicide. Simple iodine derivatives of hydrocarbons, such as iodoform (CHI3), have an antiseptic action. Organic compounds containing iodine have been used as rubber emulsifiers, chemical antioxidants, and dyes and pigments.
Production
Iodine can be produced from iodates:
IO3- + 3SO2 + 3H2O → I- + 3SO42- + 6H-
IO3- + I- + 6H+ → 3I2 + 3H2O
Iodine can also be produced from brine. This process consists of cleaning the solution (of clays and other materials), adding sulfuric acid to a pH <2.5 followed by treatment with gaseous chlorine:
2I- + Cl2 → I2 + 2Cl-
after which the Iodine is recovered by a countercurrent air blow out step. process.
Toxicity Data With Reference
| Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
|---|---|---|---|---|---|
| dog | LDLo | intravenous | 40mg/kg (40mg/kg) | "Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 5, Pg. 76, 1959. | |
| dog | LDLo | oral | 800mg/kg (800mg/kg) | "Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1289, 1935. | |
| human | LDLo | oral | 28mg/kg (28mg/kg) | GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA" GASTROINTESTINAL: OTHER CHANGES | "Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 330, 1969. |
| man | LDLo | unreported | 29mg/kg (29mg/kg) | "Poisoning; Toxicology, Symptoms, Treatments," 2nd ed., Arena, J.M., Springfield, IL, C.C. Thomas, 1970Vol. 2, Pg. 73, 1970. | |
| mouse | LD50 | oral | 22gm/kg (22000mg/kg) | Drugs of the Future. Vol. 4, Pg. 876, 1979. | |
| mouse | LD50 | subcutaneous | > 8650mg/kg (8650mg/kg) | Drugs in Japan Vol. -, Pg. 1226, 1990. | |
| rabbit | LD50 | oral | 10gm/kg (10000mg/kg) | Drugs of the Future. Vol. 4, Pg. 876, 1979. | |
| rabbit | LDLo | subcutaneous | 175mg/kg (175mg/kg) | "Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 5, Pg. 76, 1959. | |
| rat | LCLo | inhalation | 137ppm/1H (137ppm) | SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | National Technical Information Service. Vol. OTS0555278, |
| rat | LD50 | oral | 14gm/kg (14000mg/kg) | Drugs of the Future. Vol. 4, Pg. 876, 1979. | |
| rat | LD50 | subcutaneous | 10500mg/kg (10500mg/kg) | Drugs in Japan Vol. -, Pg. 1226, 1990. | |
| women | TDLo | oral | 26mg/kg/1Y-I (26mg/kg) | ENDOCRINE: EVIDENCE OF THYROID HYPERFUNCTION | Postgraduate Medical Journal. Vol. 62, Pg. 661, 1986. |
Consensus Reports
Reported in EPA TSCA Inventory.
Safety Profile
When heated to decomposition it emits toxic fumes of I− and various iodine compounds. Reacts vigorously with reducing materials.
Hazard Codes:
Xn,
N
Risk Statements: 36/37/38-50-20/21
R36/37/38:Irritating to eyes, respiratory system and skin.
R50:Very toxic to aquatic organisms.
R20/21:Harmful by inhalation and in contact with skin.
Safety Statements: 26-61-25-23
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S61:Avoid release to the environment. Refer to special instructions / safety data sheets.
S25:Avoid contact with eyes.
S23:Do not breathe vapour.
RIDADR: UN 2056 3/PG 2
WGK Germany: 2
RTECS: NN1575000
HazardClass: 8
PackingGroup: III
Standards and Recommendations
OSHA PEL: CL 0.1 ppm
ACGIH TLV: CL 0.1 ppm
DFG MAK: 0.1 ppm (1.1 mg/m3)
Analytical Methods
For occupational chemical analysis use OSHA: #ID-177 or NIOSH: Iodine, 6005.
Specification
Iodine (CAS NO.7553-56-2), its Synonyms are Actomar ; Diiodine ; Eranol ; Ethanolic solution of iodine ; Iodine Tincture USP ; Iodine colloidal ; Iodine crystals ; Iodine solution ; Iodine sublimed ; Iodine tincture ; Tincture iodine . It is violet-black crystals with a metallic luster and a sharp odor.
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