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| Arsenic trioxide | |
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Other names
Arsenic(III) oxide, |
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| Identifiers | |
| CAS number | 1327-53-3 Y |
| PubChem | 261004 |
| ChemSpider | 452539 Y |
| UNII | S7V92P67HO Y |
| EC number | 215-481-4 |
| DrugBank | DB01169 |
| KEGG | C13619 N |
| ChEMBL | CHEMBL1200978 N |
| RTECS number | CG3325000 |
| ATC code | L01XX27 |
| Jmol-3D images | Image 1 |
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SMILES
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InChI
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| Properties | |
| Molecular formula | As2O3 |
| Molar mass | 197.841 g/mol |
| Appearance | White solid |
| Density | 3.74 g/cm3 |
| Melting point |
312.2 °C, 585 K, 594 °F |
| Boiling point |
465 °C, 738 K, 869 °F |
| Solubility in water | 20 g/L (25 °C) see text |
| Solubility | soluble in dilute acids and alkalies, practically insoluble in organic solvents [2] |
| Acidity (pKa) | 9.2 |
| Structure | |
| Crystal structure | cubic (α)<180 °C monoclinic (β) >180 °C |
| Molecular shape | See text |
| Dipole moment | Zero |
| Thermochemistry | |
| Std enthalpy of formation ΔfH |
−657.4 kJ/mol |
| Standard molar entropy S |
? J.K−1.mol−1 |
| Pharmacology | |
| Protein binding | 75% bound |
| Hazards | |
| MSDS | External MSDS |
| EU classification | Very toxic (T+) Carc. Cat. 1 |
| R-phrases | R45, R28, R34, R50/53 |
| S-phrases | S53, S45, S60, S61 |
| NFPA 704 |
0
3
0
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| LD50 | 14.6 mg/kg (rat, oral) |
| Related compounds | |
| Other anions | Arsenic trisulfide |
| Other cations | Phosphorus trioxide Antimony trioxide |
| Related compounds | Arsenic pentoxide Arsenous acid |
| Supplementary data page | |
| Structure and properties |
n, εr, etc. |
| Thermodynamic data |
Phase behaviour Solid, liquid, gas |
| Spectral data | UV, IR, NMR, MS |
| N (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Arsenic trioxide is the inorganic compound with the formula As2O3. This commercially important oxide of arsenic is the main precursor to other arsenic compounds, including organoarsenic compounds. Approximately 50,000 tonnes are produced annually.[3] Many applications are controversial given the high toxicity of arsenic compounds.
Contents
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Preparation and properties [edit]
Arsenic trioxide can be generated via routine processing of arsenic compounds including the oxidation (combustion) of arsenic and arsenic-containing minerals in air. Illustrative is the roasting of orpiment, a typical arsenic sulfide ore.
- 2 As2S3 + 9 O2 → 2 As2O3 + 6 SO2
Most arsenic oxide is, however, obtained as a volatile by-product of the processing of other ores. For example, arsenopyrite, a common impurity in gold- and copper-containing ores, liberates arsenic trioxide upon heating in air. The processing of such minerals has led to numerous cases of poisonings.[4] Only in China are arsenic ores intentionally mined.[3]
Arsenic trioxide is an amphoteric oxide, and its aqueous solutions are weakly acidic. Thus, it dissolves readily in alkaline solutions to give arsenites. It is less soluble in acids, although it will dissolve in hydrochloric acid, giving chloro compounds[clarification needed], ultimately arsenic trichloride with concentrated acid. Only with strong oxidizing agents such as ozone, hydrogen peroxide, and nitric acid does it yield arsenic pentoxide, As2O5. Reduction gives elemental arsenic or arsine (AsH3) depending on conditions. In this regard, arsenic trioxide differs from phosphorus trioxide, which readily combusts to phosphorus pentoxide.
Structure [edit]
In the liquid and gas phase below 800 °C, arsenic trioxide has the formula As4O6 and is isostructural with P4O6. Above 800 °C As4O6 significantly dissociates into molecular As2O3, which adopts the same structure as N2O3. Three forms (polymorphs) are known in the solid state: cubic As4O6, containing molecular As4O6, and two related polymeric forms. The polymers, which both crystallize as monoclinic crystals, feature sheets of pyramidal AsO3 units that share O atoms.[5]
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(cubic) |
(monoclinic) |
(monoclinic) |
Uses [edit]
Large scale applications include its use as a precursor to forestry products, in colorless glass production, and in electronics.[3] Being the main compound of arsenic, the trioxide is the precursor to elemental arsenic, arsenic alloys, and arsenide semiconductors. Organoarsenic compounds, e.g. feed additives (Roxarsone) and pharmaceuticals (Neosalvarsan), are derived from arsenic trioxide. Bulk arsenic-based compounds sodium arsenite and sodium cacodylate are derived from the trioxide.
A variety of applications exploit arsenic's toxicity, including the use of the oxide as a wood preservative. Copper arsenates, which are derived from arsenic trioxide, are used on a large scale as a wood preservative in the US and Malaysia, but such materials are banned in many parts of the world. This practice remains controversial.[3] In combination with copper(II) acetate arsenic trioxide gives the vibrant pigment known as paris green used in paints and as a rodenticide. This application has been discontinued.
Medical applications [edit]
Despite the well known toxicity of arsenic, arsenic trioxide has long been of biomedical interest, dating to traditional Chinese medicine, where it is known as Pi Shuang and is still used to treat cancer and other conditions,[6] and to homeopathy, where it is called arsenicum album. Some discredited patent medicines, e.g., Fowler's solution, contained derivatives of arsenic oxide.[7] Arsenic trioxide under the trade name Trisenox (manufacturer: Cephalon) is a chemotheraputic agent of idiopathic function used to treat leukemia that is unresponsive to "first line" agents. It is suspected that arsenic trioxide induces cancer cells to undergo apoptosis. Due to the toxic nature of arsenic, this drug carries significant risks. Use as a cytostatic in the treatment of refractory promyelocytic (M3) subtype of acute myeloid leukemia.[8][9] The combination therapy of arsenic trioxide and all-trans retinoic acid (ATRA) has been approved by the U.S. Food and Drug Administration (FDA) for treatment of certain leukemias.[10] University of Hong Kong developed a liquid form of arsenic trioxide that can be administered orally.[11]
Arsenic trioxide also appears to be a promising therapeutic agent for autoimmune diseases.[12]
The enzyme thioredoxin reductase has recently been identified as a target for arsenic trioxide.[13]
Arsenic trioxide in combination with ascorbic acid and buthionine sulfoxide decrease intracellular glutathione to a greater extent, and render malignant cells more sensitive to apoptosis. Arsenic trioxide induced apoptosis was not enhanced by ascorbic acid in normal cells, suggesting that this combination may be selectively toxic to some malignant cells.[14]
Natural occurrence [edit]
Two minerals are known to possess the As2O3 chemical formula: arsenolite(regular) and claudetite (monoclinic). Both are relatively rare secondary minerals found in oxidation zones of As-rich ore deposits (these are often Co-, Ni-, Ag- and U-bearing, too). Traces of arsenic may naturally contaminate drinking water wells. Researchers at the Geological Survey of Canada have modelled relative variation in natural arsenic hazard potential in drinking water for the province of New Brunswick.[15]
Toxicology [edit]
See also: Arsenicosis
Arsenic trioxide is readily absorbed by the digestive system: toxic effects are also well known upon inhalation or upon skin contact. Elimination is rapid at first (half-life of 1–2 days), by methylation to monomethylarsonic acid and dimethylarsonic acid, and excretion in the urine, but a certain amount (30–40% in the case of repeated exposure) is incorporated into the bones, muscles, skin, hair and nails (all tissues rich in keratin) and eliminated over a period of weeks or months.
The first symptoms of acute arsenic poisoning by ingestion are digestive problems: vomiting, abdominal pains, diarrhea often accompanied by bleeding. Sub-lethal doses can lead to convulsions, cardiovascular problems, inflammation of the liver and kidneys and abnormalities in the coagulation of the blood. These are followed by the appearance of characteristic white lines (Mees stripes) on the nails and by hair loss. Lower doses lead to liver and kidney problems and to changes in the pigmentation of the skin. Even dilute solutions of arsenic trioxide are dangerous on contact with the eyes.
The poisonous properties are legendary and the subject of an extensive literature.[16][17][18]
Chronic arsenic poisoning is known as arsenicosis. This disorder affects workers in smelters, in populations whose drinking water contains high levels of arsenic (0.3–0.4 ppm), and in patients treated for long periods with arsenic-based pharmaceuticals. Similarly, studies on workers exposed in copper foundries in the U.S., Japan and Sweden indicate a risk of lung cancer 6–10 times higher for the most exposed workers compared with the general population. Long-term ingestion of arsenic trioxide either in drinking water or as a medical treatment can lead to skin cancer. Reproductive problems (high incidence of miscarriage, low birth weight, congenital deformations) have also been indicated in one study of women exposed to arsenic trioxide dust as employees or neighbours of a copper foundry.
In Austria, there lived the so-called "arsenic eaters of Styria", who ingested doses far beyond the lethal dose of arsenic trioxide without any apparent harm. Arsenic is thought to enable strenuous work at high altitudes, e.g. in the Alps.[19][20][21][22]
The current OSHA 1910.1018 occupational permissible exposure limit for inorganic arsenic compounds in breathing zone air is 0.010 mg/m3.
References [edit]
- ^ Shakhashiri, B. Z. "Chemical of the Week: Arsenic". University of Wisconsin-Madison Chemistry Dept.
- ^ Patnaik, P. (2002). Handbook of Inorganic Chemicals. McGraw-Hill. ISBN 0-07-049439-8.
- ^ a b c d Grund, S. C.; Hanusch, K.; Wolf, H. U. (2005), "Arsenic and Arsenic Compounds", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a03_113.pub2
- ^ "Giant Mine – Northwest Territories Region – Indian and Northern Affairs Canada". Retrieved 2007-08-28.
- ^ Holleman, A. F.; Wiberg, E. (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN 0-12-352651-5.
- ^ Gielen, M.; Tiekink, E. R. (2005). Metallotherapeutic Drugs and Metal-Based Diagnostic Agents. Wiley. p. 298. ISBN 0-470-86403-6.
- ^ Gibaud, S.; Jaouen, G. (2010). "Arsenic-Based Drugs: From Fowler’s Solution to Modern Anticancer Chemotherapy". Topics in Organometallic Chemistry 32: 1–20. doi:10.1007/978-3-642-13185-1_1.
- ^ Soignet, S. L.; Frankel, S. R.; Douer, D.; Tallman, M. S.; Kantarjian, H.; Calleja, E.; Stone, R. M.; Kalaycio, M.; Scheinberg, D. A. et al. (2001). "United States Multicenter Study of Arsenic Trioxide in Relapsed Acute Promyelocytic Leukemia" (pdf). Journal of Clinical Oncology 19 (18): 3852–3860. PMID 11559723.
- ^ Antman, K. H. (2001). "Introduction: The history of arsenic trioxide in cancer therapy" (pdf). Oncologist 6 (Supplement 2): 1–2. doi:10.1634/theoncologist.6-suppl_2-1. PMID 11331433.
- ^ Zhu, J.; Chen, Z.; Lallemand-Breitenbach, V.; de Thé, H. (2002). "How acute promyelocytic leukaemia revived arsenic". Nature Reviews. Cancer 2 (9): 705–714. doi:10.1038/nrc887. PMID 12209159.
- ^ Au, W.-Y.; Kumana, C. R.; Kou, M.; Mak, R.; Chan, G. C.; Lam, C.-W.; Kwong, Y.-L. (2003). "Oral arsenic trioxide in the treatment of relapsed acute promyelocytic leukemia" (pdf). Blood 102 (1): 407–408. doi:10.1182/blood-2003-01-0298. PMID 12814916.
- ^ Bobé, P.; Bonardelle, D.; Benihoud, K.; Opolon, P.; Mounira, C.-A. (2006). "Arsenic trioxide: A promising novel therapeutic agent for lymphoproliferative and autoimmune syndromes in MRL/lpr mice" (pdf). Blood 108 (13): 3967–3975. doi:10.1182/blood-2006-04-020610. PMID 16926289.
- ^ Lu, J.; Chew, E. H.; Holmgren, A. (2007). "Targeting thioredoxin reductase is a basis for cancer therapy by arsenic trioxide". Proc. Natl. Acad. Sci. U.S.A. 104 (30): 12288–12293. doi:10.1073/pnas.0701549104. PMC 1940330. PMID 17640917.
- ^ Dai, J.; Weinberg, R. S.; Waxman, S.; Jing, Y. (January 1999). "Malignant cells can be sensitized to undergo growth inhibition and apoptosis by arsenic trioxide through modulation of the glutathione redox system". Blood 93 (1): 268–277. PMID 9864170.
- ^ Klassen, R. A.; Douma, S. L.; Ford, A.; Rencz, A.; Grunsky, E. (2009). "Geoscience modelling of relative variation in natural arsenic hazard potential in New Brunswick" (pdf). Geological Survey of Canada Current Research 2009 (7).
- ^ "Stanton v Benzler 9716830". U.S. 9th Circuit Court of Appeals. 1998-06-17. Retrieved 2008-06-09. "(...) convicted by a jury of first degree murder for poisoning her ex-husband. Her ex-husband's body was found with traces of arsenic trioxide in it."
- ^ Emsley, J. (2006). "Arsenic". The Elements of Murder: A History of Poison. Oxford University Press. pp. 93–197. ISBN 978-0-19-280600-0.
- ^ Flaubert, G. (1856). Madame Bovary.
- ^ "Arsenic Eaters". New York Times. July 26, 1885.
- ^ Allesch, R. M. (1959). Arsenik. Seine Geschichte in Österreich. Archiv für vaterländische Geschichte und Topographie 54. Klagenfurt: Kleinmayr.
- ^ Przygoda, G.; Feldmann, J.; Cullen, W. R. (2001). "The arsenic eaters of Styria: a different picture of people who were chronically exposed to arsenic". Applied Organometallic Chemistry 15 (6): 457–462. doi:10.1002/aoc.126.
- ^ Whorton, J. C. (2010). The Arsenic Century. Oxford University Press. pp. 270–273. ISBN 978-0-19-960599-6.
External links [edit]
- Case Studies in Environmental Medicine: Arsenic Toxicity
- "Arsenic and Arsenic Compounds". Summaries & Evaluations. International Agency for Research on Cancer (IARC). February 1998.
- International Chemical Safety Card 0378
- NIOSH Pocket Guide to Chemical Hazards
- NTP Report on Carcinogens – Inorganic Arsenic Compounds
- Use of Arsenic Trioxide in Multiple Myeloma Treatment
- The use of Arsenic trioxide in medicine.
- Institut national de recherche et de sécurité (1989). "Trioxyde d'arsenic." Fiche toxicologique n° 89. Paris:INRS. (French)
- Institute of Chemistry Austria, speciallised on arsenic and various arsenic compounds
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English Journal
- The ratsbane and the vitamin.
- Jukes TH.
- Journal of applied biochemistry.J Appl Biochem.1983 Dec;5(6):369-70.
- PMID 6678938
- The toxic principle in seeds of Dichapetalum toxicarium (ratsbane).
- PETERS RA, WAKELIN RW, BIRKS FT, MARTIN AJ, WEBB J.
- The Biochemical journal.Biochem J.1954 Dec;58(4):xl.
- PMID 13230034
Japanese Journal
- 殺鼠剤中ワルファリンの二次元超臨界流体クロマトグラフィーによる光学分割と円二色性検出 (超臨界流体クロマトグラフィー特集号)
- Jasco report [50](-), 31-33, 2008-12
- NAID 40016452849
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