| |
| |
| Names | |
|---|---|
| IUPAC name
Arsoric acid[1] | |
Other names
| |
| Identifiers | |
3D model (JSmol) |
|
| ChEBI | |
| ChEMBL | |
| ChemSpider |
|
| ECHA InfoCard | 100.029.001 
|
| EC Number |
|
| KEGG |
|
PubChem CID |
|
| RTECS number |
|
| UNII | |
| UN number | 1553, 1554 |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| H3AsO4 | |
| Molar mass | 141.942 g·mol−1 |
| Appearance | White translucent or colorless crystals, hygroscopic |
| Density | 2.5 g/cm3 |
| Melting point | 35.5 °C (95.9 °F; 308.6 K) |
| Boiling point | 120 °C (248 °F; 393 K) decomposes |
| 16.7 g/(100 mL) | |
| Solubility | soluble in ethanol |
| Vapor pressure | 55 hPa (50 °C) |
| Acidity (pKa) | pKa1 = 2.19 pKa2 = 6.94 pKa3 = 11.5[2] |
| Conjugate base | Arsenate |
| Structure | |
| Tetrahedralatarsenic atom | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
Extremely toxic, carcinogenic, corrosive |
| GHS labelling: | |
    
| |
| Danger | |
| H301, H312, H314, H331, H350, H361, H410 | |
| P201, P202, P260, P261, P264, P270, P271, P273, P280, P281, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P308+P313, P310, P311, P312, P321, P322, P330, P363, P391, P403+P233, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | Non-flammable |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
48 mg/kg (rat, oral)
6 mg/kg (rabbit, oral) |
| Related compounds | |
Other cations |
Sodium arsenate |
Related compounds |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Arsenic acidorarsoric acid is the chemical compound with the formula H3AsO4. More descriptively written as AsO(OH)3, this colorless acid is the arsenic analogue of phosphoric acid. Arsenate and phosphate salts behave very similarly. Arsenic acid as such has not been isolated, but is only found in solution, where it is largely ionized. Its hemihydrate form (2H3AsO4·H2O) does form stable crystals. Crystalline samples dehydrate with condensation at 100 °C.[3]
It is a tetrahedral species of idealized symmetry C3v with As–O bond lengths ranging from 1.66 to 1.71 Å.[4]
Being a triprotic acid, its acidity is described by three equilibria:
These pKa values are close to those for phosphoric acid. The highly basic arsenate ion (AsO3−
4) is the product of the third ionization. Unlike phosphoric acid, arsenic acid is an oxidizer, as illustrated by its ability to convert iodidetoiodine.
Arsenic acid is prepared by treating arsenic trioxide with concentrated nitric acid. Dinitrogen trioxide is produced as a by-product.[5]
The resulting solution is cooled to give colourless crystals of the hemihydrate H3AsO4·0.5H2O (or2H3AsO4·H2O), although the dihydrate H3AsO4·2H2O is produced when crystallisation occurs at lower temperatures.[5]
Arsenic acid is slowly formed when arsenic pentoxide is dissolved in water, and when meta- or pyroarsenic acid (H4As2O7) is treated with cold water. Arsenic acid can also be prepared directly from elemental arsenic by moistening it and treating with ozone.
Commercial applications of arsenic acid are limited by its toxicity. It is a precursor to a variety of pesticides. It has found occasional use as a wood preservative, a broad-spectrum biocide, a finishing agent for glass and metal, and a reagent in the synthesis of some dyestuffs and organic arsenic compounds.[6]
Arsenic acid is extremely toxic and carcinogenic, like all arsenic compounds. It is also corrosive. The LD50 in rabbits is 6 mg/kg (0.006 g/kg).[7]
| Authority control databases: National |
|
|---|
