Mercury(II) Oxide
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Mercury II Oxide
Mercury(II) oxide
Mercury(II) oxide
Mercury(II) oxide
IUPAC name
Mercury(II) oxide
Other names
3D model (JSmol)
ECHA InfoCard 100.040.580 Edit this at Wikidata
RTECS number
  • OW8750000
UN number 1641
Molar mass  g·mol-1
Appearance Yellow or red solid
Odor odorless
Density 11.14 g/cm3
Melting point 500 °C (932 °F; 773 K) (decomposes)
0.0053 g/100 mL (25 °C)
0.0395 g/100 mL (100 °C)
Solubility insoluble in alcohol, ether, acetone, ammonia
Band gap 2.2 eV[1]
−44.0·10-6 cm3/mol
2.5 (550 nm)[1]
70 J·mol-1·K-1[2]
-90 kJ·mol-1[2]
Main hazards Highly toxic
Safety data sheet ICSC 0981
GHS pictograms GHS06: Toxic GHS08: Health hazard GHS09: Environmental hazard
NFPA 704 (fire diamond)
Flammability code 0: Will not burn. E.g. waterHealth code 4: Very short exposure could cause death or major residual injury. E.g. VX gasReactivity code 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazards (white): no codeNFPA 704 four-colored diamond
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
18 mg/kg (oral, rat)[3]
Related compounds
Other anions
Mercury sulfide
Mercury selenide
Mercury telluride
Other cations
Zinc oxide
Cadmium oxide
Related compounds
Mercury(I) oxide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Mercury(II) oxide, also called mercuric oxide or simply mercury oxide, has a formula of HgO. It has a red or orange color. Mercury(II) oxide is a solid at room temperature and pressure. The mineral form montroydite is very rarely found.


In 1774, Joseph Priestley discovered that oxygen was released by heating mercuric oxide, although he did not identify the gas as oxygen (rather, Priestley called it "dephlogisticated air," as that was the paradigm that he was working under at the time).[4]


Montroydite structure (red atoms are oxygens)
Cinnabar structure

The red form of HgO can be made by heating Hg in oxygen at roughly 350 °C, or by pyrolysis of Hg(NO3)2.[5] The yellow form can be obtained by precipitation of aqueous Hg2+ with alkali.[5] The difference in color is due to particle size, both forms have the same structure consisting of near linear O-Hg-O units linked in zigzag chains with an Hg-O-Hg angle of 108°.[5]


Under atmospheric pressure mercuric oxide has two crystalline forms: one is called montroydite (orthorhombic, 2/m 2/m 2/m, Pnma), and the second is analogous to the sulfide mineral cinnabar (hexagonal, hP6, P3221); both are characterized by Hg-O chains.[6] At pressures above 10 GPa both structures convert to a tetragonal form.[1]


HgO is sometimes used in the production of mercury as it decomposes quite easily. When it decomposes, oxygen gas is generated.

It is also used as a material for cathodes for mercury batteries.[7]

Health issues

The label on an HgO powder bottle.

Mercury oxide is a highly toxic substance which can be absorbed into the body by inhalation of its aerosol, through the skin and by ingestion. The substance is irritating to the eyes, the skin and the respiratory tract and may have effects on the kidneys, resulting in kidney impairment. In the food chain important to humans, bioaccumulation takes place, specifically in aquatic organisms. The substance is banned as a pesticide in the EU.[8]

Evaporation at 20 °C is negligible. HgO decomposes on exposure to light or on heating above 500 °C. Heating produces highly toxic mercury fumes and oxygen, which increases the fire hazard. Mercury(II) oxide reacts violently with reducing agents, chlorine, hydrogen peroxide, magnesium (when heated), disulfur dichloride and hydrogen trisulfide. Shock-sensitive compounds are formed with metals and elements such as sulfur and phosphorus.[9]


  1. ^ a b c "Mercury oxide (HgO) crystal structure, physical properties". Semiconductors · II-VI and I-VII Compounds; Semimagnetic Compounds. Landolt-Börnstein - Group III Condensed Matter. Landolt-Börnstein - Group III Condensed Matter. 41B. Springer-Verlag. 1999. pp. 1-7. doi:10.1007/b71137. ISBN 978-3-540-64964-9.
  2. ^ a b Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A22. ISBN 978-0-618-94690-7.
  3. ^ Chambers, Michael. "ChemIDplus - 21908-53-2 - UKWHYYKOEPRTIC-UHFFFAOYSA-N - Mercuric oxide [ISO] - Similar structures search, synonyms, formulas, resource links, and other chemical information".
  4. ^ Almqvist, Ebbe (2003). History of Industrial Gases. Springer. p. 23. ISBN 978-0-306-47277-0.
  5. ^ a b c Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  6. ^ Aurivillius, Karin; Carlsson, Inga-Britt; Pedersen, Christian; Hartiala, K.; Veige, S.; Diczfalusy, E. (1958). "The Structure of Hexagonal Mercury(II)oxide". Acta Chemica Scandinavica. 12: 1297-1304. doi:10.3891/acta.chem.scand.12-1297. Retrieved 2010.
  7. ^ Moore, John W.; Conrad L. Stanitski; Peter C. Jurs (2005). Chemistry: The Molecular Science. Thomson Brooks/Cole. p. 941. ISBN 978-0-534-42201-1. Mercury(II) oxide anode mercury battery.
  8. ^ Chemicals Regulation Directorate. "Banned and Non-Authorised Pesticides in the United Kingdom". Retrieved 2009.
  9. ^ "Mercury (II) oxide". International Occupational Safety and Health Information Centre. Retrieved .

External links

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