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Names | |||
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IUPAC name
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Other names
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Identifiers | |||
74-90-8 | |||
3D model (Jmol) | Interactive image | ||
3DMet | B00275 | ||
ChEBI | CHEBI:18407 | ||
ChemSpider | 748 | ||
ECHA InfoCard | 100.000.747 | ||
EC Number | 200-821-6 | ||
KEGG | C01326 | ||
MeSH | Hydrogen+Cyanide | ||
PubChem | 768 | ||
RTECS number | MW6825000 | ||
UNII | 2WTB3V159F | ||
UN number | 1051 | ||
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Properties | |||
HCN | |||
Appearance | Very pale, blue, transparent liquid or colorless gas | ||
Odor | Oil of bitter almond | ||
Density | 0.687 g mL−1 | ||
Melting point | −14 to −12 °C; 7 to 10 °F; 259 to 261 K | ||
Boiling point | 25.6 to 26.6 °C; 78.0 to 79.8 °F; 298.7 to 299.7 K | ||
Miscible | |||
Solubility in ethanol | Miscible | ||
Vapor pressure | 630 mmHg (20 °C) | ||
Henry's law
constant (kH) |
75 μmol Pa−1 kg−1 | ||
Acidity (pKa) | 9.21 | ||
Basicity (pKb) | 4.79 | ||
Refractive index (nD)
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1.2675 | ||
Viscosity | 201 μPa s | ||
Structure | |||
C∞v | |||
Linear | |||
2.98 D | |||
Thermochemistry | |||
71.00 kJ K−1 mol−1 (at 27 °C) | |||
Std molar
entropy (S |
113.01 J K−1 mol−1 | ||
Std enthalpy of
formation (ΔfH |
109.9 kJ mol−1 | ||
Std enthalpy of
combustion (ΔcH |
-426.5 kJ mol−1 | ||
Hazards | |||
GHS pictograms | |||
GHS signal word | DANGER | ||
H225, H319, H336 | |||
P210, P261, P305+351+338 | |||
EU classification (DSD)
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F+ T+ N | ||
R-phrases | R12, R26/27/28, R50/53 | ||
S-phrases | (S1/2), S16, S36/37, S38, S45, S53, S59, S61 | ||
NFPA 704 | |||
Flash point | −17.8 °C (0.0 °F; 255.3 K) | ||
538 °C (1,000 °F; 811 K) | |||
Explosive limits | 5.6% – 40.0% | ||
Lethal dose or concentration (LD, LC): | |||
LC50 (median concentration)
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501 ppm (rat, 5 min) 323 ppm (mouse, 5 min) 275 ppm (rat, 15 min) 170 ppm (rat, 30 min) 160 ppm (rat, 30 min) 323 ppm (rat, 5 min) |
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LCLo (lowest published)
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200 ppm (mammal, 5 min) 36 ppm (mammal, 2 hr) 107 ppm (human, 10 min) 759 ppm (rabbit, 1 min) 759 ppm (cat, 1 min) 357 ppm (human, 2 min) 179 ppm (human, 1 hr) |
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US health exposure limits (NIOSH): | |||
PEL (Permissible)
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TWA 10 ppm (11 mg/m3) [skin] | ||
REL (Recommended)
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ST 4.7 ppm (5 mg/m3) [skin] | ||
IDLH (Immediate danger)
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50 ppm | ||
Related compounds | |||
Related alkanenitriles
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|||
Infobox references | |||
Hydrogen cyanide (HCN), sometimes called prussic acid, is an organic compound with the chemical formula HCN. It is a colorless, extremely poisonous and flammable liquid that boils slightly above room temperature, at 25.6 °C (78.1 °F). HCN is produced on an industrial scale and is a highly valuable precursor to many chemical compounds ranging from polymers to pharmaceuticals.
Hydrogen cyanide is a linear molecule, with a triple bond between carbon and nitrogen. A minor tautomer of HCN is HNC, hydrogen isocyanide.
Hydrogen cyanide is weakly acidic with a pKa of 9.2. It partially ionizes in water solution to give the cyanide anion, CN−. A solution of hydrogen cyanide in water, represented as HCN, is called hydrocyanic acid. The salts of the cyanide anion are known as cyanides.
HCN has a faint bitter almond-like odor that some people are unable to detect owing to a recessive genetic trait. The volatile compound has been used as inhalation rodenticide and human poison, as well as for killing whales. Cyanide ions interfere with iron-containing respiratory enzymes.