Hydrogen cyanide

Hydrogen cyanide
Names
IUPAC name
Formonitrile[2]
Systematic IUPAC name
Methanenitrile[2]
Other names
  • Formic anammonide
  • Hydridonitridocarbon[1]
  • Hydrocyanic acid (aqueous)
  • Prussic acid
  • Cyanane
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.000.747
EC Number
  • 200-821-6
KEGG
MeSH Hydrogen+Cyanide
RTECS number
  • MW6825000
UNII
UN number 1051
CompTox Dashboard (EPA)
  • InChI=1S/CHN/c1-2/h1H N
    Key: LELOWRISYMNNSU-UHFFFAOYSA-N N
SMILES
  • C#N
Properties
HCN
Molar mass 27.0253 g/mol
Appearance Colorless liquid or gas
Odor bitter almond-like[3]
Density 0.6876 g/cm3[4]
Melting point −13.29 °C (8.08 °F; 259.86 K)[4]
Boiling point 26 °C (79 °F; 299 K)[4]: 4.67 
Miscible
Solubility in ethanol Miscible
Vapor pressure 100 kPa (25 °C)[4]: 6.94 
75 μmol Pa−1 kg−1
Acidity (pKa) 9.21 (in water),

12.9 (in DMSO)[5]

Basicity (pKb) 4.79 (cyanide anion)
Conjugate acid Hydrocyanonium
Conjugate base Cyanide
1.2675[6]
Viscosity 0.183 mPa·s (25 °C)[4]: 6.231 
Structure
tetragonal (>170 K)
orthorhombic (<170 K)[7]
C∞v
Molecular shape
Linear
Dipole moment
2.98 D
Thermochemistry
35.9 J K−1 mol−1 (gas)[4]: 5.19 
Std molar
entropy (S298)
201.8 J K−1 mol−1
135.1 kJ mol−1
Hazards
GHS labelling:
Pictograms
Danger
Hazard statements
H225, H300+H310+H330, H319, H336, H370, H410
Precautionary statements
P210, P261, P305+P351+P338
NFPA 704 (fire diamond)
4
4
2
Flash point −17.8 °C (0.0 °F; 255.3 K)
Autoignition
temperature
538 °C (1,000 °F; 811 K)
Explosive limits 5.6% – 40.0%[8]
Lethal dose or concentration (LD, LC):
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)[9]
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)[9]
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 10 ppm (11 mg/m3) [skin][8]
REL (Recommended)
ST 4.7 ppm (5 mg/m3) [skin][8]
IDLH (Immediate danger)
50 ppm[8]
Related compounds
Related alkanenitriles
  • Hydrogen isocyanide
  • Isocyanic acid
  • Thiocyanic acid
  • Cyanogen iodide
  • Cyanogen bromide
  • Cyanogen chloride
  • Cyanogen fluoride
  • Acetonitrile
  • Aminoacetonitrile
  • Glycolonitrile
  • Cyanogen
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Hydrogen cyanide (formerly known as prussic acid) is a chemical compound with the formula HCN and structural formula H−C≡N. It is a highly toxic 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 valued precursor to many chemical compounds ranging from polymers to pharmaceuticals. Large-scale applications are for the production of potassium cyanide and adiponitrile, used in mining and plastics, respectively.[10] It is more toxic than solid cyanide compounds due to its volatile nature. A solution of hydrogen cyanide in water, represented as HCN(aq), is called hydrocyanic acid. The salts of the cyanide anion are known as cyanides.

Whether hydrogen cyanide is an organic compound or not is a topic of debate among chemists. It is traditionally considered inorganic, but can also be considered a nitrile,[11] giving rise to its alternative names of methanenitrile and formonitrile.[2]

  1. ^ "hydrogen cyanide (CHEBI:18407)". Chemical Entities of Biological Interest. UK: European Bioinformatics Institute. 18 October 2009. Main. Retrieved 2012-06-04.
  2. ^ a b c "Hydrogen Cyanide". PubChem. National Center for Biotechnology Information.
  3. ^ Simeonova, Fina Petrova; Fishbein, Lawrence (2004). Hydrogen cyanide and cyanides : human health aspects (Report). World Health Organization. ISBN 9241530618. ISSN 1020-6167.
  4. ^ a b c d e f Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). CRC Press. ISBN 978-1439855119.
  5. ^ Evans DA. "pKa's of Inorganic and Oxo-Acids" (PDF). Archived (PDF) from the original on 2022-10-09. Retrieved June 19, 2020.
  6. ^ Patnaik P (2002). Handbook of Inorganic Chemicals. McGraw-Hill. ISBN 978-0070494398.
  7. ^ Schulz, Axel; Surkau, Jonas (2022-09-21). "Main group cyanides: from hydrogen cyanide to cyanido-complexes". Reviews in Inorganic Chemistry. 43 (1). Walter de Gruyter GmbH: 49–188. doi:10.1515/revic-2021-0044. ISSN 0193-4929.
  8. ^ a b c d NIOSH Pocket Guide to Chemical Hazards. "#0333". National Institute for Occupational Safety and Health (NIOSH).
  9. ^ a b "Hydrogen cyanide". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  10. ^ Gail, E.; Gos, S.; Kulzer, R.; Lorösch, J.; Rubo, A.; Sauer, M. "Cyano Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_159.pub2. ISBN 978-3-527-30673-2.
  11. ^ "Human Metabolome Database: Showing metabocard for Hydrogen cyanide (HMDB0060292)".