Hydrogen cyanide
Names | |
---|---|
IUPAC names
Formonitrile (substitutive)
Hydridonitridocarbon (additive) | |
Other names
Carbon hydride nitride
Formic anammonide Hydrocyanic acid Methanenitrile Prussic acid | |
Identifiers | |
Jmol-3D images | Image |
| |
Properties | |
HCN | |
Appearance | Colorless volatile liquid |
Density | 0.687 g/cm3 |
Melting point | 13.4 °C (56.1 °F; 286.5 K) |
Boiling point | 25.6 °C (78.1 °F; 298.8 K) |
Miscible | |
Solubility | Miscible with ethanol Slightly soluble in diethyl ether |
Vapor pressure | 630 mmHg (at 20 °C) |
Acidity (pKa) | 9.21 |
Thermochemistry | |
Std molar
entropy (S |
113.01 J·K−1·mol−1 |
Std enthalpy of
formation (ΔfH |
109.9 kJ·mol−1 |
Hazards | |
Safety data sheet | Matheson |
Flash point | −17.8 °C |
Related compounds | |
Related compounds
|
Acetonitrile |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Hydrogen cyanide, also known as prussic acid, is a chemical compound with the chemical formula HCN. It is a colorless, extremely poisonous and flammable liquid that boils just above room temperature, at 25.6 °C.
The exact classification of HCN as organic or inorganic remains unresolved. Going by the C-H bond definition, HCN would be organic, but in aqueous solution it dissociates into H+ and CN-, and since the cyanide ion is a pseudohalogen, this makes it inorganic. Hydrogen cyanide is considered a borderline compound.
Contents
Properties
Chemical
Hydrogen cyanide reacts with sodium hydroxide to yield sodium cyanide.
Physical
Hydrogen cyanide is a highly toxic colorless liquid with a bitter almond smell. It is miscible with water and ethanol, and slightly soluble in diethyl ether. HCN melts at -13.4 °C and boils at 25.6 °C. Its density is 0.687 g/cm3.
Availability
Anhydrous hydrogen cyanide is only available to large chemical entities and cannot be purchased by individuals or small companies.
HCN is is listed on schedule 3 of the Chemical Weapons Convention, meaning all transactions are monitored.
HCN absorbed by diatomaceous earth is somewhat easier to come by: it is sometimes sold as an industrial-strength pesticide. The most well known brand is Uragan D2 (Czech Republic). Another, very infamous brand under which this product was sold was Zyklon-B (the agent used to kill people in Nazi gas chambers).
Preparation
Due to its extreme toxicity, HCN production is generally avoided and instead sodium cyanide or other cyanide salts are used for reactions where a cyanide group is required. The procedures below should only performed if you have proper installations and experience.
Adding any strong acid to sodium cyanide will liberate hydrogen cyanide, which will rapidly evaporate due to its low boiling point.
Adding a dilute acid to Prussian blue and heating the flask will also yield hydrogen cyanide gas.
The thermal decomposition of amides, such as formamide will yield hydrogen cyanide gas.
The combustion of nitrile containing plastic materials will give off very impure hydrogen cyanide gas.
Projects
Seriously, if you really want to make experiments with cyanides, it's MUCH safer to use cyanide salts. Experimenting with hydrogen cyanide is not worth the risk.
Handling
Safety
Hydrogen cyanide is lethal. Air concentrations of 100–200 ppm in air will kill a human within 10-60 minutes, while 2000 ppm (about 2380 mg/m3) will kill a human in about 1 minute. Since it boils slightly above room temperature, open containers are a big no-no, and metal cylinders are instead employed, which severely limit its evaporation.
Contact of HCN with bases and amines may cause violent polymerization and even explosion.
Hydrogen cyanide will also attack certain plastic and rubber materials.
In case of poisoning, glucose, methylene blue or sodium thiosulfate can be used as antidotes.
Storage
DO NOT STORE HCN! EVER! If you absolutely want to, you can make your own Uragan D2 and store that.
Disposal
Hydrogen cyanide can be neutralized with a variety of chemicals, such as hydrogen peroxide, sodium hypochlorite (bleach), which will convert it to the less toxic isocyanate species. Sodium thiosulfate will convert it to thiocyanate, which is less toxic. These two products can be further oxidized to nitrogen, carbon dioxide and water with a strong oxidizer.
References
Relevant Sciencemadness threads
- Chemical pages without CAS Registry Number
- Articles without EBI source
- Chemical pages without ChemSpiderID
- Chemical pages without DrugBank identifier
- Articles without KEGG source
- Articles without InChI source
- Articles without UNII source
- Articles containing unverified chemical infoboxes
- Chembox articles without image
- Chemical compounds
- Inorganic compounds
- Organic compounds
- Hydrogen compounds
- Cyanides
- Acids
- Materials unstable in basic solution
- Things that can kill you very quickly
- Things that should NOT be messed with except by professionals
- Blood agents
- Schedule 3 chemicals