Hydrogen Cyanide - Wikipedia

Highly toxic chemical with the formula HCN "Cyanane" redirects here. For a class of synthetic dyes, see Cyanine. "Cyanide gas" redirects here. For other gaseous cyanides, see Cyanogen chloride, Cyanogen fluoride, and Cyanogen. Hydrogen cyanide

Names
IUPAC name Formonitrile[2]
Systematic IUPAC name Methanenitrile[2]
Other names Formic anammonide Hydridonitridocarbon[1] Hydrocyanic acid (aqueous) Hydrogen cyanide (gas form) Prussic acid Cyanane
Identifiers
CAS Number	74-90-8 Y
3D model (JSmol)	Interactive image
3DMet	B00275
ChEBI	CHEBI:18407 N
ChemSpider	748 N
ECHA InfoCard	100.000.747
EC Number	200-821-6
KEGG	C01326 N
MeSH	Hydrogen+Cyanide
PubChem CID	768
RTECS number	MW6825000
UNII	2WTB3V159F Y
UN number	1051
CompTox Dashboard (EPA)	DTXSID9024148
InChI InChI=1S/CHN/c1-2/h1H NKey: LELOWRISYMNNSU-UHFFFAOYSA-N N
SMILES C#N
Properties
Chemical formula	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
Solubility in water	Miscible
Solubility in ethanol	Miscible
Vapor pressure	100 kPa (25 °C)[4]: 6.94
Henry's lawconstant (kH)	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
Refractive index (nD)	1.2675[6]
Viscosity	0.183 mPa·s (25 °C)[4]: 6.231
Structure
Crystal structure	tetragonal (>170 K)orthorhombic (<170 K)[7]
Point group	C∞v
Molecular shape	Linear
Dipole moment	2.98 D
Thermochemistry
Heat capacity (C)	35.9 J K−1 mol−1 (gas)[4]: 5.19
Std molarentropy (S⦵298)	201.8 J K−1 mol−1
Std enthalpy offormation (ΔfH⦵298)	135.1 kJ mol−1
Hazards
GHS labelling:
Pictograms
Signal word	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)
Autoignitiontemperature	538 °C (1,000 °F; 811 K)
Explosive limits	5.6% – 40.0%[8]
Lethal dose or concentration (LD, LC):
LC50 (median concentration)	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]
LCLo (lowest published)	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

Chemical compound

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, 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, and opinions vary from author to author. Traditionally, it is considered inorganic by a significant number of authors. Contrary to this view, it is considered organic by other authors, because hydrogen cyanide belongs to the class of organic compounds known as nitriles which have the formula R−C≡N, where R is typically organyl group (e.g., alkyl or aryl) or hydrogen.[11] In the case of hydrogen cyanide, the R group is hydrogen H, so the other names of hydrogen cyanide are methanenitrile and formonitrile.[2]

Structure and general properties

[edit]

Hydrogen cyanide is a linear molecule, with a triple bond between carbon and nitrogen. The tautomer of HCN is HNC, hydrogen isocyanide.[citation needed]

HCN has a faint bitter almond-like odor that some people are unable to detect owing to a recessive genetic trait.[12] The volatile compound has been used as inhalation rodenticide and human poison, as well as for killing whales.[13] Cyanide ions interfere with iron-containing respiratory enzymes.[citation needed]

Chemical properties

[edit]

Hydrogen cyanide is weakly acidic with a pKa of 9.2. It partially ionizes in water to give the cyanide anion, CN−. HCN forms hydrogen bonds with its conjugate base, species such as (CN−)(HCN)n.[14]

Hydrogen cyanide reacts with alkenes to give nitriles. The conversion, which is called hydrocyanation, employs nickel complexes as catalysts.[15]

RCH=CH2 + HCN → RCH2−CH2CN

Four molecules of HCN will tetramerize into diaminomaleonitrile.[16]

Metal cyanides are typically prepared by salt metathesis from alkali metal cyanide salts, but mercuric cyanide is formed from aqueous hydrogen cyanide:[17]

HgO + 2 HCN → Hg(CN)2 + H2O

History of discovery

[edit]

Hydrogen cyanide was first isolated in 1752 by French chemist Pierre Macquer who converted Prussian blue to an iron oxide plus a volatile component and found that these could be used to reconstitute it.[18] The new component was what is now known as hydrogen cyanide. It was subsequently prepared from Prussian blue by the Swedish chemist Carl Wilhelm Scheele in 1782,[19] and was eventually given the German name Blausäure (lit. "Blue acid") because of its acidic nature in water and its derivation from Prussian blue. In English, it became known popularly as prussic acid.

In 1787, the French chemist Claude Louis Berthollet showed that prussic acid did not contain oxygen,[20] an important contribution to acid theory, which had hitherto postulated that acids must contain oxygen[21] (hence the name of oxygen itself, which is derived from Greek elements that mean "acid-former" and are likewise calqued into German as Sauerstoff). In 1811, Joseph Louis Gay-Lussac prepared pure, liquified hydrogen cyanide.[22] In 1815, Gay-Lussac deduced Prussic acid's chemical formula.[23] The radical cyanide in hydrogen cyanide was given its name from cyan, not only an English word for a shade of blue but the Greek word for blue (Ancient Greek: κύανος), again owing to its derivation from Prussian blue.

Production and synthesis

[edit]

The most important process is the Andrussow oxidation invented by Leonid Andrussow at IG Farben in which methane and ammonia react in the presence of oxygen at about 1,200 °C (2,190 °F) over a platinum catalyst:[24]

2 CH4 + 2 NH3 + 3 O2 → 2 HCN + 6 H2O

In 2006, between 500 million and 1 billion pounds (between 230,000 and 450,000 t) were produced in the US.[25] Hydrogen cyanide is produced in large quantities by several processes and is a recovered waste product from the manufacture of acrylonitrile.[10]

Of lesser importance is the Degussa process (BMA process) in which no oxygen is added and the energy must be transferred indirectly through the reactor wall:[26]

CH4 + NH3 → HCN + 3H2

This reaction is akin to steam reforming, the reaction of methane and water to give carbon monoxide and hydrogen.

In the Shawinigan Process, hydrocarbons, e.g. propane, are reacted with ammonia.

In the laboratory, small amounts of HCN are produced by the addition of acids to cyanide salts of alkali metals:

H+ + CN− → HCN

This reaction is sometimes the basis of accidental poisonings because the acid converts a nonvolatile cyanide salt into the gaseous HCN.

Hydrogen cyanide could be obtained from potassium ferricyanide and acid:

6 H+ + [Fe(CN)6]−3 → 6 HCN + Fe+3[27][28]

Historical methods of production

[edit]

The large demand for cyanides for mining operations in the 1890s was met by George Thomas Beilby, who patented a method to produce hydrogen cyanide by passing ammonia over glowing coal in 1892. This method was used until Hamilton Castner in 1894 developed a synthesis starting from coal, ammonia, and sodium yielding sodium cyanide, which reacts with acid to form gaseous HCN.

Applications

[edit]

HCN is the precursor to sodium cyanide and potassium cyanide, which are used mainly in gold and silver mining and for the electroplating of those metals. Via the intermediacy of cyanohydrins, a variety of useful organic compounds are prepared from HCN including the monomer methyl methacrylate, from acetone, the amino acid methionine, via the Strecker synthesis, and the chelating agents EDTA and NTA. Via the hydrocyanation process, HCN is added to butadiene to give adiponitrile, a precursor to Nylon-6,6.[10]

HCN is used globally as a fumigant against many species of pest insects that infest food production facilities. Both its efficacy and method of application lead to very small amounts of the fumigant being used compared to other toxic substances used for the same purpose.[29] Using HCN as a fumigant also has less environmental impact, compared to some other fumigants such as sulfuryl fluoride,[30] and methyl bromide.[31]

Occurrence

[edit]

HCN is obtainable from fruits that have a pit, such as cherries, apricots, apples, and nuts such as bitter almonds, from which almond oil and extract is made. Many of these pits contain small amounts of cyanohydrins such as mandelonitrile and amygdalin, which slowly release hydrogen cyanide.[32][33] One hundred grams of crushed apple seeds can yield about 70 mg of HCN.[34] The roots of cassava plants contain cyanogenic glycosides such as linamarin, which decompose into HCN in yields of up to 370 mg per kilogram of fresh root.[35] Some millipedes, such as Harpaphe haydeniana, Desmoxytes purpurosea, and Apheloria release hydrogen cyanide as a defense mechanism,[36] as do certain insects, such as burnet moths and the larvae of Paropsisterna eucalyptus.[37] Hydrogen cyanide is contained in the exhaust of vehicles, and in smoke from burning nitrogen-containing plastics.

On Titan

[edit]

HCN has been measured in Titan's atmosphere by four instruments on the Cassini space probe, one instrument on Voyager, and one instrument on Earth.[38] One of these measurements was in situ, where the Cassini spacecraft dipped between 1,000 and 1,100 km (620 and 680 mi) above Titan's surface to collect atmospheric gas for mass spectrometry analysis.[39] HCN initially forms in Titan's atmosphere through the reaction of photochemically produced methane and nitrogen radicals which proceed through the H2CN intermediate, e.g., (CH3 + N → H2CN + H → HCN + H2).[40][41] Ultraviolet radiation breaks HCN up into CN + H; however, CN is efficiently recycled back into HCN via the reaction CN + CH4 → HCN + CH3.[40]

On the young Earth

[edit]

It has been postulated that carbon from a cascade of asteroids (known as the Late Heavy Bombardment), resulting from interaction of Jupiter and Saturn, blasted the surface of young Earth and reacted with nitrogen in Earth's atmosphere to form HCN.[42]

In mammals

[edit]

Some authors[who?] have shown that neurons can produce hydrogen cyanide upon activation of their opioid receptors by endogenous or exogenous opioids. They have also shown that neuronal production of HCN activates NMDA receptors and plays a role in signal transduction between neuronal cells (neurotransmission). Moreover, increased endogenous neuronal HCN production under opioids was seemingly needed for adequate opioid analgesia, as analgesic action of opioids was attenuated by HCN scavengers. They considered endogenous HCN to be a neuromodulator.[43]

It has also been shown that, while stimulating muscarinic cholinergic receptors in cultured pheochromocytoma cells increases HCN production, in a living organism (in vivo) muscarinic cholinergic stimulation actually decreases HCN production.[44]

Leukocytes generate HCN during phagocytosis, and can kill bacteria, fungi, and other pathogens by generating several different toxic chemicals, one of which is hydrogen cyanide.[43]

The vasodilatation caused by sodium nitroprusside has been shown to be mediated not only by NO generation, but also by endogenous cyanide generation, which adds not only toxicity, but also some additional antihypertensive efficacy compared to nitroglycerine and other non-cyanogenic nitrates which do not cause blood cyanide levels to rise.[45]

HCN is a constituent of tobacco smoke.[46]

HCN and the origin of life

[edit]

Hydrogen cyanide has been discussed as a precursor to amino acids and nucleic acids, and is proposed to have played a part in the origin of life.[47] Although the relationship of these chemical reactions to the origin of life theory remains speculative, studies in this area have led to discoveries of new pathways to organic compounds derived from the condensation of HCN (e.g. Adenine).[48]

In space

[edit] See also: Astrochemistry

HCN has been detected in the interstellar medium[49] and in the atmospheres of carbon stars.[50] Since then, extensive studies have probed formation and destruction pathways of HCN in various environments and examined its use as a tracer for a variety of astronomical species and processes. HCN can be observed from ground-based telescopes through a number of atmospheric windows.[51] The J=1→0, J=3→2, J= 4→3, and J=10→9 pure rotational transitions have all been observed.[49][52][53]

HCN is formed in interstellar clouds through one of two major pathways:[54] via a neutral-neutral reaction (CH2 + N → HCN + H) and via dissociative recombination (HCNH+ + e− → HCN + H). The dissociative recombination pathway is dominant by 30%; however, the HCNH+ must be in its linear form. Dissociative recombination with its structural isomer, H2NC+, exclusively produces hydrogen isocyanide (HNC).

HCN is destroyed in interstellar clouds through a number of mechanisms depending on the location in the cloud.[54] In photon-dominated regions (PDRs), photodissociation dominates, producing CN (HCN + ν → CN + H). At further depths, photodissociation by cosmic rays dominate, producing CN (HCN + cr → CN + H). In the dark core, two competing mechanisms destroy it, forming HCN+ and HCNH+ (HCN + H+ → HCN+ + H; HCN + HCO+ → HCNH+ + CO). The reaction with HCO+ dominates by a factor of ~3.5. HCN has been used to analyze a variety of species and processes in the interstellar medium. It has been suggested as a tracer for dense molecular gas[55][56] and as a tracer of stellar inflow in high-mass star-forming regions.[57] Further, the HNC/HCN ratio has been shown to be an excellent method for distinguishing between PDRs and X-ray-dominated regions (XDRs).[58]

On 11 August 2014, astronomers released studies, using the Atacama Large Millimeter/Submillimeter Array (ALMA) for the first time, that detailed the distribution of HCN, HNC, H2CO, and dust inside the comae of comets C/2012 F6 (Lemmon) and C/2012 S1 (ISON).[59][60]

In February 2016, it was announced that traces of hydrogen cyanide were found in the atmosphere of the hot Super-Earth 55 Cancri e with NASA's Hubble Space Telescope.[61]

On 14 December 2023, astronomers reported the first time discovery, in the plumes of Enceladus, moon of the planet Saturn, of hydrogen cyanide, a possible chemical essential for life[62] as we know it, as well as other organic molecules, some of which are yet to be better identified and understood. According to the researchers, "these [newly discovered] compounds could potentially support extant microbial communities or drive complex organic synthesis leading to the origin of life."[63][64]

As a poison and chemical weapon

[edit] Main article: Cyanide poisoning

In World War I, hydrogen cyanide was used by the French from 1916 as a chemical weapon against the Central Powers, and by the United States and Italy in 1918. It was not found to be effective enough due to weather conditions.[65][66] The gas is lighter than air and rapidly disperses up into the atmosphere. Rapid dilution made its use in the field impractical. In contrast, denser agents such as phosgene or chlorine tended to remain at ground level and sank into the trenches of the Western Front's battlefields. Compared to such agents, hydrogen cyanide had to be present in higher concentrations in order to be fatal.

A hydrogen cyanide concentration of 100–200 ppm in breathing air will kill a human within 10 to 60 minutes.[67] A hydrogen cyanide concentration of 2000 ppm (about 2380 mg/m3) will kill a human in about one minute.[67] The toxic effect is caused by the action of the cyanide ion, which halts cellular respiration. It acts as a non-competitive inhibitor for an enzyme in mitochondria called cytochrome c oxidase. As such, hydrogen cyanide is commonly listed among chemical weapons as a blood agent.[68]

The Chemical Weapons Convention lists it under Schedule 3 as a potential weapon which has large-scale industrial uses. Signatory countries must declare manufacturing plants that produce more than 30 metric tons per year, and allow inspection by the Organisation for the Prohibition of Chemical Weapons.

Perhaps its most infamous use is Zyklon B (German: Cyclone B, with the B standing for Blausäure – prussic acid; also, to distinguish it from an earlier product later known as Zyklon A),[69] used in Nazi German extermination camps during World War II to kill Jews and other persecuted minorities en masse as part of their Final Solution genocide program. Hydrogen cyanide was also used in the camps for delousing clothing in attempts to eradicate diseases carried by lice and other parasites. One of the original Czech producers continued making Zyklon B under the trademark "Uragan D2"[70] until around 2015.[71]

During World War II, the US considered using it, along with cyanogen chloride, as part of Operation Downfall, the planned invasion of Japan, but President Harry Truman decided against it, instead using the atomic bombs developed by the secret Manhattan Project.[72]

Hydrogen cyanide was also the agent employed in judicial execution in some U.S. states, where it was produced during the execution by the action of sulfuric acid on sodium cyanide or potassium cyanide.[73]

Under the name prussic acid, HCN has been used as a killing agent in whaling harpoons, although it proved quite dangerous to the crew deploying it, and it was quickly abandoned.[13] From the middle of the 18th century it was used in a number of poisoning murders and suicides.[74]

Hydrogen cyanide gas in air is explosive at concentrations above 5.6%.[75]

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External links

[edit]

• Institut national de recherche et de sécurité (1997). "Cyanure d'hydrogène et solutions aqueuses". Fiche toxicologique n° 4, Paris:INRS, 5pp. (PDF file, in French)
• International Chemical Safety Card 0492
• Hydrogen cyanide and cyanides (CICAD 61)
• National Pollutant Inventory: Cyanide compounds fact sheet
• NIOSH Pocket Guide to Chemical Hazards
• Department of health review
• Density of Hydrogen Cyanide gas

v t e Molecules detected in outer space
Molecules	Diatomic Aluminium monochloride Aluminium monofluoride Aluminium(II) oxide Argonium Carbon cation Carbon monophosphide Carbon monosulfide Carbon monoxide Cyano radical Diatomic carbon Fluoromethylidynium Helium hydride ion Hydrogen chloride Hydrogen fluoride Hydrogen (molecular) Hydroxyl radical Iron(II) oxide Magnesium monohydride Methylidyne radical Nitric oxide Nitrogen (molecular) Imidogen Sulfur mononitride Oxygen (molecular) Phosphorus monoxide Phosphorus mononitride Potassium chloride Silicon carbide Silicon monoxide Silicon monosulfide Sodium chloride Sodium iodide Sulfanyl Sulfur monoxide Titanium(II) oxide Triatomic Aluminium(I) hydroxide Aluminium isocyanide Amino radical Carbon dioxide Carbonyl sulfide CCP radical Chloronium Diazenylium Dicarbon monoxide Disilicon carbide Ethynyl radical Formyl radical Hydrogen cyanide (HCN) Hydrogen isocyanide (HNC) Hydrogen sulfide Hydroperoxyl Iron cyanide Isoformyl Magnesium cyanide Magnesium isocyanide Methylene N2H+ Nitrous oxide Nitroxyl Ozone Methylidynephosphane Potassium cyanide Trihydrogen cation Sodium cyanide Sodium hydroxide Silicon carbonitride c-Silicon dicarbide SiNC Sulfur dioxide Thioformyl Thioxoethenylidene Titanium dioxide Tricarbon Water Fouratoms Acetylene Ammonia Isocyanic acid Cyanoethynyl Formaldehyde Fulminic acid HCCN Hydrogen peroxide Hydromagnesium isocyanide Isocyanic acid Isothiocyanic acid Ketenyl Methylene amidogen Methyl cation Methyl radical Propynylidyne Protonated carbon dioxide Protonated hydrogen cyanide Silicon tricarbide Thioformaldehyde Tricarbon monoxide Tricarbon monosulfide Thiocyanic acid Fiveatoms Ammonium ion Butadiynyl Carbodiimide Cyanamide Cyanoacetylene Cyanoformaldehyde Cyanomethyl Cyclopropenylidene Formic acid Isocyanoacetylene Ketene Methane Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Sixatoms Acetonitrile Cyanobutadiynyl radical E-Cyanomethanimine Cyclopropenone Diacetylene Ethylene Formamide HC4N Ketenimine Methanethiol Methanol Methyl isocyanide Pentynylidyne Propynal Protonated cyanoacetylene Sevenatoms Acetaldehyde Acrylonitrile Vinyl cyanide Cyanodiacetylene Ethylene oxide Glycolonitrile Hexatriynyl radical Propyne Methylamine Methyl isocyanate Vinyl alcohol Eightatoms Acetic acid Aminoacetonitrile Cyanoallene Ethanimine Glycolaldehyde Hexapentaenylidene Methylcyanoacetylene Methyl formate Acrolein Nineatoms Acetamide Cyanohexatriyne Dimethyl ether Ethanol Methyldiacetylene Octatetraynyl radical Propene Ethanethiol Propionitrile N-Methylformamide Tenatomsor more Acetone Benzene Benzonitrile Buckminsterfullerene (C60, C60+, fullerene, buckyball) C70 fullerene Cyanodecapentayne Ethylene glycol Ethyl formate Methyl acetate Methyl-cyano-diacetylene Methyltriacetylene Propionaldehyde Butyronitrile Pyrimidine Heptatrienyl radical
Deuteratedmolecules	Ammonia Ammonium ion Formaldehyde Formyl radical Heavy water Hydrogen cyanide Hydrogen deuteride Hydrogen isocyanide Propyne N2D+ Trihydrogen cation
Unconfirmed	Anthracene Dihydroxyacetone Methoxyethane Glycine Graphene Hemolithin H2NCO+ Linear C5 Naphthalene cation Phosphine Pyrene Silylidyne
Related	Abiogenesis Astrobiology Astrochemistry Atomic and molecular astrophysics Chemical formula Circumstellar dust Circumstellar envelope Cosmic dust Cosmic ray Cosmochemistry Diffuse interstellar band Earliest known life forms Extraterrestrial life Extraterrestrial liquid water Forbidden mechanism Homochirality Intergalactic dust Interplanetary medium Interstellar medium Photodissociation region Iron–sulfur world theory Kerogen Molecules in stars Nexus for Exoplanet System Science Organic compound Outer space PAH world hypothesis Pseudo-panspermia Polycyclic aromatic hydrocarbon (PAH) RNA world hypothesis Spectroscopy Tholin
Category:Astrochemistry Outer space portal Astronomy portal Chemistry portal

v t e Agents used in chemical warfare incapacitation riot control
Blood agents	Cyanogen Cyanogen bromide Cyanogen chloride (CK) Hydrogen cyanide (AC) Arsine Cacodyl cyanide Cacodyl oxide Hydrogen sulfide Phosphine Carbon monoxide Phosphorus trifluoride Methyl cyanoformate Iron pentacarbonyl Nickel tetracarbonyl 2,3,7,8-Tetrachlorodibenzodioxin Glycolonitrile Lactonitrile Acetone cyanohydrin Stibine Chloral cyanohydrin
Blister agents	Arsenicals Ethyldichloroarsine (ED) Methyldichloroarsine (MD) Phenyldichloroarsine (PD) Lewisite (L) Lewisite 2 (L2) Lewisite 3 (L3) Sulfur mustards Levinstein mustard (EA-229) T Q CEES Nitrogen mustards HN1 HN2 HN3 TL-301 Nettle agents Phosgene oxime (CX) Other KB-16 Dibutylchloromethyltin chloride Selenium oxychloride
Nerve agents	G-agents Tabun (GA) Sarin (GB) Chlorosarin (ClGB) Thiosarin (SGB) Soman (GD) Chlorosoman (ClGD) Ethylsarin (GE) GH Cyclosarin (GF) GP Fluorotabun EA-1356 EA-4352 Crotylsarin V-agents EA-2192 EA-3148 VE VG VM VP VR VS VX EA-1763 Chinese VX V-sub x (GD-7) GV agents GV (EA-5365) Novichok agents A-208 A-232 A-234 A-242 A-262 C01-A035 C01-A039 C01-A042 Carbamates Dimethylcarbamoyl fluoride EA-3887 EA-3887A EA-3966 EA-3990 EA-4056 T-1123 T-1152 T-1194 Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide) TL-599 TL-1238 TL-1299 TL-1317 Miotine (AR-28/T-1843) 3152 CT 4-686-293-01 (Agent 1-10) Other Diisopropyl fluorophosphate Dicyclohexyl phosphorofluoridate EA-2012 EA-2054 EA-2098 EA-2613 2-Ethoxycarbonyl-1-methylvinyl cyclohexyl methylphosphonate Neopentylene fluorophosphate Selenophos Phospholine R-16661 Ro 3-0422 Methanesulfonyl fluoride Dimefox (TL-792) MSPI Precursors Acetonitrile AT ATO AlP A.P.C. complex Chlorosarin Chlorosoman Cyclohexanol 1,8-Dibromooctane N,N-Diisopropylaminoethanol (KB) EA-1250 DIHP ZS DEHP EA-1224 Dimethylamidophosphoric dichloride Dimethylamidophosphoric dicyanide DMHP Ethylphosphonoselenoic dichloride Formaldoxime Nital 4-Hydroxycoumarin Isopropyl alcohol (TB) Methyldichlorophosphine (SW) Methylphosphonyl difluoride (difluoro) (DF) Methylphosphonyl dichloride (dichloro) Nitromethane OPA mixture Phosphoryl chloride Phosphorus pentachloride Phosphorus trichloride (TH) Pinacolone Pinacolyl alcohol Phenacyl chloride QL 2,4,5-Trichlorophenol 3,3,5-Trimethylcyclohexanol Triethyl phosphite Trimethyl phosphite TC TG
Neurotoxins	Anatoxin-a Saxitoxin (TZ) Bungarotoxin Botulinum toxin (BTX) Tetanospasmin (TeNT) Ryanodine Ciguatoxin (CTX) Guanitoxin (GTX) Chlorophenylsilatrane Palytoxin (PTX) Maitotoxin (MTX) Tetrodotoxin Aconitine Brevetoxin (PbTX) Strychnine Antillatoxin (ATX) Tetraethyllead Dimethylmercury HN1 hydrochloride HN2 hydrochloride HN3 hydrochloride A-8564 Picrotoxin Sulfuryl fluoride Tremorine Oxotremorine Batrachotoxin Tetramethylenedisulfotetramine (TETS) Bicyclic phosphates IPTBO TBPO TBPS Cloflubicyne Trimethylolpropane phosphite Domoic acid
Pulmonary/choking agents	Chlorine Bromine Phosgene (CG) Fluorine Perfluoroisobutene Chloropicrin (PS) Dimethyl(trifluoromethylthio)arsine Diphosgene (DP) Disulfur decafluoride (Z) Acrolein Ethyl bromoacetate Perchloromethyl mercaptan Phenylcarbylamine chloride Tetranitromethane Tetrachlorodinitroethane Chlorine trifluoride Perchloryl fluoride Cadmium oxide Cadmium chloride Mercuric chloride Selenium dioxide Selenoyl fluoride Trifluoronitrosomethane Trichloronitrosomethane Nitric oxide Nitrogen dioxide Dinitrogen tetroxide Sulfur dioxide Phosphorus trichloride Methyl isocyanate Ethenone Methyl vinyl ketone Trifluoroacetyl chloride Salcomine Fluomine Uranium hexafluoride Diborane Green Cross
Vomiting agents	Adamsite (DM) Chloropicrin Litharge-glycerine Diphenylchlorarsine Diphenylcyanoarsine Cacodyl cyanide o-Dianisidine
Incapacitatingagents	BZ (CS-4030) Apomorphine Butyrophenone EA-4941 (CS-4640) Etorphine EA-2092 CS-4297 Etoxadrol Dimethylheptylpyran (DMHP) EA-2148 EA-3167 EA-3443 Pethidine EA-3580 Ibogaine EA-3834 Kolokol-1 LSD-25 PAVA spray Psilocybin Sleeping gas Carfentanil JB-318 JB-336 CS-27349 CAR-226,086 CAR-301,060 CAR-302,196 CAR-302,282 CAR-302,668 Benperidol Desflurane Enflurane Bufotenin Isoflurane Halothane Sevoflurane Pentazocine Procarbazine Fluphenazine Chlorpromazine
Lachrymatoryagents	Xylyl bromide Pepper spray (OC) Mace (spray) CN CS CR CNS Benzyl chloride Benzyl bromide Benzyl iodide Bromobenzyl cyanide Thiophosgene Chloroacetone Bromoacetone Bromomethyl ethyl ketone Acrolein Phenacyl bromide Chloroacetophenone oxime Ethyl bromoacetate Ethyl iodoacetate Iodoacetone Allyl isothiocyanate Hexamethylene diisocyanate Crotonaldehyde DRC-5593
Malodorant agents	Thioacetone Allicin Skatole Cadaverine Putrescine
Cornea-clouding agents	Lewisite CX KB-16 Methyl cyanoacrylate N-Methylmorpholine Allyl alcohol Osmium tetroxide Acrolein
Biological toxins	Abrin Aconitine Cyclopiazonic acid Histrionicotoxins Aflatoxins Anatoxin-a Batrachotoxin Botulinum toxin Brevetoxin Ciguatoxin Domoic acid Enterotoxin type B Grayanotoxin Guanitoxin Maitotoxin Modeccin Palytoxin Ricin Saxitoxin Shiga toxin T-2 mycotoxin Tetanospasmin Tetrodotoxin Volkensin Veratridine
Other	Methyl fluoroacetate Napalm (variants and mixtures) Fluoroethyl fluoroacetate Depleted uranium post-combustion uranium oxides Plutonium and its compounds Polonium White phosphorus
List of chemical warfare agents CB military symbol

v t e Salts and covalent derivatives of the cyanide ion

HCN He LiCN Be(CN)2 B(CN)3 C(CN)4C2(CN)2 NH4CNONCNO2NCNN3CN OCN−-NCOO(CN)2 FCN Ne NaCN Mg(CN)2 Al(CN)3 Si(CN)4(CH3)3SiCN P(CN)3 SCN−-NCS(SCN)2S(CN)2 ClCN Ar KCN Ca(CN)2 Sc(CN)3 Ti V Cr(CN)63− Mn Fe(CN)2Fe(CN)64−Fe(CN)63− Co(CN)2Co(CN)3−5 Ni(CN)2Ni(CN)42−Ni(CN)44− CuCN Zn(CN)2 Ga(CN)3 Ge(CN)2Ge(CN)4 As(CN)3(CH3)2AsCN(C6H5)2AsCN SeCN−(SeCN)2Se(CN)2 BrCN Kr RbCN Sr(CN)2 Y(CN)3 Zr Nb Mo(CN)84− Tc Ru Rh Pd(CN)2 AgCN Cd(CN)2 In(CN)3 Sn(CN)2 Sb(CN)3 Te(CN)2Te(CN)4 ICN Xe CsCN Ba(CN)2 * Lu(CN)3 Hf Ta W(CN)84− Re Os Ir Pt(CN)42-Pt(CN)64- AuCNAu(CN)2- Hg2(CN)2Hg(CN)2 TlCN Pb(CN)2 Bi(CN)3 Po At Rn Fr Ra ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og   * La(CN)3 Ce(CN)3 Ce(CN)4 Pr(CN)3 Nd Pm Sm(CN)3 Eu(CN)3 Gd(CN)3 Tb Dy(CN)3 Ho(CN)3 Er Tm Yb(CN)3 ** Ac(CN)3 Th(CN)4 Pa UO2(CN)2 Np Pu Am Cm Bk Cf Es Fm Md No

v t e Nitrogen species
Hydrides	NH3 NH+4 NH−2 N3− NH2OH N2H4 HN3 N−3 NH5 (?)
Organic	NR3 >C=NR −CONR2 −CN HCN CN− (CN)2 H2NCN HOCN HNCO HNCS CH2N2 −NO −NO2
Oxides	NO / (NO)2 N2O3 HNO2 / NO−2 / NO+ NO2 / (NO2)2 N2O5 HNO3 / NO−3 / NO+2 NO3 HNO / (HON)2 / N2O−2 / N2O H2NNO2 HO2NO / ONOO− HO2NO2 / O2NOO− NO−4 H4N2O4 / N2O2−3
Halides	NF NF2 NF3 NF5 (?) NCl3 NBr3 NI3 FN3 ClN3 BrN3 IN3 NH2F N2F2 NH2Cl NHF2 NHCl2 NHBr2 NHI2
Oxidation states	−3, −2, −1, 0, +1, +2, +3, +4, +5 (a strongly acidic oxide)

v t e Hydrogen compounds

H3AsO3 H3AsO4 HArF HAt HSO3F H[BF4] HBr HBrO HBrO2 HBrO3 HBrO4 HCl HClO HClO2 HClO3 HClO4 HCN HCNO H2CrO4/H2Cr2O7 H2CO3 H2CS3 HF HFO HI HIO HIO2 HIO3 HIO4 HMnO4 H2MnO4 H2MoO4 HNC NaHCO3 HNCO HNO HNO2 HNO3 H2N2O2 HNO5S H3NSO3 H2O H2O2 H2O3 H2O4 H2O5 H3PO2 H3PO3 H3PO4 H4P2O7 H5P3O10 H2[PtCl6] H2S H2S2 H2Se H2SeO3 H2SeO4 H4SiO4 H2[SiF6] HSCN HNCS H2SO3 H2SO4 H2SO5 H2S2O3 H3O H2S2O6 H2S2O7 H2S2O8 CF3SO3H H2Te H2TeO3 H6TeO6 H4TiO4 H2Po H[Co(CO)4]

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