Product Code Database
Example Keywords: games -stockings $99-170
barcode-scavenger
   » » Wiki: Cyanide
Tag Wiki 'Cyanide'.
Tag

In , cyanide () is an chemical compound that contains a . This group, known as the cyano group, consists of a atom to a atom.

Ionic cyanides contain the cyanide . This anion is extremely poisonous. Soluble cyanide salts such as (NaCN), potassium cyanide (KCN) and tetraethylammonium cyanide () are highly toxic.

cyanides contain the group, and are usually called if the group is linked by a to atom. For example, in , the cyanide group is bonded to . In tetracyanomethane , four cyano groups are bonded to carbon. Although nitriles generally do not release cyanide ions, the do and are thus toxic. The cyano group may be covalently bonded to atoms different than carbon, e.g., in , phosphorus tricyanide and trimethylsilyl cyanide .

, or , is a highly volatile toxic liquid that is produced on a large scale industrially. It is obtained by of cyanide salts.


Bonding
The cyanide ion is with and with molecular N≡N. A triple bond exists between C and N. The negative charge is concentrated on C.Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd Edn.), Oxford:Butterworth-Heinemann. .G. L. Miessler and D. A. Tarr "Inorganic Chemistry" 3rd Ed, Pearson/Prentice Hall publisher, .


Occurrence

In nature
Cyanides are produced by certain , , and . It is an in a number of plants. Cyanides are found in substantial amounts in certain seeds and fruit stones, e.g., those of , , , and . Chemical compounds that can release cyanide are known as cyanogenic compounds. In plants, cyanides are usually bound to molecules in the form of cyanogenic and defend the plant against . roots (also called manioc), an important -like food grown in tropical countries (and the base from which is made), also contain cyanogenic glycosides.

The bamboo Cathariostachys madagascariensis produces cyanide as a deterrent to grazing. In response, the golden bamboo lemur, which eats the bamboo, has developed a high tolerance to cyanide.

The enzymes contain cyanide attached to iron in their active sites. The biosynthesis of cyanide in the proceeds from carbamoyl phosphate, which converts to , the donor.


Interstellar medium
The CN has been identified in interstellar space. , , is used to measure the temperature of .


Pyrolysis and combustion product
Hydrogen cyanide is produced by the combustion or of certain materials under oxygen-deficient conditions. For example, it can be detected in the of internal combustion engines and smoke. Certain , especially those derived from , release hydrogen cyanide when heated or burnt.


Organic derivatives
In IUPAC nomenclature, that have a are called .IUPAC Gold Book nitrilesNCBI-MeSH Nitriles An example of a nitrile is , . Nitriles usually do not release cyanide ions. A functional group with a hydroxyl and cyanide bonded to the same carbon atom is called (). Unlike nitriles, cyanohydrins do release poisonous .


Reactions

Protonation
Cyanide is basic. The p Ka of hydrogen cyanide is 9.21. Thus, addition of stronger than hydrogen cyanide to solutions of cyanide salts releases .


Hydrolysis
Cyanide is unstable in water, but the reaction is slow until about 170 °C. It undergoes to give and , which are far less toxic than cyanide:
Cyanide hydrolase is an that this reaction.


Alkylation
Because of the cyanide anion's high , cyano groups are readily introduced into organic molecules by displacement of a group (e.g., the on ). In general, organic cyanides are called nitriles. In organic synthesis, cyanide is a C-1 ; i.e., it can be used to lengthen a carbon chain by one, while retaining the ability to be .


Redox
The cyanide ion is a and is by strong such as molecular (), (), and hydrogen peroxide (). These oxidizers are used to destroy cyanides in from . Https://engg.ksu.edu/HSRC/95Proceed/young.pdf< /ref>Botz Michael M. Overview of cyanide treatment methods. Elbow Creek Engineering, Inc. http://www.botz.com/MEMCyanideTreatment.pdf


Metal complexation
The cyanide anion reacts with transition metals to form . This reaction is the basis of cyanide's toxicity.Sharpe, A. G. The Chemistry of Cyano Complexes of the Transition Metals; Academic Press: London, 1976 The high affinities of metals for this can be attributed to its negative charge, compactness, and ability to engage in π-bonding.

Among the most important cyanide coordination compounds are the potassium ferrocyanide and the pigment , which are both essentially nontoxic due to the tight binding of the cyanides to a central iron atom.

(2025). 9780123526519, Academic Press.
Prussian blue was first accidentally made around 1706, by heating substances containing iron and carbon and nitrogen, and other cyanides made subsequently (and named after it). Among its many uses, Prussian blue gives the blue color to , bluing, and .


Manufacture
The principal process used to manufacture cyanides is the Andrussow process in which gaseous is produced from and in the presence of and a .

Sodium cyanide, the precursor to most cyanides, is produced by treating with :


Toxicity
Among the most toxic cyanides are (HCN), (NaCN), potassium cyanide (KCN), and (). The cyanide anion is an of the cytochrome c oxidase (also known as aa3), the fourth complex of the electron transport chain found in the inner membrane of the of cells. It attaches to the iron within this protein. The binding of cyanide to this enzyme prevents transport of electrons from to oxygen. As a result, the electron transport chain is disrupted, meaning that the cell can no longer aerobically produce ATP for energy.
(2025). 9781572591530, . .
Tissues that depend highly on aerobic respiration, such as the central nervous system and the , are particularly affected. This is an example of histotoxic hypoxia.
(2025). 9780781779067, Lippincott Williams & Wilkins.

Hydrogen cyanide, which is a gas, kills by inhalation. For this reason, working with hydrogen cyanide requires wearing an air respirator supplied by an external oxygen source. Hydrogen cyanide can be produced by adding acid to a solution containing a cyanide salt. Alkaline solutions of cyanide are safer to use because they do not evolve hydrogen cyanide gas. Oral ingestion of a small quantity of solid cyanide or a cyanide solution of as little as 200 mg, or exposure to airborne cyanide of 270 ppm, is sufficient to cause death within minutes.

Organic do not readily release cyanide ions, and so have low toxicities.


Disposal
Due to toxicity considerations, the disposal of cyanide is subject to stringent regulations. Industrial cyanide effluent is typically destroyed by oxidation using peroxysulfuric acid, hydrogen peroxide, /copper salts ("Inco process") or all three ("Combiox Process"). Use of sodium hypochlorite, traditional for laboratory-scale wastes, is impractical on a commercial scale. Hydrolysis at higher temperatures is highly effective, but requires specialized equipment. Lastly, cyanide wastes can be acidified for recovery of .
(2025). 9783527303854


Antidote
reacts with cyanide to form , which can be safely eliminated by the kidneys. This method has the advantage of avoiding the formation of methemoglobin (see below). This antidote kit is sold under the brand name Cyanokit and was approved by the U.S. FDA in 2006.

An older cyanide antidote kit included administration of three substances: pearls (administered by inhalation), , and sodium thiosulfate. The goal of the antidote was to generate a large pool of iron () to compete for cyanide with cytochrome a3 (so that cyanide will bind to the antidote rather than the enzyme). The to , which competes with cytochrome oxidase for the cyanide ion. Cyanmethemoglobin is formed and the cytochrome oxidase enzyme is restored. The major mechanism to remove the cyanide from the body is by enzymatic conversion to by the enzyme . Thiocyanate is a relatively non-toxic molecule and is excreted by the kidneys. To accelerate this detoxification, sodium thiosulfate is administered to provide a sulfur donor for , needed in order to produce thiocyanate.


Sensitivity
Minimum risk levels (MRLs) may not protect for delayed health effects or health effects acquired following repeated sublethal exposure, such as hypersensitivity, , or . MRLs may be revised after sufficient data accumulates.


Applications

Mining
Cyanide is mainly produced for the of and : It helps dissolve these metals allowing separation from the other solids. In the , finely ground high-grade ore is mixed with the cyanide (at a ratio of about 1:500 parts NaCN to ore); low-grade ores are stacked into heaps and sprayed with a cyanide solution (at a ratio of about 1:1000 parts NaCN to ore). The precious metals are complexed by the cyanide to form soluble derivatives, e.g., (dicyanoargentate(I)) and (dicyanoaurate(I)).
(2025). 9783527303854
Silver is less than gold and often occurs as the sulfide, in which case redox is not invoked (no is required). Instead, a displacement reaction occurs:
The "pregnant liquor" containing these ions is separated from the solids, which are discarded to a or spent heap, the recoverable gold having been removed. The metal is recovered from the "pregnant solution" by reduction with dust or by onto . This process can result in environmental and health problems. A number of environmental disasters have followed the overflow of tailing ponds at gold mines. Cyanide contamination of waterways has resulted in numerous cases of human and aquatic species mortality.

Aqueous cyanide is hydrolyzed rapidly, especially in sunlight. It can mobilize some heavy metals such as mercury if present. Gold can also be associated with arsenopyrite (FeAsS), which is similar to (fool's gold), wherein half of the sulfur atoms are replaced by . Gold-containing arsenopyrite ores are similarly reactive toward inorganic cyanide.


Industrial organic chemistry
The second major application of alkali metal cyanides (after mining) is in the production of CN-containing compounds, usually nitriles. are produced from acyl chlorides and cyanide. , cyanogen chloride, and the trimer cyanuric chloride are derived from alkali metal cyanides.


Medical uses
The cyanide compound sodium nitroprusside is used mainly in clinical chemistry to measure mainly as a follow-up to patients. On occasion, it is used in emergency medical situations to produce a rapid decrease in in humans; it is also used as a in vascular research. The cobalt in artificial vitamin B12 contains a cyanide ligand as an artifact of the purification process; this must be removed by the body before the vitamin molecule can be activated for biochemical use. During World War I, a copper cyanide compound was briefly used by physicians for the treatment of and .


Illegal fishing and poaching
Cyanides are illegally used to capture live fish near for the and seafood markets. The practice is controversial, dangerous, and damaging but is driven by the lucrative exotic fish market.Dzombak, David A; Ghosh, Rajat S; Wong-Chong, George M. Cyanide in Water and Soil. , 2006, Chapter 11.2: "Use of Cyanide for Capturing Live Reef Fish".

Poachers in Africa have been known to use cyanide to poison waterholes, to kill elephants for their ivory. Poachers kill 80 elephants with cyanide in Zimbabwe ABC News, 25 September 2013. Retrieved 30 October 2015.


Pest control
M44 cyanide devices are used in the United States to kill and other canids. Cyanide is also used for pest control in , particularly for possums, an introduced marsupial that threatens the conservation of native species and spreads amongst cattle. Possums can become bait shy but the use of pellets containing the cyanide reduces bait shyness. Cyanide has been known to kill native birds, including the endangered kiwi. Cyanide is also effective for controlling the , another introduced marsupial pest in New Zealand. A licence is required to store, handle and use cyanide in New Zealand.

Cyanides are used as for fumigating ships. Cyanide salts are used for killing ants, and have in some places been used as rat poison (the less toxic poison is more common).


Niche uses
Potassium ferrocyanide is used to achieve a blue color on cast during the final finishing stage of the sculpture. On its own, it will produce a very dark shade of blue and is often mixed with other chemicals to achieve the desired tint and hue. It is applied using a torch and paint brush while wearing the standard safety equipment used for any patina application: rubber gloves, safety glasses, and a respirator. The actual amount of cyanide in the mixture varies according to the recipes used by each foundry.

Cyanide is also used in -making and certain kinds of such as .

Although usually thought to be toxic, cyanide and cyanohydrins increase germination in various plant species.


Human poisoning
Deliberate cyanide poisoning of humans has occurred many times throughout history.
(2025). 9780160813207, Government Printing Off. .
, Extract p. 41
Common salts such as are involatile but water-soluble, so are poisonous by ingestion. is a gas, making it more indiscriminately dangerous, however it is lighter than air and rapidly disperses up into the atmosphere, which makes it ineffective as a .


Food additive
Because of the high stability of their complexation with , ferrocyanides (Sodium ferrocyanide E535, Potassium ferrocyanide E536, and Calcium ferrocyanide E538
(1997). 9781855734753, Woodhead Publishing. .
Extract of page 459
) do not decompose to lethal levels in the human body and are used in the food industry as, e.g., an in .
(2025). 9783527277667, Wiley-VCH. .


Chemical tests for cyanide
Cyanide is quantified by potentiometric titration, a method widely used in gold mining. It can also be determined by titration with silver ion. Some analyses begin with an air-purge of an acidified boiling solution, sweeping the vapors into a basic absorber solution. The cyanide salt absorbed in the basic solution is then analyzed.


Qualitative tests
Because of the notorious toxicity of cyanide, many methods have been investigated. Benzidine gives a blue coloration in the presence of . Iron(II) sulfate added to a solution of cyanide, such as the filtrate from the sodium fusion test, gives . A solution of para-benzoquinone in DMSO reacts with inorganic cyanide to form a cyano, which is . Illumination with a gives a green/blue glow if the test is positive.


External links

Safety data (French)

Page 1 of 1
1
Page 1 of 1
1

Account

Social:
Pages:  ..   .. 
Items:  .. 

Navigation

General: Atom Feed Atom Feed  .. 
Help:  ..   .. 
Category:  ..   .. 
Media:  ..   .. 
Posts:  ..   ..   .. 

Statistics

Page:  .. 
Summary:  .. 
1 Tags
10/10 Page Rank
5 Page Refs
2s Time