| Dictionary: sodium cyanide |
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| Chemistry Dictionary: sodium cyanide |
A white or colourless crystalline solid, NaCN, deliquescent, soluble in water and in liquid ammonia, and slightly soluble in ethanol; cubic; m.p. 564°C; b.p. 1496°C. Sodium cyanide is now made by absorbing hydrogen cyanide in sodium hydroxide or sodium carbonate solution. The compound is extremely poisonous because it reacts with the iron in haemoglobin in the blood, so preventing oxygen reaching the tissues of the body. It is used in the extraction of precious metals and in electroplating industries. Aqueous solutions are alkaline due to salt hydrolysis.
| WordNet: sodium cyanide |
The noun has one meaning:
Meaning #1:
a white poisonous salt (NaCN) used in electroplating
| Wikipedia: Sodium cyanide |
| Sodium cyanide | |
|---|---|
| Identifiers | |
| CAS number | |
| PubChem | |
| UN number | 1689 |
| RTECS number | VZ7525000 |
| Properties | |
| Molecular formula | NaCN |
| Molar mass | 49.0072 g/mol |
| Appearance | white solid |
| Density | 1.595 g/cm3 |
| Melting point |
563.7 °C |
| Boiling point |
1496 °C |
| Solubility in water | 58 g/100 ml (20 °C) (hydrate solubility), 82 g/100 ml (34.7 °C) |
| Refractive index (nD) | 1.45 |
| Hazards | |
| MSDS | ICSC 1118 |
| EU Index | 006-007-00-5 |
| EU classification | Very toxic (T+) Dangerous for the environment (N) |
| R-phrases | R26/27/28, R32, R50/53 |
| S-phrases | (S1/2), S7, S28, S29, S45, S60, S61 |
| NFPA 704 | |
| Flash point | Non-flammable |
| LD50 | 5.8–15 mg/kg (oral in rats, mice)[1] |
| Related compounds | |
| Other cations | Potassium cyanide |
| Related compounds | Hydrogen cyanide |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Sodium cyanide is an inorganic compound with the formula NaCN. This highly toxic colourless salt is used mainly in gold mining but has other niche applications. It is an inorganic salt derived from neutralisation reactions involving the weak acid hydrogen cyanide.
Contents |
Sodium cyanide is produced by treating hydrogen cyanide with sodium hydroxide:[2]
Worldwide production was estimated at 500,000 tons in the year 2006. In former times, it was prepared by the Castner-Kellner process involving the reaction of sodium amide with carbon at elevated temperatures.
The structure of solid NaCN is related to that of sodium chloride.[3] The anions and cations are each six-coordinate (KCN has a similar structure). Each Na+ forms pi-bonds to two CN- groups as well as two "bent" K---CN and two "bent "K---NC links.[4]
Because the salt is derived from a weak acid, NaCN readily reverts back to HCN by hydrolysis: the moist solid emits small amounts of hydrogen cyanide, which smells like bitter almonds (not everyone can smell it—the ability thereof is due to a genetic trait[5]). Sodium cyanide reacts rapidly with strong acids to release hydrogen cyanide. This dangerous process represents a significant risk associated with cyanide salts. It is detoxified most efficiently with hydrogen peroxide:[2]
Sodium cyanide can be produced by treating formamide with sodium hydroxide. HCONH2 + NaOH → NaCN + 2H2O
Sodium cyanide is mainly used to extract gold and other precious metals in mining. This application exploits the high affinity of gold(I) for cyanide, which induces gold metal to oxidize and dissolve in the presence of air and water.
Few alternative methods exist for this extraction process.
Several commercially significant chemical compounds are derived from cyanide, including cyanuric chloride, cyanogen chloride, and many nitriles. In organic synthesis, cyanide, which is classified as a strong nucleophile, is used to prepare nitriles, which occur widely in many specialty chemicals, including pharmaceuticals.
Being highly toxic, sodium cyanide is used to kill or stun rapidly such as in illegal cyanide fishing and in collecting jars used by entomologists.
Cyanide salts are among the most rapidly acting of all known poisons. Cyanide is a potent inhibitor of respiration, acting on mitochondrial cytochrome oxidase and hence blocking electron transport. This results in decreased oxidative metabolism and oxygen utilization. Lactic acidosis then occurs as a consequence of anaerobic metabolism.
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![]() | Chemistry Dictionary. A Dictionary of Chemistry. Sixth Edition. Copyright © Market House Books Ltd, 2008. All rights reserved. Read more | |
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