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Sodium chloride
IUPC name Sodium chloride
Other names Common salt; halite; table salt
Molecular formula NaCl
Molar mass 58.44277 g/mol
Appearance White or colorless crystals or powder
Odor Odourless
Density 2.16 g/cm³, solid
Melting point

801 °C

Boiling point

1465 °C (1738 K)

Solubility in water 35.9 g/100 mL (25 °C)
Crystal structure Face centered cubic
Related compounds
Other anions NaF, NaBr, NaI
Other cations LiCl, KCl, RbCl,
CsCl, MgCl2, CaCl2
Related salts Sodium acetate
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)
Infobox references

Sodium chloride, also known as common salt, table salt, or halite, is a chemical compound with the formula NaCl. Sodium chloride is the salt most responsible for the salinity of the ocean and of the extracellular fluid of many multicellular organisms. As the major ingredient in edible salt, it is commonly used as a condiment and food preservative.

Production and use

Salt is currently mass-produced by evaporation of seawater or brine from other sources, such as brine wells and salt lakes, and by mining rock salt, called halite. In 2002, world production was estimated at 210 million metric tonnes, the top five producers being the United States (40.3 million tonnes), China (32.9), Germany (17.7), India (14.5), and Canada (12.3).[1]

As well as the familiar uses of salt in cooking, salt is used in many applications, from manufacturing pulp and paper, to setting dyes in textiles and fabric, to producing soaps, detergents, and other bath products.It is the major source of industrial chlorine and sodium hydroxide, and used in almost every industry.

In cold countries, large quantities of rock salt are used to help clear highways of ice during winter, although "Road Salt" loses its melting ability at temperatures below -15°C to -20°C (5°F to -4°F). Sodium chloride is sometimes used as a cheap and safe desiccant due to its hygroscopic properties, making salting an effective method of food preservation historically. Even though more effective desiccants are available, few are safe for humans to ingest.

]Synthetic uses

Sodium chloride is also the raw material used to produce chlorine which itself is required for the production of many modern materials including PVC and pesticides. Industrially, elemental chlorine is usually produced by the electrolysis of sodium chloride dissolved in water. Along with chlorine, this chloralkali process yields hydrogen gas and sodium hydroxide, according to the chemical equation

2NaCl + 2H2O → Cl2 + H2 + 2NaOH

Sodium metal is produced commercially through the electrolysis of liquid sodium chloride. This is now done in a Down's cell in which sodium chloride is mixed with calcium chloride to lower the melting point below 700 °C. As calcium is more electropositive than sodium, no calcium will be formed at the cathode. This method is less expensive than the previous method of electrolyzing sodium hydroxide.

Sodium chloride is used in other chemical processes for the large-scale production of compounds containing sodium or chlorine. In the Solvay process, sodium chloride is used for producing sodium carbonate and calcium chloride. In the Mannheim process and in the Hargreaves process, it is used for the production of sodium sulfate and hydrochloric acid.


Biological uses

Many microorganisms cannot live in an overly salty environment: water is drawn out of their cells by osmosis. For this reason salt is used to preserve some foods, such as smoked bacon or fish and can also be used to detach leeches that have attached themselves to feed. It has also been used to disinfect wounds.

Household uses

Since at least medieval times, people have used salt as a cleansing agent rubbed on household surfaces. It is also used in many brands of shampoo.

Biological functions

In humans, a high-salt intake has long been known to generally raise blood pressure, especially in certain individuals. More recently, it was demonstrated to attenuate nitric oxide production. Nitric oxide (NO) contributes to vessel homeostasis by inhibiting vascular smooth muscle contraction and growth, platelet aggregation, and leukocyte adhesion to the endothelium.[2][3]

Crystal structure

The crystal structure of sodium chloride. Each atom has six nearest neighbors, with octahedral geometry.Sodium chloride forms crystals with cubic symmetry. In these, the larger chloride ions, shown to the right as green spheres, are arranged in a cubic close-packing, while the smaller sodium ions, shown to the right as silver spheres, fill the octahedral gaps between them.Each ion is surrounded by six ions of the other kind. This same basic structure is found in many other minerals, and is known as the halite structure. This arrangement is known as cubic close packed (ccp). It can be represented as two interpenetrating face-centered cubic (fcc) lattices, or one fca lattic with a two atom basis. It is most commonly known as the rocksalt crystal structure.It is held together with an ionic bond and electrostatic forces.


Table salt sold for consumption today is not pure sodium chloride. In 1911 magnesium carbonate was first added to salt to make it flow more freely.[4] In 1924 trace amounts of iodine in form of sodium iodide, potassium iodide or potassium iodate were first added, to reduce the incidence of simple goiter.[5]

Salt for de-icing in the UK typically contains sodium hexacyanoferrate (II) at less than 100ppm as an anti-caking agent. In recent years this additive has also been used in table salt.

Common chemicals

Chemicals used in de-icing salts are mostly found to be sodium chloride (NaCl) or calcium chloride (CaCl2). Both are similar and are effective in de-icing roads. When these chemicals are produced, they are mined/made, crushed to fine granules, then treated with an anti-caking agent. Adding salt lowers the freezing point of the water, which allows the liquid to be stable at lower temperatures and allows the ice to melt. Alternative de-icing chemicals have also been used. Chemicals such as calcium magnesium acetate and potassium formate are being produced. These chemicals have few of the negative chemical effects on the environment commonly associated with NaCl and CaCl2.[6][7]



  1. Susan R. Feldman. Sodium chloride. Kirk-Othmer Encyclopedia of Chemical Technology. John Wiley & Sons, Inc. Published online 2005. doi:10.1002/0471238961.1915040902051820.a01.pub2
  2. [ Relationship between Salt Intake, Nitric Oxide and Asymmetric Dimethylarginine and Its Relevance to Patients with End-Stage]
  3. Dietary sodium and cardiovascular and renal disease risk factors: dark horse or phantom entry?
  4. "Morton Salt FAQ".
  5. Markel H (1987). ""When it rains it pours": endemic goiter, iodized salt, and David Murray Cowie, MD". American journal of public health 77 (2): 219-29. PMID 3541654. 
  6. Finnish Environment Institute (1/9/2007). "Migration of alternative de-icing chemicals in aquifers (MIDAS)". Press release.
  7. Finnish Environment Institute (2/10/2004). "Alternative de-icer found". Press release.






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