Names | |
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IUPAC name Calcium chloride | |
Other names
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Identifiers | |
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3D model (JSmol) |
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ChEBI | |
ChEMBL | |
ChemSpider | |
DrugBank | |
ECHA InfoCard | 100.030.115 |
EC Number |
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E number | E509 (acidity regulators, ...) |
PubChem CID | |
RTECS number |
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UNII |
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CompTox Dashboard (EPA) | |
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Properties | |
CaCl2 | |
Molar mass | 110.98 g·mol−1 |
Appearance | White hygroscopic powder |
Odor | Odorless |
Density |
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Melting point | 772–775 °C (1,422–1,427 °F; 1,045–1,048 K) anhydrous [2] 260 °C (500 °F; 533 K) monohydrate, decomposes 175 °C (347 °F; 448 K) dihydrate, decomposes 45.5 °C (113.9 °F; 318.6 K) tetrahydrate, decomposes [2] 30 °C (86 °F; 303 K) hexahydrate, decomposes [1] |
Boiling point | 1,935 °C (3,515 °F; 2,208 K) anhydrous [1] |
Anhydrous: 74.5 g/100 mL (20 °C) [3] Hexahydrate: 49.4 g/100 mL (−25 °C) 59.5 g/100 mL (0 °C) 65 g/100 mL (10 °C) 81.1 g/100 mL (25 °C) [1] 102.2 g/100 mL (30.2 °C) α-Tetrahydrate: 90.8 g/100 mL (20 °C) 114.4 g/100 mL (40 °C) Dihydrate: 134.5 g/100 mL (60 °C) 152.4 g/100 mL (100 °C) [4] | |
Solubility |
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Solubility in ethanol |
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Solubility in methanol |
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Solubility in acetone | 0.1 g/kg (20 °C) [5] |
Solubility in pyridine | 16.6 g/kg [5] |
Acidity (pKa) |
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−5.47·10−5 cm3/mol [1] | |
Refractive index (nD) | 1.52 |
Viscosity |
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Structure | |
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α = 90°, β = 90°, γ = 90° | |
Octahedral at Ca2+ centres (anhydrous) | |
Thermochemistry | |
Heat capacity (C) | |
Std molar entropy (S⦵298) | 108.4 J/(mol·K) [1] [2] |
Std enthalpy of formation (ΔfH⦵298) | |
Gibbs free energy (ΔfG⦵) | −748.81 kJ/mol [1] [2] |
Pharmacology | |
A12AA07 ( WHO ) B05XA07 ( WHO ), G04BA03 ( WHO ) | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards | Irritant |
GHS labelling: | |
[7] | |
Warning | |
H319 [7] | |
P305+P351+P338 [7] | |
NFPA 704 (fire diamond) | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) | 1,000-1,400 mg/kg (rats, oral) [9] |
Related compounds | |
Other anions | |
Other cations | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Calcium chloride is an inorganic compound, a salt with the chemical formula CaCl2. It is a white crystalline solid at room temperature, and it is highly soluble in water. It can be created by neutralising hydrochloric acid with calcium hydroxide.
Calcium chloride is commonly encountered as a hydrated solid with generic formula CaCl2·nH2O, where n = 0, 1, 2, 4, and 6. These compounds are mainly used for de-icing and dust control. Because the anhydrous salt is hygroscopic and deliquescent, it is used as a desiccant. [10]
Calcium chloride was apparently discovered in the 15th century but wasn't studied properly until the 18th century. [11] It was historically called "fixed sal ammoniac" (Latin : sal ammoniacum fixum [12] ) because it was synthesized during the distillation of ammonium chloride with lime and was nonvolatile (while the former appeared to sublime); in more modern times (18th-19th cc.) it was called "muriate of lime" (Latin : murias calcis, calcaria muriatica [12] ). [13]
By depressing the freezing point of water, calcium chloride is used to prevent ice formation and is used to de-ice. This application consumes the greatest amount of calcium chloride. Calcium chloride is relatively harmless to plants and soil. As a de-icing agent, it is much more effective at lower temperatures than sodium chloride. When distributed for this use, it usually takes the form of small, white spheres a few millimeters in diameter, called prills. Solutions of calcium chloride can prevent freezing at temperatures as low as −52 °C (−62 °F), making it ideal for filling agricultural implement tires as a liquid ballast, aiding traction in cold climates. [14]
It is also used in domestic and industrial chemical air dehumidifiers. [15]
The second largest application of calcium chloride exploits its hygroscopic nature and the tackiness of its hydrates; calcium chloride is highly hygroscopic and its hydration is an exothermic process. A concentrated solution keeps a liquid layer on the surface of dirt roads, which suppresses the formation of dust. It keeps the finer dust particles on the road, providing a cushioning layer. If these are allowed to blow away, the large aggregate begins to shift around and the road breaks down. Using calcium chloride reduces the need for grading by as much as 50% and the need for fill-in materials as much as 80%. [16]
In the food industry, calcium chloride is frequently employed as a firming agent in canned vegetables, particularly for canned tomatoes and cucumber pickles. [17] [18] [19] [20] It is also used in firming soybean curds into tofu and in producing a caviar substitute from vegetable or fruit juices. [21] [22] [23] It is also used to enhance the texture of various other products, such as whole apples, whole hot peppers, whole and sliced strawberries, diced tomatoes, and whole peaches. [24] [25]
The firming effect of calcium chloride can be attributed to several mechanisms: [24]
Calcium chloride's freezing-point depression properties are used to slow the freezing of the caramel in caramel-filled chocolate bars.[ citation needed ] Also, it is frequently added to sliced apples to maintain texture. [26]
In brewing beer, calcium chloride is sometimes used to correct mineral deficiencies in the brewing water. It affects flavor and chemical reactions during the brewing process, and can also affect yeast function during fermentation. [27] [28] [29] [30] [31]
In cheesemaking, calcium chloride is sometimes added to processed (pasteurized/homogenized) milk to restore the natural balance between calcium and protein in casein. It is added before the coagulant. [32]
Calcium chloride is also commonly used as an "electrolyte" in sports drinks and other beverages; as a food additive used in conjunction with other inorganic salts it adds taste to bottled water. [33] [34] [35]
The average intake of calcium chloride as food additives has been estimated to be 160–345 mg/day. [36] Calcium chloride is permitted as a food additive in the European Union for use as a sequestrant and firming agent with the E number E509. [37] It is considered as generally recognized as safe (GRAS) by the U.S. Food and Drug Administration. [38] Its use in organic crop production is generally prohibited under the US National Organic Program. [39]
The elemental calcium content in calcium chloride hexahydrate (CaCl2·6H2O) is approximately 27.2%. This means that for every gram of calcium chloride hexahydrate, there are about 272 milligrams of elemental calcium.
For anhydrous calcium chloride (CaCl2), the elemental calcium content is slightly higher, around 28.4% (for every gram of anhydrous calcium chloride there are about 284 milligrams of elemental calcium).
Calcium chloride has a very salty taste and can cause mouth and throat irritation at high concentrations, so it is typically not the first choice for long-term oral supplementation (as a calcium supplement). [40] [41] Calcium chloride, characterized by its low molecular weight and high water solubility, readily breaks down into calcium and chloride ions when exposed to water. These ions are efficiently absorbed from the intestine. [42] However, caution should be exercised when handling calcium chloride, for it has the potential to release heat energy upon dissolution in water. This release of heat can lead to trauma and burns in the mouth, throat, esophagus, and stomach. In fact, there have been reported cases of stomach necrosis resulting from burns caused by accidental ingestions of big amounts of undissolved calcium chloride. [43] [44]
The extremely salty taste of calcium chloride is used to flavor pickles without increasing the food's sodium content. [45]
Calcium chloride is used to prevent cork spot and bitter pit on apples by spraying on the tree during the late growing season. [46]
Drying tubes are frequently packed with calcium chloride. Kelp is dried with calcium chloride for use in producing sodium carbonate. Anhydrous calcium chloride has been approved by the FDA as a packaging aid to ensure dryness (CPG 7117.02). [47]
The hydrated salt can be dried for re-use but will dissolve in its own water of hydration if heated quickly and form a hard amalgamated solid when cooled.
Similarly, CaCl2 is used as a flux and electrolyte in the FFC Cambridge electrolysis process for titanium production, where it ensures the proper exchange of calcium and oxygen ions between the electrodes.
Calcium chloride infusions may be used as an intravenous therapy to prevent hypocalcemia. [48] [49] [50] [51] [52]
Calcium chloride is a highly soluble calcium salt. Hexahydrate calcium chloride (CaCl2·6H2O) has solubility in water of 811 g/L at 25 °C. [1] Calcium chloride when taken orally completely dissociates into calcium ions (Ca2+) in the gastrointestinal tract, resulting in readily bioavailable calcium. The high concentration of calcium ions facilitates efficient absorption in the small intestine. [42] [53] However, the use of calcium chloride as a source of calcium taken orally is less common compared to other calcium salts because of potential adverse effects such as gastrointestinal irritation and discomfort. [53] [54] [55]
When tasted, calcium chloride exhibits a distinctive bitter flavor alongside its salty taste. The bitterness is attributable to the calcium ions and their interaction with human taste receptors: certain members of the TAS2R family of bitter taste receptors respond to calcium ions; the bitter perception of calcium is thought to be a protective mechanism to avoid ingestion of toxic substances, as many poisonous compounds taste bitter. While chloride ions (Cl⁻) primarily contribute to saltiness, at higher concentrations, they can enhance the bitter sensation. The combination of calcium and chloride ions intensifies the overall bitterness. At lower concentrations, calcium chloride may taste predominantly salty. The salty taste arises from the electrolyte nature of the compound, similar to sodium chloride (table salt). As the concentration increases, the bitter taste becomes more pronounced: the increased presence of calcium ions enhances the activation of bitterness receptors. [56] [57] [58]
This section needs additional citations for verification .(May 2020) |
Calcium chloride is used in concrete mixes to accelerate the initial setting, but chloride ions lead to corrosion of steel rebar, so it should not be used in reinforced concrete. [59] The anhydrous form of calcium chloride may also be used for this purpose and can provide a measure of the moisture in concrete. [60]
Calcium chloride is included as an additive in plastics and in fire extinguishers, in blast furnaces as an additive to control scaffolding (clumping and adhesion of materials that prevent the furnace charge from descending), and in fabric softener as a thinner.[ citation needed ]
The exothermic dissolution of calcium chloride is used in self-heating cans and heating pads.[ citation needed ]
Calcium chloride is used as a water hardener in the maintenance of hot tub water, as insufficiently hard water can lead to corrosion and foaming.[ citation needed ]
In the oil industry, calcium chloride is used to increase the density of solids-free brines. It is also used to provide inhibition of swelling clays in the water phase of invert emulsion drilling fluids.[ citation needed ]
Calcium chloride (CaCl
2) acts as flux material, decreasing the melting point, in the Davy process for the industrial production of sodium metal through the electrolysis of molten NaCl.[ citation needed ]
Calcium chloride is also used in the production of activated charcoal.[ citation needed ]
Calcium chloride can be used to precipitate fluoride ions from water as insoluble CaF
2.[ citation needed ]
Calcium chloride is also an ingredient used in ceramic slipware. It suspends clay particles so that they float within the solution, making it easier to use in a variety of slipcasting techniques.[ citation needed ]
For watering plants to use as a fertilizer, a moderate concentration of calcium chloride is used to avoid potential toxicity: 5 to 10 mM (millimolar) is generally effective and safe for most plants—that is 0.55–1.11 grams (0.019–0.039 oz) of anhydrous calcium chloride (CaCl
2) per liter of water or 1.10–2.19 grams (0.039–0.077 oz) of calcium chloride hexahydrate (CaCl
2·6H
2O) per liter of water. [61] [62] Calcium chloride solution is used immediately after preparation to prevent potential alterations in its chemical composition. [63] [64] Besides that, calcium chloride is highly hygroscopic, meaning it readily absorbs moisture from the air. [65] If the solution is left standing, it can absorb additional water vapor, leading to dilution and a decrease in the intended concentration. [65] Prolonged standing may lead to the precipitation of calcium hydroxide or other insoluble calcium compounds, reducing the availability of calcium ions in the solution [66] and reducing the effectiveness of the solution as a calcium source for plants. [66] Nutrient solutions can become a medium for microbial growth if stored for extended periods. [67] Microbial contamination may alter the composition of the solution and potentially introduce pathogens to the plants. [67] When dissolved in water, calcium chloride can undergo hydrolysis, especially over time, which can lead to the formation of small amounts of hydrochloric acid and calcium hydroxide: Ca+
2+2H
2O ⇌ Ca(OH)
2+2H+
. This reaction can lower the pH of the solution, making it more acidic. [68] Acidic solutions may harm plant tissues and disrupt nutrient uptake. [69]
Calcium chloride dihydrate (20 percent by weight) dissolved in ethanol (95 percent ABV) has been used as a sterilant for male animals. The solution is injected into the testes of the animal. Within one month, necrosis of testicular tissue results in sterilization. [70] [71] [ non-primary sources needed ]
Cocaine producers in Colombia import tons of calcium chloride to recover solvents that are on the INCB Red List and are more tightly controlled. [72]
Although the salt is non-toxic in small quantities when wet, the strongly hygroscopic properties of non-hydrated calcium chloride present some hazards. It can act as an irritant by desiccating moist skin. Solid calcium chloride dissolves exothermically, and burns can result in the mouth and esophagus if it is ingested. Ingestion of concentrated solutions or solid products may cause gastrointestinal irritation or ulceration. [73]
Consumption of calcium chloride can lead to hypercalcemia. [74]
Calcium chloride dissolves in water, producing chloride and the aquo complex [Ca(H2O)6]2+. In this way, these solutions are sources of "free" calcium and free chloride ions. This description is illustrated by the fact that these solutions react with phosphate sources to give a solid precipitate of calcium phosphate:
Calcium chloride has a very high enthalpy change of solution, indicated by considerable temperature rise accompanying dissolution of the anhydrous salt in water. This property is the basis for its largest-scale application.
Aqueous solutions of calcium chloride tend to be slightly acidic due to the influence of the chloride ions on the hydrogen ion concentration in water. The slight acidity of calcium chloride solutions is primarily due to the increased ionic strength of the solution, which can influence the activity of hydrogen ions and lower the pH slightly. The pH of calcium chloride in aqueous solution is the following: [75] [76]
Concentration (mol/L) | Approximate pH |
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0.01 | 6.5 – 7.0 |
0.1 | 6.0 – 6.5 |
1.0 | 5.5 – 6.0 |
Molten calcium chloride can be electrolysed to give calcium metal and chlorine gas:
In much of the world, calcium chloride is derived from limestone as a by-product of the Solvay process, which follows the net reaction below: [10]
North American consumption in 2002 was 1,529,000 tonnes (3.37 billion pounds). [77] In the US, most calcium chloride is obtained by purification from brine. As with most bulk commodity salt products, trace amounts of other cations from the alkali metals and alkaline earth metals (groups 1 and 2) and other anions from the halogens (group 17) typically occur. [10]
Calcium chloride occurs as the rare evaporite minerals sinjarite (dihydrate) and antarcticite (hexahydrate). [78] [79] [80] Another natural hydrate known is ghiaraite – a tetrahydrate. [81] [80] The related minerals chlorocalcite (potassium calcium chloride, KCaCl3) and tachyhydrite (calcium magnesium chloride, Ca Mg 2 Cl 6·12H2O ) are also very rare. [82] [83] [80] The same is true for rorisite, CaClF (calcium chloride fluoride). [84] [80]
The term chloride refers to a compound or molecule that contains either a chlorine anion, which is a negatively charged chlorine atom, or a non-charged chlorine atom covalently bonded to the rest of the molecule by a single bond. Many inorganic chlorides are salts. Many organic compounds are chlorides. The pronunciation of the word "chloride" is.
Sodium carbonate is the inorganic compound with the formula Na2CO3 and its various hydrates. All forms are white, odourless, water-soluble salts that yield alkaline solutions in water. Historically, it was extracted from the ashes of plants grown in sodium-rich soils, and because the ashes of these sodium-rich plants were noticeably different from ashes of wood, sodium carbonate became known as "soda ash". It is produced in large quantities from sodium chloride and limestone by the Solvay process, as well as by carbonating sodium hydroxide which is made using the chloralkali process.
Potassium chloride is a metal halide salt composed of potassium and chlorine. It is odorless and has a white or colorless vitreous crystal appearance. The solid dissolves readily in water, and its solutions have a salt-like taste. Potassium chloride can be obtained from ancient dried lake deposits. KCl is used as a fertilizer, in medicine, in scientific applications, domestic water softeners, and in food processing, where it may be known as E number additive E508.
Sodium hypochlorite is an alkaline inorganic chemical compound with the formula NaOCl. It is commonly known in a dilute aqueous solution as bleach or chlorine bleach. It is the sodium salt of hypochlorous acid, consisting of sodium cations and hypochlorite anions.
Magnesium sulfate or magnesium sulphate is a chemical compound, a salt with the formula MgSO4, consisting of magnesium cations Mg2+ (20.19% by mass) and sulfate anions SO2−4. It is a white crystalline solid, soluble in water but not in ethanol.
Iron(III) chloride describes the inorganic compounds with the formula FeCl3(H2O)x. Also called ferric chloride, these compounds are some of the most important and commonplace compounds of iron. They are available both in anhydrous and in hydrated forms, which are both hygroscopic. They feature iron in its +3 oxidation state. The anhydrous derivative is a Lewis acid, while all forms are mild oxidizing agents. It is used as a water cleaner and as an etchant for metals.
Zinc sulfate describes a family of inorganic compounds with the formula ZnSO4(H2O)x. All are colorless solids. The most common form includes water of crystallization as the heptahydrate, with the formula ZnSO4·7H2O. As early as the 16th century it was prepared on the large scale, and was historically known as "white vitriol" (the name was used, for example, in 1620s by the collective writing under the pseudonym of Basil Valentine). Zinc sulfate and its hydrates are colourless solids.
Magnesium chloride is an inorganic compound with the formula MgCl2. It forms hydrates MgCl2·nH2O, where n can range from 1 to 12. These salts are colorless or white solids that are highly soluble in water. These compounds and their solutions, both of which occur in nature, have a variety of practical uses. Anhydrous magnesium chloride is the principal precursor to magnesium metal, which is produced on a large scale. Hydrated magnesium chloride is the form most readily available.
Zinc chloride is an inorganic chemical compound with the formula ZnCl2·nH2O, with n ranging from 0 to 4.5, forming hydrates. Zinc chloride, anhydrous and its hydrates, are colorless or white crystalline solids, and are highly soluble in water. Five hydrates of zinc chloride are known, as well as four forms of anhydrous zinc chloride.
Sodium sulfate (also known as sodium sulphate or sulfate of soda) is the inorganic compound with formula Na2SO4 as well as several related hydrates. All forms are white solids that are highly soluble in water. With an annual production of 6 million tonnes, the decahydrate is a major commodity chemical product. It is mainly used as a filler in the manufacture of powdered home laundry detergents and in the Kraft process of paper pulping for making highly alkaline sulfides.
In chemistry, hypochlorite, or chloroxide is an anion with the chemical formula ClO−. It combines with a number of cations to form hypochlorite salts. Common examples include sodium hypochlorite and calcium hypochlorite. The Cl-O distance in ClO− is 1.69 Å.
Barium chloride is an inorganic compound with the formula BaCl2. It is one of the most common water-soluble salts of barium. Like most other water-soluble barium salts, it is a white powder, highly toxic, and imparts a yellow-green coloration to a flame. It is also hygroscopic, converting to the dihydrate BaCl2·2H2O, which are colourless crystals with a bitter salty taste. It has limited use in the laboratory and industry.
Aluminium chloride, also known as aluminium trichloride, is an inorganic compound with the formula AlCl3. It forms a hexahydrate with the formula [Al(H2O)6]Cl3, containing six water molecules of hydration. Both the anhydrous form and the hexahydrate are colourless crystals, but samples are often contaminated with iron(III) chloride, giving them a yellow colour.
Manganese(II) chloride is the dichloride salt of manganese, MnCl2. This inorganic chemical exists in the anhydrous form, as well as the dihydrate (MnCl2·2H2O) and tetrahydrate (MnCl2·4H2O), with the tetrahydrate being the most common form. Like many Mn(II) species, these salts are pink, with the paleness of the color being characteristic of transition metal complexes with high spin d5 configurations.
Copper(II) chloride, also known as cupric chloride, is an inorganic compound with the chemical formula CuCl2. The monoclinic yellowish-brown anhydrous form slowly absorbs moisture to form the orthorhombic blue-green dihydrate CuCl2·2H2O, with two water molecules of hydration. It is industrially produced for use as a co-catalyst in the Wacker process.
Chromium(III) chloride (also called chromic chloride) is an inorganic chemical compound with the chemical formula CrCl3. It forms several hydrates with the formula CrCl3·nH2O, among which are hydrates where n can be 5 (chromium(III) chloride pentahydrate CrCl3·5H2O) or 6 (chromium(III) chloride hexahydrate CrCl3·6H2O). The anhydrous compound with the formula CrCl3 are violet crystals, while the most common form of the chromium(III) chloride are the dark green crystals of hexahydrate, CrCl3·6H2O. Chromium chlorides find use as catalysts and as precursors to dyes for wool.
Nickel(II) chloride (or just nickel chloride) is the chemical compound NiCl2. The anhydrous salt is yellow, but the more familiar hydrate NiCl2·6H2O is green. Nickel(II) chloride, in various forms, is the most important source of nickel for chemical synthesis. The nickel chlorides are deliquescent, absorbing moisture from the air to form a solution. Nickel salts have been shown to be carcinogenic to the lungs and nasal passages in cases of long-term inhalation exposure.
Calcium lactate is a white crystalline salt with formula C
6H
10CaO
6, consisting of two lactate anions H
3C(CHOH)CO−
2 for each calcium cation Ca2+
. It forms several hydrates, the most common being the pentahydrate C
6H
10CaO
6·5H
2O.
Calcium hypochlorite is an inorganic compound with chemical formula Ca(ClO)2, also written as Ca(OCl)2. It is a white solid, although commercial samples appear yellow. It strongly smells of chlorine, owing to its slow decomposition in moist air. This compound is relatively stable as a solid and solution and has greater available chlorine than sodium hypochlorite. "Pure" samples have 99.2% active chlorine. Given common industrial purity, an active chlorine content of 65-70% is typical. It is the main active ingredient of commercial products called bleaching powder, used for water treatment and as a bleaching agent.
Ytterbium(III) chloride (YbCl3) is an inorganic chemical compound. It reacts with NiCl2 to form a very effective catalyst for the reductive dehalogenation of aryl halides. It is poisonous if injected, and mildly toxic by ingestion. It is an experimental teratogen, known to irritate the skin and eyes.
Its toxicity upon ingestion, is indicated by the test on rats: oral LD50 (rat) is 1.0–1.4 g/kg (the lethal dose for half of the test animals, in this case rats...)
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