Calcium Pyrophosphate

Calcium pyrophosphate
Names
	IUPAC name Calcium diphosphate
	Other names Diphosphoric acid, calcium salt (1:2); Dicalcium diphosphate; Dicalcium pyrophosphate
Identifiers
CAS Number	7790-76-3 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:32598 ;
ChemSpider	23034 ;
MeSH	Calcium+pyrophosphate
PubChem CID	24632;
UNII	X69NU20D19 ;
	InChI InChI=1S/2Ca.H4O7P2/c;;1-8(2,3)7-9(4,5)6/h;;(H2,1,2,3)(H2,4,5,6)/q2+2;/p-4 Key: JUNWLZAGQLJVLR-UHFFFAOYSA-J ; InChI=1/2Ca.H4O7P2/c;;1-8(2,3)7-9(4,5)6/h;;(H2,1,2,3)(H2,4,5,6)/q2+2;/p-4 Key: JUNWLZAGQLJVLR-XBHQNQODAN;
	SMILES [Ca+2].[Ca+2].[O-]P([O-])(=O)OP([O-])([O-])=O;
Properties
Chemical formula	Ca2O7P2
Molar mass	254.053 g/mol
Appearance	White powder
Density	3.09 g/cm3
Melting point	1,353 °C (2,467 °F; 1,626 K)
Solubility in water	insoluble
Solubility	soluble in HCl, nitric acids
Refractive index (nD)	1.585
Hazards
NFPA 704 (fire diamond)	0 2 0
Flash point	Non-flammable
Related compounds
Other anions	Calcium phosphate
Other cations	Magnesium pyrophosphate; Sodium pyrophosphate
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Calcium pyrophosphate (Ca₂P₂O₇) is a chemical compound, an insoluble calcium salt containing the pyrophosphate anion. There are a number of forms reported: an anhydrous form, a dihydrate, Ca₂P₂O₇·2H₂O and a tetrahydrate, Ca₂P₂O₇·4H₂O. Deposition of dihydrate crystals in cartilage are responsible for the severe joint pain in cases of calcium pyrophosphate deposition disease (pseudo gout) whose symptoms are similar to those of gout.^[1] Ca₂P₂O₇ is commonly used as a mild abrasive agent in toothpastes,^{[citation needed]} because of its insolubility and nonreactivity toward fluoride.^[2]

Preparation

Crystals of the tetrahydrate can be prepared by reacting sodium pyrophosphate, Na₄P₂O₇ with calcium nitrate, Ca(NO₃)₂, at carefully controlled pH and temperature:^[3]

Na₄P₂O₇(aq)+2 Ca(NO₃)₂(aq)→ Ca₂P₂O₇·4 H₂O + 4 NaNO₃

The dihydrate, sometimes termed CPPD, can be formed by the reaction of pyrophosphoric acid with calcium chloride:^{[citation needed]}

CaCl₂ + H₄P₂O₇(aq) → Ca₂P₂O₇·2 H₂O + HCl.

The anhydrous forms can be prepared by heating dicalcium phosphate:^{[citation needed]}

2 CaHPO₄ → Ca₂P₂O₇ + H₂O

At 240-500 °C an amorphous phase is formed, heating to 750 °C forms β-Ca₂P₂O₇, heating to 1140 - 1350 °C forms the α-Ca₂P₂O₇.

Structure of anhydrous and hydrated forms

The stable tetrahydrate was originally reported to be rhombohedral but is now believed to be monoclinic. Additionally there is an unstable monoclinic form.^[3]

The dihydrate is triclinic, with hydrogen bonding between the two water molecules and hydrogen bonds to the O atoms on the anion.^{[citation needed]} An hexagonal dihydrate has also been reported.^[4]

The anhydrous form has 3 polymorphs, α-, β-, and metastable γ^[5] (T_α/β=1140ºС^[6]). The high temperature form α- is monoclinic (P2₁/n, a=12.66(1)Å, b=8.542(8)Å, c=5.315(5)Å, Z=4, ρ_α=2.95 g/cm³), with 8 coordinate calcium, the lower temperature form β- is tetragonal (P4₁, a=b=6.684Å, c=24.144Å, V=915.40Å³, Z=8, ρ_β=3.128 g/cm³), with calcium in four different coordination environments, 2 that are 7 coordinate, one eight and one 9. In both the pyrophosphates are essentially eclipsed.^[7]^[8]^[9]

References

↑ Calcium Pyrophosphate Deposition Disease at eMedicine
↑ Klaus Schrödter; Gerhard Bettermann; Thomas Staffel; Friedrich Wahl; Thomas Klein; Thomas Hofmann (2012). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_465.pub3.
↑ ^3.0 ^3.1 Christoffersen, Margaret R.; Balic-Zunic, Tonci; Pehrson, Søren; Christoffersen, Jørgen (2000). "Growth and precipitation of a monoclinic calcium pyrophosphate tetrahydrate indicating auto-inhibition at pH7". Journal of Crystal Growth 212 (3–4): 500–506. doi:10.1016/S0022-0248(00)00231-1. Bibcode: 2000JCrGr.212..500C.
↑ Mandel, Gretchen S.; Renne, Kathleen M.; Kolbach, Ann M.; Kaplan, Wayne D.; Miller, Jay D.; Mandel, Neil S. (1988). "Calcium pyrophosphate crystal deposition disease: Preparation and characterization of crystals". Journal of Crystal Growth 87 (4): 453–462. doi:10.1016/0022-0248(88)90093-0. Bibcode: 1988JCrGr..87..453M.
↑ Parodi, J. A.; Hickok, R. L.; Segelken, W. G.; Cooper, J. R. (1965). "Electronic Paramagnetic Resonance Study of the Thermal Decomposition of Dibasic Calcium Orthophosphate" (in en). Journal of the Electrochemical Society 112 (7): 688. doi:10.1149/1.2423665. Bibcode: 1965JElS..112..688P. https://iopscience.iop.org/article/10.1149/1.2423665.
↑ Hill, W L; Reynolds, D S; Hendbicks, S B; Jacob, K D (1945-02-01). "Nutritive Evaluation of Defluorinated Phosphates and Other Phosphorus Supplements. I. Preparation and Properties of the Samples". Journal of AOAC International 28 (1): 105–118. doi:10.1093/jaoac/28.1.105. ISSN 0095-9111. https://doi.org/10.1093/jaoac/28.1.105.
↑ Calvo, C. (1968-07-01). "Crystal structure of .alpha.-calcium pyrophosphate". Inorganic Chemistry 7 (7): 1345–1351. doi:10.1021/ic50065a019. ISSN 0020-1669. https://doi.org/10.1021/ic50065a019.
↑ Parodi, J. A.; Hickok, R. L.; Segelken, W. G.; Cooper, J. R. (1965). "Electronic Paramagnetic Resonance Study of the Thermal Decomposition of Dibasic Calcium Orthophosphate". Journal of the Electrochemical Society 112 (7): 688. doi:10.1149/1.2423665. Bibcode: 1965JElS..112..688P.
↑ Webb, N. C. (1966). "The crystal structure of β-Ca2P2O". Acta Crystallographica 21 (6): 942–948. doi:10.1107/S0365110X66004225.

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Original source: https://en.wikipedia.org/wiki/Calcium pyrophosphate. Read more

[emedicine1-1] Calcium Pyrophosphate Deposition Disease at eMedicine

[Ullmann-2] Klaus Schrödter; Gerhard Bettermann; Thomas Staffel; Friedrich Wahl; Thomas Klein; Thomas Hofmann (2012). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_465.pub3.

[Christofferson-3] 3.0 ^3.1 Christoffersen, Margaret R.; Balic-Zunic, Tonci; Pehrson, Søren; Christoffersen, Jørgen (2000). "Growth and precipitation of a monoclinic calcium pyrophosphate tetrahydrate indicating auto-inhibition at pH7". Journal of Crystal Growth 212 (3–4): 500–506. doi:10.1016/S0022-0248(00)00231-1. Bibcode: 2000JCrGr.212..500C.

[Mandel1983-4] Mandel, Gretchen S.; Renne, Kathleen M.; Kolbach, Ann M.; Kaplan, Wayne D.; Miller, Jay D.; Mandel, Neil S. (1988). "Calcium pyrophosphate crystal deposition disease: Preparation and characterization of crystals". Journal of Crystal Growth 87 (4): 453–462. doi:10.1016/0022-0248(88)90093-0. Bibcode: 1988JCrGr..87..453M.

[5] Parodi, J. A.; Hickok, R. L.; Segelken, W. G.; Cooper, J. R. (1965). "Electronic Paramagnetic Resonance Study of the Thermal Decomposition of Dibasic Calcium Orthophosphate" (in en). Journal of the Electrochemical Society 112 (7): 688. doi:10.1149/1.2423665. Bibcode: 1965JElS..112..688P. https://iopscience.iop.org/article/10.1149/1.2423665.

[6] Hill, W L; Reynolds, D S; Hendbicks, S B; Jacob, K D (1945-02-01). "Nutritive Evaluation of Defluorinated Phosphates and Other Phosphorus Supplements. I. Preparation and Properties of the Samples". Journal of AOAC International 28 (1): 105–118. doi:10.1093/jaoac/28.1.105. ISSN 0095-9111. https://doi.org/10.1093/jaoac/28.1.105.

[7] Calvo, C. (1968-07-01). "Crystal structure of .alpha.-calcium pyrophosphate". Inorganic Chemistry 7 (7): 1345–1351. doi:10.1021/ic50065a019. ISSN 0020-1669. https://doi.org/10.1021/ic50065a019.

[ParodiHickok1965-8] Parodi, J. A.; Hickok, R. L.; Segelken, W. G.; Cooper, J. R. (1965). "Electronic Paramagnetic Resonance Study of the Thermal Decomposition of Dibasic Calcium Orthophosphate". Journal of the Electrochemical Society 112 (7): 688. doi:10.1149/1.2423665. Bibcode: 1965JElS..112..688P.

[Webb1966-9] Webb, N. C. (1966). "The crystal structure of β-Ca2P2O". Acta Crystallographica 21 (6): 942–948. doi:10.1107/S0365110X66004225.