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Tricalcium phosphate

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Title: Tricalcium phosphate  
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Subject: Dicalcium phosphate, Bone char, Tetracalcium phosphate, Monocalcium phosphate, Calcium
Collection: Calcium Compounds, Phosphates
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Tricalcium phosphate

Tricalcium phosphate
IUPAC name
Tricalcium bis(phosphate)
Other names
Tribasic calcium phosphate
ATC code A12
ChemSpider  Y
Jmol-3D images Image
Molar mass 310.17 g·mol−1
Appearance White amorphous powder
Density 3.14 g/cm3
Melting point Liquifies under high pressure at 1670 K (1391 °C)
0.002 g/100 g
-4126 kcal/mol (α-form)[1]
NFPA 704
Flash point Non-flammable
Related compounds
Other anions
Calcium pyrophosphate
Other cations
Trimagnesium phosphate
Trisodium phosphate
Tripotassium phosphate
Related compounds
Monocalcium phosphate
Dicalcium phosphate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 Y  (: Y/N?)

Tricalcium phosphate (sometimes abbreviated TCP) is a

  1. ^ Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A21.  
  2. ^ Yacoubou, Jeanne, MS. Vegetarian Journal's Guide To Food Ingredients "Guide to Food Ingredients". The Vegetarian Resource Group, n.d. Web. 14 Sept. 2012.
  3. ^ a b Destainville, A., Champion, E., Bernache-Assollant, D., Laborde, E. (2003). "Synthesis, characterization and thermal behavior of apatitic tricalcium phosphate". Materials Chemistry and Physics 80 (1): 269–277.    – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  4. ^ a b c d Rey, C.; Combes, C.; Drouet, C.; Grossin, D. (2011). "1.111 - Bioactive Ceramics: Physical Chemistry". In Ducheyne, Paul. Comprehensive Biomaterials 1. Elsevier. pp. 187–281.    – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  5. ^ Dorozhkin, Sergey V. (December 2012). "Amorphous calcium (ortho)phosphates". Acta Biomaterialia 6 (12): 4457–4475.    – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  6. ^ a b Carrodeguas, R.G.; De Aza, S. (2011). "α-Tricalcium phosphate: Synthesis, properties and biomedical applications". Acta Biomaterialia 7 (10): 3536–3546.    – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  7. ^ Daculsi, G.; Legeros, R. (2008). "17 - Tricalcium phosphate/hydroxyapatite biphasic ceramics". In Kokubo, Tadashi. Bioceramics and their Clinical Applications. Woodhead Publishing. pp. 395–423.    – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  8. ^ Salinas, Antonio J.; Vallet-Regi, Maria (2013). "Bioactive ceramics: from bone grafts to tissue engineering". RSC Advances ( 
  9. ^ Elliott, J.C. (1994). "3 - Hydroxyapatite and Nonstoichiometric Apatites". Studies in Inorganic Chemistry 18. Elsevier. pp. 111–189.    – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  10. ^ Vallet-Regí, M.;Rodríguez-Lorenzo, L.M. (November 1997). "Synthesis and characterisation of calcium deficient apatite". Solid State Ionics. 101–103, Part 2: 1279–1285.    – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  11. ^ Ober, JA, Phosphate Rock: U.S. Geological Survey Mineral Information (PDF) 
  12. ^ Bonjour JP, Carrie AL, Ferrari S, Clavien H, Slosman D, Theintz G, Rizzoli R (March 1997). "Calcium-enriched foods and bone mass growth in prepubertal girls: a randomized, double-blind, placebo-controlled trial".  
  13. ^ Straub DA (June 2007). "Calcium supplementation in clinical practice: a review of forms, doses, and indications".  
  14. ^ Paderni S, Terzi S, Amendola L (September 2009). "Major bone defect treatment with an osteoconductive bone substitute".  
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  16. ^ Lange TA, Zerwekh JE, Peek RD, Mooney V, Harrison BH (1986). "Granular tricalcium phosphate in large cancellous defects".  
  17. ^ Cao H, Kuboyama N (September 2009). "A biodegradable porous composite scaffold of PGA/beta-TCP for bone tissue engineering".  
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Calcium triphosphate is used to remove fluoride from water in water filtration systems.[21]

Another practical application of the compound is its use in gene transfection. The calcium ions can make a cell competent to allow exogenous genes to enter the cell by diffusion. A heat shock afterwards then invokes the cell to repair itself. This is a quick and easy method for transfection, albeit a rather inefficient one.

Porous beta-Tricalcium phosphate scaffolds are employed as drug carrier systems for local drug delivery in bone.[20]

It can be used as a tissue replacement for repairing bony defects when autogenous bone graft is not feasible or possible.[14][15][16] It may be used alone or in combination with a biodegradable, resorbable polymer such as polyglycolic acid.[17] It may also be combined with autologous materials for a bone graft.[18][19]

It is commonly used in porcelain and dental powders, and medically as an antacid or calcium supplement, although calcium carbonate is more common in this regard.

It is also used as a nutritional supplement[12] and occurs naturally in cow milk , although the most common and economical forms for supplementation are calcium carbonate (which should be taken with food) and calcium citrate (which can be taken without food).[13] There is some debate about the different bioavailabilities of the different calcium salts.

Calcium phosphate is also a raising agent (food additive) E341. As a mineral salt found in rocks and bones, it is used in cheese products.

Calcium phosphate is an important raw material for the production of phosphoric acid and fertilizers, for example in the Odda process. Phosphate ore quality and quantity is often specified as percent BPL (bone phosphate of lime), where 1% BPL is equivalent to 0.458% P2O5.[11]

Tricalcium phosphate is used in powdered spices as an anticaking agent. It is also found in baby powder.


β-TCP can contain impurities, for example calcium pyrophosphate, CaP2O7 and apatite. β-TCP is bioresorbable. The biodegradation of BCP involves faster dissolution of the β-TCP phase followed by elimination of HA crystals. β-TCP does not dissolve in body fluids at physiological pH levels, dissolution requires cell activity producing acidic pH.[4]

Ca10-δ(PO4)6-δ(HPO4)δ(OH)2-δ → (1-δ)Ca10(PO4)6(OH)2 + 3δCa3(PO4)2

Biphasic tricalcium phosphate, BCP, was originally reported as tricalcium phosphate but X-Ray diffraction techniques showed that the material was an intimate mixture of two phases, hydroxyapatite, HA, and β-tricalcium phosphate.[7] It is a ceramic.[8] Preparation involves the sintering causing the irreversible decomposition of calcium deficient apatites[4] alternatively termed non-stoichiometric apatites or basic calcium phosphate,[9] an example is:[10]

Biphasic tricalcium phosphate, BCP

  • as a rock in Morocco, Israel, Philippines, Egypt, and Kola (Russia) and in smaller quantities in some other countries. The natural form is not completely pure, and there are some other components like sand and lime which can change the composition. In terms of P2O5, most calcium phosphate rocks have a content of 30% to 40% P2O5 in weight.
  • in the skeletons and teeth of vertebrate animals
  • in milk.

Tricalcium phosphate occurs naturally in several forms, including:

Natural occurrence

There are differences in chemical and biological properties between the beta and alpha forms, the alpha form is more soluble and biodegradeable. Both forms are available commercially and are present in formulations used in medical and dental applications.[6]

Tricalcium phosphate has three recognised polymorphs, the rhombohedral β- form, and two high temperature forms, monoclinic α- and hexagonal α'-. β-tricalcium phosphate has a crystallographic density of 3.066 g cm−3 while the high temperature forms are less dense, α-tricalcium phosphate has a density of 2.866 g cm−3 and α'-tricalcium phosphate has a density of 2.702 g cm−3 They all have complex structures and have been described as containing "columns" of cations and anions. The β-form has two types of columns, each containing calcium and phosphate ions. The high temperature forms each have two types of columns, one containing only calcium ions and the other both calcium and phosphate.[6]

Crystal structure of β-, α- and α'- Ca3(PO4)2 polymorphs

CaCO3 + Ca2P2O7 → Ca3(PO4)2 + CO2

An alternative to a wet procedure is to heat a dry mixture of a calcium phosphate and calcium carbonate which has an overall Ca/P ratio of 3:2, for example:[4]

It is generally believed that tricalcium phosphate cannot be precipitated directly from aqueous solution. Typically a double decomposition reaction involving a soluble phosphate and calcium salts (e.g. (NH4)2HPO4 + Ca(NO3)2)[3] is performed under carefully controlled pH conditions. The precipitate will either be "amorphous tricalcium phosphate", ATCP, or calcium deficient hydroxypatite, CDHA, Ca9(HPO4)(PO4)5(OH), (note CDHA is sometimes termed apatitic calcium triphosphate).[3][4][5] Crystalline tricalcium phosphate can be obtained by calcining the precipitate. β-Ca3(PO4)2 is generally formed, higher temperatures are required to produce α-Ca3(PO4)2.

Preparation of pure Ca3(PO4)2

Calcium phosphate refers to minerals containing calcium ions (Ca2+) together with orthophosphates (PO43−), metaphosphates or pyrophosphates (P2O74−) and occasionally hydrogen or hydroxide ions. Especially, the common mineral apatite has formula Ca5(PO4)3X, where X is F, Cl, OH, or a mixture; it is hydroxyapatite if the extra ion is mainly hydroxide. Much of the "tricalcium phosphate" on the market is actually powdered hydroxyapatite.



  • Nomenclature 1
  • Preparation of pure Ca3(PO4)2 2
  • Crystal structure of β-, α- and α'- Ca3(PO4)2 polymorphs 3
  • Natural occurrence 4
  • Biphasic tricalcium phosphate, BCP 5
  • Uses 6
  • References 7

It has three crystalline polymorphs α, α' and β. The α and α' states are formed at high temperatures. As rock, it is found in Whitlockite.


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