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Chemistry

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Also known as: 62-54-4, Calcium diacetate, Acetic acid, calcium salt, Lime acetate, Phoslo, Lime pyrolignite
Molecular Formula
C4H6CaO4
Molecular Weight
158.17  g/mol
InChI Key
VSGNNIFQASZAOI-UHFFFAOYSA-L
FDA UNII
Y882YXF34X

Calcium Acetate
Calcium Acetate is a calcium salt of acetic acid. Calcium is a mineral essential for many cellular functions including nerve impulse transmission, muscle contraction, cardiac function, bone formation, and capillary and cell membrane permeability. Calcium acetate is administered orally to prevent or treat calcium deficiency and to treat hyperphosphatemia due to its phosphate-binding properties.
1 2D Structure

Calcium Acetate

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
calcium;diacetate
2.1.2 InChI
InChI=1S/2C2H4O2.Ca/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
2.1.3 InChI Key
VSGNNIFQASZAOI-UHFFFAOYSA-L
2.1.4 Canonical SMILES
CC(=O)[O-].CC(=O)[O-].[Ca+2]
2.2 Other Identifiers
2.2.1 UNII
Y882YXF34X
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Acetic Acid, Calcium Salt

2. Acetic Acid, Calcium Salt (2:1)

3. Phoslo

2.3.2 Depositor-Supplied Synonyms

1. 62-54-4

2. Calcium Diacetate

3. Acetic Acid, Calcium Salt

4. Lime Acetate

5. Phoslo

6. Lime Pyrolignite

7. Acetate Of Lime

8. Brown Acetate

9. Acetic Acid Calcium Salt

10. Gray Acetate Of Lime

11. Brown Acetate Of Lime

12. Phoslyra

13. Calcium;diacetate

14. Calcium Ethanoate

15. Fema No. 2228

16. Calcarea Acetica

17. Calcium(ii) Acetate

18. Acetic Acid, Calcium Salt (2:1)

19. Calcium Acetate Anhydrous

20. Calcium Acetate, Anhydrous

21. Chebi:3310

22. Ins No.263

23. Y882yxf34x

24. Teltozan

25. Sorbo-calcion

26. Vinegar Salts

27. Gray Acetate

28. Ins-263

29. Phoslo Gelcaps

30. Calcium Di(acetate)

31. E-263

32. Ca(oac)2

33. Eliphos

34. Sanopan

35. Ccris 4921

36. Hsdb 928

37. Einecs 200-540-9

38. Calcium Acetate [usp:jan]

39. Unii-y882yxf34x

40. Ai3-02903

41. Calcium Acetate Salt

42. Phoslo (tn)

43. Calcium Acetate, Fcc

44. Calcium Acetate (usp)

45. Ec 200-540-9

46. Calcium Acetate 23% 10m

47. Schembl23872

48. Calcium Acetate [ii]

49. Calcium Acetate [mi]

50. Calcium Acetate [fcc]

51. Calcium Acetate [fhfi]

52. Calcium Acetate [hsdb]

53. Calcium Acetate [inci]

54. Calcarea Acetica [hpus]

55. Calcium Acetate [vandf]

56. Calcium Acetate [mart.]

57. Chembl1200800

58. Dtxsid0020234

59. Calcium Acetate [usp-rs]

60. Calcium Acetate [who-dd]

61. Calcium Acetate (fragrance Grade)

62. Amy23411

63. Mfcd00012448

64. Calcium Acetate [orange Book]

65. Akos015904560

66. Calcium Acetate [ep Monograph]

67. Calcium Acetate [usp Monograph]

68. Db00258

69. E263

70. Ft-0623376

71. Ft-0623377

72. D00931

73. Calcium Acetate, Anhydrous [ep Impurity]

74. Cis,cis-1,3,5-cyclohexanetricarboxylicacid

75. Q409251

76. Calcium Diacetate, Cac - Acetic Acid, Calcium Salt

77. J-519530

2.4 Create Date
2005-03-27
3 Chemical and Physical Properties
Molecular Weight 158.17 g/mol
Molecular Formula C4H6CaO4
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass157.9891995 g/mol
Monoisotopic Mass157.9891995 g/mol
Topological Polar Surface Area80.3 Ų
Heavy Atom Count9
Formal Charge0
Complexity25.5
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count3
4 Drug and Medication Information
4.1 Drug Information
1 of 6  
Drug NameCalcium acetate
PubMed HealthCalcium Acetate (By mouth)
Drug ClassesCalcium Supplement, Phosphate Binder
Drug LabelEach white, round tablet (stamped CYP910) contains 667 mg calcium acetate, USP (anhydrous; Ca(CH3COO)2; MW=158.17 grams) equal to 169 mg (8.45 mEq) calcium, polyethylene glycol 8000 NF; sodium lauryl sulfate, NF; and crospovidone, NF. ELIPHOS...
Active IngredientCalcium acetate
Dosage FormTablet; Capsule
RouteOral
Strengtheq 169mg calcium
Market StatusPrescription
CompanyAmneal Pharms; Paddock; Invagen Pharms; Roxane

2 of 6  
Drug NamePhoslo gelcaps
Active IngredientCalcium acetate
Dosage FormCapsule
RouteOral
Strengtheq 169mg calcium
Market StatusPrescription
CompanyFresenius Medcl

3 of 6  
Drug NameProcalamine
Active Ingredientcalcium acetate; sodium chloride; magnesium acetate; sodium acetate; phosphoric acid; glycerin; potassium chloride; Amino acids
Dosage FormInjectable
RouteInjection
Strength200mg/100ml; 150mg/100ml; 26mg/100ml; 54mg/100ml; 120mg/100ml; 3gm/100ml; 41mg/100ml; 3%
Market StatusPrescription
CompanyB Braun

4 of 6  
Drug NameCalcium acetate
PubMed HealthCalcium Acetate (By mouth)
Drug ClassesCalcium Supplement, Phosphate Binder
Drug LabelEach white, round tablet (stamped CYP910) contains 667 mg calcium acetate, USP (anhydrous; Ca(CH3COO)2; MW=158.17 grams) equal to 169 mg (8.45 mEq) calcium, polyethylene glycol 8000 NF; sodium lauryl sulfate, NF; and crospovidone, NF. ELIPHOS...
Active IngredientCalcium acetate
Dosage FormTablet; Capsule
RouteOral
Strengtheq 169mg calcium
Market StatusPrescription
CompanyAmneal Pharms; Paddock; Invagen Pharms; Roxane

5 of 6  
Drug NamePhoslo gelcaps
Active IngredientCalcium acetate
Dosage FormCapsule
RouteOral
Strengtheq 169mg calcium
Market StatusPrescription
CompanyFresenius Medcl

6 of 6  
Drug NameProcalamine
Active Ingredientcalcium acetate; sodium chloride; magnesium acetate; sodium acetate; phosphoric acid; glycerin; potassium chloride; Amino acids
Dosage FormInjectable
RouteInjection
Strength200mg/100ml; 150mg/100ml; 26mg/100ml; 54mg/100ml; 120mg/100ml; 3gm/100ml; 41mg/100ml; 3%
Market StatusPrescription
CompanyB Braun

4.2 Therapeutic Uses

... Used to restrict phosphate absorption in patients with chronic renal failure and oxalate absorption in patients with inflammatory bowel disease.

Hardman, J.G., L.E. Limbird, P.B. Molinoff, R.W. Ruddon, A.G. Goodman (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 9th ed. New York, NY: McGraw-Hill, 1996., p. 1523


Calcium acetate is indicated in patients with end-stage renal failure to lower serum phosphate concentrations. It does not promote aluminum absorption. /Included in US product labeling/

USP. Convention. USPDI - Drug Information for the Health Care Professional. 19th ed. Volume I.Micromedex, Inc. Englewood, CO., 1999. Content Prepared by the U.S. Pharmacopieal Convention, Inc., p. 719


4.3 Drug Warning

Except under special circumstances, this medication /calcium acetate/ should not be used when the following medical problem exists: hypercalcemia (calcium acetate may exacerbate the condition).

USP. Convention. USPDI - Drug Information for the Health Care Professional. 19th ed. Volume I.Micromedex, Inc. Englewood, CO., 1999. Content Prepared by the U.S. Pharmacopieal Convention, Inc., p. 719


Concurrent use /with digitalis glycosides/ is not recommended because calcium acetate may cause hypercalcemia, which could precipitate cardiac arrhythmias.

USP. Convention. USPDI - Drug Information for the Health Care Professional. 19th ed. Volume I.Micromedex, Inc. Englewood, CO., 1999. Content Prepared by the U.S. Pharmacopieal Convention, Inc., p. 719


4.4 Drug Indication

Calcium acetate is one of a number of calcium salts used to treat hyperphosphatemia (too much phosphate in the blood) in patients with kidney disease.


FDA Label


5 Pharmacology and Biochemistry
5.1 Pharmacology

Patients with advanced renal insufficiency (creatinine clearance less than 30 ml/min) exhibit phosphate retention and some degree of hyperphosphatemia. The retention of phosphate plays a pivotal role in causing secondary hyperparathyroidism associated with osteodystrophy, and soft-tissue calcification. The mechanism by which phosphate retention leads to hyperparathyroidism is not clearly delineated. Therapeutic efforts directed toward the control of hyperphosphatemia include reduction in the dietary intake of phosphate, inhibition of absorption of phosphate in the intestine with phosphate binders, and removal of phosphate from the body by more efficient methods of dialysis. The rate of removal of phosphate by dietary manipulation or by dialysis is insufficient. Dialysis patients absorb 40% to 80% of dietary phosphorus. Therefore, the fraction of dietary phosphate absorbed from the diet needs to be reduced by using phosphate binders in most renal failure patients on maintenance dialysis. Calcium acetate when taken with meals combines with dietary phosphate to form insoluble calcium phosphate which is excreted in the feces. Maintenance of serum phosphorus below 6.0 mg/dl is generally considered as a clinically acceptable outcome of treatment with phosphate binders. Calcium acetate is highly soluble at neutral pH, making the calcium readily available for binding to phosphate in the proximal small intestine.


5.2 MeSH Pharmacological Classification

Chelating Agents

Chemicals that bind to and remove ions from solutions. Many chelating agents function through the formation of COORDINATION COMPLEXES with METALS. (See all compounds classified as Chelating Agents.)


5.3 FDA Pharmacological Classification
5.3.1 Pharmacological Classes
Calcium [CS]; Cations, Divalent [CS]; Increased Coagulation Factor Activity [PE]; Blood Coagulation Factor [EPC]
5.4 ATC Code

V - Various

V03 - All other therapeutic products

V03A - All other therapeutic products

V03AE - Drugs for treatment of hyperkalemia and hyperphosphatemia

V03AE07 - Calcium acetate


5.5 Absorption, Distribution and Excretion

Absorption

40% is absorbed in the fasting state and approximately 30% is absorbed in the nonfasting state following oral administration.


Route of Elimination

Calcium acetate when taken with meals, combines with dietary phosphate to form insoluble calcium phosphate which is excreted in the feces.


5.6 Mechanism of Action

Calcium acetate and other calcium salts are phosphate binders. They work by binding with the phosphate in the food you eat, so that it is eliminated from the body without being absorbed.


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08-Jan-2021
08-Jan-2025
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DOSAGE - CAPSULE;ORAL - 667MG

USFDA APPLICATION NUMBER - 21160

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DOSAGE - SOLUTION;ORAL - 667MG/5ML

USFDA APPLICATION NUMBER - 22581

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ABOUT THIS PAGE

Looking for 62-54-4 / Calcium Acetate API manufacturers, exporters & distributors?

Calcium Acetate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Calcium Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Calcium Acetate manufacturer or Calcium Acetate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Acetate manufacturer or Calcium Acetate supplier.

PharmaCompass also assists you with knowing the Calcium Acetate API Price utilized in the formulation of products. Calcium Acetate API Price is not always fixed or binding as the Calcium Acetate Price is obtained through a variety of data sources. The Calcium Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Calcium Acetate

Synonyms

62-54-4, Calcium diacetate, Acetic acid, calcium salt, Lime acetate, Phoslo, Lime pyrolignite

Cas Number

62-54-4

Unique Ingredient Identifier (UNII)

Y882YXF34X

About Calcium Acetate

Calcium Acetate is a calcium salt of acetic acid. Calcium is a mineral essential for many cellular functions including nerve impulse transmission, muscle contraction, cardiac function, bone formation, and capillary and cell membrane permeability. Calcium acetate is administered orally to prevent or treat calcium deficiency and to treat hyperphosphatemia due to its phosphate-binding properties.

Phoslo Gelcaps Manufacturers

A Phoslo Gelcaps manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phoslo Gelcaps, including repackagers and relabelers. The FDA regulates Phoslo Gelcaps manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phoslo Gelcaps API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Phoslo Gelcaps manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Phoslo Gelcaps Suppliers

A Phoslo Gelcaps supplier is an individual or a company that provides Phoslo Gelcaps active pharmaceutical ingredient (API) or Phoslo Gelcaps finished formulations upon request. The Phoslo Gelcaps suppliers may include Phoslo Gelcaps API manufacturers, exporters, distributors and traders.

click here to find a list of Phoslo Gelcaps suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Phoslo Gelcaps USDMF

A Phoslo Gelcaps DMF (Drug Master File) is a document detailing the whole manufacturing process of Phoslo Gelcaps active pharmaceutical ingredient (API) in detail. Different forms of Phoslo Gelcaps DMFs exist exist since differing nations have different regulations, such as Phoslo Gelcaps USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Phoslo Gelcaps DMF submitted to regulatory agencies in the US is known as a USDMF. Phoslo Gelcaps USDMF includes data on Phoslo Gelcaps's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Phoslo Gelcaps USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Phoslo Gelcaps suppliers with USDMF on PharmaCompass.

Phoslo Gelcaps CEP

A Phoslo Gelcaps CEP of the European Pharmacopoeia monograph is often referred to as a Phoslo Gelcaps Certificate of Suitability (COS). The purpose of a Phoslo Gelcaps CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Phoslo Gelcaps EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Phoslo Gelcaps to their clients by showing that a Phoslo Gelcaps CEP has been issued for it. The manufacturer submits a Phoslo Gelcaps CEP (COS) as part of the market authorization procedure, and it takes on the role of a Phoslo Gelcaps CEP holder for the record. Additionally, the data presented in the Phoslo Gelcaps CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Phoslo Gelcaps DMF.

A Phoslo Gelcaps CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Phoslo Gelcaps CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Phoslo Gelcaps suppliers with CEP (COS) on PharmaCompass.

Phoslo Gelcaps WC

A Phoslo Gelcaps written confirmation (Phoslo Gelcaps WC) is an official document issued by a regulatory agency to a Phoslo Gelcaps manufacturer, verifying that the manufacturing facility of a Phoslo Gelcaps active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Phoslo Gelcaps APIs or Phoslo Gelcaps finished pharmaceutical products to another nation, regulatory agencies frequently require a Phoslo Gelcaps WC (written confirmation) as part of the regulatory process.

click here to find a list of Phoslo Gelcaps suppliers with Written Confirmation (WC) on PharmaCompass.

Phoslo Gelcaps NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Phoslo Gelcaps as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Phoslo Gelcaps API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Phoslo Gelcaps as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Phoslo Gelcaps and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Phoslo Gelcaps NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Phoslo Gelcaps suppliers with NDC on PharmaCompass.

Phoslo Gelcaps GMP

Phoslo Gelcaps Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Phoslo Gelcaps GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Phoslo Gelcaps GMP manufacturer or Phoslo Gelcaps GMP API supplier for your needs.

Phoslo Gelcaps CoA

A Phoslo Gelcaps CoA (Certificate of Analysis) is a formal document that attests to Phoslo Gelcaps's compliance with Phoslo Gelcaps specifications and serves as a tool for batch-level quality control.

Phoslo Gelcaps CoA mostly includes findings from lab analyses of a specific batch. For each Phoslo Gelcaps CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Phoslo Gelcaps may be tested according to a variety of international standards, such as European Pharmacopoeia (Phoslo Gelcaps EP), Phoslo Gelcaps JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Phoslo Gelcaps USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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