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1. Acetate, Potassium
1. 127-08-2
2. Diuretic Salt
3. Acetic Acid, Potassium Salt
4. Potassium Ethanoate
5. Potassium;acetate
6. Fema No. 2920
7. Koac
8. Acetic Acid Potassium Salt
9. Kali Aceticum
10. Potassium Acetates
11. Acok
12. Mfcd00012458
13. Acetic Acid, Potassium Salt (1:1)
14. Ch3co2k
15. E261
16. Ins No.261
17. Potassium Acetate Solution, 5m
18. Chebi:32029
19. Ins-261
20. Ins-261(i)
21. E-261
22. M911911u02
23. Octan Draselny [czech]
24. Potassiumacetate
25. Potassium Acetate [jan]
26. Potassium Acetate (tn)
27. Einecs 204-822-2
28. Potassium Acetate In Plastic Container
29. Kaliumazetat
30. Potassium Acetate [usp:jan]
31. Potasium Acetate
32. Potassium Acetat
33. Potassium-acetate
34. Unii-m911911u02
35. Meco2k
36. Ch3cook
37. Potassium Acetate Solution
38. Dsstox_cid_7043
39. Ec 204-822-2
40. Dsstox_rid_78289
41. Dsstox_gsid_27043
42. Kali Aceticum [hpus]
43. Potassium Acetate (jan/usp)
44. Potassium Acetate [ii]
45. Potassium Acetate [mi]
46. Chembl1201058
47. Dtxsid7027043
48. Potassium Acetate [fhfi]
49. Potassium Acetate [inci]
50. Hy-y0319b
51. Potassium Acetate [vandf]
52. Potassium Acetate [mart.]
53. Potassium Acetate A.c.s. Reagent
54. Potassium Acetate [usp-rs]
55. Potassium Acetate [who-dd]
56. Potassium Acetate, Biochemical Grade
57. Tox21_202740
58. S4843
59. Akos003052760
60. Akos015901668
61. Ccg-266027
62. Cs-w020131
63. Db14498
64. Potassium Acetate [orange Book]
65. Potassium Acetate Acs Grade 1kg
66. Potassium Acetate, 8m Aqueous Solution
67. Potassium Acetate [ep Monograph]
68. Ncgc00260288-01
69. Potassium Acetate [usp Monograph]
70. Bp-21033
71. Cas-127-08-2
72. Ft-0645118
73. P2786
74. 4-chloro-n-furfuryl-5-sulfamoylanthranlic Acid
75. D01154
76. Potassium Acetate, Trace Metals Grade 99.98%
77. Potassium Acetate, 1m Aqueous Solution, Ph 7.5
78. Q409199
79. J-005461
80. Potassium Acetate, 8m Aqueous Solution, Rnase Free
81. Potassium Acetate, 1m Aqueous Solution, Ph 7.5, Rnase Free
| Molecular Weight | 98.14 g/mol |
|---|---|
| Molecular Formula | C2H3KO2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 97.97701082 g/mol |
| Monoisotopic Mass | 97.97701082 g/mol |
| Topological Polar Surface Area | 40.1 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 34.6 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
| 1 of 2 | |
|---|---|
| Drug Name | Potassium acetate in plastic container |
| Active Ingredient | Potassium acetate |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | 2meq/ml |
| Market Status | Prescription |
| Company | Hospira |
| 2 of 2 | |
|---|---|
| Drug Name | Potassium acetate in plastic container |
| Active Ingredient | Potassium acetate |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | 2meq/ml |
| Market Status | Prescription |
| Company | Hospira |
Potassium is used to regulate hypokalemia as a primary condition or secondary to other medical conditions.
B - Blood and blood forming organs
B05 - Blood substitutes and perfusion solutions
B05X - I.v. solution additives
B05XA - Electrolyte solutions
B05XA17 - Potassium acetate
Route of Elimination
Mostly urine but also skin and feces.
Potassium is the major cation (positive ion) inside animal cells, while sodium is the major cation outside animal cells. The concentration differences of these charged particles causes a difference in electric potential between the inside and outside of cells, known as the membrane potential. The balance between potassium and sodium is maintained by ion pumps in the cell membrane. The cell membrane potential created by potassium and sodium ions allows the cell generate an action potentiala "spike" of electrical discharge. The ability of cells to produce electrical discharge is critical for body functions such as neurotransmission, muscle contraction, and heart function. Potassium is also an essential mineral needed to regulate water balance, blood pressure and levels of acidity.
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PharmaCompass offers a list of Potassium 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 Potassium Acetate manufacturer or Potassium Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Acetate manufacturer or Potassium Acetate supplier.
PharmaCompass also assists you with knowing the Potassium Acetate API Price utilized in the formulation of products. Potassium Acetate API Price is not always fixed or binding as the Potassium Acetate Price is obtained through a variety of data sources. The Potassium Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KOAc manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KOAc, including repackagers and relabelers. The FDA regulates KOAc manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KOAc 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 KOAc manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KOAc supplier is an individual or a company that provides KOAc active pharmaceutical ingredient (API) or KOAc finished formulations upon request. The KOAc suppliers may include KOAc API manufacturers, exporters, distributors and traders.
click here to find a list of KOAc suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KOAc DMF (Drug Master File) is a document detailing the whole manufacturing process of KOAc active pharmaceutical ingredient (API) in detail. Different forms of KOAc DMFs exist exist since differing nations have different regulations, such as KOAc USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A KOAc DMF submitted to regulatory agencies in the US is known as a USDMF. KOAc USDMF includes data on KOAc's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The KOAc USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of KOAc suppliers with USDMF on PharmaCompass.
A KOAc CEP of the European Pharmacopoeia monograph is often referred to as a KOAc Certificate of Suitability (COS). The purpose of a KOAc CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of KOAc EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of KOAc to their clients by showing that a KOAc CEP has been issued for it. The manufacturer submits a KOAc CEP (COS) as part of the market authorization procedure, and it takes on the role of a KOAc CEP holder for the record. Additionally, the data presented in the KOAc CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the KOAc DMF.
A KOAc CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. KOAc 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 KOAc suppliers with CEP (COS) on PharmaCompass.
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 KOAc as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for KOAc API and other APIs are published in this directory by the FDA.
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 KOAc 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.
The NDC directory also contains data on finished compounded human drug products that contain KOAc and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a KOAc NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of KOAc suppliers with NDC on PharmaCompass.
KOAc 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 KOAc 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 KOAc GMP manufacturer or KOAc GMP API supplier for your needs.
A KOAc CoA (Certificate of Analysis) is a formal document that attests to KOAc's compliance with KOAc specifications and serves as a tool for batch-level quality control.
KOAc CoA mostly includes findings from lab analyses of a specific batch. For each KOAc 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.
KOAc may be tested according to a variety of international standards, such as European Pharmacopoeia (KOAc EP), KOAc JP (Japanese Pharmacopeia) and the US Pharmacopoeia (KOAc USP).
