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1. 631-61-8
2. Acetic Acid, Ammonium Salt
3. Ammoniumacetate
4. Azanium;acetate
5. Acetic Acid Ammonium Salt
6. Ammonium Ethanoate
7. Aconh4
8. Ch3coonh4
9. Ch3co2nh4
10. Rre756s6q2
11. Ammonia Acetate
12. Mfcd00013066
13. Azanium Acetate
14. Amoniumacetate
15. Unii-rre756s6q2
16. Ammonium-acetate
17. Hsdb 556
18. Acetic Acid Amine
19. Ammonium Acetate-
20. Ammonia Acetate Salt
21. Einecs 211-162-9
22. Acetic Acid Ammoniate
23. Ammonium Acetate Acs
24. Nh4oac
25. Ammonium Aceticum
26. Ai3-26540
27. Ec 211-162-9
28. Ammonium Acetate [ii]
29. Ammonium Acetate [mi]
30. Ammonium Acetate Solution, 5m
31. Ins No. 264
32. Ammonium Acetate [hsdb]
33. Ammonium Acetate [inci]
34. Ammonium Aceticum [hpus]
35. Dtxsid5023873
36. Chebi:62947
37. Ammonium Acetate [mart.]
38. Ammonium Acetate [who-dd]
39. Ammonium Acetate, Biochemical Grade
40. Acetic Acid, Ammonium Salt (1:1)
41. Akos015904610
42. Ammonium Acetate, 5m Aqueous Solution
43. E264
44. E 264
45. E-264
46. Ft-0622306
| Molecular Weight | 77.08 g/mol |
|---|---|
| Molecular Formula | C2H7NO2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 77.047678466 g/mol |
| Monoisotopic Mass | 77.047678466 g/mol |
| Topological Polar Surface Area | 41.1 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 25.5 |
| 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 |
Diuretic
Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 82
MEDICATION (VET): AS NUTRIENT
Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 15
MEDICATION (VET): Formerly a diuretic, antipyretic
Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 82
ALTHOUGH PRECISE MECHANISM OF SYSTEMIC AMMONIA INTOXICATION REMAINS TO BE ELUCIDATED, EVIDENCE EXISTS TO SUGGEST THAT AN INTERFERENCE WITH CEREBRAL OXIDATIVE ENERGY METABOLISM IS INVOLVED. IN RATS MADE COMATOSE WITH AMMONIUM ACETATE, SAMPLES OF BASILAR BRAIN STRUCTURES SHOWED SIGNIFICANT DECR IN GLYCOGEN, GLUCOSE, ATP, & ESPECIALLY IN PHOSPHOCREATINE.
Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. III-23
The effects of ammonium ions on the release of glutamic acid from the rat cerebral cortex were measured in vivo using cortical cups & multiple ion detection technique. The results indicate that ammonium ions increase the release & the formation of glutamic acid in the brain. The resulting increased concn of this amino acid in extracellular spaces may be one of the mechanisms of ammonia toxicity in vivo. /Ammonium ions/
PMID:6131108 Moroni F et al; J Neurochem 40 (3): 850-4 (1983)
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A Ammonium Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ammonium Acetate, including repackagers and relabelers. The FDA regulates Ammonium Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ammonium Acetate 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 Ammonium Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ammonium Acetate supplier is an individual or a company that provides Ammonium Acetate active pharmaceutical ingredient (API) or Ammonium Acetate finished formulations upon request. The Ammonium Acetate suppliers may include Ammonium Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Ammonium Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ammonium Acetate DMF (Drug Master File) is a document detailing the whole manufacturing process of Ammonium Acetate active pharmaceutical ingredient (API) in detail. Different forms of Ammonium Acetate DMFs exist exist since differing nations have different regulations, such as Ammonium Acetate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ammonium Acetate DMF submitted to regulatory agencies in the US is known as a USDMF. Ammonium Acetate USDMF includes data on Ammonium Acetate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ammonium Acetate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ammonium Acetate suppliers with USDMF on PharmaCompass.
Ammonium Acetate 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 Ammonium Acetate 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 Ammonium Acetate GMP manufacturer or Ammonium Acetate GMP API supplier for your needs.
A Ammonium Acetate CoA (Certificate of Analysis) is a formal document that attests to Ammonium Acetate's compliance with Ammonium Acetate specifications and serves as a tool for batch-level quality control.
Ammonium Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Ammonium Acetate 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.
Ammonium Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ammonium Acetate EP), Ammonium Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ammonium Acetate USP).
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