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1. 6890-40-0
2. 2-(1h-imidazol-4-yl)ethanamine Phosphate
3. 2-(1h-imidazol-4-yl)ethan-1-amine Phosphate
4. 2-(1h-imidazol-4-yl)ethan-1-amine Xphosphate
5. 73239-81-3
6. 2-(1h-imidazol-4-yl)ethanamine Bis(phosphate) Xhydrate
7. 207386-84-3
8. 706-43-4
9. Schembl123244
10. Dtxsid40218980
11. 1h-imidazole-4-ethanamine Phosphate
12. Akos015901547
13. Q20817118
14. Histamine Phosphate;1h-imidazole-4-ethanamine Phosphate (1:2)
Molecular Weight | 209.14 g/mol |
---|---|
Molecular Formula | C5H12N3O4P |
Hydrogen Bond Donor Count | 5 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 2 |
Exact Mass | 209.05654287 g/mol |
Monoisotopic Mass | 209.05654287 g/mol |
Topological Polar Surface Area | 133 Ų |
Heavy Atom Count | 13 |
Formal Charge | 0 |
Complexity | 115 |
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 |
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PharmaCompass offers a list of Histamine Diphosphate Monohydrate 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 Histamine Diphosphate Monohydrate manufacturer or Histamine Diphosphate Monohydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Histamine Diphosphate Monohydrate manufacturer or Histamine Diphosphate Monohydrate supplier.
PharmaCompass also assists you with knowing the Histamine Diphosphate Monohydrate API Price utilized in the formulation of products. Histamine Diphosphate Monohydrate API Price is not always fixed or binding as the Histamine Diphosphate Monohydrate Price is obtained through a variety of data sources. The Histamine Diphosphate Monohydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Histamine Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histamine Phosphate, including repackagers and relabelers. The FDA regulates Histamine Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histamine Phosphate 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 Histamine Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histamine Phosphate supplier is an individual or a company that provides Histamine Phosphate active pharmaceutical ingredient (API) or Histamine Phosphate finished formulations upon request. The Histamine Phosphate suppliers may include Histamine Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Histamine Phosphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Histamine Phosphate 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 Histamine Phosphate 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 Histamine Phosphate GMP manufacturer or Histamine Phosphate GMP API supplier for your needs.
A Histamine Phosphate CoA (Certificate of Analysis) is a formal document that attests to Histamine Phosphate's compliance with Histamine Phosphate specifications and serves as a tool for batch-level quality control.
Histamine Phosphate CoA mostly includes findings from lab analyses of a specific batch. For each Histamine Phosphate 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.
Histamine Phosphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Histamine Phosphate EP), Histamine Phosphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Histamine Phosphate USP).