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1. 32p Radioisotope
2. P-32 Radioisotope
1. Phosphorus P-32
2. 14596-37-3
3. Phosphorus, Isotope Of Mass 32
4. Phosphorus32
5. Phosphorus-32 Atom
6. (~32~p)phosphane
7. Chebi:37972
8. Dtxsid80932734
9. Db14551
10. (32)p
11. C19162
12. (32)15p
13. Q2174657
| Molecular Weight | 34.998 g/mol |
|---|---|
| Molecular Formula | H3P |
| XLogP3 | -0.1 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 34.9973827 g/mol |
| Monoisotopic Mass | 34.9973827 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 1 |
| Formal Charge | 0 |
| Complexity | 0 |
| Isotope Atom Count | 1 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
API SUPPLIERS
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USDMF
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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ABOUT THIS PAGE
A Phosphorus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phosphorus, including repackagers and relabelers. The FDA regulates Phosphorus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phosphorus API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Phosphorus supplier is an individual or a company that provides Phosphorus active pharmaceutical ingredient (API) or Phosphorus finished formulations upon request. The Phosphorus suppliers may include Phosphorus API manufacturers, exporters, distributors and traders.
click here to find a list of Phosphorus suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Phosphorus DMF (Drug Master File) is a document detailing the whole manufacturing process of Phosphorus active pharmaceutical ingredient (API) in detail. Different forms of Phosphorus DMFs exist exist since differing nations have different regulations, such as Phosphorus USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Phosphorus DMF submitted to regulatory agencies in the US is known as a USDMF. Phosphorus USDMF includes data on Phosphorus's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Phosphorus USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Phosphorus suppliers with USDMF on PharmaCompass.
Phosphorus 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 Phosphorus 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 Phosphorus GMP manufacturer or Phosphorus GMP API supplier for your needs.
A Phosphorus CoA (Certificate of Analysis) is a formal document that attests to Phosphorus's compliance with Phosphorus specifications and serves as a tool for batch-level quality control.
Phosphorus CoA mostly includes findings from lab analyses of a specific batch. For each Phosphorus 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.
Phosphorus may be tested according to a variety of international standards, such as European Pharmacopoeia (Phosphorus EP), Phosphorus JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Phosphorus USP).
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