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1. Myo-inositol Hexakisphosphate(12-)
2. (1s,2s,3s,4s,5s,6s)-cyclohexane-1,2,3,4,5,6-hexayl Hexaphosphate
3. 3929-21-3
4. 2lha
5. 3eeb
6. 3fzy
7. Insp6
8. Chebi:58130
9. Dtxsid001168213
10. Q27125203
11. Myo-inositol, Hexakis(dihydrogen Phosphate), Ion(12-)
12. 1-o,2-o,3-o,4-o,5-o,6-o-hexaphosphonato-myo-inositol
13. (1r,2s,3r,4r,5s,6s)-cyclohexane-1,2,3,4,5,6-hexayl Hexakis(phosphate)
14. Myo-inositol, 1,2,3,4,5,6-hexakis(dihydrogen Phosphate), Ion(12-)
| Molecular Weight | 647.94 g/mol |
|---|---|
| Molecular Formula | C6H6O24P6-12 |
| XLogP3 | -11.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 24 |
| Rotatable Bond Count | 6 |
| Exact Mass | 647.76747304 g/mol |
| Monoisotopic Mass | 647.76747304 g/mol |
| Topological Polar Surface Area | 435 Ų |
| Heavy Atom Count | 36 |
| Formal Charge | -12 |
| Complexity | 749 |
| 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 | 1 |
ABOUT THIS PAGE
A Insp6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Insp6, including repackagers and relabelers. The FDA regulates Insp6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Insp6 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 Insp6 supplier is an individual or a company that provides Insp6 active pharmaceutical ingredient (API) or Insp6 finished formulations upon request. The Insp6 suppliers may include Insp6 API manufacturers, exporters, distributors and traders.
Insp6 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 Insp6 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 Insp6 GMP manufacturer or Insp6 GMP API supplier for your needs.
A Insp6 CoA (Certificate of Analysis) is a formal document that attests to Insp6's compliance with Insp6 specifications and serves as a tool for batch-level quality control.
Insp6 CoA mostly includes findings from lab analyses of a specific batch. For each Insp6 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.
Insp6 may be tested according to a variety of international standards, such as European Pharmacopoeia (Insp6 EP), Insp6 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Insp6 USP).
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