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1. 7789-80-2
2. Lautarite
3. Calcium Diiodate
4. Calcium;diiodate
5. L8mn4y57br
6. Autarite
7. Iodic Acid, Calcium Salt
8. Unii-l8mn4y57br
9. Calcium Iodate (ca(io3)2)
10. Hsdb 986
11. Iodic Acid (hio3), Calcium Salt
12. Einecs 232-191-3
13. Mfcd00036265
14. Iodic Acid Calcium Salt
15. Ec 232-191-3
16. Calcium Iodate [mi]
17. Calcium Iodate [fcc]
18. Calcium Iodate [hsdb]
19. Calcium Iodate [vandf]
20. Dtxsid40960972
21. Akos015853993
22. Q2185998
23. 40563-56-2
| Molecular Weight | 389.88 g/mol |
|---|---|
| Molecular Formula | CaI2O6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 0 |
| Exact Mass | 389.74102 g/mol |
| Monoisotopic Mass | 389.74102 g/mol |
| Topological Polar Surface Area | 114 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 36.5 |
| 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 | 3 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Calcium Iodate 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 Calcium Iodate manufacturer or Calcium Iodate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Iodate manufacturer or Calcium Iodate supplier.
PharmaCompass also assists you with knowing the Calcium Iodate API Price utilized in the formulation of products. Calcium Iodate API Price is not always fixed or binding as the Calcium Iodate Price is obtained through a variety of data sources. The Calcium Iodate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lautarite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lautarite, including repackagers and relabelers. The FDA regulates Lautarite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lautarite 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 Lautarite manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lautarite supplier is an individual or a company that provides Lautarite active pharmaceutical ingredient (API) or Lautarite finished formulations upon request. The Lautarite suppliers may include Lautarite API manufacturers, exporters, distributors and traders.
click here to find a list of Lautarite suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Lautarite 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 Lautarite 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 Lautarite GMP manufacturer or Lautarite GMP API supplier for your needs.
A Lautarite CoA (Certificate of Analysis) is a formal document that attests to Lautarite's compliance with Lautarite specifications and serves as a tool for batch-level quality control.
Lautarite CoA mostly includes findings from lab analyses of a specific batch. For each Lautarite 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.
Lautarite may be tested according to a variety of international standards, such as European Pharmacopoeia (Lautarite EP), Lautarite JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lautarite USP).
