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1. 174-77-6
2. 2,6-diazaspiro[3.3]heptan
3. 2,6-diazaspiro[3,3]heptane
4. 2,6-diazaspiro[3.3]heptane;
5. Dtxsid00617011
6. Udsajfsyjmhnfi-uhfffaoysa-n
7. Bcp27220
8. Akos006352459
9. Sy018644
10. Db-000814
11. Am20090039
12. D87943
13. En300-1600550
| Molecular Weight | 98.15 g/mol |
|---|---|
| Molecular Formula | C5H10N2 |
| XLogP3 | -1 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 24.1 |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 66.6 |
| 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
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PharmaCompass offers a list of CD-001 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 CD-001 manufacturer or CD-001 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred CD-001 manufacturer or CD-001 supplier.
PharmaCompass also assists you with knowing the CD-001 API Price utilized in the formulation of products. CD-001 API Price is not always fixed or binding as the CD-001 Price is obtained through a variety of data sources. The CD-001 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2,6-Diazaspiro[3.3]heptane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2,6-Diazaspiro[3.3]heptane, including repackagers and relabelers. The FDA regulates 2,6-Diazaspiro[3.3]heptane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2,6-Diazaspiro[3.3]heptane 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 2,6-Diazaspiro[3.3]heptane supplier is an individual or a company that provides 2,6-Diazaspiro[3.3]heptane active pharmaceutical ingredient (API) or 2,6-Diazaspiro[3.3]heptane finished formulations upon request. The 2,6-Diazaspiro[3.3]heptane suppliers may include 2,6-Diazaspiro[3.3]heptane API manufacturers, exporters, distributors and traders.
2,6-Diazaspiro[3.3]heptane 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 2,6-Diazaspiro[3.3]heptane 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 2,6-Diazaspiro[3.3]heptane GMP manufacturer or 2,6-Diazaspiro[3.3]heptane GMP API supplier for your needs.
A 2,6-Diazaspiro[3.3]heptane CoA (Certificate of Analysis) is a formal document that attests to 2,6-Diazaspiro[3.3]heptane's compliance with 2,6-Diazaspiro[3.3]heptane specifications and serves as a tool for batch-level quality control.
2,6-Diazaspiro[3.3]heptane CoA mostly includes findings from lab analyses of a specific batch. For each 2,6-Diazaspiro[3.3]heptane 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.
2,6-Diazaspiro[3.3]heptane may be tested according to a variety of international standards, such as European Pharmacopoeia (2,6-Diazaspiro[3.3]heptane EP), 2,6-Diazaspiro[3.3]heptane JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2,6-Diazaspiro[3.3]heptane USP).
