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1. 3-((adamantan-1-yl)carbonyl)-1-pentylindole
2. Ab-001
1. Ab-001
2. 1345973-49-0
3. 1-adamantyl-(1-pentylindol-3-yl)methanone
4. Chembl4088147
5. H657dia015
6. Adamantyl(1-pentylindol-3-yl)methanone
7. Jwh 018 Adamantyl Analog
8. Unii-h657dia015
9. Ab 001
10. Ab-001 (cannabinoid)
11. Schembl17308094
12. Dtxsid90158822
13. Jwh-018 Adamantyl Analog
14. Bdbm50257739
15. Zinc71746268
16. Bcp9000212
17. Bcp0726000224
18. J3.184.805i
19. 10.14272/shwdycmmuppwqm-uhfffaoysa-n.1
20. Ab-001 (adamantyl(1-pentylindol-3-yl)methanone)
21. Adamantan-1-yl(1-pentyl-1h-indol-3-yl)methanone
22. Doi:10.14272/shwdycmmuppwqm-uhfffaoysa-n.1
23. Q4649999
24. Ab-001 (adamantyl(1-pentylindol-3-yl)methanone) 0.1 Mg/ml In Acetonitrile
25. Ab-001 (adamantyl(1-pentylindol-3-yl)methanone) 1.0 Mg/ml In Acetonitrile
26. Methanone, (1-pentyl-1h-indol-3-yl)tricyclo(3.3.1.13,7)dec-1-yl-
| Molecular Weight | 349.5 g/mol |
|---|---|
| Molecular Formula | C24H31NO |
| XLogP3 | 6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 6 |
| Exact Mass | 349.240564612 g/mol |
| Monoisotopic Mass | 349.240564612 g/mol |
| Topological Polar Surface Area | 22 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 499 |
| 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 AB001 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 AB001 manufacturer or AB001 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred AB001 manufacturer or AB001 supplier.
PharmaCompass also assists you with knowing the AB001 API Price utilized in the formulation of products. AB001 API Price is not always fixed or binding as the AB001 Price is obtained through a variety of data sources. The AB001 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AB001 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AB001, including repackagers and relabelers. The FDA regulates AB001 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AB001 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 AB001 supplier is an individual or a company that provides AB001 active pharmaceutical ingredient (API) or AB001 finished formulations upon request. The AB001 suppliers may include AB001 API manufacturers, exporters, distributors and traders.
AB001 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 AB001 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 AB001 GMP manufacturer or AB001 GMP API supplier for your needs.
A AB001 CoA (Certificate of Analysis) is a formal document that attests to AB001's compliance with AB001 specifications and serves as a tool for batch-level quality control.
AB001 CoA mostly includes findings from lab analyses of a specific batch. For each AB001 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.
AB001 may be tested according to a variety of international standards, such as European Pharmacopoeia (AB001 EP), AB001 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AB001 USP).
