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1. 147025-53-4
2. Talsaclidine [inn]
3. (3r)-3-prop-2-ynoxy-1-azabicyclo[2.2.2]octane
4. 1o8vsl798t
5. 1-azabicyclo[2.2.2]octane, 3-(2-propyn-1-yloxy)-, (3r)-
6. Unii-1o8vsl798t
7. (3r)-3-(2-propynyloxy)quinuclidine
8. Schembl195367
9. Talsaclidine [who-dd]
10. (r)-3-(2-propynyloxy)-1-azabicyclo[2.2.2]octane
11. Chembl2111051
12. Schembl12390535
13. Dtxsid20163565
14. Zinc1547638
15. Bdbm50119648
16. Akos025294534
17. Talsaclidine, >=98% (hplc), Oil
18. Db12287
19. Ncgc00485383-01
20. Hy-128855
21. Cs-0101277
22. (r)-3-(2-propynyloxy)-1-azabicyclo[2.2.2]octan
23. Q7680323
24. (3r)-3-(prop-2-yn-1-yloxy)-1-azabicyclo[2.2.2]octane
25. 3-(2-propynyloxy)-1-azabicyclo(2.2.2)octane, (r)-
| Molecular Weight | 165.23 g/mol |
|---|---|
| Molecular Formula | C10H15NO |
| XLogP3 | 0.8 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 165.115364102 g/mol |
| Monoisotopic Mass | 165.115364102 g/mol |
| Topological Polar Surface Area | 12.5 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 197 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
57
PharmaCompass offers a list of Talsaclidine 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 Talsaclidine manufacturer or Talsaclidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Talsaclidine manufacturer or Talsaclidine supplier.
PharmaCompass also assists you with knowing the Talsaclidine API Price utilized in the formulation of products. Talsaclidine API Price is not always fixed or binding as the Talsaclidine Price is obtained through a variety of data sources. The Talsaclidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Talsaclidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Talsaclidine, including repackagers and relabelers. The FDA regulates Talsaclidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Talsaclidine 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 Talsaclidine supplier is an individual or a company that provides Talsaclidine active pharmaceutical ingredient (API) or Talsaclidine finished formulations upon request. The Talsaclidine suppliers may include Talsaclidine API manufacturers, exporters, distributors and traders.
Talsaclidine 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 Talsaclidine 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 Talsaclidine GMP manufacturer or Talsaclidine GMP API supplier for your needs.
A Talsaclidine CoA (Certificate of Analysis) is a formal document that attests to Talsaclidine's compliance with Talsaclidine specifications and serves as a tool for batch-level quality control.
Talsaclidine CoA mostly includes findings from lab analyses of a specific batch. For each Talsaclidine 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.
Talsaclidine may be tested according to a variety of international standards, such as European Pharmacopoeia (Talsaclidine EP), Talsaclidine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Talsaclidine USP).
