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1. 14080-23-0
2. Pyrimidine-2-carbonitrile
3. 2-pyrimidinecarbonitrile
4. 2-cyano-pyrimidine
5. 2-cyano Pyrimidine
6. Mfcd00160513
7. Cyanopyrimidine
8. Pyrimidin-2-carbonitrile
9. Schembl151679
10. 2-pyrimidinecarbonitrile, 97%
11. Chembl3352946
12. Dtxsid40864466
13. Act01350
14. Albb-006249
15. Bcp27301
16. Cs-d1157
17. Hy-y0241
18. Zinc2531032
19. S5611
20. Stk503786
21. Akos000279271
22. Ac-1955
23. Pb27459
24. Ps-9303
25. Ncgc00185023-01
26. Bp-10841
27. Db-006101
28. Am20080306
29. Bb 0216629
30. Ft-0601166
31. En300-43565
32. 080c230
33. Q-200266
34. F2173-0037
35. Z1201023047
| Molecular Weight | 105.10 g/mol |
|---|---|
| Molecular Formula | C5H3N3 |
| XLogP3 | -0.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 105.032697108 g/mol |
| Monoisotopic Mass | 105.032697108 g/mol |
| Topological Polar Surface Area | 49.6 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 106 |
| 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 2-Cyanopyrimidine 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 2-Cyanopyrimidine manufacturer or 2-Cyanopyrimidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 2-Cyanopyrimidine manufacturer or 2-Cyanopyrimidine supplier.
PharmaCompass also assists you with knowing the 2-Cyanopyrimidine API Price utilized in the formulation of products. 2-Cyanopyrimidine API Price is not always fixed or binding as the 2-Cyanopyrimidine Price is obtained through a variety of data sources. The 2-Cyanopyrimidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Provastatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Provastatin, including repackagers and relabelers. The FDA regulates Provastatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Provastatin 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 Provastatin supplier is an individual or a company that provides Provastatin active pharmaceutical ingredient (API) or Provastatin finished formulations upon request. The Provastatin suppliers may include Provastatin API manufacturers, exporters, distributors and traders.
Provastatin 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 Provastatin 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 Provastatin GMP manufacturer or Provastatin GMP API supplier for your needs.
A Provastatin CoA (Certificate of Analysis) is a formal document that attests to Provastatin's compliance with Provastatin specifications and serves as a tool for batch-level quality control.
Provastatin CoA mostly includes findings from lab analyses of a specific batch. For each Provastatin 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.
Provastatin may be tested according to a variety of international standards, such as European Pharmacopoeia (Provastatin EP), Provastatin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Provastatin USP).
