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1. Kt-ii-115
2. Chembl4746439
3. Schembl18717800
4. Kt-ii 115
5. Fblnzoctnrxjqd-yfkpbyrvsa-n
6. Ov329
7. Bdbm50561618
8. Ex-a13983
9. Nsc793877
10. Ov-329
11. Nsc-793877
12. (3s)-3-amino-4-(difluoromethylidene)cyclopentene-1-carboxylic Acid
13. (3s)-3-amino-4-(difluoromethylene)-1-cyclopentene-1-carboxylic Acid
14. (s)-3-amino-4-(difluoromethylenyl)cyclopent-1-ene-1-carboxylic Acid
15. 1-cyclopentene-1-carboxylic Acid, 3-amino-4-(difluoromethylene)-, (3s)-
16. 2093928-28-8
| Molecular Weight | 175.13 g/mol |
|---|---|
| Molecular Formula | C7H7F2NO2 |
| XLogP3 | -2.6 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 63.3 |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 279 |
| 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
61
PharmaCompass offers a list of V3796Ljk8G API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right V3796Ljk8G manufacturer or V3796Ljk8G supplier for your needs.
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A V3796Ljk8G manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of V3796Ljk8G, including repackagers and relabelers. The FDA regulates V3796Ljk8G manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. V3796Ljk8G 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 V3796Ljk8G supplier is an individual or a company that provides V3796Ljk8G active pharmaceutical ingredient (API) or V3796Ljk8G finished formulations upon request. The V3796Ljk8G suppliers may include V3796Ljk8G API manufacturers, exporters, distributors and traders.
V3796Ljk8G 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 V3796Ljk8G GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right V3796Ljk8G GMP manufacturer or V3796Ljk8G GMP API supplier for your needs.
A V3796Ljk8G CoA (Certificate of Analysis) is a formal document that attests to V3796Ljk8G's compliance with V3796Ljk8G specifications and serves as a tool for batch-level quality control.
V3796Ljk8G CoA mostly includes findings from lab analyses of a specific batch. For each V3796Ljk8G 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.
V3796Ljk8G may be tested according to a variety of international standards, such as European Pharmacopoeia (V3796Ljk8G EP), V3796Ljk8G JP (Japanese Pharmacopeia) and the US Pharmacopoeia (V3796Ljk8G USP).
