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1. 72155-48-7
2. Boc-ahppa
3. (3s,4s)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-phenylpentanoic Acid
4. Boc-(3s,4s)-4-amino-3-hydroxy-5-phenylpentanoic Acid
5. Schembl8787243
6. Zinc2539198
7. Mfcd00065553
8. Akos027340117
9. As-56148
10. D87006
11. A837436
12. (3s,4s)-3-hydroxy-4-(tert-butoxycarbonylamino)-5-phenylpentanoic Acid
13. (3s,4s)-4-((tert-butoxycarbonyl)amino)-3-hydroxy-5-phenylpentanoicacid
14. (3s,4s)-4-(tert-butoxycarbonylamino)-3-hydroxy-5-phenylpentanoic Acid
15. L-threo-pentonic Acid,2,4,5-trideoxy-4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-phenyl-
| Molecular Weight | 309.36 g/mol |
|---|---|
| Molecular Formula | C16H23NO5 |
| XLogP3 | 1.8 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 8 |
| Exact Mass | 309.15762283 g/mol |
| Monoisotopic Mass | 309.15762283 g/mol |
| Topological Polar Surface Area | 95.9 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 371 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| 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 Ambotzbaa1319 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 Ambotzbaa1319 manufacturer or Ambotzbaa1319 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ambotzbaa1319 manufacturer or Ambotzbaa1319 supplier.
PharmaCompass also assists you with knowing the Ambotzbaa1319 API Price utilized in the formulation of products. Ambotzbaa1319 API Price is not always fixed or binding as the Ambotzbaa1319 Price is obtained through a variety of data sources. The Ambotzbaa1319 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ambotzbaa1319 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ambotzbaa1319, including repackagers and relabelers. The FDA regulates Ambotzbaa1319 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ambotzbaa1319 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 Ambotzbaa1319 supplier is an individual or a company that provides Ambotzbaa1319 active pharmaceutical ingredient (API) or Ambotzbaa1319 finished formulations upon request. The Ambotzbaa1319 suppliers may include Ambotzbaa1319 API manufacturers, exporters, distributors and traders.
Ambotzbaa1319 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 Ambotzbaa1319 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 Ambotzbaa1319 GMP manufacturer or Ambotzbaa1319 GMP API supplier for your needs.
A Ambotzbaa1319 CoA (Certificate of Analysis) is a formal document that attests to Ambotzbaa1319's compliance with Ambotzbaa1319 specifications and serves as a tool for batch-level quality control.
Ambotzbaa1319 CoA mostly includes findings from lab analyses of a specific batch. For each Ambotzbaa1319 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.
Ambotzbaa1319 may be tested according to a variety of international standards, such as European Pharmacopoeia (Ambotzbaa1319 EP), Ambotzbaa1319 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ambotzbaa1319 USP).
