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1. 609-06-3
2. L-(-)-xylose
3. L(+)-xylose
4. Aldehydo-l-xylose
5. L-xylo-pentose
6. Xylose, L-
7. L-xyl
8. A4jw0v2mya
9. Mfcd00151096
10. L(-)-xylose
11. Linear L-xylose
12. Nsc-26213
13. Einecs 210-174-1
14. Nsc 26213
15. Unii-a4jw0v2mya
16. Schembl59766
17. Gtpl4720
18. Chebi:17979
19. Dtxsid50883340
20. 25990-60-7
21. L-(-)-xylose, Mixture Of Anomers
22. Zinc8552145
23. S5830
24. Akos024437975
25. Am83960
26. Cs-w009191
27. Ac-30677
28. Hy-78139
29. X0021
30. L-(-)-xylose, Mixture Of Anomers, >=99%
31. H10761
32. A833906
33. Q27082478
34. 52e637a7-1509-4d9b-bf82-19c9c5a6b38b
| Molecular Weight | 150.13 g/mol |
|---|---|
| Molecular Formula | C5H10O5 |
| XLogP3 | -2.3 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 150.05282342 g/mol |
| Monoisotopic Mass | 150.05282342 g/mol |
| Topological Polar Surface Area | 98 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 104 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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ABOUT THIS PAGE
A L-Xylose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Xylose, including repackagers and relabelers. The FDA regulates L-Xylose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Xylose 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 L-Xylose supplier is an individual or a company that provides L-Xylose active pharmaceutical ingredient (API) or L-Xylose finished formulations upon request. The L-Xylose suppliers may include L-Xylose API manufacturers, exporters, distributors and traders.
L-Xylose 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 L-Xylose 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 L-Xylose GMP manufacturer or L-Xylose GMP API supplier for your needs.
A L-Xylose CoA (Certificate of Analysis) is a formal document that attests to L-Xylose's compliance with L-Xylose specifications and serves as a tool for batch-level quality control.
L-Xylose CoA mostly includes findings from lab analyses of a specific batch. For each L-Xylose 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.
L-Xylose may be tested according to a variety of international standards, such as European Pharmacopoeia (L-Xylose EP), L-Xylose JP (Japanese Pharmacopeia) and the US Pharmacopoeia (L-Xylose USP).
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