Synopsis
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1. Altritol
2. L-altritol
3. Talitol
1. D-talitol
2. 643-03-8
3. Altritol
4. Talitol
5. D-talitol-1-13c
6. (2r,3r,4s,5r)-hexane-1,2,3,4,5,6-hexaol
7. 5552-13-6
8. Altritol, D-
9. (2r,3r,4s,5r)-hexane-1,2,3,4,5,6-hexol
10. (2r,3s,4r,5r)-hexane-1,2,3,4,5,6-hexol
11. 83bxr29ekj
12. Wurcs=2.0/1,1,0/[h1222h]/1/
13. 9td9l8s68n
14. Altro-hexitol
15. Tlz
16. Mfcd00191491
17. Unii-83bxr29ekj
18. Unii-9td9l8s68n
19. Schembl15040
20. Chebi:134311
21. Zinc18010484
22. As-64096
23. Cs-0226038
24. T1398
25. C21524
26. D95360
27. W-203390
28. Q27466520
| Molecular Weight | 182.17 g/mol |
|---|---|
| Molecular Formula | C6H14O6 |
| XLogP3 | -3.1 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 5 |
| Exact Mass | 182.07903816 g/mol |
| Monoisotopic Mass | 182.07903816 g/mol |
| Topological Polar Surface Area | 121 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 105 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| 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 D-Talitol 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 D-Talitol manufacturer or D-Talitol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred D-Talitol manufacturer or D-Talitol supplier.
PharmaCompass also assists you with knowing the D-Talitol API Price utilized in the formulation of products. D-Talitol API Price is not always fixed or binding as the D-Talitol Price is obtained through a variety of data sources. The D-Talitol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A altro-hexitol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of altro-hexitol, including repackagers and relabelers. The FDA regulates altro-hexitol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. altro-hexitol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of altro-hexitol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A altro-hexitol supplier is an individual or a company that provides altro-hexitol active pharmaceutical ingredient (API) or altro-hexitol finished formulations upon request. The altro-hexitol suppliers may include altro-hexitol API manufacturers, exporters, distributors and traders.
click here to find a list of altro-hexitol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
altro-hexitol 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 altro-hexitol 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 altro-hexitol GMP manufacturer or altro-hexitol GMP API supplier for your needs.
A altro-hexitol CoA (Certificate of Analysis) is a formal document that attests to altro-hexitol's compliance with altro-hexitol specifications and serves as a tool for batch-level quality control.
altro-hexitol CoA mostly includes findings from lab analyses of a specific batch. For each altro-hexitol 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.
altro-hexitol may be tested according to a variety of international standards, such as European Pharmacopoeia (altro-hexitol EP), altro-hexitol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (altro-hexitol USP).
