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1. D-cellbiose
2. (2r,3r,4r,5r)-2,3,5,6-tetrahydroxy-4-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl)oxy)hexanal
3. (2r,3r,4r,5r)-2,3,5,6-tetrahydroxy-4-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanal
4. (3s,4r,6s)-2-(hydroxymethyl)-6-[(3s,4s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
5. Cellobiose [mi]
6. D-(+)-cellobiose, 98%
7. Schembl617749
8. D-(+)-cellobiose, >=98%
9. Zinc13541008
10. Akos025312436
11. 4-beta-d-glucopyransoyl-d-glucopyranose
12. Ak162390
13. 4-o-.beta.-d-glucopyranosyl-d-glucose
14. D-(+)-cellobiose, For Microbiology, >=99.0%
15. 4-.beta.-d-glucopyranosyl-d-glucopyranose
16. Wurcs=2.0/2,2,1/[o2122h][a2122h-1b_1-5]/1-2/a4-b1
17. (2r,3r,4r,5r)-2,3,5,6-tetrahydroxy-4-((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yloxy)hexanal
| Molecular Weight | 342.30 g/mol |
|---|---|
| Molecular Formula | C12H22O11 |
| XLogP3 | -5 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 8 |
| Exact Mass | 342.11621151 g/mol |
| Monoisotopic Mass | 342.11621151 g/mol |
| Topological Polar Surface Area | 197 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 367 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 9 |
| 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-Cellbiose 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-Cellbiose manufacturer or D-Cellbiose supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred D-Cellbiose manufacturer or D-Cellbiose supplier.
PharmaCompass also assists you with knowing the D-Cellbiose API Price utilized in the formulation of products. D-Cellbiose API Price is not always fixed or binding as the D-Cellbiose Price is obtained through a variety of data sources. The D-Cellbiose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A D-Cellbiose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D-Cellbiose, including repackagers and relabelers. The FDA regulates D-Cellbiose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D-Cellbiose 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 D-Cellbiose supplier is an individual or a company that provides D-Cellbiose active pharmaceutical ingredient (API) or D-Cellbiose finished formulations upon request. The D-Cellbiose suppliers may include D-Cellbiose API manufacturers, exporters, distributors and traders.
D-Cellbiose 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 D-Cellbiose 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 D-Cellbiose GMP manufacturer or D-Cellbiose GMP API supplier for your needs.
A D-Cellbiose CoA (Certificate of Analysis) is a formal document that attests to D-Cellbiose's compliance with D-Cellbiose specifications and serves as a tool for batch-level quality control.
D-Cellbiose CoA mostly includes findings from lab analyses of a specific batch. For each D-Cellbiose 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.
D-Cellbiose may be tested according to a variety of international standards, such as European Pharmacopoeia (D-Cellbiose EP), D-Cellbiose JP (Japanese Pharmacopeia) and the US Pharmacopoeia (D-Cellbiose USP).
