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1. 2-fucosyllactose - Synthetic
2. W-202697
3. 2'-fucosyl-d-lactose, From Human Milk, >=98% (hpae/pad)
4. (3r,4r,5s,6r)-5-((2s,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-((2r,3s,4r,5s,6s)-3,4,5-trihydroxy-6-methyltetrahydro-2h-pyran-2-yloxy)tetrahydro-2h-pyran-2-yloxy)-6-(hydroxymethyl)tetrahydro-2h-pyran-2,3,4-triol
| Molecular Weight | 488.4 g/mol |
|---|---|
| Molecular Formula | C18H32O15 |
| XLogP3 | -5.8 |
| Hydrogen Bond Donor Count | 10 |
| Hydrogen Bond Acceptor Count | 15 |
| Rotatable Bond Count | 6 |
| Exact Mass | 488.17412031 g/mol |
| Monoisotopic Mass | 488.17412031 g/mol |
| Topological Polar Surface Area | 248 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 626 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 14 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A 2-Fucosyllactose-Synthetic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-Fucosyllactose-Synthetic, including repackagers and relabelers. The FDA regulates 2-Fucosyllactose-Synthetic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-Fucosyllactose-Synthetic 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 2-Fucosyllactose-Synthetic supplier is an individual or a company that provides 2-Fucosyllactose-Synthetic active pharmaceutical ingredient (API) or 2-Fucosyllactose-Synthetic finished formulations upon request. The 2-Fucosyllactose-Synthetic suppliers may include 2-Fucosyllactose-Synthetic API manufacturers, exporters, distributors and traders.
2-Fucosyllactose-Synthetic 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 2-Fucosyllactose-Synthetic 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 2-Fucosyllactose-Synthetic GMP manufacturer or 2-Fucosyllactose-Synthetic GMP API supplier for your needs.
A 2-Fucosyllactose-Synthetic CoA (Certificate of Analysis) is a formal document that attests to 2-Fucosyllactose-Synthetic's compliance with 2-Fucosyllactose-Synthetic specifications and serves as a tool for batch-level quality control.
2-Fucosyllactose-Synthetic CoA mostly includes findings from lab analyses of a specific batch. For each 2-Fucosyllactose-Synthetic 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.
2-Fucosyllactose-Synthetic may be tested according to a variety of international standards, such as European Pharmacopoeia (2-Fucosyllactose-Synthetic EP), 2-Fucosyllactose-Synthetic JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-Fucosyllactose-Synthetic USP).
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