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1. 161713-86-6
2. G0398
| Molecular Weight | 772.7 g/mol |
|---|---|
| Molecular Formula | C34H44O20 |
| XLogP3 | -2.7 |
| Hydrogen Bond Donor Count | 11 |
| Hydrogen Bond Acceptor Count | 20 |
| Rotatable Bond Count | 10 |
| Exact Mass | 772.24259379 g/mol |
| Monoisotopic Mass | 772.24259379 g/mol |
| Topological Polar Surface Area | 313 Ų |
| Heavy Atom Count | 54 |
| Formal Charge | 0 |
| Complexity | 1230 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 15 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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ABOUT THIS PAGE
A Alpha-Glucosyl Hesperidin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alpha-Glucosyl Hesperidin, including repackagers and relabelers. The FDA regulates Alpha-Glucosyl Hesperidin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alpha-Glucosyl Hesperidin 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 Alpha-Glucosyl Hesperidin supplier is an individual or a company that provides Alpha-Glucosyl Hesperidin active pharmaceutical ingredient (API) or Alpha-Glucosyl Hesperidin finished formulations upon request. The Alpha-Glucosyl Hesperidin suppliers may include Alpha-Glucosyl Hesperidin API manufacturers, exporters, distributors and traders.
Alpha-Glucosyl Hesperidin 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 Alpha-Glucosyl Hesperidin 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 Alpha-Glucosyl Hesperidin GMP manufacturer or Alpha-Glucosyl Hesperidin GMP API supplier for your needs.
A Alpha-Glucosyl Hesperidin CoA (Certificate of Analysis) is a formal document that attests to Alpha-Glucosyl Hesperidin's compliance with Alpha-Glucosyl Hesperidin specifications and serves as a tool for batch-level quality control.
Alpha-Glucosyl Hesperidin CoA mostly includes findings from lab analyses of a specific batch. For each Alpha-Glucosyl Hesperidin 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.
Alpha-Glucosyl Hesperidin may be tested according to a variety of international standards, such as European Pharmacopoeia (Alpha-Glucosyl Hesperidin EP), Alpha-Glucosyl Hesperidin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Alpha-Glucosyl Hesperidin USP).
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