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1. 9-kcme
1. 135415-65-5
2. 9-kcme
3. Dtxsid10928983
4. (6ar,10ar)-1-methoxy-6,6-dimethyl-3-pentyl-7,8,10,10a-tetrahydro-6ah-benzo[c]chromen-9-one
5. 9h-dibenzo(b,d)pyran-9-one, 6,6a,7,8,10,10a-hexahydro-1-methoxy-6,6-dimethyl-3-pentyl-, Trans-(+-)-
6. 1-methoxy-6,6-dimethyl-3-pentyl-6,6a,7,8,10,10a-hexahydro-9h-dibenzo[b,d]pyran-9-one
Molecular Weight | 330.5 g/mol |
---|---|
Molecular Formula | C21H30O3 |
XLogP3 | 4.8 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 5 |
Exact Mass | 330.21949481 g/mol |
Monoisotopic Mass | 330.21949481 g/mol |
Topological Polar Surface Area | 35.5 Ų |
Heavy Atom Count | 24 |
Formal Charge | 0 |
Complexity | 444 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 2 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Global Sales Information
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ABOUT THIS PAGE
A 9-Keto-Cannabinoid Methyl Ether manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 9-Keto-Cannabinoid Methyl Ether, including repackagers and relabelers. The FDA regulates 9-Keto-Cannabinoid Methyl Ether manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 9-Keto-Cannabinoid Methyl Ether 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 9-Keto-Cannabinoid Methyl Ether supplier is an individual or a company that provides 9-Keto-Cannabinoid Methyl Ether active pharmaceutical ingredient (API) or 9-Keto-Cannabinoid Methyl Ether finished formulations upon request. The 9-Keto-Cannabinoid Methyl Ether suppliers may include 9-Keto-Cannabinoid Methyl Ether API manufacturers, exporters, distributors and traders.
9-Keto-Cannabinoid Methyl Ether 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 9-Keto-Cannabinoid Methyl Ether 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 9-Keto-Cannabinoid Methyl Ether GMP manufacturer or 9-Keto-Cannabinoid Methyl Ether GMP API supplier for your needs.
A 9-Keto-Cannabinoid Methyl Ether CoA (Certificate of Analysis) is a formal document that attests to 9-Keto-Cannabinoid Methyl Ether's compliance with 9-Keto-Cannabinoid Methyl Ether specifications and serves as a tool for batch-level quality control.
9-Keto-Cannabinoid Methyl Ether CoA mostly includes findings from lab analyses of a specific batch. For each 9-Keto-Cannabinoid Methyl Ether 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.
9-Keto-Cannabinoid Methyl Ether may be tested according to a variety of international standards, such as European Pharmacopoeia (9-Keto-Cannabinoid Methyl Ether EP), 9-Keto-Cannabinoid Methyl Ether JP (Japanese Pharmacopeia) and the US Pharmacopoeia (9-Keto-Cannabinoid Methyl Ether USP).
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