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1. 1,3-benzenediol, 2-(3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl)-5-pentyl-, (1r-trans)-
2. Cannabidiol
3. Epidiolex
1. 1,3-benzenediol, 2-(3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl)-5-pentyl-, (1r-trans)-
2. Cbd Hemp Oil
3. Schembl122259
4. 2-(6-isopropenyl-3-methyl-2-cyclohexen-1-yl)-5-pentyl-1,3-benzenediol #
5. 2-(6-isopropenyl-3-methyl-cyclohex-2-enyl)-5-pentyl-benzene-1,3-diol
6. 1,3-benzenediol, 2-[3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-, (1r-trans)-
7. L000157
8. 2-(3-methyl-6-isopropenyl-2-cyclohexenyl)-5-pentylresorcinol
Molecular Weight | 314.5 g/mol |
---|---|
Molecular Formula | C21H30O2 |
XLogP3 | 6.5 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 6 |
Exact Mass | 314.224580195 g/mol |
Monoisotopic Mass | 314.224580195 g/mol |
Topological Polar Surface Area | 40.5 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 414 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Anticonvulsants
Drugs used to prevent SEIZURES or reduce their severity. (See all compounds classified as Anticonvulsants.)
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PharmaCompass offers a list of CBD Hemp Oil 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 CBD Hemp Oil manufacturer or CBD Hemp Oil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred CBD Hemp Oil manufacturer or CBD Hemp Oil supplier.
PharmaCompass also assists you with knowing the CBD Hemp Oil API Price utilized in the formulation of products. CBD Hemp Oil API Price is not always fixed or binding as the CBD Hemp Oil Price is obtained through a variety of data sources. The CBD Hemp Oil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Epidiolex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Epidiolex, including repackagers and relabelers. The FDA regulates Epidiolex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Epidiolex 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 Epidiolex supplier is an individual or a company that provides Epidiolex active pharmaceutical ingredient (API) or Epidiolex finished formulations upon request. The Epidiolex suppliers may include Epidiolex API manufacturers, exporters, distributors and traders.
Epidiolex 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 Epidiolex 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 Epidiolex GMP manufacturer or Epidiolex GMP API supplier for your needs.
A Epidiolex CoA (Certificate of Analysis) is a formal document that attests to Epidiolex's compliance with Epidiolex specifications and serves as a tool for batch-level quality control.
Epidiolex CoA mostly includes findings from lab analyses of a specific batch. For each Epidiolex 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.
Epidiolex may be tested according to a variety of international standards, such as European Pharmacopoeia (Epidiolex EP), Epidiolex JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Epidiolex USP).