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1. (1r, 4s)-1,4,5,6,7,7-hexachloro-3-methylbicyclohept-5-ene-2-carbaldehyde
| Molecular Weight | 342.9 g/mol |
|---|---|
| Molecular Formula | C9H6Cl6O |
| XLogP3 | 3.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 341.852031 g/mol |
| Monoisotopic Mass | 339.854981 g/mol |
| Topological Polar Surface Area | 17.1 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 405 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 2 |
| 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 Endosulfan Monoaldehyde 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 Endosulfan Monoaldehyde manufacturer or Endosulfan Monoaldehyde supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Endosulfan Monoaldehyde manufacturer or Endosulfan Monoaldehyde supplier.
PharmaCompass also assists you with knowing the Endosulfan Monoaldehyde API Price utilized in the formulation of products. Endosulfan Monoaldehyde API Price is not always fixed or binding as the Endosulfan Monoaldehyde Price is obtained through a variety of data sources. The Endosulfan Monoaldehyde Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Endosulfan Monoaldehyde manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Endosulfan Monoaldehyde, including repackagers and relabelers. The FDA regulates Endosulfan Monoaldehyde manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Endosulfan Monoaldehyde 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 Endosulfan Monoaldehyde supplier is an individual or a company that provides Endosulfan Monoaldehyde active pharmaceutical ingredient (API) or Endosulfan Monoaldehyde finished formulations upon request. The Endosulfan Monoaldehyde suppliers may include Endosulfan Monoaldehyde API manufacturers, exporters, distributors and traders.
Endosulfan Monoaldehyde 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 Endosulfan Monoaldehyde 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 Endosulfan Monoaldehyde GMP manufacturer or Endosulfan Monoaldehyde GMP API supplier for your needs.
A Endosulfan Monoaldehyde CoA (Certificate of Analysis) is a formal document that attests to Endosulfan Monoaldehyde's compliance with Endosulfan Monoaldehyde specifications and serves as a tool for batch-level quality control.
Endosulfan Monoaldehyde CoA mostly includes findings from lab analyses of a specific batch. For each Endosulfan Monoaldehyde 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.
Endosulfan Monoaldehyde may be tested according to a variety of international standards, such as European Pharmacopoeia (Endosulfan Monoaldehyde EP), Endosulfan Monoaldehyde JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Endosulfan Monoaldehyde USP).
