Synopsis
Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Chlorhydroxyquinoline
2. Halquinol
1. Sq 16,401
2. 5-chloroquinolin-8-ol;7-chloroquinolin-8-ol;5,7-dichloroquinolin-8-ol
3. Tarquinor
4. 8-quinolinol, 5,7-dichloro-, Mixt. With 5-chloro-8-quinolinol And 7-chloro-8-quinolinol
5. Halquinols [usan]
6. Unii-z7z4bx535u
7. Z7z4bx535u
8. Chembl3833358
9. Dtxsid90230490
10. Mfcd28978222
11. 5-chloroquinolin-8-ol; 7-chloroquinolin-8-ol; 5,7-dichloroquinolin-8-ol
12. 5,7-dichloro-8-quinolinol Mixt. With 5-chloro-8-quinolinol And 7-chloro-8-quinolinol
13. 5,7-dichloro-8-quinolinol, 5-chloro-8-quinolinol, And 7-chloro-8-quinolinol In Proportions Resulting Naturally From Chlorination Of 8-quinolinol
14. Sq-16401
15. Sy272205
16. So 16,401
17. Ft-0626854
18. A839963
19. 5,7-dichloro-8-quinolino & 5-chloro-8-quinolino & 7-chloro-8-quinnolinol
20. 5-chloro-8-quinolinol; 7-chloro-8-quinolinol; 5,7-dichloro-8-quinolinol
21. 5,7-bis(chloranyl)quinolin-8-ol; 5-chloranylquinolin-8-ol; 7-chloranylquinolin-8-ol
Molecular Weight | 573.2 g/mol |
---|---|
Molecular Formula | C27H17Cl4N3O3 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 0 |
Exact Mass | 572.999452 g/mol |
Monoisotopic Mass | 571.002402 g/mol |
Topological Polar Surface Area | 99.4 Ų |
Heavy Atom Count | 37 |
Formal Charge | 0 |
Complexity | 520 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 3 |
ABOUT THIS PAGE
A Halquinols manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Halquinols, including repackagers and relabelers. The FDA regulates Halquinols manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Halquinols API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Halquinols manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Halquinols supplier is an individual or a company that provides Halquinols active pharmaceutical ingredient (API) or Halquinols finished formulations upon request. The Halquinols suppliers may include Halquinols API manufacturers, exporters, distributors and traders.
click here to find a list of Halquinols suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Halquinols 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 Halquinols 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 Halquinols GMP manufacturer or Halquinols GMP API supplier for your needs.
A Halquinols CoA (Certificate of Analysis) is a formal document that attests to Halquinols's compliance with Halquinols specifications and serves as a tool for batch-level quality control.
Halquinols CoA mostly includes findings from lab analyses of a specific batch. For each Halquinols 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.
Halquinols may be tested according to a variety of international standards, such as European Pharmacopoeia (Halquinols EP), Halquinols JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Halquinols USP).
LOOKING FOR A SUPPLIER?