Synopsis
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USDMF
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1. Biotetrussin
2. Chlorodimenol
3. Clobutinol Hydrochloride
4. Kat 250
5. Petoxil
6. Silomat
1. 14860-49-2
2. Clobutinol [inn]
3. Clobutinolum
4. Iversal
5. 1-(4-chlorophenyl)-4-(dimethylamino)-2,3-dimethylbutan-2-ol
6. Clobutinol (inn)
7. Iversal (tn)
8. 1-(4-chlorophenyl)-2,3-dimethyl-4-dimethylamino-2-butanol
9. C14h22clno
10. 1ny2ix043a
11. R05db03
12. Kat 256 [as Hydrochloride]
13. Clobutinolum [inn-latin]
14. Benzeneethanol, 4-chloro-.alpha.-[2-(dimethylamino)-1-methylethyl]-.alpha.-methyl-
15. Ncgc00159437-02
16. Einecs 238-926-4
17. Brn 2843490
18. Unii-1ny2ix043a
19. Benzeneethanol, 4-chloro-.alpha.-(2-(dimethylamino)-1-methylethyl)-.alpha.-methyl-
20. Clobutinol [mi]
21. 4-chloro-alpha(2-(dimethylamino)-1-methylethyl)alpha-methylbenzeneethanol
22. Benzeneethanol, 4-chloro-alpha-(2-(dimethylamino)-1-methyl)-alpha-methyl-
23. Benzeneethanol, 4-chloro-alpha-(2-(dimethylamino)-1-methylethyl)-alpha-methyl-
24. P-chloro-alpha-(2-(dimethylamino)-1-methylethyl)-alpha-methyl-phenethyl Alcohol
25. Clobutinol [who-dd]
26. P-cloro-alpha-(2-(dimetilamino)-1-metiletil)-alpha-metil Fenetil Alcool [italian]
27. Kat 256 Free Base
28. Kat-256 Free Base
29. Schembl148543
30. Chembl1474889
31. Dtxsid2022838
32. Chebi:94381
33. P-chloro-alpha-(2-(dimethylamino)-1-methylethyl)-alpha-methylphenethyl Alcohol
34. P-cloro-alpha-(2-(dimetilamino)-1-metiletil)-alpha-metil Fenetil Alcool
35. Db09004
36. Phenethyl Alcohol, P-chloro-.alpha.-[2-(dimethylamino)-1-methylethyl]-.alpha.-methyl-
37. Phenethyl Alcohol, P-chloro-alpha-(2-(dimethylamino)-1-methylethyl)-alpha-methyl-
38. Hy-148144
39. Cs-0613654
40. Ft-0714887
41. D07716
42. Diethylenetriamine Crosslinked With Epichlorohydrin
43. Q415654
44. Brd-a43809092-003-01-3
45. 1-(4-chlorophenyl)-4-(dimethylamino)-2,3-dimethyl-2-butanol
46. (2s)-1-(4-chlorophenyl)-4-(dimethylamino)-2,3-dimethylbutan-2-ol
47. Benzeneethanol, 4-chloro-.alpha.-(2-(dimethylamino)-1-methyl)-.alpha.-methyl-
48. P-chloro-.alpha.-(2-(dimethylamino)-1-methylethyl)-.alpha.-methyl-phenethyl Alcohol
49. P-chloro-.alpha.-(2-(dimethylamino)-1-methylethyl)-.alpha.-methylphenethyl Alcohol
50. P-chloro-.alpha.-[2-(dimethylamino)-1-methylethyl]-.alpha.-methylphenyl Alcohol
51. P-cloro-.alpha.-(2-(dimetilamino)-1-metiletil)-.alpha.-metil Fenetil Alcool
Molecular Weight | 255.78 g/mol |
---|---|
Molecular Formula | C14H22ClNO |
XLogP3 | 3.2 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 5 |
Exact Mass | 255.1389920 g/mol |
Monoisotopic Mass | 255.1389920 g/mol |
Topological Polar Surface Area | 23.5 Ų |
Heavy Atom Count | 17 |
Formal Charge | 0 |
Complexity | 226 |
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 |
Antitussive Agents
Agents that suppress cough. They act centrally on the medullary cough center. EXPECTORANTS, also used in the treatment of cough, act locally. (See all compounds classified as Antitussive Agents.)
R - Respiratory system
R05 - Cough and cold preparations
R05D - Cough suppressants, excl. combinations with expectorants
R05DB - Other cough suppressants
R05DB03 - Clobutinol
ABOUT THIS PAGE
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PharmaCompass offers a list of Clobutinol HCl 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 Clobutinol HCl manufacturer or Clobutinol HCl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clobutinol HCl manufacturer or Clobutinol HCl supplier.
PharmaCompass also assists you with knowing the Clobutinol HCl API Price utilized in the formulation of products. Clobutinol HCl API Price is not always fixed or binding as the Clobutinol HCl Price is obtained through a variety of data sources. The Clobutinol HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Silomat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Silomat, including repackagers and relabelers. The FDA regulates Silomat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Silomat 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 Silomat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Silomat supplier is an individual or a company that provides Silomat active pharmaceutical ingredient (API) or Silomat finished formulations upon request. The Silomat suppliers may include Silomat API manufacturers, exporters, distributors and traders.
click here to find a list of Silomat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Silomat 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 Silomat 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 Silomat GMP manufacturer or Silomat GMP API supplier for your needs.
A Silomat CoA (Certificate of Analysis) is a formal document that attests to Silomat's compliance with Silomat specifications and serves as a tool for batch-level quality control.
Silomat CoA mostly includes findings from lab analyses of a specific batch. For each Silomat 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.
Silomat may be tested according to a variety of international standards, such as European Pharmacopoeia (Silomat EP), Silomat JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Silomat USP).