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1. N-(2-(3-methoxyphenyl)-2-ethylbutyl-(1))-gamma-hydroxybutyramide
1. Embutane
2. 15687-14-6
3. Embutramid
4. N-[2-ethyl-2-(3-methoxyphenyl)butyl]-4-hydroxybutanamide
5. T-61
6. Butanamide, N-(2-ethyl-2-(3-methoxyphenyl)butyl)-4-hydroxy-
7. Hoe 18 680
8. 3p4tqg94t1
9. Hoe-18680
10. Hoe-18-680
11. Embutramida
12. Embutramidum
13. Butanamide, N-[2-ethyl-2-(3-methoxyphenyl)butyl]-4-hydroxy-
14. N-(.beta.,.beta.-diethyl-m-methoxyphenethyl)-4-hydroxybutyramide
15. Embutramidum [inn-latin]
16. Embutramida [inn-spanish]
17. Embutramide [usan:inn:ban]
18. Einecs 239-780-4
19. Hoe 18,680
20. Unii-3p4tqg94t1
21. Tributane
22. Embutane (tn)
23. N-(beta,beta-diethyl-m-methoxyphenethyl)-4-hydroxybutyramide
24. Embutramide [inn]
25. Embutramide (usan/inn)
26. Embutramide [usan]
27. Dsstox_cid_31443
28. Dsstox_rid_97329
29. Embutramide [mart.]
30. Dsstox_gsid_57654
31. Schembl294224
32. Dea No. 2020
33. Embutramid [green Book]
34. Chembl2104668
35. Dtxsid7057654
36. Zinc2018676
37. Tox21_113716
38. Hy-u00009
39. Cs-6631
40. Db01487
41. Embutramide 1.0 Mg/ml In Acetonitrile
42. Hoe-18 680
43. Ncgc00253572-01
44. Cas-15687-14-6
45. D03984
46. Q908240
47. N-[2-ethyl-2-(3-methoxyphenyl)butyl]-4-hydroxybutanamide #
48. N-(.beta.,.beta.-dimethyl-m-methoxyphenethyl)-4-hydroxybutyramide
| Molecular Weight | 293.4 g/mol |
|---|---|
| Molecular Formula | C17H27NO3 |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 9 |
| Exact Mass | 293.19909372 g/mol |
| Monoisotopic Mass | 293.19909372 g/mol |
| Topological Polar Surface Area | 58.6 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 302 |
| 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 | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Embutramide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Embutramide manufacturer or Embutramide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Embutramide manufacturer or Embutramide supplier.
A Embutramida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Embutramida, including repackagers and relabelers. The FDA regulates Embutramida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Embutramida 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 Embutramida supplier is an individual or a company that provides Embutramida active pharmaceutical ingredient (API) or Embutramida finished formulations upon request. The Embutramida suppliers may include Embutramida API manufacturers, exporters, distributors and traders.
click here to find a list of Embutramida suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Embutramida DMF (Drug Master File) is a document detailing the whole manufacturing process of Embutramida active pharmaceutical ingredient (API) in detail. Different forms of Embutramida DMFs exist exist since differing nations have different regulations, such as Embutramida USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Embutramida DMF submitted to regulatory agencies in the US is known as a USDMF. Embutramida USDMF includes data on Embutramida's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Embutramida USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Embutramida suppliers with USDMF on PharmaCompass.
Embutramida 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 Embutramida GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Embutramida GMP manufacturer or Embutramida GMP API supplier for your needs.
A Embutramida CoA (Certificate of Analysis) is a formal document that attests to Embutramida's compliance with Embutramida specifications and serves as a tool for batch-level quality control.
Embutramida CoA mostly includes findings from lab analyses of a specific batch. For each Embutramida 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.
Embutramida may be tested according to a variety of international standards, such as European Pharmacopoeia (Embutramida EP), Embutramida JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Embutramida USP).
