Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
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
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. 19961-27-4
2. 2-propanamine, N-ethyl-
3. Ethylisopropylamine
4. N-ethylpropan-2-amine
5. Diethylamine, 1-methyl-
6. Isopropylethylamine
7. N-ethyl-2-propanamine
8. Ethyl(propan-2-yl)amine
9. N-ethyl-n-isopropylamine
10. Isopropylamine, N-ethyl-
11. Ethyl(isopropyl)amine
12. Ethyl-isopropyl-amine
13. W87tph94ob
14. Nsc-165659
15. Isopropyl Ethylamine
16. Isopropylethyl-amine
17. Einecs 243-442-1
18. 1-methyldiethylamine
19. Mfcd00015105
20. Nsc165659
21. Isopropyl Ethyl Amine
22. Isopropyl(ethyl)amine
23. Neipa
24. Nsc 165659
25. N-ethyl Isopropylamine
26. Unii-w87tph94ob
27. (ch3)2chnhch2ch3
28. N-ethylisopropylamine, 98%
29. 2-(ethylamino)propane
30. Dtxsid4066547
31. (c2h5)(i-c3h7)nh
32. Rividppyrintth-uhfffaoysa-
33. Amy13342
34. Str05935
35. Zinc1648991
36. (ethyl)(1-methylethyl)amine
37. Akos000154426
38. Bp-10645
39. Db-000324
40. E0343
41. Ft-0704583
42. En300-40181
43. D77967
44. J-012895
45. Z137545702
Molecular Weight | 87.16 g/mol |
---|---|
Molecular Formula | C5H13N |
XLogP3 | 0.9 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 2 |
Exact Mass | 87.104799419 g/mol |
Monoisotopic Mass | 87.104799419 g/mol |
Topological Polar Surface Area | 12 Ų |
Heavy Atom Count | 6 |
Formal Charge | 0 |
Complexity | 25.1 |
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 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
82
PharmaCompass offers a list of N-Ethylisopropylamine 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 N-Ethylisopropylamine manufacturer or N-Ethylisopropylamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred N-Ethylisopropylamine manufacturer or N-Ethylisopropylamine supplier.
PharmaCompass also assists you with knowing the N-Ethylisopropylamine API Price utilized in the formulation of products. N-Ethylisopropylamine API Price is not always fixed or binding as the N-Ethylisopropylamine Price is obtained through a variety of data sources. The N-Ethylisopropylamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N-Ethylisopropylamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-Ethylisopropylamine, including repackagers and relabelers. The FDA regulates N-Ethylisopropylamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-Ethylisopropylamine 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 N-Ethylisopropylamine supplier is an individual or a company that provides N-Ethylisopropylamine active pharmaceutical ingredient (API) or N-Ethylisopropylamine finished formulations upon request. The N-Ethylisopropylamine suppliers may include N-Ethylisopropylamine API manufacturers, exporters, distributors and traders.
N-Ethylisopropylamine 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 N-Ethylisopropylamine 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 N-Ethylisopropylamine GMP manufacturer or N-Ethylisopropylamine GMP API supplier for your needs.
A N-Ethylisopropylamine CoA (Certificate of Analysis) is a formal document that attests to N-Ethylisopropylamine's compliance with N-Ethylisopropylamine specifications and serves as a tool for batch-level quality control.
N-Ethylisopropylamine CoA mostly includes findings from lab analyses of a specific batch. For each N-Ethylisopropylamine 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.
N-Ethylisopropylamine may be tested according to a variety of international standards, such as European Pharmacopoeia (N-Ethylisopropylamine EP), N-Ethylisopropylamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (N-Ethylisopropylamine USP).