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1. 168127-08-0
2. 61832-41-5
3. Methyl[(z)-1-(methylsulfanyl)-2-nitroethenyl]amine
4. N-methyl-1-(methylthio)-2-nitroethenamine
5. 856lu0gv8h
6. N-methyl-1-(methylthio)-2-nitroethylen-1-amine
7. (z)-n-methyl-1-methylsulfanyl-2-nitroethenamine
8. Ethenamine, N-methyl-1-(methylthio)-2-nitro-, (1z)-
9. (z)-n-methyl-1-(methylthio)-2-nitroethenamine
10. N-methyl-1-(methylsulfanyl)-2-nitro-1-ethylenamine
11. 1-methylamino-1-methylthio-2-nitroethylene
12. 1-methylthio-1-methylamino-2-nitroethylene
13. Methyl[1-(methylsulfanyl)-2-nitroethenyl]amine
14. Unii-856lu0gv8h
15. Schembl85718
16. Mls006011658
17. Str00714
18. Zinc1385210
19. Akos015900644
20. Smr004703410
21. 1-methylamino-1-(methylthio)-2-nitroethylene
22. 1b-021
23. 832m415
24. (z)-1-(methylthio)-1-(methylamino)-2-nitroethene
25. (z)-n-methyl-1-(methylsulfanyl)-2-nitroethenamine
26. Q27269602
| Molecular Weight | 148.19 g/mol |
|---|---|
| Molecular Formula | C4H8N2O2S |
| XLogP3 | 1 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 148.03064868 g/mol |
| Monoisotopic Mass | 148.03064868 g/mol |
| Topological Polar Surface Area | 83.2 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 129 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Unii-856Lu0Gv8H manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Unii-856Lu0Gv8H, including repackagers and relabelers. The FDA regulates Unii-856Lu0Gv8H manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Unii-856Lu0Gv8H 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 Unii-856Lu0Gv8H supplier is an individual or a company that provides Unii-856Lu0Gv8H active pharmaceutical ingredient (API) or Unii-856Lu0Gv8H finished formulations upon request. The Unii-856Lu0Gv8H suppliers may include Unii-856Lu0Gv8H API manufacturers, exporters, distributors and traders.
click here to find a list of Unii-856Lu0Gv8H suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Unii-856Lu0Gv8H DMF (Drug Master File) is a document detailing the whole manufacturing process of Unii-856Lu0Gv8H active pharmaceutical ingredient (API) in detail. Different forms of Unii-856Lu0Gv8H DMFs exist exist since differing nations have different regulations, such as Unii-856Lu0Gv8H USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Unii-856Lu0Gv8H DMF submitted to regulatory agencies in the US is known as a USDMF. Unii-856Lu0Gv8H USDMF includes data on Unii-856Lu0Gv8H's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Unii-856Lu0Gv8H USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Unii-856Lu0Gv8H suppliers with USDMF on PharmaCompass.
Unii-856Lu0Gv8H 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 Unii-856Lu0Gv8H 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 Unii-856Lu0Gv8H GMP manufacturer or Unii-856Lu0Gv8H GMP API supplier for your needs.
A Unii-856Lu0Gv8H CoA (Certificate of Analysis) is a formal document that attests to Unii-856Lu0Gv8H's compliance with Unii-856Lu0Gv8H specifications and serves as a tool for batch-level quality control.
Unii-856Lu0Gv8H CoA mostly includes findings from lab analyses of a specific batch. For each Unii-856Lu0Gv8H 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.
Unii-856Lu0Gv8H may be tested according to a variety of international standards, such as European Pharmacopoeia (Unii-856Lu0Gv8H EP), Unii-856Lu0Gv8H JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Unii-856Lu0Gv8H USP).
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