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1. Ethyl 2-(2-methoxyphenoxy)acetate
2. 13078-21-2
3. Ethyl 2-methoxyphenoxyacetate
4. Acetic Acid, (2-methoxyphenoxy)-, Ethyl Ester
5. Fj76e63kzh
6. Einecs 235-977-4
7. Ai3-10576
8. Unii-fj76e63kzh
9. Ethyl-2-methoxyphenoxyacetate
10. Schembl5318188
11. Dtxsid40156737
12. Albb-023455
13. Amy18100
14. Cs-d0564
15. Zinc2149930
16. Mfcd00082657
17. Stk399864
18. Akos000308020
19. (2-methoxyphenoxy)acetic Acid Ethyl Este
20. (o-methoxyphenoxy)acetic Acid Ethyl Ester
21. Ds-15465
22. (2-methoxyphenoxy)acetic Acid Ethyl Ester
23. Db-041985
24. 2-(o-methoxyphenoxy)acetic Acid Ethyl Ester
25. E1241
26. Ft-0608885
27. Ft-0625752
28. A806144
29. Acetic Acid, 2-(2-methoxyphenoxy)-, Ethyl Ester
| Molecular Weight | 210.23 g/mol |
|---|---|
| Molecular Formula | C11H14O4 |
| XLogP3 | 1.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 6 |
| Exact Mass | 210.08920892 g/mol |
| Monoisotopic Mass | 210.08920892 g/mol |
| Topological Polar Surface Area | 44.8 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 193 |
| 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 13078-21-2 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 13078-21-2 manufacturer or 13078-21-2 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 13078-21-2 manufacturer or 13078-21-2 supplier.
PharmaCompass also assists you with knowing the 13078-21-2 API Price utilized in the formulation of products. 13078-21-2 API Price is not always fixed or binding as the 13078-21-2 Price is obtained through a variety of data sources. The 13078-21-2 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 13078-21-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 13078-21-2, including repackagers and relabelers. The FDA regulates 13078-21-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 13078-21-2 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 13078-21-2 supplier is an individual or a company that provides 13078-21-2 active pharmaceutical ingredient (API) or 13078-21-2 finished formulations upon request. The 13078-21-2 suppliers may include 13078-21-2 API manufacturers, exporters, distributors and traders.
13078-21-2 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 13078-21-2 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 13078-21-2 GMP manufacturer or 13078-21-2 GMP API supplier for your needs.
A 13078-21-2 CoA (Certificate of Analysis) is a formal document that attests to 13078-21-2's compliance with 13078-21-2 specifications and serves as a tool for batch-level quality control.
13078-21-2 CoA mostly includes findings from lab analyses of a specific batch. For each 13078-21-2 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.
13078-21-2 may be tested according to a variety of international standards, such as European Pharmacopoeia (13078-21-2 EP), 13078-21-2 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (13078-21-2 USP).
