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1. Cis-anethol
2. Dsstox_cid_86
3. Dsstox_rid_75355
4. Dsstox_gsid_20086
5. Nauli ''gum''
6. P-(1-propenyl)anisole
7. Cas-104-46-1
8. 4-(1-propenyl)anisole
9. 1-(p-methoxyphenyl)propene
10. Chebi:2716
11. Mfcd00009284
12. 1-methoxy-4-[1-propenyl]benzene #
13. 1-methoxy-4-prop-1-enylbenzene
14. Ncgc00091493-01
15. Spectrum_001629
16. Specplus_000644
17. Spectrum2_000538
18. Spectrum3_001109
19. Spectrum4_001950
20. Kbiogr_002362
21. Kbioss_002109
22. 1-methoxy-4-propenyl-benzene
23. Divk1c_006740
24. Spbio_000555
25. Chembl3185908
26. Dtxsid4020086
27. Kbio1_001684
28. Kbio2_002109
29. Kbio2_004677
30. Kbio2_007245
31. Kbio3_002038
32. 1-(1-propenyl)-4-methoxybenzene
33. Tox21_111139
34. Tox21_202001
35. Tox21_111139_1
36. Ncgc00091493-09
37. Ncgc00259550-01
38. Sy019737
39. Ft-0600040
40. Ft-0623935
41. Ft-0686721
42. Q27105777
| Molecular Weight | 148.20 g/mol |
|---|---|
| Molecular Formula | C10H12O |
| XLogP3 | 3.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 148.088815002 g/mol |
| Monoisotopic Mass | 148.088815002 g/mol |
| Topological Polar Surface Area | 9.2 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 121 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 1 |
| Covalently Bonded Unit Count | 1 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Anethole 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 Anethole manufacturer or Anethole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Anethole manufacturer or Anethole supplier.
PharmaCompass also assists you with knowing the Anethole API Price utilized in the formulation of products. Anethole API Price is not always fixed or binding as the Anethole Price is obtained through a variety of data sources. The Anethole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anethole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anethole, including repackagers and relabelers. The FDA regulates Anethole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anethole 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 Anethole supplier is an individual or a company that provides Anethole active pharmaceutical ingredient (API) or Anethole finished formulations upon request. The Anethole suppliers may include Anethole API manufacturers, exporters, distributors and traders.
Anethole 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 Anethole 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 Anethole GMP manufacturer or Anethole GMP API supplier for your needs.
A Anethole CoA (Certificate of Analysis) is a formal document that attests to Anethole's compliance with Anethole specifications and serves as a tool for batch-level quality control.
Anethole CoA mostly includes findings from lab analyses of a specific batch. For each Anethole 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.
Anethole may be tested according to a variety of international standards, such as European Pharmacopoeia (Anethole EP), Anethole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Anethole USP).
