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1. Butyl 2-hydroxybenzoate
2. 2052-14-4
3. N-butyl Salicylate
4. Benzoic Acid, 2-hydroxy-, Butyl Ester
5. Butyl O-hydroxybenzoate
6. N-butyl O-hydroxybenzoate
7. Salicylic Acid, Butyl Ester
8. Salicylic Acid Butyl Ester
9. Salicylic Acid N-butyl Ester
10. Fema No. 3650
11. Butyl (2-hydroxyphenyl)formate
12. 1322-01-6
13. Nsc 1511
14. Benzoic Acid, Hydroxy-, Butyl Ester
15. Nsc 403676
16. 2-hydroxybenzoic Acid Butyl Ester
17. Qpr9lm8vzo
18. Nsc-1511
19. 2-hydroxy-benzoic Acid, Butyl Ester
20. Nsc-403676
21. Wln: 4ovr Bq
22. Unii-qpr9lm8vzo
23. Einecs 218-142-9
24. Brn 2208904
25. Brunol
26. Ai3-00512
27. Butoxycarbonylphenol
28. Butyl 2-oxidanylbenzoate
29. Butyl Salicylate, >=99%
30. Schembl62565
31. Salicylic Acid, N-butyl Ester
32. Butyl Salicylate [fhfi]
33. Chembl2260713
34. Dtxsid8062153
35. Fema 3650
36. Yfduwsbgvpbwkf-uhfffaoysa-
37. Nsc1511
38. Chebi:173949
39. 2-hydroxy-benzoic Acid Butyl Ester
40. Zinc1576866
41. Mfcd00020038
42. Nsc403676
43. Akos015890784
44. Cs-w010656
45. Bs-42154
46. Ft-0603583
47. S0010
48. A814643
49. Q27287442
| Molecular Weight | 194.23 g/mol |
|---|---|
| Molecular Formula | C11H14O3 |
| XLogP3 | 4.6 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 194.094294304 g/mol |
| Monoisotopic Mass | 194.094294304 g/mol |
| Topological Polar Surface Area | 46.5 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 179 |
| 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 |
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ABOUT THIS PAGE
A Butyl Salicylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Butyl Salicylate, including repackagers and relabelers. The FDA regulates Butyl Salicylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Butyl Salicylate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Butyl Salicylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Butyl Salicylate supplier is an individual or a company that provides Butyl Salicylate active pharmaceutical ingredient (API) or Butyl Salicylate finished formulations upon request. The Butyl Salicylate suppliers may include Butyl Salicylate API manufacturers, exporters, distributors and traders.
click here to find a list of Butyl Salicylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Butyl Salicylate 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 Butyl Salicylate 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 Butyl Salicylate GMP manufacturer or Butyl Salicylate GMP API supplier for your needs.
A Butyl Salicylate CoA (Certificate of Analysis) is a formal document that attests to Butyl Salicylate's compliance with Butyl Salicylate specifications and serves as a tool for batch-level quality control.
Butyl Salicylate CoA mostly includes findings from lab analyses of a specific batch. For each Butyl Salicylate 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.
Butyl Salicylate may be tested according to a variety of international standards, such as European Pharmacopoeia (Butyl Salicylate EP), Butyl Salicylate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Butyl Salicylate USP).
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