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1. 2-hydroxypropionic Acid Dodecyl Ester
2. Dodecyl 2-hydroxypropionate
3. Eutanol G
4. Lauryl Lactate
1. 6283-92-7
2. Lauryl Lactate
3. Dodecyl 2-hydroxypropanoate
4. Dodecyl Lactate
5. Cyclochem Lvl
6. Lactic Acid Dodecyl Ester
7. Ceraphyl 31
8. Lactic Acid, Dodecyl Ester
9. G5su0bfk7o
10. Nsc-7752
11. Crodamol Ll
12. Propanoic Acid,2-hydroxy-, Dodecyl Ester
13. Nsc 7752
14. Unii-g5su0bfk7o
15. Ceraphyl 3
16. Einecs 228-504-8
17. Lauryl Lactate, Aldrichcpr
18. Lauryl Lactate [ii]
19. Schembl33838
20. Lauryl Lactate [inci]
21. (+/-)-lauryl Lactate
22. Fema No. 4482
23. Dtxsid40863737
24. Nsc7752
25. Amy22510
26. Lauryl Lactate, (+/-)-
27. Akos015950776
28. 2-hydroxypropanoic Acid, Dodecyl Ester
29. Ft-0670699
30. 10.14272/qqqmublxdafbrh-uhfffaoysa-n
31. Doi:10.14272/qqqmublxdafbrh-uhfffaoysa-n
32. Q27278801
33. 196321-22-9
| Molecular Weight | 258.40 g/mol |
|---|---|
| Molecular Formula | C15H30O3 |
| XLogP3 | 5.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 13 |
| Exact Mass | 258.21949481 g/mol |
| Monoisotopic Mass | 258.21949481 g/mol |
| Topological Polar Surface Area | 46.5 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 192 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Cyclochem Lvl 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 Cyclochem Lvl manufacturer or Cyclochem Lvl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclochem Lvl manufacturer or Cyclochem Lvl supplier.
PharmaCompass also assists you with knowing the Cyclochem Lvl API Price utilized in the formulation of products. Cyclochem Lvl API Price is not always fixed or binding as the Cyclochem Lvl Price is obtained through a variety of data sources. The Cyclochem Lvl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eutanol G manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eutanol G, including repackagers and relabelers. The FDA regulates Eutanol G manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eutanol G 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 Eutanol G supplier is an individual or a company that provides Eutanol G active pharmaceutical ingredient (API) or Eutanol G finished formulations upon request. The Eutanol G suppliers may include Eutanol G API manufacturers, exporters, distributors and traders.
Eutanol G 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 Eutanol G 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 Eutanol G GMP manufacturer or Eutanol G GMP API supplier for your needs.
A Eutanol G CoA (Certificate of Analysis) is a formal document that attests to Eutanol G's compliance with Eutanol G specifications and serves as a tool for batch-level quality control.
Eutanol G CoA mostly includes findings from lab analyses of a specific batch. For each Eutanol G 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.
Eutanol G may be tested according to a variety of international standards, such as European Pharmacopoeia (Eutanol G EP), Eutanol G JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eutanol G USP).
