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1. Solutol Hs 15
2. Solutol-hs15
1. Solutol Hs 15
2. 61909-81-7
3. 105109-85-1
4. 6284-41-9
5. Schembl505106
6. Chebi:9194
7. Dtxsid90909336
8. Nsc7395
9. Chebi:177412
10. Bcp34187
11. Nsc-7395
12. 2-hydroxyethyl-12-hydroxyoctadecanoate
| Molecular Weight | 344.5 g/mol |
|---|---|
| Molecular Formula | C20H40O4 |
| XLogP3 | 5.9 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 19 |
| Exact Mass | 344.29265975 g/mol |
| Monoisotopic Mass | 344.29265975 g/mol |
| Topological Polar Surface Area | 66.8 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 268 |
| 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 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Solutol Hs 15 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Solutol Hs 15 manufacturer or Solutol Hs 15 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Solutol Hs 15 manufacturer or Solutol Hs 15 supplier.
A 2-hydroxyethyl 12-hydroxyoctadecanoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-hydroxyethyl 12-hydroxyoctadecanoate, including repackagers and relabelers. The FDA regulates 2-hydroxyethyl 12-hydroxyoctadecanoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-hydroxyethyl 12-hydroxyoctadecanoate 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 2-hydroxyethyl 12-hydroxyoctadecanoate supplier is an individual or a company that provides 2-hydroxyethyl 12-hydroxyoctadecanoate active pharmaceutical ingredient (API) or 2-hydroxyethyl 12-hydroxyoctadecanoate finished formulations upon request. The 2-hydroxyethyl 12-hydroxyoctadecanoate suppliers may include 2-hydroxyethyl 12-hydroxyoctadecanoate API manufacturers, exporters, distributors and traders.
click here to find a list of 2-hydroxyethyl 12-hydroxyoctadecanoate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A 2-hydroxyethyl 12-hydroxyoctadecanoate DMF (Drug Master File) is a document detailing the whole manufacturing process of 2-hydroxyethyl 12-hydroxyoctadecanoate active pharmaceutical ingredient (API) in detail. Different forms of 2-hydroxyethyl 12-hydroxyoctadecanoate DMFs exist exist since differing nations have different regulations, such as 2-hydroxyethyl 12-hydroxyoctadecanoate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 2-hydroxyethyl 12-hydroxyoctadecanoate DMF submitted to regulatory agencies in the US is known as a USDMF. 2-hydroxyethyl 12-hydroxyoctadecanoate USDMF includes data on 2-hydroxyethyl 12-hydroxyoctadecanoate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 2-hydroxyethyl 12-hydroxyoctadecanoate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 2-hydroxyethyl 12-hydroxyoctadecanoate suppliers with USDMF on PharmaCompass.
2-hydroxyethyl 12-hydroxyoctadecanoate 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 2-hydroxyethyl 12-hydroxyoctadecanoate GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right 2-hydroxyethyl 12-hydroxyoctadecanoate GMP manufacturer or 2-hydroxyethyl 12-hydroxyoctadecanoate GMP API supplier for your needs.
A 2-hydroxyethyl 12-hydroxyoctadecanoate CoA (Certificate of Analysis) is a formal document that attests to 2-hydroxyethyl 12-hydroxyoctadecanoate's compliance with 2-hydroxyethyl 12-hydroxyoctadecanoate specifications and serves as a tool for batch-level quality control.
2-hydroxyethyl 12-hydroxyoctadecanoate CoA mostly includes findings from lab analyses of a specific batch. For each 2-hydroxyethyl 12-hydroxyoctadecanoate 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.
2-hydroxyethyl 12-hydroxyoctadecanoate may be tested according to a variety of international standards, such as European Pharmacopoeia (2-hydroxyethyl 12-hydroxyoctadecanoate EP), 2-hydroxyethyl 12-hydroxyoctadecanoate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-hydroxyethyl 12-hydroxyoctadecanoate USP).
