Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. Dodecanoyl Chloride
2. 112-16-3
3. N-dodecanoyl Chloride
4. Lauroylchloride
5. Lauric Acid Chloride
6. Dodecanoic Acid, Chloride
7. 9lhl10777i
8. Mfcd00000740
9. Unii-9lhl10777i
10. Dodecanoylchloride
11. Hsdb 5567
12. Einecs 203-941-7
13. Lauric Acid, Chloride
14. Ai3-52409
15. Lauroyl Chloride, 98%
16. Ec 203-941-7
17. Schembl160647
18. Ch3(ch2)10c(o)cl
19. Dodecanoic Acid,chloride
20. Chembl3561663
21. Dtxsid5044368
22. Dodecanoyl Chloride [hsdb]
23. Str10231
24. Zinc2041056
25. Tox21_303812
26. Akos009031493
27. Db14670
28. Ncgc00357016-01
29. Cas-112-16-3
30. Db-041047
31. D0972
32. Ft-0627725
33. Dodecanoyl Chloride, Purum, >=97.5% (gc)
34. En300-19952
35. 1,3-dimethyl-1-methylazo-urea;lauroyl Chloride
36. A802503
37. W-108656
38. Q27272707
1. N-dodecanoyl Chloride
2. Lauric Acid Chloride
3. Laurel Acetyl Chlorine
4. Dodecanoyl Chloride
5. Lauroylchloride
6. Cas 112-16-3
7. Dodecanoic Acid, Chloride
| Molecular Weight | 218.76 g/mol |
|---|---|
| Molecular Formula | C12H23ClO |
| XLogP3 | 5.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 10 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 17.1 |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 134 |
| 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
23
PharmaCompass offers a list of EN300-19952 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 EN300-19952 manufacturer or EN300-19952 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred EN300-19952 manufacturer or EN300-19952 supplier.
PharmaCompass also assists you with knowing the EN300-19952 API Price utilized in the formulation of products. EN300-19952 API Price is not always fixed or binding as the EN300-19952 Price is obtained through a variety of data sources. The EN300-19952 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EN300-19952 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EN300-19952, including repackagers and relabelers. The FDA regulates EN300-19952 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EN300-19952 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 EN300-19952 supplier is an individual or a company that provides EN300-19952 active pharmaceutical ingredient (API) or EN300-19952 finished formulations upon request. The EN300-19952 suppliers may include EN300-19952 API manufacturers, exporters, distributors and traders.
EN300-19952 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 EN300-19952 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 EN300-19952 GMP manufacturer or EN300-19952 GMP API supplier for your needs.
A EN300-19952 CoA (Certificate of Analysis) is a formal document that attests to EN300-19952's compliance with EN300-19952 specifications and serves as a tool for batch-level quality control.
EN300-19952 CoA mostly includes findings from lab analyses of a specific batch. For each EN300-19952 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.
EN300-19952 may be tested according to a variety of international standards, such as European Pharmacopoeia (EN300-19952 EP), EN300-19952 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (EN300-19952 USP).
