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1. 1,2-dioleoyl-sn-glycero-3-phospho(1-rac-glycerol)
2. 1,2-dioleoyl-sn-glycero-3-phosphoglycerol
3. 1,2-dioleoyl-sn-glycero-3-phosphoglycerol, (r-(r*,s*))-(z)-isomer
4. 1,2-dioleoyl-sn-glycero-3-phosphoglycerol, (z)-isomer
5. 1,2-dioleoylphosphatidylglycerol
6. Di-c18-1(c)-pg
7. Dopg
1. Dopg Na, L-
2. Dopg Na, R-
3. Dopg-na, L-
4. Dopg-na, R-
5. 67254-28-8
6. T40u11pg20
7. 1,2-dioleoyl-sn-glycero-3-(phospho-rac-(1-glycerol)), Sodium Salt
8. 1,2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol), Sodium Salt
9. Sodium;[(2r)-2,3-bis[[(z)-octadec-9-enoyl]oxy]propyl] 2,3-dihydroxypropyl Phosphate
10. 9-octadecenoic Acid (9z)-, 1,1'-(1-((((2,3-dihydroxypropoxy)hydroxyphosphinyl)oxy)methyl)-1,2-ethanediyl) Ester, Sodium Salt (1:1)
11. 1,2-dioleoyl-sn-glycero-3-phospho(1-rac-glycerol)
12. Sodium 1,2-dioleoyl-sn-glycero-3-(phospho-rac-(1-glycerol))
13. Sodium (r)-2,3-bis(oleoyloxy)propyl (2,3-dihydroxypropyl) Phosphate
14. 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) Sodium Salt
15. Unii-t40u11pg20
16. Dopg Sodium Salt
17. Dopg-na
18. 1,2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium Salt)
19. Mfcd00070069
20. Dioleoylphosphatidylglycerol Sodium Salt
21. Bp-26300
22. D5318
23. Q27289636
24. 1,2-dioleoyl-sn-glycero-3-phosphoglycerol, Sodium Salt
25. 1-boc-4-phenyl-pyrrolidine-2-carbothioicacidamide
26. 1,2-dioleoyl-sn-glycero-3-(phospho-rac-(1-glycerol)) Sodium
27. 1, 2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol),dioleoyl Phosphatidylglycerole
28. 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) Sodium Salt, >=98.0% (tlc)
29. 18:1 (delta9-cis) Pg, 1,2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium Salt), Chloroform
30. 18:1 (delta9-cis) Pg, 1,2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium Salt), Powder
1. Dopg
| Molecular Weight | 797.0 g/mol |
|---|---|
| Molecular Formula | C42H78NaO10P |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 42 |
| Exact Mass | 796.52302996 g/mol |
| Monoisotopic Mass | 796.52302996 g/mol |
| Topological Polar Surface Area | 152 Ų |
| Heavy Atom Count | 54 |
| Formal Charge | 0 |
| Complexity | 948 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A DOPG manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DOPG, including repackagers and relabelers. The FDA regulates DOPG manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DOPG 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 DOPG supplier is an individual or a company that provides DOPG active pharmaceutical ingredient (API) or DOPG finished formulations upon request. The DOPG suppliers may include DOPG API manufacturers, exporters, distributors and traders.
click here to find a list of DOPG suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DOPG DMF (Drug Master File) is a document detailing the whole manufacturing process of DOPG active pharmaceutical ingredient (API) in detail. Different forms of DOPG DMFs exist exist since differing nations have different regulations, such as DOPG USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DOPG DMF submitted to regulatory agencies in the US is known as a USDMF. DOPG USDMF includes data on DOPG's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DOPG USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DOPG suppliers with USDMF on PharmaCompass.
DOPG 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 DOPG 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 DOPG GMP manufacturer or DOPG GMP API supplier for your needs.
A DOPG CoA (Certificate of Analysis) is a formal document that attests to DOPG's compliance with DOPG specifications and serves as a tool for batch-level quality control.
DOPG CoA mostly includes findings from lab analyses of a specific batch. For each DOPG 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.
DOPG may be tested according to a variety of international standards, such as European Pharmacopoeia (DOPG EP), DOPG JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DOPG USP).
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