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1. Ampholan
2. Ampholyt G
3. Ddeg
4. Desimex I
5. Dodecyldi(aminoethyl)glycine
6. Dodecyldiaminoethylglycine
7. Dodicin
8. Dodicin Monohydrochloride
9. Dodicin Monosodium Salt
10. Tego 51
1. 36895-38-2
2. 2-[2-(carboxymethylamino)ethylamino]ethyl-dodecylazanium;chloride
3. Lebon 15 Hydrochloride
4. Tego 51
5. Glycine, N-(2-((2-(dodecylamino)ethyl)amino)ethyl)-, Hydrochloride
| Molecular Weight | 366.0 g/mol |
|---|---|
| Molecular Formula | C18H40ClN3O2 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 19 |
| Exact Mass | 365.2809052 g/mol |
| Monoisotopic Mass | 365.2809052 g/mol |
| Topological Polar Surface Area | 78 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 250 |
| 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 | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Dodicin Hydrochloride 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 Dodicin Hydrochloride manufacturer or Dodicin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dodicin Hydrochloride manufacturer or Dodicin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dodicin Hydrochloride API Price utilized in the formulation of products. Dodicin Hydrochloride API Price is not always fixed or binding as the Dodicin Hydrochloride Price is obtained through a variety of data sources. The Dodicin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tego 51 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tego 51, including repackagers and relabelers. The FDA regulates Tego 51 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tego 51 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 Tego 51 supplier is an individual or a company that provides Tego 51 active pharmaceutical ingredient (API) or Tego 51 finished formulations upon request. The Tego 51 suppliers may include Tego 51 API manufacturers, exporters, distributors and traders.
Tego 51 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 Tego 51 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 Tego 51 GMP manufacturer or Tego 51 GMP API supplier for your needs.
A Tego 51 CoA (Certificate of Analysis) is a formal document that attests to Tego 51's compliance with Tego 51 specifications and serves as a tool for batch-level quality control.
Tego 51 CoA mostly includes findings from lab analyses of a specific batch. For each Tego 51 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.
Tego 51 may be tested according to a variety of international standards, such as European Pharmacopoeia (Tego 51 EP), Tego 51 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tego 51 USP).
