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1. Schembl27413
2. Sodium Dodecyl Benzenesulphonate
3. Sodium Dodecylbenzene Sulphonate
4. Sodium N-dodecylbenzenesulfonate
5. Sodium N-dode Cylbenzenesulfonate
6. Sodium N-dodecylbenzene-sulfonate
7. A817670
Molecular Weight | 349.5 g/mol |
---|---|
Molecular Formula | C18H30NaO3S |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 13 |
Exact Mass | 349.18133527 g/mol |
Monoisotopic Mass | 349.18133527 g/mol |
Topological Polar Surface Area | 51.8 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 340 |
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 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Sodium Dodecylbenzenesulphonate 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 Sodium Dodecylbenzenesulphonate manufacturer or Sodium Dodecylbenzenesulphonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Dodecylbenzenesulphonate manufacturer or Sodium Dodecylbenzenesulphonate supplier.
PharmaCompass also assists you with knowing the Sodium Dodecylbenzenesulphonate API Price utilized in the formulation of products. Sodium Dodecylbenzenesulphonate API Price is not always fixed or binding as the Sodium Dodecylbenzenesulphonate Price is obtained through a variety of data sources. The Sodium Dodecylbenzenesulphonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Dodecylbenzenesulphonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Dodecylbenzenesulphonate, including repackagers and relabelers. The FDA regulates Sodium Dodecylbenzenesulphonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Dodecylbenzenesulphonate 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 Sodium Dodecylbenzenesulphonate supplier is an individual or a company that provides Sodium Dodecylbenzenesulphonate active pharmaceutical ingredient (API) or Sodium Dodecylbenzenesulphonate finished formulations upon request. The Sodium Dodecylbenzenesulphonate suppliers may include Sodium Dodecylbenzenesulphonate API manufacturers, exporters, distributors and traders.
Sodium Dodecylbenzenesulphonate 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 Sodium Dodecylbenzenesulphonate 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 Sodium Dodecylbenzenesulphonate GMP manufacturer or Sodium Dodecylbenzenesulphonate GMP API supplier for your needs.
A Sodium Dodecylbenzenesulphonate CoA (Certificate of Analysis) is a formal document that attests to Sodium Dodecylbenzenesulphonate's compliance with Sodium Dodecylbenzenesulphonate specifications and serves as a tool for batch-level quality control.
Sodium Dodecylbenzenesulphonate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Dodecylbenzenesulphonate 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.
Sodium Dodecylbenzenesulphonate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Dodecylbenzenesulphonate EP), Sodium Dodecylbenzenesulphonate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Dodecylbenzenesulphonate USP).