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1. 68585-34-2
2. Disodium;1-dodecoxydodecane;sulfate
3. 1335-72-4
4. Sodiumlaurylethersulfate
5. Ft-0775147
| Molecular Weight | 496.7 g/mol |
|---|---|
| Molecular Formula | C24H50Na2O5S |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 22 |
| Exact Mass | 496.31743443 g/mol |
| Monoisotopic Mass | 496.31743443 g/mol |
| Topological Polar Surface Area | 97.9 Ų |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 254 |
| 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 | 4 |
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ABOUT THIS PAGE
A Sodium Lauryl Ether Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Lauryl Ether Sulfate, including repackagers and relabelers. The FDA regulates Sodium Lauryl Ether Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Lauryl Ether Sulfate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Sodium Lauryl Ether Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Lauryl Ether Sulfate supplier is an individual or a company that provides Sodium Lauryl Ether Sulfate active pharmaceutical ingredient (API) or Sodium Lauryl Ether Sulfate finished formulations upon request. The Sodium Lauryl Ether Sulfate suppliers may include Sodium Lauryl Ether Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Lauryl Ether Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Sodium Lauryl Ether Sulfate 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 Lauryl Ether Sulfate 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 Lauryl Ether Sulfate GMP manufacturer or Sodium Lauryl Ether Sulfate GMP API supplier for your needs.
A Sodium Lauryl Ether Sulfate CoA (Certificate of Analysis) is a formal document that attests to Sodium Lauryl Ether Sulfate's compliance with Sodium Lauryl Ether Sulfate specifications and serves as a tool for batch-level quality control.
Sodium Lauryl Ether Sulfate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Lauryl Ether Sulfate 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 Lauryl Ether Sulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Lauryl Ether Sulfate EP), Sodium Lauryl Ether Sulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Lauryl Ether Sulfate USP).
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