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1. 2717-15-9
2. 2,2',2''-nitrilotriethanol Oleate
| Molecular Weight | 431.6 g/mol |
|---|---|
| Molecular Formula | C24H49NO5 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 21 |
| Exact Mass | 431.36107366 g/mol |
| Monoisotopic Mass | 431.36107366 g/mol |
| Topological Polar Surface Area | 101 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 289 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 1 |
| Covalently Bonded Unit Count | 2 |
2. 2= SLIGHTLY TOXIC. PROBABLE ORAL LETHAL DOSE (HUMANS) IS 5-15 G/KG; BETWEEN 1 PINT AND 1 QUART FOR 70 KG PERSON (150 LB).
Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. II-276
ABOUT THIS PAGE
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PharmaCompass offers a list of Triethanolamine Oleate 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 Triethanolamine Oleate manufacturer or Triethanolamine Oleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triethanolamine Oleate manufacturer or Triethanolamine Oleate supplier.
PharmaCompass also assists you with knowing the Triethanolamine Oleate API Price utilized in the formulation of products. Triethanolamine Oleate API Price is not always fixed or binding as the Triethanolamine Oleate Price is obtained through a variety of data sources. The Triethanolamine Oleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Triethanolamine Oleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triethanolamine Oleate, including repackagers and relabelers. The FDA regulates Triethanolamine Oleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triethanolamine Oleate 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 Triethanolamine Oleate supplier is an individual or a company that provides Triethanolamine Oleate active pharmaceutical ingredient (API) or Triethanolamine Oleate finished formulations upon request. The Triethanolamine Oleate suppliers may include Triethanolamine Oleate API manufacturers, exporters, distributors and traders.
Triethanolamine Oleate 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 Triethanolamine Oleate 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 Triethanolamine Oleate GMP manufacturer or Triethanolamine Oleate GMP API supplier for your needs.
A Triethanolamine Oleate CoA (Certificate of Analysis) is a formal document that attests to Triethanolamine Oleate's compliance with Triethanolamine Oleate specifications and serves as a tool for batch-level quality control.
Triethanolamine Oleate CoA mostly includes findings from lab analyses of a specific batch. For each Triethanolamine Oleate 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.
Triethanolamine Oleate may be tested according to a variety of international standards, such as European Pharmacopoeia (Triethanolamine Oleate EP), Triethanolamine Oleate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Triethanolamine Oleate USP).
