Product Name:11-Aminoundecanoic acid

IUPAC Name:11-aminoundecanoic acid

CAS:2432-99-7
Molecular Formula:C11H23NO2
Purity:97%
Catalog Number:CM251633
Molecular Weight:201.31

Packing Unit Available Stock Price($) Quantity
CM251633-500g 1-2 Weeks ȌȌƼ

For R&D use only.

Inquiry Form

   refresh    

Product Details

CAS NO:2432-99-7
Molecular Formula:C11H23NO2
Melting Point:-
Smiles Code:NCCCCCCCCCCC(O)=O
Density:
Catalog Number:CM251633
Molecular Weight:201.31
Boiling Point:334.9°C at 760 mmHg
MDL No:MFCD00008150
Storage:Keep in dark place, inert atmosphere, store at 2-8°C.

Category Infos

PROTAC-Linkers
PROTACs (Proteolytic Targeting Chimeric Molecules) are heterobifunctional protein degraders and are promising targeted therapy candidates for cancer. PROTAC is composed of three parts, one end is connected with the ligand bound by E3 ligase, the other end is connected with the ligand bound by the target protein, and the middle is the linker.
Protac Linkers
where to buy PROTAC-Linkers, Chemenu is research-based manufacturer of pharmaceutical intermediates. We supply Protac Linkers with low price.Warmly welcome new and old customers to visit!

Related Products



Product Other Information

Product Overview 11-Aminoundecanoic acid (11-AUA) is a naturally occurring fatty acid found in a variety of species, including mammals, fish, and insects. It is a non-essential fatty acid, meaning that it is not required for normal metabolic functions. 11-AUA is a long-chain fatty acid, with a molecular weight of 201.31 g/mol, which makes it one of the longest-chain fatty acids found in nature. 11-AUA has been studied for its potential use in a variety of scientific and medical applications, including its use as a drug delivery system, its role in the regulation of gene expression, and its potential to reduce inflammation.
Synthesis and Application 11-Aminoundecanoic acid can be synthesized in a laboratory using a variety of methods. The most common method is to use the reaction of 11-bromoundecanoic acid with an alcohol in the presence of sodium hydroxide. This reaction produces 11-Aminoundecanoic acid and 11-bromoethanol. Other synthetic methods include the reaction of 11-chloroundecanoic acid with an alcohol in the presence of a base, and the reaction of 11-iodoundecanoic acid with an alcohol in the presence of a base. 11-Aminoundecanoic acid has been studied extensively for its potential use in a variety of scientific and medical applications. It has been found to have potential as a drug delivery system, and has been studied for its role in the regulation of gene expression. In addition, 11-Aminoundecanoic acid has been found to have anti-inflammatory effects, and has been studied for its potential to reduce inflammation.
Future Directions Future research into 11-Aminoundecanoic acid could include further studies into its mechanism of action and its potential therapeutic applications. Additionally, further studies into its potential use as a drug delivery system and its role in the regulation of gene expression could be beneficial. Additionally, further studies into its biochemical and physiological effects, as well as its potential to reduce inflammation, could lead to a better understanding of its potential therapeutic uses. Finally, further studies into its potential to reduce the production of certain hormones, such as cortisol and testosterone, could lead to a better understanding of its potential therapeutic uses.