2536-38-1

Usage

Uses

Used in Chemical Synthesis:
Octadecanoic acid, 18-bromois used as a chemical intermediate for the synthesis of various compounds. Its reactive bromine atom allows for easy substitution in chemical reactions, making it a valuable component in the production of other organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Octadecanoic acid, 18-bromois used as a precursor in the development of new drugs. Its unique structure and reactivity can contribute to the creation of novel therapeutic agents with potential applications in various medical fields.
Used in Research and Development:
Octadecanoic acid, 18-bromois utilized in research and development settings to study the properties and reactions of alpha-bromo carboxylic acids. Its presence in certain marine organisms also makes it a subject of interest for researchers exploring natural sources of chemical compounds and their potential applications.
Used in Specialty Chemicals Production:
Due to its unique properties, Octadecanoic acid, 18-bromois used in the production of specialty chemicals that cater to specific industries. These may include industries that require high-performance materials or those that need to develop new chemical processes.

Upstream product

• 3155-42-8 18-hydroxystearic acid 
• 55362-80-6 9-bromononan-1-ol 
• 55695-90-4 2-(9-bromononyloxy)tetrahydropyran 
• 3155-43-9 octadecane-1,18-diol 
• 59101-17-6 18-bromooctadecan-1-ol 

Downstream Products

• 59101-17-6 18-bromooctadecan-1-ol 
• 70794-53-5 <1-(ethoxycarbonyl)decyl>triphenylphosphonium iodide 
• 96303-16-1 28-(tetrahydropyran-2-yloxy)-19-octacosynoic acid 
• 96303-22-9 (Z)-28-hydroxy-19-octacosenoic acid 
• 96303-18-3 28-hydroxy-19-octacosynoic acid 
• 506-17-2 cis-vaccenic acid 
• 6198-58-9 methyl (Z)-vaccenate 
• 137202-20-1 ethyl (11Z)-octadec-11-enoate 
• 59100-67-3 4-(18-Mercapto-octadecyloxy)-benzoic acid 
• 59100-04-8 4-(18-Hydroxy-octadecyloxy)-benzoic acid methyl ester 
• 59100-18-4 4-(18-Acetylsulfanyl-octadecyloxy)-benzoic acid methyl ester 
• 59100-11-7 4-(18-Methanesulfonyloxy-octadecyloxy)-benzoic acid methyl ester 
• 1199580-32-9 tert-butyl 18-bromooctadecanoate 

Relevant academic research and scientific papers

Compositions and methods for binding lysophosphatidic acid

Compositions and methods for making and using anti-LPA agents, for example, monoclonal antibodies, are described. Variable domain and complementarity determining region amino acid sequences of several monoclonal antibodies against LPA are disclosed, as is a consensus anti-LPA monoclonal antibody variable domain sequence.

New GM1 ganglioside derivatives for selective single and double labelling of the natural glycosphingolipid skeleton

Selective single and double labelling of the natural ganglioside GM1. enables one to introduce various markers into different parts of the glycosphingolipid molecule without changing the natural skeleton. To that end, N-Fmoc-2amino-, N-Fmoc-18-amino- and S-(ethoxythiocarbonyl)-18mercaptostearic acids have been prepared, and. coupled with the primary amino group in the sphingosine part of lyso-GM1 and. deAc-deAcyl-GM1. gangliosides. The products of these coupling reactions - building blocks 16a, 16b, 16c, 26 and 27 - may be used for the synthesis of GM1 derivatives with one or two fluorescent dye moieties or other labels of various polarities. Examples of various labelling strategies, using hydrophilic and lipophilic photostable fluorescent dyes, have been made available. The GM1. derivatives 17a, 22a and 23c labelled with the fluorescent dye ATTO 647N or the doubly labelled derivative 25b can be used as probes in fluorescence correlation spectroscopy (in conventional, microscopy or stimulated emission depletion nanoscopy) to study the diffusion of lipid analogues in model or live cell membranes.