63632-65-5

Basic information

• Product Name: 11-iodoundecanoic acid
• Synonyms: undecanoic acid, 11-iodo-
• CAS NO: 63632-65-5
• Molecular Formula: C₁₁H₂₁IO₂
• Molecular Weight: 312.1877
• Mol File: 63632-65-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 371.385°C at 760 mmHg
• Flash Point: 178.407°C
• Density: 1.396g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.516
• CAS DataBase Reference: 11-iodoundecanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 11-iodoundecanoic acid(63632-65-5)
• EPA Substance Registry System: 11-iodoundecanoic acid(63632-65-5)

Safety Data

• Hazardous Substances Data: 63632-65-5(Hazardous Substances Data)

Usage

Type of compound

Iodinated fatty acid derivative

Common use

Pharmaceutical research as a tracer for the study of fatty acid metabolism and oxidation

Specific applications

Studying the uptake and metabolism of fatty acids in various tissues and cells, research on the mechanisms of heart disease, diabetes, and obesity

Additional use

Radiotracer in positron emission tomography (PET) imaging studies to visualize and quantify fatty acid metabolism in the body

Importance

Applications in both basic research and medical imaging for the study of fatty acid metabolism and related diseases.

Upstream product

• 2834-05-1 11-bromoundecanoic acid 
• 112-38-9 10-undecenoic acid 
• 2777-65-3 undec-10-ynoic acid 
• 1725-03-7 oxacyclododecan-2-one 

Downstream Products

• 53821-20-8 ethyl 11-iodoundecanoate 
• 14502-46-6 ω-tridecyn-1-oic acid 
• 105962-63-8 11-Phenylsulfanyl-undecanoic acid methyl ester 
• 123053-76-9 ethyl 11-(phenylthio)undecanoate 
• 18202-11-4 tridec-12-yn-1-ol 
• 53821-24-2 Ethyl 17-Benzoxyheptadecanoat 
• 53821-23-1 21-docosenoic acid 
• 71310-21-9 11-mercaptounadecanoic acid 
• 108045-05-2 methyl (Z)-hexacos-17-enoate 
• 4082-55-7 nonacosanoic acid methyl ester 
• 19307-16-5 Octadec-17-ensaeure 
• 850347-60-3 (Z)-Docos-11-enedioic acid benzyl ester (S)-2-tert-butoxycarbonylamino-1-undecanoyloxymethyl-ethyl ester 
• 850347-54-5 (Z)-Docos-11-enedioic acid benzyl ester 3-hydroxy-2-hydroxymethyl-2-methyl-propyl ester 
• 850347-51-2 (Z)-21-(4-Methyl-2,6,7-trioxa-bicyclo[2.2.2]oct-1-yl)-henicos-11-enoic acid benzyl ester 

Relevant articles and documents

Testing Theoretical Models of Micelles. The Acetylenic Probe

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Design and synthesis of asymmetric acyclic phospholipid bolaamphiphiles

(Chemical Equation Presented) A synthetic route was devised for the generation of asymmetric lipid bolaamphiphiles through the sequential esterification of an alkyldioic acid, bearing distinct terminal protecting groups, with propanylamine and lyso-phosph

Synthesis of Very Long Fatty Acid Methyl Esters

Phosphoranes, produced by treating alkyltriphenylphosphonium bromides with lithium hexamethyldisilazide, reacted with ω-oxo esters to give modest yields of the corresponding methyl cis-alkenoates.By an alternative method, treatment of ω-iodo esters with the complexes formed from reactions of alkylcopper(I) and Grignard reagents gave methyl alkanoates, cis-alkenoates, and methylene-interrupted cis,cis-alka-dienoates and cis,cis,cis-trienoates.The stereochemical integrity of the esters was determined by 13C NMR spectroscopy.