107827-77-0

Basic information

• Product Name: 5-Dodecanoylaminofluorescein
• Synonyms: 5-(N-dodecanoyl)aminofluorescein;DAF [5-DodecanoylaMinofluorescein];N-(3',6'-dihydroxy-3-oxospiro[2-benzofuran-1,9'-xanthene]-5-yl)dodecanamide
• CAS NO: 107827-77-0
• Molecular Formula: C32H35NO6
• Molecular Weight: 529.25
• Mol File: 107827-77-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 773.655 °C at 760 mmHg
• Flash Point: 421.692 °C
• Appearance: /
• Density: 1.309 g/cm³
• Vapor Pressure: 8.28E-25mmHg at 25°C
• Refractive Index: 1.648
• CAS DataBase Reference: 5-Dodecanoylaminofluorescein(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Dodecanoylaminofluorescein(107827-77-0)
• EPA Substance Registry System: 5-Dodecanoylaminofluorescein(107827-77-0)

Safety Data

• Hazardous Substances Data: 107827-77-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C32H35NO6/c1-2-3-4-5-6-7-8-9-10-11-30(36)33-21-12-15-25-24(18-21)31(37)39-32(25)26-16-13-22(34)19-28(26)38-29-20-23(35)14-17-27(29)32/h12-20,34-35H,2-11H2,1H3,(H,33,36)

Upstream product

• 112-16-3 n-dodecanoyl chloride 
• 3326-34-9 fluoresceinamine 

Related news

5-Dodecanoylaminofluorescein (cas 107827-77-0) as a probe for the determination of critical micelle concentration of detergents using fluorescence anisotropy08/16/2019

A method for determining the critical micelle concentration (CMC) of various detergents based on fluorescence polarization (anisotropy) of the lipophilic probe 5-dodecanoylaminofluorescein is presented. Nonionic, cationic, anionic, and steroid-based detergents can all be evaluated by this method...detailed

Relevant articles and documents

Development of a Gemini Interfacial Antioxidant for Oil in Water Emulsion with Gallic Acid and Dodecyl Gemini Chains

In this study, development of the gemini gallate (GG) interfacial antioxidant for oil in water (O/W) emulsion was performed employing Steglich esterification with gallic acid and dodecyl gemini chains through a prepacked column and peristaltic pump-based purification system. The structural identity and purity of the prepared GG and monogallate (MG) were confirmed by NMR, Fourier transform infrared spectroscopy, and high-performance liquid chromatography-mass spectrometry. Further evaluation revealed that the GG possessed excellent radical scavenging activity and superior antioxidant activity in an O/W emulsion relative to the MG, especially under the condition of a reduced amount of the emulsifier. Microscopic investigation by a fluorescent probe and transmission electron microscopy (TEM) unveiled that the extraordinary antioxidant performance in the O/W emulsion was presumably attributed to preferable interfacial location because of the unique gemini molecular architecture. The superior antioxidant activity of the gemini antioxidant holds great promise for antioxidation in O/W emulsions.