24632-92-6

Basic information

• Product Name: phenyl hexadecanoate
• Synonyms: hexadecanoic acid, phenyl ester; Phenyl palmitate
• CAS NO: 24632-92-6
• Molecular Formula: C₂₂H₃₆O₂
• Molecular Weight: 332.52
• Mol File: 24632-92-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 424.4°C at 760 mmHg
• Flash Point: 137.1°C
• Density: 0.928g/cm³
• Vapor Pressure: 2.07E-07mmHg at 25°C
• Refractive Index: 1.483
• CAS DataBase Reference: phenyl hexadecanoate(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl hexadecanoate(24632-92-6)
• EPA Substance Registry System: phenyl hexadecanoate(24632-92-6)

Safety Data

• Hazardous Substances Data: 24632-92-6(Hazardous Substances Data)

Upstream product

• 57-10-3 1-hexadecylcarboxylic acid 
• 108-95-2 phenol 
• 112-67-4 n-hexadecanoyl chloride 

Downstream Products

• 57-10-3 1-hexadecylcarboxylic acid 
• 108-95-2 phenol 
• 1162025-36-6 bis(2-hydroxy-5-n-hexadecylphenyl)methane 
• 1071581-75-3 C₂₂H₃₈N₂O 
• 2589-78-8 4-hexadecylphenol 
• 629-50-5 Tridecane 
• 2589-76-6 1-(4-hydroxyphenyl)hexadecane-1-one 
• 2589-84-6 2-hexadecanoyl phenol 
• 7530-93-0 thiopalmitic acid 

Relevant articles and documents

Synthesis and critical micelle concentration of a series of gemini alkylphenol polyoxyethylene nonionic surfactants

A series of gemini n-alkylphenol polyoxyethylene surfactants (GAP) were successfully synthesized and their molecular structure were confirmed by NMR and FTIR spectrum. Using the same synthesis route, a Gemini nonylphenol polyoxyethylene surfactant (GNP) was synthesized using an industrial nonylphenol product and paraformaldehyde, and its molecular structure was also characterized by 1H-NMR and FTIR spectra. The optimal reaction conditions were established. The critical micelle concentration (CMC) values of GAP were determined by means of Wilhelmy plate method and steady-state fluorescence probe method. The experimental results show how the lengths of the hydrophilic polyoxyethylene chain and the hydrophobic tail alter the CMC values. The CMC values of the GAP are found to be much lower than those of corresponding conventional single tail nonionic surfactants of the polyethoxylated alkylphenol type, which indicates that the gemini species exhibit a better surface activity. AOCS 2011.

Cytotoxicity and antiestrogenicity of a novel series of basic diphenylethylenes

On the premise that it is necessary to develop antiestrogens with a higher cytotoxic component in order to reduce the risks of the development of heterogeneous malignant cell populations in breast cancer, we studied a novel series of basic diphenylethylenes, for the most part devoid of estrogenic activity, with low antiestrogenicity but much enhanced cytotoxicity compared to the reference drug tamoxifen. The main structural features associated with cytotoxicity were E isomery, substituents of five to eight carbons on the ethylene bond, and dibasicity.