isononylphenol

• CAT Number: M065035
• CAS Number: 11066-49-2
• Molecular Formula: C15H24O
• Molecular Weight: 220.35
• Purity: ≥95%
• Synonyms: 3-Nonylphenol; m-Nonylphenol.
• Storage: Store at -20°C
• IUPAC Name: 2-(7-methyloctyl)phenol
• InChI: InChI=1S/C15H24O/c1-13(2)9-5-3-4-6-10-14-11-7-8-12-15(14)16/h7-8,11-13,16H,3-6,9-10H2,1-2H3
• InChIKey: UZVAZDQMPUOHKP-UHFFFAOYSA-N
• SMILES: CC(C)CCCCCCC1=CC=CC=C1O

Isononylphenol（Cat No.:M065035）, a type of alkylphenol, is a compound used in various industrial applications, notably in the production of detergents, lubricants, and plasticizers. It’s also found in certain consumer products like paints and pesticides. However, concerns have been raised regarding its potential environmental and health impacts. Studies suggest it may disrupt hormone systems in aquatic organisms, leading to adverse effects on reproduction and development.

Reference

[1]. Magn Reson Chem. 2013 Jul;51(7):424-30. doi: 10.1002/mrc.3968. Epub 2013 May 23.
Micelle structure and molecular self-diffusion in isononylphenol ethoxylate-water systems.
Arkhipov VP(1), Potapova EF, Antzutkin ON, Filippov AV.
Author information: (1)Kazan National Research Technological University, 420015, Kazan, Russia.
The structure and dynamic properties of micellar solutions of nonionic surfactants of a series of isononylphenol ethoxylates, C9H19C6H4O(C2H4O)(n)H (where n = 6,8,9,10, and 12), were studied by NMR diffusometry, dynamic light scattering, and viscosimetry. The sizes of the micelles were determined for different surfactants and at different surfactant concentrations. The numbers of water molecules bound by a micelle and by one oxyethylene group of the surfactant were estimated.
DOI: 10.1002/mrc.3968 PMID: 23703737

[2]. Micelles of Oxyethylated Isononylphenols in Aqueous Solutions and Hydrophilic–Lipophilic Balance
Victor P. Arkhipov, Ruslan Arkhipov, and Andrei Filippov
Abstract:
We have measured the self-diffusion coefficients and calculated the effective hydrodynamic radii of micelles of ethoxylated isononylphenols in aqueous solutions in the presence of sodium chloride, as well as in their binary mutual mixtures, when approaching cloudy conditions. These cloudy conditions were created by an increase in temperature, a change in the concentration of an electrolyte in the solution, or a mutual ratio of neonols in their binary mixtures. The results are discussed within the concept of the hydrophilic–lipophilic balance.
ACS Omega 2020 5 (43), 28224-28232
DOI: 10.1021/acsomega.0c04041