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| | 4-NONYLPHENOL Basic information |
| | 4-NONYLPHENOL Chemical Properties |
| Melting point | 43-44°C | | Boiling point | 293-297 °C | | density | 0.937 g/mL at 25 °C(lit.) | | vapor pressure | 0.109Pa at 25℃ | | refractive index | n20/D 1.511(lit.) | | Fp | >230 °F | | storage temp. | APPROX 20°C
| | solubility | Sparingly Soluble (0.020 g/L) at 25°C. | | form | neat | | pka | 10.15±0.15(Predicted) | | color | Clear colorless | | Specific Gravity | ~1.057 | | Odor | Phenol like | | PH Range | 6 - 8 | | Water Solubility | 6.35mg/L(25 ºC) | | BRN | 2047450 | | Stability: | Stable. Incompatible with strong oxidizing agents. | | LogP | 5.76 | | CAS DataBase Reference | 104-40-5(CAS DataBase Reference) | | EPA Substance Registry System | p-Nonylphenol (104-40-5) |
| | 4-NONYLPHENOL Usage And Synthesis |
| Chemical Properties | viscous colourless liquid with a phenol-like smell | | Uses | 4-nonylphenol is used in the process for the manufacture of 5-nonyl salicylaldoxime, which is used for the selective purification and concentration of copper ions.
| | Uses | Principal use as an intermediate in the
production of nonionic ethoxylated surfactants;
as an intermediate in the manufacture of phosphite
antioxidants used for the plastics and
rubber industries | | Uses | weevil pheromone, shows estrogenic activity | | Definition | ChEBI: A member of the class of phenols that is phenol which is para-substituted with a nonyl group. | | Health Hazard | Nonylphenol is a severe irritant
of the eyes and skin. | | Carcinogenicity | Nonylphenol has recently been shown to
have estrogenic properties, triggering mitotic
activity in rat endometrium and cell proliferation
in estrogen-sensitive tumor cells.9 Potential
toxicity to humans who may be exposed to
nonylphenol through leaching of plastics has
not been determined. |
| | 4-NONYLPHENOL Preparation Products And Raw materials |
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