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IUPAC name 4-Nonylphenol
Other names p-Nonylphenol
CAS number 104-40-5
PubChem 1752
Molecular formula C15H24O
Molar mass 220.35 g/mol
Appearance White crystals
Density 0.94
Melting point

43-45 °C

Boiling point

180-181 °C

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Nonylphenol is an organic compound of the wider family of alkylphenols. It is a product of industrial synthesis formed during the alkylation process of phenols, particularly in the synthesis of polyethoxylate detergents. Because of their man-made origins, nonylphenols are classified as xenobiotics. In nonylphenols, a hydrocarbon chain of nine carbon atoms is attached to the phenol ring in either the ortho (2), meta (3), or para (4) position, with the most common ring isomers being ortho or para (e.g. figure 1 para-nonylphenol). Moreover, the alkyl chains can exist as either linear n-alkyl chains, or complex branched chains. Nonylphenol is commonly obtained as a mixture of isomers, and is thus usually found as a pale yellow liquid at room temperature with a freezing point of -10°C and a boiling point of 295-320°C. However, pure isomers of nonylphenol crystallize readily at room temperatures and for example, para-n-nonylphenol, forms white crystals at room temperature.

Additional recommended knowledge

Ethoxylated alkylphenols, alkylphenol ethoxylates (APE), are used as industrial surfactants in manufacture of wool and metal, as emulsifiers for emulsion polymerization, in laboratory detergents, and pesticides. APEs are a component of some household detergents outside of Europe; within Europe, due to environmental concerns, they are replaced by more expensive but safer alcohol ethoxylates.

Nonoxynol-9, one of the APEs, is used as a surfactant in cleaning and cosmetic products, and as a spermicide in contraceptives.

Nonylphenol, and a related compound tert-octylphenol, were first detected as an air pollutant in New York City and New Jersey, probably due to its evaporation from the Hudson river and other smaller rivers in the region that routinely receive municipal wastewaters. It is possible that the atmosphere is a destructive sink for nonylphenol as it is probably reactive with atomspheric radicals and/or is photoactive.

Nonylphenol and nonyphenol ethoxylates have been banned in the European Union as a hazard to human and environmental safety.

Biochemically, p-nonylphenol and many of its derivatives act as a xenoestrogen.

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Nonylphenol". A list of authors is available in Wikipedia.
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