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Sigma-Aldrich

4-Octylphenol

99%

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Synonym(s):
4-Octylphenol, 4-n-Octylphenol, p-(n-Octyl)phenol, p-Octylphenol
Linear Formula:
CH3(CH2)7C6H4OH
CAS Number:
1806-26-4
Molecular Weight:
206.32
EC Number:
217-302-5
MDL number:
MFCD00036134
UNSPSC Code:
12352100
PubChem Substance ID:
24863997
NACRES:
NA.22

Quality Level

100

Assay

99%

form

solid

bp

150 °C/4 mmHg (lit.)

mp

44-45 °C (lit.)

density

0.961 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCc1ccc(O)cc1

InChI

1S/C14H22O/c1-2-3-4-5-6-7-8-13-9-11-14(15)12-10-13/h9-12,15H,2-8H2,1H3

InChI key

NTDQQZYCCIDJRK-UHFFFAOYSA-N

Gene Information

rat ... Ar(24208)

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Carme Valls-Cantenys et al.
Journal of separation science, 37(24), 3706-3713 (2014-10-10)
Simple, precise, and low-cost methods for the simultaneous determination of phenolic endocrine disrupting compounds such as bisphenol A, trichlorophenol, pentachlorophenol, 4-nonylphenol, and 4-octylphenol in water samples were developed. The Direct, in situ derivatization methods are based on polydimethylsiloxane rod extraction
Yu-Hai Liu et al.
Huan jing ke xue= Huanjing kexue, 35(6), 2209-2215 (2014-08-28)
The 206 nm irradiation from excilamp was able to directly photo-degrade 4-nonylphenol (4-NP) and 4-octylphenol (4-OP), but it could not oxidize them completely into CO2. Under the same irradiation condition, the removal efficiency of 4-OP was higher than that of
Ana-Maria Gurban et al.
Talanta, 85(4), 2007-2013 (2011-08-30)
Simple and low cost biosensor based on screen-printed electrode for sensitive detection of some alkylphenols was developed, by entrapment of HRP in a nanocomposite gel based on single-walled carbon nanotubes (SWCNTs) and 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF(6)]) ionic liquid. Raman and FTIR
Jayne V Brian et al.
Environmental health perspectives, 113(6), 721-728 (2005-06-03)
Existing environmental risk assessment procedures are limited in their ability to evaluate the combined effects of chemical mixtures. We investigated the implications of this by analyzing the combined effects of a multicomponent mixture of five estrogenic chemicals using vitellogenin induction
R White et al.
Endocrinology, 135(1), 175-182 (1994-07-01)
We show that a number of alkylphenolic compounds, used in a variety of commercial products and found in river water, are estrogenic in fish, birds, and mammals. 4-Octylphenol (OP), 4-nonylphenol, 4-nonylphenoxycarboxylic acid, and 4-nonylphenoldiethoxylate were each capable of stimulating vitellogenin
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