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Supelco

4-Octylphenol

analytical standard

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About This Item

Linear Formula:
CH3(CH2)7C6H4OH
CAS Number:
Molecular Weight:
206.32
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 500 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

150 °C/4 mmHg (lit.)

mp

44-45 °C (lit.)

density

0.961 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-30°C

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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General description

4-Octylphenol belongs to the class of alkylphenolpolyethoxylates, commonly used as non-ionic surfactants in a variety of commercial and industrial applications.

Application

4-Octylphenol may be used as an analytical reference standard for the quantification of the analyte in biological samples and environmental samples using different chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

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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Certificates of Analysis (COA)

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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
Chih-Hsing Hung et al.
Environmental health perspectives, 118(1), 67-72 (2010-01-09)
Exposure to environmental endocrine-disrupting chemicals (EDCs) is often associated with dysregulated immune homeostasis, but the mechanisms of action remain unclear. The aim of this study was to test a hypothesis that EDCs regulate the functions of human dendritic cells, a
Countering matrix effects in environmental liquid chromatography--electrospray ionization tandem mass spectrometry water analysis for endocrine disrupting chemicals
Benijts T, et al.
Journal of Chromatography A, 1029(1-2), 15-15 (2004)
Sumiko Tayama et al.
Mutation research, 649(1-2), 114-125 (2007-10-05)
Some environmental estrogen-like compounds, such as bisphenol A (BPA), 4-nonylphenol (NP), 4-octylphenol (OP), propyl p-hydroxybenzoate (P-PHBA), and butyl p-hydroxybenzoate (B-PHBA), synthetic estrogen, diethylstilbestrol (DES), and natural estrogen, 17beta-estradiol (E2), were studied for their genotoxicity in CHO-K1 cells using sister-chromatid exchange

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