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Supelco

4-Octylphenol

analytical standard

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About This Item

Linear Formula:
CH3(CH2)7C6H4OH
CAS Number:
1806-26-4
Molecular Weight:
206.32
EC Number:
217-302-5
MDL number:
MFCD00036134
UNSPSC Code:
12000000
PubChem Substance ID:
24868025

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
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
LRAD4735
LRAD2121
LRAC4180
LRAB8046
LC26027V

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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)
Qian Bian et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 44(8), 1355-1361 (2006-04-25)
The aim of the present study is to investigate the toxic effect of 4-tert-octylphenol (OP) on testicular functions of rats. Male Sprague-Dawley rats were orally administered different doses of OP at the levels of 0 (control), 50, 150 and 450
K A Langdon et al.
Chemosphere, 84(11), 1556-1562 (2011-06-28)
Land application of biosolids is common practice in many countries, however, there are some potential risks associated with the presence of contaminants within the biosolids. This laboratory study examined the degradation of four commonly found organic compounds, 4-nonylphenol, 4-t-octylphenol, bisphenol
Marie-Claude Perron et al.
Environmental research, 111(4), 520-529 (2011-03-29)
Among the numerous toxics found in the aquatic environment, endocrine disrupters can interfere with the normal functioning of the endocrine system of several organisms, leading to important consequences. Even if algae and cyanobacteria are non-target organisms without endocrine system, our
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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