Skip to Content
Merck
CN

384445

4-Octylphenol

99%

Synonym(s):

4-Octylphenol, 4-n-Octylphenol, p-(n-Octyl)phenol, p-Octylphenol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
CH3(CH2)7C6H4OH
CAS Number:
1806-26-4
Molecular Weight:
206.32
NACRES:
NA.22
PubChem Substance ID:
24863997
UNSPSC Code:
12352100
EC Number:
217-302-5
MDL number:
MFCD00036134
Assay:
99%
Form:
solid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

bp

150 °C/4 mmHg (lit.)

mp

44-45 °C (lit.)

InChI key

NTDQQZYCCIDJRK-UHFFFAOYSA-N

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

SMILES string

CCCCCCCCc1ccc(O)cc1

assay

99%

form

solid

density

0.961 g/mL at 25 °C (lit.)

Quality Level

100

Gene Information

rat ... Ar(24208)

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCZ8785
MKCP9386
MKCC6434
MKBW6803V
MKBR5305V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service