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Merck

442850

Supelco

4-Octylphenol

analytical standard

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About This Item

Lineare Formel:
CH3(CH2)7C6H4OH
CAS-Nummer:
Molekulargewicht:
206.32
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12000000
PubChem Substanz-ID:

Qualität

analytical standard

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

ampule of 500 mg

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

150 °C/4 mmHg (lit.)

mp (Schmelzpunkt)

44-45 °C (lit.)

Dichte

0.961 g/mL at 25 °C (lit.)

Anwendung(en)

environmental

Format

neat

Lagertemp.

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

InChIKey

NTDQQZYCCIDJRK-UHFFFAOYSA-N

Angaben zum Gen

rat ... Ar(24208)

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Allgemeine Beschreibung

4-Octylphenol belongs to the class of alkylphenolpolyethoxylates, commonly used as non-ionic surfactants in a variety of commercial and industrial applications.[1]

Anwendung

4-Octylphenol may be used as an analytical reference standard for the quantification of the analyte in biological samples[1] and environmental samples[2] 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.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

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
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
Haidong Zhou et al.
Environmental monitoring and assessment, 161(1-4), 107-121 (2009-02-03)
Occurrence and fate of eight kinds of selected endocrine-disrupting compounds (EDCs) in three sewage treatment plants (STPs) of Beijing, China was investigated. These EDCs, composed of 4-octylphenol (4-OP), 4-n-nonylphenol (4-n-NP), bisphenol A (BPA), estrone (E1), 17alpha-estradiol (17alpha-E2), 17beta-estradiol (E2), estriol
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

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