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4-tert.-Octylphenol -Lösung

1000 μg/mL in acetone, analytical standard

Synonym(e):

4-(1,1,3,3-Tetramethyl-butyl)-phenol -Lösung

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About This Item

Empirische Formel (Hill-System):
C14H22O
CAS-Nummer:
140-66-9
Molekulargewicht:
206.32
MDL-Nummer:
MFCD00002368
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329754229
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Haltbarkeit

limited shelf life, expiry date on the label

Konzentration

1000 μg/mL in acetone

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

environmental

Format

single component solution

Lagertemp.

−20°C

SMILES String

CC(C)(C)CC(C)(C)c1ccc(O)cc1

InChI

1S/C14H22O/c1-13(2,3)10-14(4,5)11-6-8-12(15)9-7-11/h6-9,15H,10H2,1-5H3

InChIKey

ISAVYTVYFVQUDY-UHFFFAOYSA-N

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Allgemeine Beschreibung

4-tert-Octylphenols are classified under the alkylphenol family of compounds.

Anwendung

4-tert-Octylphenol may be used as an analytical reference standard for the determination of the analyte in:
  • Human biological samples and water samples by stir bar sorptive extraction (SBSE) and thermal desorption–gas chromatography-mass spectrometry (TD-GC-MS) operating in the selected ion monitoring (SIM) mode of detection.
  • Surface water samples by GC-MS with SIM detection.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Ähnliches Produkt

Produkt-Nr.
Beschreibung
Preisangaben

442858

4-tert-Octylphenol, analytical standard

Piktogramme

FlameExclamation mark
GHS02,GHS07

Signalwort

Danger

Gefahreneinstufungen

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Zielorgane

Central nervous system

Zusätzliche Gefahrenhinweise

EUH066

WGK

WGK 2

Flammpunkt (°F)

1.4 °F

Flammpunkt (°C)

-17.0 °C

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCK5257
BCCJ6819
BCCH3160
BCCG4742
BCCF1257

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Die Dokumentenbibliothek aufrufen

Determination of 4-tert-octylphenol, 4-nonylphenol and bisphenol A in surface waters from the Haihe River in Tianjin by gas chromatography-mass spectrometry with selected ion monitoring.
Jin X, et al.
Chemosphere, 56(11), 1113-1119 (2004)
Determination of 4-nonylphenol and 4-tert.-octylphenol in water samples by stir bar sorptive extraction and thermal desorption-gas chromatography-mass spectrometry.
Kawaguchi M, et al.
Analytica Chimica Acta, 505(2), 217-222 (2004)
Stir bar sorptive extraction and thermal desorption-gas chromatography-mass spectrometry for the measurement of 4-nonylphenol and 4-tert-octylphenol in human biological samples.
Kawaguchi M, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 799(1), 119-125 (2004)
Yonglan Xu et al.
Chemosphere, 85(5), 790-796 (2011-07-13)
Direct and indirect (sensitized) photolysis of p-tert-octylphenol (OP), 4-octylphenoxy-acetic acid (OP1EC), and ibuprofen (IBU) were investigated in laboratory water and surface water under simulated and natural sunlight conditions. Photodegradation obeyed apparent-first order kinetics with rates increasing in the presence of
Yanlin Wu et al.
Environmental science and pollution research international, 20(1), 3-9 (2012-07-21)
4-Tert-octylphenol (4-t-OP), a kind of endocrine-disrupting compounds, is widely distributed in natural water surroundings but can hardly be biodegraded. The advanced oxidation processes (AOPs) have been proved to be an efficient method to degrade 4-t-OP. In this study, the photodegradation
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