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33557

Supelco

4-tert-Octylphenol-3,5-d2 solution

10 μg/mL in acetone, analytical standard

Synonym(s):

4-(1,1,3,3-Tetramethylbutyl)phenol-3,5-d2, 4-tert-OP-D2

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About This Item

Empirical Formula (Hill Notation):
C14D2H20O
CAS Number:
Molecular Weight:
208.34
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

concentration

10 μg/mL in acetone

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

mass shift

M+2

storage temp.

−20°C

SMILES string

[2H]c1cc(O)cc([2H])c1C(C)(C)CC(C)(C)C

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/i6D,7D

InChI key

ISAVYTVYFVQUDY-QFIQSOQBSA-N

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General description

Certan Vial

Application

4-tert-Octylphenol-3,5-d2 solution is an deuterated standard used for the analysis of mono and di-ethoxylates of nonylphenol (NP) and octylphenol (OP) in environmental samples using solid-phase micro extraction followed by gas chromatography with mass spectrometry (SPME-GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

1.4 °F - Information refers to the main ingredient.

flash_point_c

-17 °C - Information refers to the main ingredient.


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Protocols

Alkylphenols are starting materials for the synthesis of alkylphenol ethoxylates, which are widely used as non ionic tensides, dispersive agents in paper and leather manufacturing, emulsifiers for pesticide formulations and as auxiliary agents for drilling and flotation.

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

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