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Merck

40057

Supelco

2,4-Dinitrophenol -Lösung

reference material, 5000 μg/mL in methanol

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About This Item

CAS-Nummer:
UNSPSC-Code:
41116105

Qualität

reference material

Qualitätsniveau

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

ampule of 1 mL

Konzentration

5000 μg/mL in methanol

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

cleaning products
cosmetics
environmental
food and beverages
personal care

Format

single component solution

Lagertemp.

2-8°C

InChI

1S/C6H4N2O5/c9-6-2-1-4(7(10)11)3-5(6)8(12)13/h1-3,9H

InChIKey

UFBJCMHMOXMLKC-UHFFFAOYSA-N

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Anwendung

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

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Zielorgane

Eyes,Central nervous system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

51.8 °F

Flammpunkt (°C)

11 °C


Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number

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

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K Srinivasan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 94, 89-100 (2012-04-21)
The formation of host-guest inclusion complex of 2,4-dinitrophenol (2,4-DNP) with nano-hydrophobic cavity of β-cyclodextrin (β-CD) in solution phase was studied by UV-visible spectrophotometer and electrochemical method (cyclic voltammetry, CV). The prototropic behaviors of 2,4-DNP with and without β-CD and the
L V Grubskaia et al.
Ukrains'kyi biokhimichnyi zhurnal (1999 ), 84(1), 45-52 (2012-06-12)
The influence of ionizing radiation with low absorbed dose rate (55 mGy x min(-1)) in 1, 12 and 24 hours after irradiation in doses of 0.1; 0.5 and 1.0 Gy on functional state of the electron transfer chain of the
Sean Marrache et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(40), 16288-16293 (2012-09-20)
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Michelle Medeiros et al.
The Journal of organic chemistry, 77(23), 10907-10913 (2012-11-22)
This work presents a detailed kinetic and mechanistic study of biologically interesting dephosphorylation reactions involving the exceptionally reactive nucleophilic group, hydroxamate. We compare results for hydroxamate groups anchored on the simple molecular backbone of benzohydroxamate (BHA) and on the more

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