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36070

Sigma-Aldrich

2,6-Dichloro-4-nitrophenol

98%

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About This Item

Empirical Formula (Hill Notation):
C6H3Cl2NO3
CAS Number:
618-80-4
Molecular Weight:
208.00
Beilstein:
1245045
EC Number:
210-563-6
MDL number:
MFCD00014715
UNSPSC Code:
12352100
PubChem Substance ID:
57649441

Assay

≥97.5% (HPLC)
98%

form

solid

mp

123-126 °C (dec.)

solubility

methanol: soluble 1 g/10 mL, clear, slightly yellow to deep greenish-yellow

SMILES string

Oc1c(Cl)cc(cc1Cl)[N+]([O-])=O

InChI

1S/C6H3Cl2NO3/c7-4-1-3(9(11)12)2-5(8)6(4)10/h1-2,10H

InChI key

PXSGFTWBZNPNIC-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBJ9934V
BCBF6288V
1402975

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S K Hong et al.
Journal of toxicology and environmental health. Part A, 57(1), 47-62 (1999-05-13)
The agricultural fungicide N-(3,5-dichlorophenyl)succinimide (NDPS) is an acute nephrotoxicant in rats. Our previous studies suggested that sulfate conjugation of NDPS metabolites might be a bioactivation step mediating NDPS nephrotoxicity. In this study, effects of substrates and/or inhibitors of sulfation on
T Walle et al.
Biochemical pharmacology, 50(5), 731-734 (1995-08-25)
The natural product quercetin was a potent inhibitor of the human P-form phenolsulfo-transferase with an IC50 value of 0.10 +/- 0.03 microM (mean +/- SEM; N = 5), which was three to four orders of magnitude more potent than its
V M Seah et al.
Biochemical pharmacology, 47(10), 1743-1749 (1994-05-18)
2,6-Dichloro-4-nitrophenol (DCNP)-35sulfate was identified and quantified by an HPLC-radiometric assay following its biosynthesis in vitro from 35S-labeled 3'-phosphoadenosine-5'-phosphosulfate (PAP35S) by phenolsulfotransferase (PST) of rat liver cytosol. Acid hydrolysis of DCNP-35sulfate produced almost stoichiometric release of inorganic 35sulfate and DCNP. In
Khairia M Al-Ahmary et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 126, 260-269 (2014-03-13)
Proton transfer reaction between the proton donor 2,6-dichloro-4-nitrophenol (DCNP) with the proton acceptor 4-aminopyridine (4APy) has been investigated spectrophotometrically in different solvents included the aprotic solvent acetonitrile (MeCN), the protic one methanol (MeOH) and a mixture consists of 50% acetonitrile+50%
Andreas Wild et al.
Chemical communications (Cambridge, England), 48(7), 964-966 (2011-12-14)
Water-based Zn(II) bisterpyridine systems were used as fluorometric sensors for the detection of the nerve gas G mimics DMMP, DCP and DCNP. Analyte concentrations in the range of 10(-7) to 10(-6) M are detectable in solution. The utilization of a
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