2,6-Dichloro-4-nitrophenol

Name: 2,6-Dichloro-4-nitrophenol
Brand: ALDRICH

98%

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A propos de cet article

Formule empirique (notation de Hill) :

C₆H₃Cl₂NO₃

Numéro CAS:

618-80-4

Poids moléculaire :

208.00

EC Number:

210-563-6

UNSPSC Code:

12352100

PubChem Substance ID:

57649441

Beilstein/REAXYS Number:

1245045

MDL number:

MFCD00014715

Assay:

≥97.5% (HPLC), 98%

Form:

solid

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InChI key

PXSGFTWBZNPNIC-UHFFFAOYSA-N

InChI

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

SMILES string

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

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

pictograms

GHS07

signalword

Warning

hcodes

H302 + H312 + H332,H315,H319

pcodes

P261 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338

Hazard Classifications

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

Classe de stockage

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

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number

BCBJ9934V

BCBF6288V

1402975

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Bioactivation of 3-n-butylphthalide via sulfation of its major metabolite 3-hydroxy-NBP: mediated mainly by sulfotransferase 1A1.

Xingxing Diao et al.

Drug metabolism and disposition: the biological fate of chemicals, 42(4), 774-781 (2014-01-29)

3-n-Butylphthalide (NBP) [(±)-3-butyl-1(3H)-isobenzofuranone] is an anti-cerebral-ischemia drug. Moderate hepatotoxicity has been observed in clinical applications. One of the major metabolites, 3-N-acetylcysteine-NBP, has been detected in human urine, indicating the formation of a reactive metabolite. We elucidated the formation mechanism of

Suicidal differential housekeeping gene activity in apoptosis induced by DCNP.

L Qi et al.

Apoptosis : an international journal on programmed cell death, 5(4), 379-388 (2001-03-03)

Previous suggestions of CpG-specific apoptotic commitment implied critical epigenetic modulation of housekeeping genes which have canonical CpG islands at 5' promoter regions. Differential housekeeping gene activity however has not been shown. Using a focussed microarray (genechip) of 22 housekeeping genes

N-sulphation of desipramine in the rat brain.

K O Wong et al.

Xenobiotica; the fate of foreign compounds in biological systems, 26(1), 17-26 (1996-01-01)

1. Amine N-sulphotransferase (NST) activity with desipramine (DMI) as substrate was assayed in vitro in various areas of the rat brain. Biosynthesis of 3'-phosphoadenosine-5'-phospho35sulphate (PAPS) from sodium 35sulphate and ATP was also measured by coupling it to the sulphation of

Selective inhibition of sulfate conjugation in the rat: pharmacokinetics and characterization of the inhibitory effect of 2,6-dichloro-4-nitrophenol.

H Koster et al.

Biochemical pharmacology, 31(10), 1919-1924 (1982-05-15)

The pharmacokinetics of 2,6-dichloro-4-nitrophenol (DCNP) have been studied in the rat. Upon i.v. injection the plasma decay curve of DCNP showed a rapid distribution phase. After 30 min the plasma concentration reached a value that was constant for at least

Metabolism and toxicity of benzophenone in isolated rat hepatocytes and estrogenic activity of its metabolites in MCF-7 cells.

Y Nakagawa et al.

Toxicology, 156(1), 27-36 (2001-02-13)

The metabolism and cytotoxicity of benzophenone and estrogenic activity of its metabolites have been studied in freshly isolated rat hepatocytes and cultured MCF-7 human breast cancer cells, respectively. The incubation of hepatocytes with benzophenone (0.25-1.0 mM) elicited a concentration- and

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