N15553
4-Nitrocatechol
≥96.0%
Synonym(s):
1,2-Dihydroxy-4-nitrobenzene, 4-Nitropyrocatechol
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About This Item
Linear Formula:
O2NC6H3-1,2-(OH)2
CAS Number:
Molecular Weight:
155.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-009-0
Beilstein/REAXYS Number:
1867508
MDL number:
Assay:
≥96.0%
Form:
powder
assay
≥96.0%
form
powder
mp
173-177 °C (lit.)
SMILES string
Oc1ccc(cc1O)[N+]([O-])=O
InChI
1S/C6H5NO4/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,8-9H
InChI key
XJNPNXSISMKQEX-UHFFFAOYSA-N
Gene Information
rat ... Nos1(24598)
Storage Class
11 - Combustible Solids
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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W Tassaneeyakul et al.
Biochemical pharmacology, 46(11), 1975-1981 (1993-12-03)
The involvement of human cytochrome P450 (CYP) 2E1 in the hydroxylation of 4-nitrophenol (4NP) to 4-nitrocatechol (4NC) has been investigated using cDNA expression and liver microsomal kinetic and inhibitor techniques. 4NP hydroxylation by human liver microsomes and cDNA-expressed human CYP2E1
Chong Shen et al.
Chemico-biological interactions, 162(1), 53-61 (2006-06-27)
An important application of primary hepatocyte cultures is for hepatotoxicity research. In this paper, gel entrapment culture of rat hepatocytes in miniaturized BAL system were evaluated as a potential in vitro model for hepatotoxicity studies in comparison to monolayer cultures.
Archana Chauhan et al.
Environmental science & technology, 44(9), 3435-3441 (2010-04-03)
Microbial degradation studies have pointed toward the occurrence of two distinct PNP catabolic pathways in Gram positive and Gram negative bacteria. The former involves 4-nitrocatechol (4-NC), 1,2,4-benzenetriol (BT), and maleylacetate (MA) as major degradation intermediates, whereas the later proceeds via
Global Trade Item Number
| SKU | GTIN |
|---|---|
| N15553-1G | 04061826285640 |
| N15553-5G | 04061834109556 |