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经验公式(希尔记法):
C12H10N2O2
化学文摘社编号:
分子量:
214.22
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-108-2
Beilstein/REAXYS Number:
170877
MDL number:
InChI
1S/C12H10N2O2/c15-14(16)12-3-1-10(2-4-12)9-11-5-7-13-8-6-11/h1-8H,9H2
InChI key
MNHKUCBXXMFQDM-UHFFFAOYSA-N
SMILES string
[O-][N+](=O)c1ccc(Cc2ccncc2)cc1
assay
≥98.0% (NT)
form
crystals
quality
for spectrophotometric det. of phosphorus-containing pesticides
technique(s)
thin layer chromatography (TLC): suitable
ign. residue
≤0.1%
mp
69-71 °C (lit.)
Quality Level
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Application
用于环氧化物和甲基化试剂的检测;用于含磷杀虫剂的分光光度测定
Other Notes
用于检测烷化剂的试剂
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Spectrophotometric determination of organophosphorus pesticides with 4-(4-nitrobenzyl)pyridine.
C R Turner
The Analyst, 99(180), 431-434 (1974-07-01)
Studies on chemical carcinogens. XXIII. A simple method for characterization of the alkylating ability of compounds by using 4-(p-nitrobenzyl)-pyridine.
Y Kawazoe et al.
Chemical & pharmaceutical bulletin, 30(6), 2077-2086 (1982-06-01)
Marina González-Pérez et al.
Chemical research in toxicology, 25(12), 2755-2762 (2012-11-23)
The chemical reactivity of the mutagenic epoxides (EP) propylene oxide (PO), 1,2-epoxybutane (1,2-EB), and cis- and trans-2,3-epoxybutane (cis- and trans-2,3-EB) with 4-(p-nitrobenzyl)pyridine (NBP), a bionucleophile model for S(N)2 alkylating agents with high affinity for the guanine-N7 position, was investigated kinetically.
K Futagami et al.
Journal of chromatography. B, Biomedical sciences and applications, 704(1-2), 369-373 (1998-03-28)
We developed a rapid and simple method for identifying 25 commonly used organophosphorus insecticides in human serum using high-performance thin-layer chromatography (HPTLC). These organophosphates were separated on plates with three different developing systems within 6-18 min and detected by means
Erwin Eder et al.
Chemico-biological interactions, 164(1-2), 76-84 (2006-10-03)
Six monofunctional alkylating methanesulphonates of widely varying structures were investigated in the in vitro micronucleus assay with Syrian hamster embryo fibroblast cells. The results were compared with the alkylating activities measured in the 4-(nitrobenzyl)pyridine test (NBP-test) and the N-methyl mercaptoimidazole
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