D67820
2,6-二氯-4-硝基苯胺
96%
别名:
Dichloran
方案
96%
表单
powder
mp
190-192 °C (lit.)
SMILES字符串
Nc1c(Cl)cc(cc1Cl)[N+]([O-])=O
InChI
1S/C6H4Cl2N2O2/c7-4-1-3(10(11)12)2-5(8)6(4)9/h1-2H,9H2
InChI key
BIXZHMJUSMUDOQ-UHFFFAOYSA-N
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警示用语:
Danger
危险分类
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 1 - STOT RE 2
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Liming Fan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 239, 118467-118467 (2020-05-31)
Two ternary cadmium(II) coordination polymers, with the formulas being {[Cd(tptc)0.5(bpz)(H2O)]·0.5H2O}n (CP 1), and [Cd(tptc)0.5(bpy)]n (CP 2), were designed through mixed ligands strategy. Benefiting from the excellent chemical stability and luminescent property, two Cd(II) CPs possessing efficient multi-functional fluorescent responses toward
T Deak et al.
International journal of food microbiology, 43(1-2), 91-95 (1998-10-07)
A collaborative study was made to evaluate the effectivity of a general purpose medium, tryptone glucose yeast extract (TGY) agar on the detection and enumeration of yeasts from food. Nine laboratories participated in the study and compared five media (four
H A Hasan
Folia microbiologica, 38(4), 295-298 (1993-01-01)
The effect of fungicides on the production of aflatoxin by Aspergillus flavus IMI 89717, diacetoxyscirpenol and zearalenone by Fusarium graminearum was studied. In a yeast extract-sucrose medium, dicloran, iprodione and vinclozolin fungicides significantly inhibited mycelial growth of A. flavus at
Danielle Palma de Oliveira et al.
Environmental toxicology and chemistry, 28(9), 1881-1884 (2009-05-05)
2,6-Dichloro-4-nitroaniline (dicloran) is a mutagenic aromatic amine used as an agricultural fungicide and in the synthesis of disperse dyes. It is a known mutagen (Salmonella/microsome assay) in strains TA98 and TA100. Dicloran was initially detected, but not quantified, in the
L A Myers et al.
Toxicology and applied pharmacology, 95(1), 139-152 (1988-08-01)
The metabolism of 2,6-dichloro-4-nitroaniline (DCNA) to a unique denitrosated product, 3,5-dichloro-p-aminophenol (DCAP), was investigated in rat hepatic microsomes using an HPLC system containing a reverse-phase column and an electrochemical detector. The parent compound appears to induce its own metabolism. The
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