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Merck
CN

D67820

2,6-Dichloro-4-nitroaniline

96%

Synonym(s):

Dichloran

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About This Item

Linear Formula:
Cl2C6H2(NO2)NH2
CAS Number:
99-30-9
Molecular Weight:
207.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894047
EC Number:
202-746-4
Beilstein/REAXYS Number:
1459581
MDL number:
MFCD00007677

Key Documents

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Product Name

2,6-Dichloro-4-nitroaniline, 96%

InChI key

BIXZHMJUSMUDOQ-UHFFFAOYSA-N

InChI

1S/C6H4Cl2N2O2/c7-4-1-3(10(11)12)2-5(8)6(4)9/h1-2H,9H2

SMILES string

Nc1c(Cl)cc(cc1Cl)[N+]([O-])=O

assay

96%

form

powder

mp

190-192 °C (lit.)

Quality Level

200

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Related Categories

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

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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Certificates of Analysis (COA)

Lot/Batch Number
SDBB1326
STBK6275
STBK4779
STBJ6678
STBJ3361

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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
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
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
E Käfer
Mutation research, 241(1), 49-66 (1990-05-01)
Both bleomycin, an antineoplastic drug, and botran (2,6-dichloro-4-nitro-aniline), a fungicide, are known to inhibit growth and induce genetic segregation in diploid tester strains of Aspergillus nidulans when present in agar media. To identify primary effects, samples of induced apparent crossover
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