D67820
2,6-Dichloro-4-nitroaniline
96%
Synonym(s):
Dichloran
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About This Item
Linear Formula:
Cl2C6H2(NO2)NH2
CAS Number:
Molecular Weight:
207.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-746-4
Beilstein/REAXYS Number:
1459581
MDL number:
Assay:
96%
Form:
powder
Quality Level
assay
96%
form
powder
mp
190-192 °C (lit.)
SMILES string
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
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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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
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
Ryota Uehara et al.
Cell motility and the cytoskeleton, 65(2), 100-115 (2007-10-31)
Phosphorylation of myosin regulatory light chain (RLC) at Ser19 (mono-phosphorylation) promotes filament assembly and enhances actin-activated ATPase activity of non-muscle myosin, while phosphorylation at both Ser19 and Thr18 (di-phosphorylation) further enhances the ATPase activity. However, it has not well been
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D67820-5G | 04061833587881 |
| D67820-100G | 04061833587874 |
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