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D67820

Sigma-Aldrich

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
Beilstein:
1459581
EC Number:
202-746-4
MDL number:
MFCD00007677
UNSPSC Code:
12352100
PubChem Substance ID:
24894047
NACRES:
NA.22

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

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Related Categories

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

D67820-500G:
D67820-100G:
D67820-BULK:
D67820-VAR:
D67820-5G:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
Acute toxicity of cadmium, copper, zinc, ammonia, 3,3'-dichlorobenzidine, 2,6-dichloro-4-nitroaniline, methylene chloride, and 2,4,6-trichlorophenol to juvenile grass shrimp and killifish.
D T Burton et al.
Bulletin of environmental contamination and toxicology, 44(5), 776-783 (1990-05-01)
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
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