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45435

Supelco

Dichloran

PESTANAL®, analytical standard

Synonym(s):

2,6-Dichloro-4-nitroaniline, 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:
41116107
PubChem Substance ID:
329756731

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

190-192 °C (lit.)

application(s)

agriculture
environmental

format

neat

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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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH0324
BCCC6544
BCBS2325V
SZBF103XV
SZBB166XV

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Chloramphenicol ≥98% (HPLC)

Sigma-Aldrich

C0378

Chloramphenicol

Proteose-Peptone suitable for microbiology

Millipore

82450

Proteose-Peptone

Rose bengal ≥96% (HPLC), Dye content 95 %

Sigma-Aldrich

330000

Rose bengal

Florina Uzefovsky et al.
Emotion (Washington, D.C.), 14(4), 712-721 (2014-05-29)
Increasing evidence points to a role of dopaminergic pathways in modulating social behavior. Specifically, a polymorphic region in the third exon of the Dopamine D4 receptor (DRD4) has been associated with a host of social behaviors, often in an environment-sensitive
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
U Thrane
International journal of food microbiology, 29(2-3), 149-156 (1996-04-01)
At the Second International Workshop on Standardisation of Methods for the Mycological Examination of Foods in Baarn, 1990, three selective media for food-borne Fusarium species were recommended: Czapek-Dox Iprodione Dichloran Agar (CZID), Dichloran Chloramphenicol Peptone agar (DCPA) and Pentachloronitrobenzene Peptone
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
L R Beuchat et al.
International journal of food microbiology, 29(2-3), 161-166 (1996-04-01)
Dichloran 18% glycerol agar base supplemented with 100 micrograms of chloramphenicol ml-1 (DG18 agar) was compared to DG18 agar supplemented with 100 micrograms of Triton X-301 ml-1 (DG18T) and DG18 agar supplemented with 1 microgram of iprodione [3-(3,5-dichlorophenyl)-N-(1-methyl-ethyl)-2,4-dioxo-1-imidazolidine- carboxamide] ml-1
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