Skip to Content
Merck
CN
All Photos(1)

Key Documents

View All Documentation

Safety Information

36030

Sigma-Aldrich

2,4-Dichloro-1-nitrobenzene

purum, ≥98.0% (GC)

Synonym(s):

1,3-Dichloro-4-nitrobenzene, asym.-Nitro-m-dichlorobenzene

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
Cl2C6H3NO2
CAS Number:
611-06-3
Molecular Weight:
192.00
Beilstein:
1451655
EC Number:
210-248-3
MDL number:
MFCD00007071
UNSPSC Code:
12352100
PubChem Substance ID:
329755254

grade

purum

Assay

≥98.0% (GC)

bp

258 °C (lit.)

mp

29-32 °C (lit.)
30-32 °C

SMILES string

[O-][N+](=O)c1ccc(Cl)cc1Cl

InChI

1S/C6H3Cl2NO2/c7-4-1-2-6(9(10)11)5(8)3-4/h1-3H

InChI key

QUIMTLZDMCNYGY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

replaced by

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B - Muta. 2 - Skin Sens. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

305.6 °F

Flash Point(C)

152 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Makoto Ohnishi et al.
The Journal of toxicological sciences, 34(2), 233-237 (2009-04-02)
Oral administration of 2,4-dichloro-1-nitrobenzene (2,4-DCNB) causes kidney tumors in the rat. The objective of the present study was to identify the chemical structure of 2,4-DCNB metabolites in urine. Urine from 2,4-DCNB fed rats was more yellow than urine from control
P A Botham et al.
The British journal of dermatology, 117(1), 1-9 (1987-07-01)
The fate of 2,4-dinitrochlorobenzene, a potent contact sensitizing chemical, and 2,4-dichloronitrobenzene, a non-sensitizer, was compared following their application to the skin of BALB/c mice. Although both chemicals were able to bind to protein in vitro and were capable of being
Maja Aleksic et al.
Toxicology in vitro : an international journal published in association with BIBRA, 22(5), 1169-1176 (2008-04-29)
A large proportion of allergic skin reactions are considered to be the result of skin exposure to small organic chemicals that possess the intrinsic ability to covalently modify skin proteins, either directly or following activation. In the absence of information
A Bu-Abbas et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 36(8), 617-621 (1998-09-12)
Aqueous extracts of green tea, at concentrations of 2.5. 5.0 and 7.5%, were administered to rats as the sole drinking fluid for 4 weeks. Hepatic glutathione S-transferase (GST) activity, determined using 1-chloro-2,4-dinitrobenzene (CDNB) and 3,4-dichloronitrobenzene (DCNB) as substrates, and UDP-glucuronosyl
Hirokazu Kano et al.
Archives of toxicology, 86(11), 1763-1772 (2012-06-26)
Carcinogenicity and chronic toxicity of 2,4-dichloro-1-nitrobenzene (2,4-DCNB) were examined by dietary administration to F344/DuCrj rats and Crj:BDF(1) mice of both sexes for 2 years. Dietary administration commenced when the animals were 6 weeks old. The dietary concentration of 2,4-DCNB was 0 (control)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service