Skip to Content
Merck
All Photos(2)

Key Documents

161365

Sigma-Aldrich

3,4-Dichlorotoluene

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3C6H3Cl2
CAS Number:
Molecular Weight:
161.03
Beilstein:
1931687
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.547 (lit.)

bp

200.5 °C/741 mmHg (lit.)

density

1.251 g/mL at 25 °C (lit.)

SMILES string

Cc1ccc(Cl)c(Cl)c1

InChI

1S/C7H6Cl2/c1-5-2-3-6(8)7(9)4-5/h2-4H,1H3

InChI key

WYUIWKFIFOJVKW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

3,4-Dichlorotoluene is added as growth supplement in culture medium of Ralstonia sp. strain PS12.

Application

3,4-Dichlorotoluene was used in determination of enthalpy of formation for molecular complexes of I2 with chloromethylbenzene molecules in CCl4.

Pictograms

Environment

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

185.0 °F

Flash Point(C)

85 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

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

Visit the Document Library

Thermochemistry of molecular complexes. 4. Molecular complexes of I2 with chloromethylbenzenes.
Greaux JB, et al.
J. Incl. Phenom. Mol. Recog. Chem., 13(3), 245-248 (1992)
Katrin Pollmann et al.
Journal of bacteriology, 184(19), 5261-5274 (2002-09-10)
Ralstonia sp. strain PS12 is able to use 2,4-, 2,5-, and 3,4-dichlorotoluene as growth substrates. Dichloromethylcatechols are central intermediates that are formed by TecA tetrachlorobenzene dioxygenase-mediated activation at two adjacent unsubstituted carbon atoms followed by TecB chlorobenzene dihydrodiol dehydrogenase-catalyzed rearomatization

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