All Photos(1)
Synonym(s):
1,3-Dichloro-4-methylbenzene, 2,4-Dichloro-1-methylbenzene
Linear Formula:
CH3C6H3Cl2
CAS Number:
Molecular Weight:
161.03
Beilstein:
1931691
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.546 (lit.)
bp
200 °C (lit.)
density
1.246 g/mL at 25 °C (lit.)
SMILES string
Cc1ccc(Cl)cc1Cl
InChI
1S/C7H6Cl2/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3
InChI key
FUNUTBJJKQIVSY-UHFFFAOYSA-N
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Application
2,4-Dichlorotoluene was used as an oxidant and a solvent during anaerobic catalytic oxidation of secondary alcohols by using an in situ (N-heterocyclic carbene)-Ni(0) system. It was used as growth supplement in the culture media of Ralstonia sp. strain PS12. It was used to develop a sensitive method based on solid-phase microextraction followed by gas chromatography-tandem mass spectrometry for the analysis of chlorotoluenes in water samples.
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2
WGK
WGK 2
Flash Point(F)
174.2 °F
Flash Point(C)
79 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Certificates of Analysis (COA)
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[Gas chromatographic determination of 2,4-dichlorotoluene in water].
T A Kozeĭko et al.
Gigiena i sanitariia, (3)(3), 44-45 (1988-03-01)
Omid Khakshoor et al.
Journal of the American Chemical Society, 134(6), 3154-3163 (2012-02-04)
We address the recent debate surrounding the ability of 2,4-difluorotoluene (F), a low-polarity mimic of thymine (T), to form a hydrogen-bonded complex with adenine in DNA. The hydrogen bonding ability of F has been characterized as small to zero in
[Hygienic standards for 2,4-dichlorotoluene in reservoir water].
G V Tolstpiatova et al.
Gigiena i sanitariia, (2)(2), 80-81 (1988-02-01)
Christophe Berini et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(23), 6857-6860 (2010-05-11)
The selective, anaerobic catalytic oxidation of secondary alcohols at room temperature by using an in situ (N-heterocyclic carbene)-Ni(0) system is presented. The use of non-anhydrous, non-degassed 2,4-dichlorotoluene as both the oxidant and the solvent allows for very short reaction times
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
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