2,4-Dichlorotoluene

2,4-Dichlorotoluene

Benzene,2,4-dichloro-1-methyl-;Toluene,2,4-dichloro-;2,4-Dichloro-1-methylbenzene;2,4-Dichlorotoluene;1,3-Dichloro-4-methylbenzene;NSC 8764

95-73-8

C7H6Cl2

InChIKey=FUNUTBJJKQIVSY-UHFFFAOYSA-N

161.03

161.03

1931691

202-445-8

3S32N6LG3X

1727

8764

2810|3082

DTXSID5040702

Colorless liquid

29036990

Pesticide Intermediates

0

4.24

Clear colorless Liquid

1.2476 g/cm³ @ Temp: 20 °C

-13.5 °C

201 °C @ Press: 760 Torr

175 °F

1.543

Solubility in water, g/100ml at 20°C: (very poor)

Store below +30°C.

Vapour pressure, kPa at 50°C: 0.4

Relative vapour density (air = 1): 5.56

Oral-rat LD50: 2400 mg/kg;Oral-Mouse LD50: 2400 mg/kg

Open flame is flammable; burning releases toxic chloride fumes

vol% in air: 1.9.5

Weight 10.34 lb/gal|The use of global and substituent physicochemical structure descriptors for quantitative structure-property relationship studies has been evaluated through direct and autocorrelated applications. Partial least squares analysis has been used to predict the partition coefficient for octanol/water, log P, for chlorinated alkylbenzenes. This investigation revealed that various of the physicochemical parameters considered were highly correlated with the partition coefficient and that partial least square models based on global, direct or autocorrelated substituent parameters all seem to be adequate for prediction of log P, as compared to results obtained experimentally or by means of standard substituent calculation schemes. However, the use of autocorrelation vectors of connectivity, steric and electronic effects may be preferably due to a high degree of explanation of the molecular descriptor variance.

Insoluble in water.

Aryl Halides

Simple aromatic halogenated organic compounds, such as 2,4-DICHLOROTOLUENE, are very unreactive. Halogenated organics generally become less reactive as more of their hydrogen atoms are replaced with halogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

As a result of flow, agitation, etc., electrostatic charges can be generated.