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Featured Results:
 2,4-dichlorophenol : Carcinogenic Potency Database
2,4-dichlorophenol: Carcinogenic Potency Database
potency.berkeley.edu
 
2,4-Dichlorophenol
2,4-Dichlorophenol.png
IUPAC name
Identifiers
CAS number 120-83-2 Yes check.svgY
PubChem 8449
SMILES
InChI
InChI key HFZWRUODUSTPEG-UHFFFAOYAU
ChemSpider ID 8140
Properties
Molecular formula C6H4Cl2O
Molar mass 163.00 g/mol
Appearance White/Off-white crystalline solid
Odor Phenolic
Density 1.38g/cm3
Melting point

42.5 °C, 316 K, 109 °F (This is an average of the range 42°C - 43°C)

Boiling point

209.5 °C, 483 K, 409 °F (This is an average of the range 209°C - 210°C)

Solubility in water 5 g/100mL
Hazards
MSDS http://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSPage.do
R-phrases R22, R24, R34, R51/53
S-phrases S26, S36/37/39, S45, S61
NFPA 704
NFPA 704.svg
1
 
0
COR
Flash point 114°C
 Yes check.svgY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

2,4-Dichlorophenol (2,4-DCP) is a chlorinated derivative of phenol with the molecular formula C6H4Cl2O. 2,4-DCP is used primarily as intermediate in the preparation of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). Annual worldwide production is estimated at 88 million pounds.[1]

2,4-DCP is readily absorbed through the skin and contact with large amounts may be fatal.[2]

[edit] See also

[edit] References

  1. ^ Desmurs J, Ratton S. Chlorophenols. In: Kirk-Othmer Encyclopedia of Chemical Technology, 4th Edition. Kroschwitz JI, Howe-Grant M, eds. New York: John Wiley and Sons, 1993;6:156-168
  2. ^ Kintz P, Tracqui A, Mangin P (1992). "Accidental death caused by the absorption of 2,4-dichlorophenol through the skin". Arch. Toxicol. 66 (4): 298–9. doi:10.1007/BF02307178. PMID 1514931. 



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