Chlorobenzilate

From Wikipedia, the free encyclopedia
Chlorobenzilate[1]
Skeletal formula of chlorobenzilate
Ball-and-stick model of the chlorobenzilate molecule
Names
Preferred IUPAC name
Ethyl bis(4-chlorophenyl)hydroxyacetate
Other names
Chlorbenzylate; Chlorobenzylate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.374 Edit this at Wikidata
EC Number
  • 208-110-2
KEGG
RTECS number
  • DD2275000
UNII
UN number 2996
  • InChI=1/C16H14Cl2O3/c1-2-21-15(19)16(20,11-3-7-13(17)8-4-11)12-5-9-14(18)10-6-12/h3-10,20H,2H2,1H3
    Key: RAPBNVDSDCTNRC-UHFFFAOYAH
  • Clc1ccc(cc1)C(O)(c2ccc(Cl)cc2)C(=O)OCC
Properties
C16H14Cl2O3
Molar mass 325.19 g·mol−1
Appearance Colorless to pale yellow solid
Density 1.28 g/cm3
Melting point 37 °C (99 °F; 310 K)
Hazards
GHS labelling:
GHS07: Exclamation markGHS09: Environmental hazard
Signal word
 Warning
H302, H410
P264, P270, P273, P301+P312, P330, P391, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Chlorobenzilate is a pesticide that is not currently used in the United States or Europe. It was originally developed by Ciba-Geigy and introduced in 1952.[2] It was used as an acaricide against mites on citrus trees, including deciduous fruit trees.[3] It has been detected as a residue on tomatoes found in Japanese markets in 2005.[4] It is a non-systemic pesticide that works through contact and as a neurotoxin: it disrupts the functioning of the nervous system.

In the pure state, chlorobenzilate is a colorless to pale yellow solid, but the commercial product is a brownish liquid.[3] It is only slightly soluble in water, but miscible with acetone, toluene and methanol.

Toxicity[]

There is no data on the carcinogenic effects of chlorobenzilate in humans. However, when mice were administered the substance orally, carcinogenic effects were observed.[3] The U.S. Environmental Protection Agency has therefore classified chlorobenzilate as a probable human carcinogen (Group B2).[5] The International Agency for Research on Cancer has concluded that there is insufficient information available to evaluate the carcinogenicity of chlorobenzilate in humans.[2]

Chlorobenzilate is a persistent organic pollutant and is very toxic to aquatic invertebrates.

Regulation[]

After carcinogenicity was established in mice, the use of chlorobenzilate was banned in the United States in 1979, except for citrus cultivation. After 1999, it was banned completely. In the European Union, its use is also currently banned.

International trade in chlorobenzilate is regulated by the Rotterdam Convention.

References[]

  1. ^ International Chemical Safety Card for chlorobenzilate, National Institute for Occupational Safety and Health
  2. ^ a b Chlorobenzilate, International Agency for Research on Cancer
  3. ^ a b c Chlorobenzilate, U.S. Environmental Protection Agency
  4. ^ Ochiai, Nobuo (2005). "Optimization of a multi-residue screening method for the determination of 85 pesticides in selected food matrices by stir bar sorptive extraction and thermal desorption GC-MS". Journal of Separation Science. 28: 1083–1092. doi:10.1002/jssc.200500017.
  5. ^ U.S. Environmental Protection Agency. Health Effects Assessment Summary Tables. FY 1997 Update. Solid Waste and Emergency Response, Office of Emergency and Remedial Response, Cincinnati, OH. EPA/540/R-97-036. 1997.
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