A phenylurea herbicide
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Chlorotoluron

Item No. 24225

Technical Information
Formal Name
N'-(3-chloro-4-methylphenyl)-N,N-dimethyl-urea
CAS Number
15545-48-9
Molecular Formula
C10H13ClN2O
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
Chloroform: slightly solubleMethanol: slightly soluble
λmax
244 nm
SMILES
ClC1=C(C)C=CC(NC(N(C)C)=O)=C1
InChi Code
InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)
InChi Key
JXCGFZXSOMJFOA-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Chlorotoluron is a phenylurea herbicide.1 It is genotoxic, inducing the formation of chromosome aberrations and sister chromatid exchange (SCE) in CHEL liver epithelial cells in a concentration-dependent manner.2 Chlorotoluron (625-5,000 mg/kg) induces testicular anaplasia as well as looseness and incrassation to the basement membrane that destroys the blood-testis barrier, increases superoxide dismutase (SOD) activity, and degrades testis mitochondria in mice.3 It reduces food intake and body weight and induces hemolytic anemia, hemosiderosis of the spleen, and brown atrophy in dogs when administered at a dose of 9,200 ppm in the diet.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Banyiova, K., Cup, P., and Kohoutek, J. An experimentally refined tool to assess the risks of the human dermal exposure to herbicide chlorotoluron. Environ. Sci. Pollut. Res. Int. 22(14), 10713-10720 (2015).

    2. Federico, C., Motta, S., Palmieri, C., et alPhenylurea herbicides induce cytogenetic effects in Chinese hamster cell lines. Mutat. Res. 721(1), 89-94 (2011).

    3. Mu, H., Zhang, P., and Xu, J. Testicular toxicity and mechanisms of chlorotoluron compounds in the mouse. Toxicol. Mech. Methods 17(8), 483-488 (2007).

    4. Zak, F., and Sachsse, K. Oral toxicity of the herbibide chlortoluron [N-(3-chloro-4-methylphenyl)-N,N'-dimethylurea] in rats and dogs. Proc. Eur. Soc. Study Drug Tox. 12, 272-281 (1971).