Nematicidal and annelicidal activities of 4-phenylazophenol derivatives, which had shown remarkable toxicity against animal parasitic nematodes (
Rhabdias bufonis, Ascaris lumbricoides, Anchylostoma canninum) and
Eisenia foetida, were evaluated against
Panagrellus redivivus and two species of aquatic oligochaetes (
Branchiura sowerbyi, Criodrilus bathybates) by applying the immersion test. The most effective compounds against
Panagrellus were P-11, 13, and 73, which result from the substitution of Cl, Br or CH
3 in the
p-position of the benzen ring. Many NO
2 substituted derivatives were very effective against
Branchiura. In particular, P-10, 62 and 99, which derive from the substitution of NO
2 and halogen in the
p-position of the benzen ring and the 3, 5-position of the phenol ring, showed a high toxicity. The most effective compound against
Criodrilus was P-62. When the toxicity of the azo compounds aginst the four species of nematodes was compared, the effect on
Panagrellus was similar to that on
Anchylostoma but different from that on
Rhabdias. No remarkable difference of toxicity among the three species of oligochates was observed.
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