Ectoparasitic insect pest controllers for animals and their usage

Abstract

1

Description

TECHNICAL FIELD

[0001] This invention relates to novel ectoparasitic insect pest controllers for animals containing a hydrazine derivative as the active ingredient, and method for application of the same.

BACKGROUND ART

[0002] The hydrazine derivatives represented by the general formula (I) which are used as an active ingredient of the ectoparasitic insect pest controllers for animals of this invention are known compounds disclosed in JP-A-5-4958, JP-A-5-17428, JP-A-5-32603 and JP-A-5-262712, wherein is mentioned that these compounds, as an agrihorticultural insecticide, have a controlling effect on Lepidopterous insect pests such as diamondback moth (Plutella xylostella (Linnaeus)), rice leafroller (Cnaphalocrosis medinalis (Guenee)), etc.; Hemipterous insect pests such as tea green leafhopper (Empoasca onukii Matsuda), pear lace bug (Stephanitis nashi Esaki et Takeya), etc.; Coleopterous insect pests such as twenty-eight-spotted ladybird (Epilachna vigintioctopunctata (Fabricius)), maize weevil (Sitophilus zeamais Motschulsky), etc.; Dipterous insect pests such as melon fly (Dacus (Zeugodacus) cucurbitae Coquillett), muscid flies (Muscidae), Culex pipiens molestus, etc.; and tylenchid insect pests such as coffee root lesion nematode (Pratylenchus coffeae (Zimmermann) Filipjev et Schuurmans Stekhoven), root-knot nematode (Meloidogyne sp.), etc. However, in the above-mentioned prior arts, neither mention nor suggestion is made as to the insecticidal effect of these compounds on the ectoparasitic insect pests of animals such as insect pests belonging to fleas, lice and ticks.

[0003] A variety of chemicals have so far been proposed as an agent for controlling the ectoparasitic insect pests harmful to bred animals such as domestic and pet animals. However, an agent capable of exhibiting a high controlling effect on the ectoparasitic insect pests at a low dose is not yet known, and creation of such a novel agent is waited for.

[0004] The present inventors have conducted extensive studies with the aim of creating a novel agent exerting a remarkable controlling effect on the ectoparasitic insect pests of domestic and pet animals at a low dose. As a result, it has been found that some of the compounds selected from the hydrazine derivatives described in the above-mentioned prior arts have a remarkable controlling effect on the ectoparasitic insect pests of animals. Based on this finding, this invention has been accomplished.

DISCLOSURE OF THE INVENTION

[0005] This invention relates to an ectoparasitic insect pest controller for animals which contains, as active ingredient thereof, a hydrazine derivative represented by the following general formula (I): 2

[0006] wherein A represents 3

[0007] (in this formula, R4 represents a hydrogen atom or a C1-6alkyl group; X which may be the same or different represents one to five substituents selected from the group consisting of hydrogen atom, halogen atom, C1-6alkyl group and halo C1-6alkyl group); 4

[0008] (in this formula, R4 and X are as defined above, and R5 represents a hydrogen atom, a C1-6alkylcarbonyl group or a phenylcarbonyl group which may optionally have one or two, the same or different substituents selected from C1-6alkyl groups); 5

[0009] (in this formula, R4 and X are as defined above), or 6

[0010] (in this formula, R4 and X are as defined above);

[0011] R1 represents a hydrogen atom or a C1-6alkyl group;

[0012] R2 and R3 which may be the same or different, each represents a hydrogen atom, a hydroxyl group, a C1-6alkyl group, a C1-6alkoxy group, a C1-6alkylcarbonyl group or a phenylcarbonyl group;

[0013] Y which may be the same or different, represents one to five substituents selected from the group consisting of hydrogen atom, halogen atom, nitro group and cyano group;

[0014] Z represents a halogen atom, a cyano group, a C1-6alkyl group, a halo C1-6alkyl group, a C1-6alkoxy group, a halo C1-6alkoxy group, a halo C1-6alkylthio group, a halo C1-6alkylsulfinyl group or a halo C1-6alkylsulfonyl group; and

[0015] W represents an oxygen atom or a sulfur atom; and to a method for using said insect pest controller.

[0016] The ectoparasitic insect pest controller for animals of this invention exerts a remarkable controlling effect on the parasitic insect pests harmful to domestic and pet animals, such as fleas, lice, ticks, etc.

BEST MODE FOR CARRYING OUT THE INVENTION

[0017] In the definition of the general formula (I) of this invention, “halogen atom” means chlorine atom, bromine atom, iodine atom or fluorine atom; “C1-6alkyl” means a straight or branched chain alkyl group having 1-6 carbon atoms; and “halo C1-6alkyl” means an alkyl group having 1-6 carbon atoms, substituted with at least one halogen atoms which may be the same or different. The hydrazine derivatives represented by the general formula (I) used as an active ingredient of the ectoparasitic insect pesst controller for animals of this invention can be produced according to the production processes mentioned in JP-A-5-4958, JP-A-5-17428, JP-A-5-32603 and JP-A-5-262712.

[0018] Among the hydrazine derivatives of this invention represented by the general formula (I), preferable are the hydrazine derivatives represented by the general formulas (I-1) and (I-2) and, in such preferable compounds, the substituent W is an oxygen atom, the substituent X is a trifluoromethyl group, the substituent Y is a cyano group, the substituent Z is a trifluoromethoxy group, and R1, R2, R3 and R4 simultaneously represent a hydrogen atom. As a further preferable compound, for example, (E)-2-[2-(4-cyanophenyl)-1-(3-trifluoromethylphenyl)ethylidene]-N-(4-trifluoromethoxyphenyl)hydrazine carboxamide can be referred to.

[0019] Next, typical examples of the hydrazine derivative represented by the general formula (I) which is an active ingredient of the ectoparasitic insect pest controller for animals of this invention will be shown in the following Tables 1 to 4. This invention, however, is not limited by these compounds. In the tables, Ph means a phenyl group.

TABLE 1
General formula (I-1)
(I-1)
7
No	R1	R2	R3	R4	X	Y	Z	W	mp° C.
1	H	H	H	H	H	H	Cl	O	199
2	H	H	H	H	H	H	OCF3	O	149
3	H	H	H	H	H	4-Cl	Cl	O	206
4	H	H	H	H	H	4-Cl	OCF3	O	197
5	H	H	H	H	H	4-CN	Cl	O	217
6	H	H	H	H	H	4-CN	Cl	S	128
7	H	H	H	H	H	4-CN	OCF3	S	116
8	H	H	H	H	H	4-CN	OCF3	O	214
									E-form
9	H	H	H	H	H	4-CN	OCF3	O	159
									Z-form
10	H	H	H	H	H	4-NO2	Cl	O	222
11	H	H	H	H	H	4-NO2	Cl	S	206
12	H	H	H	H	H	4-NO2	OCF3	O	189
13	H	H	H	H	H	4-NO2	OCF3	S	139
14	H	H	H	H	H	4-NO2	SCF3	O	200
15	H	H	H	H	3-Cl	H	OCF3	O	212
16	H	H	H	H	3-Cl	4-Cl	OCF3	O	201
17	H	H	H	H	3-Cl	4-CN	Cl	O	206
18	H	H	H	H	3-Cl	4-CN	OCF3	O	187
									E-form
19	H	H	H	H	3-Cl	4-CN	OCF3	O	148
									Z-form
20	H	H	H	H	3-Cl	4-CN	OCF3	S	199
21	H	H	H	H	3-Cl	4-CN	SCF3	O	215
22	H	H	H	H	3-Cl	4-CN	SOCF3	O	205
23	H	H	H	H	3-Cl	4-CN	SO2CF3	O	212
24	H	H	H	H	3-Br	H	Cl	O	191
25	H	H	H	H	3-Br	H	OCF3	O	209
26	H	H	H	H	3-Br	4-CN	Cl	O	205
27	H	H	H	H	3-Br	4-CN	OCF3	O	176
28	H	H	H	H	3-Br	4-CN	SCF3	O	206
29	H	H	H	H	3-Br	4-CN	SCF3	O	216
30	H	H	H	H	3-Br	4-CN	SO2CF3	O	215
31	H	H	H	H	3-F	H	Cl	O	206
32	H	H	H	H	3-F	H	OCF3	O	200
33	H	H	H	H	3-F	4-Cl	OCF3	O	191
34	H	H	H	H	3-F	4-Cl	Cl	O	208
35	H	H	H	H	3-F	4-CN	OCF3	O	202
36	H	H	H	H	3-I	4-CN	Cl	O	213
37	H	H	H	H	3-I	4-CN	OCF3	O	201
38	H	H	H	H	3-CH3	H	Cl	O	185
39	H	H	H	H	3-CH3	H	OCF3	O	198
40	H	H	H	H	3-CH3	4-CN	Cl	O	200
41	H	H	H	H	3-CH3	4-CN	OCF3	O	189
42	H	H	H	H	3-CF3	H	Cl	O	206
43	H	H	H	H	3-CF3	H	OCF3	O	210
44	H	H	H	H	3-CF3	4-CN	OCF3	O	191
45	H	H	H	H	3-CF3	4-CN	OCF3	S	149
46	CH3	H	H	H	H	H	Cl	O	132
47	CH3	H	H	H	H	H	OCF3	O	108
48	H	CH3	H	H	H	H	Cl	O	98
49	H	CH3	H	H	H	H	Br	O	85
50	H	CH3	H	H	H	H	OCF3	O	115
									EZ-form
51	H	CH3	H	H	H	H	OCF3	O	95
									E-form
52	H	CH3	H	H	H	H	OCF3	O	66
									Z-form
53	H	CH3	H	H	H	4-Cl	Cl	O	121
54	H	CH3	H	H	H	4-Cl	OCF3	O	105
55	H	CH3	H	H	3-Cl	4-CN	Cl	O	140
56	H	CH3	H	H	3-Cl	4-CN	OCF3	O	98
57	H	H	OH	H	H	H	Cl	O	188
58	H	H	OH	H	H	H	OCF3	O	170
59	H	H	OH	H	H	4-Cl	Cl	O	Viscous
									material
60	H	H	OH	H	H	4-Cl	OCF3	O	185
									E-form
61	H	H	OH	H	H	4-Cl	OCF3	O	95
									Z-form
62	H	H	OH	H	H	4-CN	Cl	O	Viscous
									material
63	H	H	OH	H	H	4-CN	OCF3	O	113
64	H	H	CH3	H	H	H	Cl	O	164
65	H	H	CH3	H	H	H	OCF3	S	118
66	H	H	OCH3	H	H	H	Cl	O	183
67	H	H	OCH3	H	H	H	OCF3	O	181
68	H	H	C3H7-i	H	H	H	Cl	O	155
69	H	H	C3H7-i	H	H	H	OCF3	O	193
70	H	H	OC4H9-i	H	H	H	Cl	O	176
71	H	H	OC4H9-i	H	H	H	OCF3	O	184
72	H	H	O—CO—CH3	H	H	H	OCF3	O	182
73	H	H	O—CO—Ph	H	H	H	OCF3	O	168
74	H	H	OH	CH3	H	H	Cl	O	115
75	H	H	OH	CH3	H	H	OCF3	O	130
76	H	H	H	H	3-F	4-CN	SCF3	O	214
77	H	H	H	H	3-F	4-CN	SOCF3	O	214
78	H	H	H	H	4-F	4-CN	SO2CF3	O	165
79	H	H	H	H	3-Cl	4-CN	SOCF3	O	157
80	H	H	H	H	3-CF3	4-CN	SCF3	O	215
81	H	H	H	H	3-CF3	4-CN	SOCF3	O	210
82	H	H	H	H	3-CF3	4-CN	OCF3	O	152
									Z-form
83	H	H	H	H	3-CF3	4-CN	Cl	O	165

[0020]

TABLE 2
General Formula (I-2)
(I-2)
8
(R1 and R3 are hydrogen atoms.)
No	R2	R4	R5	X	Y	Z	W	mp° C.
84	H	H	H	H	H	Cl	O	211
85	H	H	H	H	H	OCF3	O	194
86	H	H	H	H	4-Cl	OCF3	O	209
87	H	H	H	H	4-CN	OCF3	O	204
88	H	H	H	H	4-NO2	OCF3	O	203
89	H	H	H	3-F	4-Cl	OCF3	O	203
90	H	H	H	3-Cl	4-Cl	OCF3	O	176
91	H	H	H	3-Cl	4-CN	OCF3	O	193
92	H	H	H	3-Cl	4-CN	SCF3	O	177
93	H	H	H	3-Cl	4-CN	SOCF3	O	178
94	H	H	H	3-Cl	4-CN	SO2CF3	O	170
95	H	H	H	3-Br	4-CN	OCF3	O	187
96	H	H	H	3-CF3	4-CN	OCF3	O	165
97	H	H	H	3-CF3	4-CN	SCF3	O	164
98	H	H	H	H	4-Cl	OCF3	S	171
99	H	H	H	3-Cl	4-CN	OCF3	S	149
100	H	H	H	3-CF3	4-CN	OCF3	S	209
101	H	H	CO—CH3	3-Cl	4-CN	OCF3	O	178
102	H	H	CO—Ph	3-Cl	4-CN	OCF3	O	221
103	H	H	CONHC2H5	3-Cl	4-CN	OCF3	O	201
104	H	OH	H	H	H	OCF3	O	190
105	H	OCH3	H	H	H	Cl	O	195
106	H	OCH3	H	H	H	OCF3	O	183
107	H	OCH3	H	H	H	OCF3	O	186
108	CH3	H	H	3-Cl	4-CN	OCF3	O	156
109	H	H	H	H	4-F	OCF3	O	209
110	H	H	H	H	4-Br	Cl	O	233
111	H	H	H	H	4-Br	OCF3	O	201
112	H	H	H	H	3-CN	OCF3	O	176
113	H	H	H	H	2-NO2	OCF3	O	197
114	H	H	H	3-F	4-CN	OCF3	O	189
115	H	H	H	3-F	4-CN	SCF3	O	189
116	H	H	H	3-F	4-CN	SOCF3	O	166
117	H	H	H	3-CF3	4-CN	OCF3	O	131
								−Isomer
118	H	H	H	3-CF3	4-CN	OCF3	O	126
								+Isomer
119	H	H	H	3-CF3	4-CN	SOCF3	O	Glassy
								material
120	H	H	H	3-CF3	4-CN	SO2CF3	O	Glassy
								material
121	H	H	H	H	3-CN	OCF3	O	120
Notes: In this table, Ph represents a phenyl group. Compound Nos. 106 and 107 are diastereomers. Compound No. 106 is higher than Compound No. 107 in Rf value.

[0021]

TABLE 3
General formula (I-3)
(I-3)
9
(In this table, R2 and R3 are hydrogen atoms,
and W is an oxygen atom.)
						mp° C.
No	R1	R4	X	Y	X	Refractive index
122	H	H	H	H	OCF3	113.3-114.0
123	H	H	H	4-Cl	OCF3	137.8
124	H	H	H	4-CN	Cl	163
125	H	H	H	4-CN	OCF3	138
126	H	H	3-Cl	4-Cl	Cl	143.5-144.0
127	H	H	3-Cl	4-Cl	OCF3	139.6-141.5
128	H	H	3-Cl	4-NO2	Cl	174.0-176.5
129	H	H	3-Cl	4-NO2	OCF3	151.6-151.7
130	H	H	3-Cl	4-CN	Cl	191.0-192.0
131	H	H	3-Cl	4-CN	OCF3	160.5-162.0
132	H	H	3-Cl	4-CN	SCF3	188.0
133	H	H	3-Cl	4-CN	SOCF3	206.1
134	H	H	3-F	4-CN	Cl	154-156
135	H	H	3-F	4-CN	OCF3	155.9-156.8
136	H	H	3-CH3	4-CN	Cl	127
137	H	H	3-CH3	4-CN	OCF3	166
138	H	H	3-CF3	4-CN	Cl	164-165
139	H	H	3-CF3	4-CN	OCF3	151.0
140	H	CH3	3-Cl	4-CN	OCF3	nD 1.5950(25° C.)
141	CH3	H	3-CF3	4-CN	Cl	209-211
142	H	H	3-Cl	2-CN	OCF3	148

[0022]

TABLE 4
General formula (I-4)
(I-4)
10
(In this formula, R1, R2, R3 and R4 are hydrogen
atoms, and W is an oxygen atom.)
				mp° C.
No	X	Y	Z	Refractive index
143	H	H	OCF3	51.0-53.0
144	H	4-Cl	OCF3	92.1
145	H	4-CN	Cl	106-108
146	H	4-CN	OCF3	nD 1.5685 (27° C.)
147	3-Cl	4-Cl	Cl	105.3-106.4
148	3-Cl	4-Cl	OCF3	38.0
149	3-Cl	4-NO2	Cl	Viscous material
150	3-Cl	4-NO2	OCF3	Viscous material
151	3-Cl	4-CN	Cl	153.1
152	3-Cl	4-CN	OCF3	43.5-45.0
153	3-F	4-CN	Cl	164-165
154	3-F	4-CN	OCF3	nD 1.5615 (27° C.)
155	3-CH3	4-CN	Cl	138-139
156	3-CH3	4-CN	OCF3	nD 1.5315 (28° C.)
157	3-CF3	4-CN	Cl	43
158	3-CF3	4-CN	OCF3	153.1

[0023] Some of the compounds shown in Tables 1 to 4 are viscous substances or glassy substances. 1H-NMR date of these compounds are shown in Table 5.

No  1H-NMR [CDCl3/TMS, δ value (ppm)]
59  6.29(s, 1H), 7.65-7.92(m, 13H), 9.14(bs, 1H),
    10.70(bs, 1H). (DMSO-d6)
62  3.88(bs, 1H), 3.87(s, 1H), 6.91-7.55(m, 13H),
    7.73(s, 1H), 8.13(bs, 1H).
119 3.12(dd, 1H), 3.23(dd, 1H), 4.12-4.32(m, 2H),
    6.13(bs, 1H), 7.24-7.93(m, 12H), 8.08(bs, 1H).
120 3.11(dd, 1H), 3.23(dd, 1H), 4.13-4.28(m, 2H),
    5.97(s, 1H), 7.25-7.75(m, 12H), 7.90-8.00(bs, 1H).
149 3.65(d, 2H), 4.20(t, 1H), 4.70(s, 2H),
    6.85(dd, 1H), 6.93(dd, 1H), 7.08(dd, 1H), 7.15-
    7.21 (m, 3H), 7.24(d, 2H), 7.40(d, 2H), 8.13(d, 2H),
    8.40 (s, 1H).
150 3.64(s, 2H), 4.69(s, 2H), 6.84(dd, 1H),
    6.94 (dd, 1H), 7.09(m, 3H), 7.23(t, 1H),
    7.29(d, 2H), 7.40(d, 2H), 8.12(d, 2H), 8.40(s, 1H).

[0024] The ectoparasitic insect pest controller for animals of this invention can be used for domestic animals such as cattle, horse, sheep, etc.; and pets such as dog, cat, etc.; as well as for Rodential animals such as mouse, rat, hamster, squirrel, etc.; Lagomorphous animals, Carnivorous animals such as ferret, etc.; and birds such as duck, chicken, pigeon, etc. As the ectoparasitic pest insects of these animals, for example, the insects belonging to fleas such as

cat flea                   (Ctenocephalides felis),
dog flea                   (Ctenocephalides canis),
oriental rat flea          (Xenopsylla cheopis), etc.; the
                           insects belonging to ticks such as
Haemaphysalis longicornis, (Boophilus microplus), etc.; and
cattle tick                the insects belonging to lice such as
cattle louse               (Haematopinus eurysternus),
sheep louse                (Damalinia ovis), etc. can be
                           referred to.

[0025] For an effective use of the ectoparasitic insect pest controllers for animals of this invention represented by the general formula (1), the controller is compounded with an appropriate solid carrier and/or liquid carrier and, if necessary, adjuvants and the like in an appropriate proportion according to the conventional recipe in the drug making and fixed on the carriers by dissolution, suspension, mixing, impregnation, adsorption or adhesion. The resulting mixture is formed into an appropriate preparation form such as liquid preparation, emulsion, cream, ointment, suspension, aerosol, etc. according to the purpose of the use, and then the formed preparation is put to use.

[0026] The solid or liquid carriers used in this invention may be the carriers conventionally used for agents for animals. From the viewpoint of easiness of treatment on the objective animals, the use of liquid carriers is preferable. As examples of the liquid carrier, alcohols such as methyl alcohol, ethyl alcohol, isopropyl alcohol, tertiary butyl alcohol, benzyl alcohol and the like; propylene carbonate; N-methyl-2-pyrrolidone; water, etc. can be referred to.

[0027] According to the need, adjuvants can be incorporated into the controller of this invention. As the adjuvants, surfactants, antioxidants, emulsifiers, etc. can be referred to. More specific examples of the adjuvants include surfactants such as polyoxyethylene alkylaryl ether, polyoxyethylene sorbitan monolaurate, alkylaryl sorbitan monolaurate, alkylbenzenesulfonates, alkylnaphthalene-sulfonic acid, ligninsulfonic acid salts, higher alcohol sulfate salts, glycol monoalkyl ethers, glycols, and the like; emulsifiers such as sorbitan monooleate, sorbitan monolaurate, caprylic acid monoglyceride, capric acid monoglyceride, isostearic acid monoglyceride, propylene glycol monocaprylate, etc; and antioxidants such as BHA, BHT, etc.

[0028] The ectoparasitic insect pest controller composition for animals of this invention can contain the insect pest controller of this invention as an active ingredient in an amount of 0.01-80.0% by weight per 100 parts by weight of the present composition.

[0029] The methods for using the ectoparasitic insect pest controller for animals of this invention include a pot-on treatment which comprises dropping a liquid agent onto the skin of the back shoulder region of the objective animal and thereby controlling the ectoparasitic insect pest; and a local treatment such as pore-on which comprises applying a liquid agent along the back center line of the objective animal and the allowing the applied agent to diffuse on the body surface and thereby controlling the ectoparasitic insect pest; as well as a treatment method of supporting the agent on a collar or the like from which the agent is released; a treatment method of directly coating a liquid agent or an ointment onto the body surface; a treatment method of applying an aerosol of a liquid agent by means of spray or the like; etc. The dose of the agent may be appropriately selected from a range of about 0.1 to 500 mg as expressed in terms of active ingredient compound, and from a range of about 0.01 to 20 ml as expressed in terms of the insect pest controller of this invention, both per kilogram of body weight of the objective animal.

[0030] According to the need, the ectoparasitic insect pest controller for animals of this invention may be used in combination with other active ingredients. As said “other active ingredient”, for example, the following can be referred to:

[0031] pyrethroid compounds such as permethrin, phenothrin, allethrin, pyrethrin, prallethrin, cyphenothrin, cyfluthrin, fenvalerate, fenpropathrin, transfluthrin, etc.;

[0032] organic phosphorus compounds such as dichlorvos, tetrachlorvinphos, fenthion, chlorpyrifos, diazinon, etc.;

[0033] N-phenylpyrazole compounds such as fipronil, etc.;

[0034] carbamate compounds such as propoxur, carbaryl, metoxadiazone, fenocarb, etc.;

[0035] neonicotinoid compounds; etc.

EXAMPLES

Example 1

[0036]

A compound shown in Tables 1-4 5 parts
Hexylene glycol                50 parts
Isopropanol                    45 parts

[0037] The above-mentioned ingredients were uniformly mixed and dissolved together to obtain a liquid formulation.

Example 2

[0038]

A compound shown in Tables 1-4   10 parts
Polyoxyethylene styrylphenyl ether 10 parts
Cylohexanone                     80 parts

[0039] The above-mentioned ingredients were uniformly mixed and dissolved together to obtain an emulsifier.

Test Example 1

[0040] A spot-on agent was prepared by mixing and dissolving 10 parts by weight of Compound 44 or Compound 96 in 90 parts by weight of diethylene glycol monoethyl ether. One day before the day of administration, 30 fleas [adult worm of cat flea (Ctenocephalides felis)] were made to parasitize a cat, and the cat was let wear an Elizabeth collar on the neck. Then, 0.4 ml of a test agent was applied to the skin of back shoulder area of the cat (alive body weight 3.2 kg). One day after and three days after the treatment using the agent, the number of parasitic fleas was counted by means of a flea-catching comb. After counting the number of parasitic fleas, the whole fleas were again made to parasitize the cat. As a blank test, fleas were made to parasitize an untreated cat in the same manner as above, and the number of parasitic fleas was counted. The controlling rate was calculated according to the following formula, and the result was judged according to the criterion shown below.

1Controlling⁢ ⁢rate⁢ ⁢(%)=Parasitic⁢ ⁢ratein⁢ ⁢untreatedgroup-Parasitic⁢ ⁢ratein⁢ ⁢treatedgroupParasitic⁢ ⁢rate⁢ ⁢inuntreated⁢ ⁢group×100
Criterion of judgement Controlling rate (%)
A                      100
B                      99-90
C                      89-80
D                      79-50

[0041] Thus, both the ectoparasitic insect pest controllers for animals containing Compound No. 44 and Compound No. 96 of this invention gave a judgement of A.

Claims

1. (Amended) An ectoparasitic insect pest controller for animals which contains, as active ingredient thereof, a hydrazine derivative represented by the following general formula (I):

2. (Amended) An ectoparasitic insect pest controller for animals according to claim 1, represented by the following general formula (I-1):

3. An ectoparasitic insect pest controller for animals according to claim 1, represented by the following general formula (I-2):

4. An ectoparasitic insect pest controller for animals according to claim 1, represented by the following general formula (I-3):

5. An ectoparasitic insect pest controller for animals according to claim 1, represented by the following general formula (I-4):

6. A method for using an ectoparasitic insect pest controller for animals, characterized by treating the body surface of an animal with an effective quantity of the ectoparasitic insect pest controller for animals according to any one of claims 1-5.