Acaricidal

Karathane A trade name for 2,4-dinitro-6-( 1 -methylheptyl)phenyl crotonate, CJ8H24N2O6, a compound which has both acaricidal and fungicidal activity. It is a red-brown oil of high boiling point, insoluble in water but soluble in most organic solvents. Karathane is used for the control of powdery mildew, and is nontoxic to mammals. 

Carbamates such as Aldicarb undergo degradation under both aerobic and anaerobic conditions. Indeed the oxidation of the sulfur moiety to the sulfoxide and sulfone is part of the activation of the compound to its most potent form. Subsequent aerobic metaboHsm can completely mineralize the compound, although this process is usually relatively slow so that it is an effective iasecticide, acaricide and nematocide. Anaerobically these compounds are hydrolyzed, and then mineralized by methanogens (61). 

Dicofol [54532-36-4] l,l-bis(/)-chlorophenyl)-2,2,2-trichloroethanol, R = Cl (139), is a white crystalline soHd (mp 79°C). This compound is insoluble in water and soluble in organic solvents, and in the presence of alkaU forms the inactive/),/) -dichloroben2ophenone and chloroform. Dicofol is a long-lasting acaricide and is active against all stages of mites. The rat oral LD qS are 809, 684 mg/kg. 

Cyhexatin [13121 -70-5], tricyclohexylhydroxystannane (147) (mp 195°C), rat oral 540 mg/kg, and fenbutatin oxide [13356-08-6], hexakis-(2-methyl-2-phenylpropyl)distannoxane (148) (mp 138°C), rat oral LD q 2630 mg/kg, are two novel tin acaricides used on deciduous fmits. They are inhibitors of oxidative phosphorylation. 

Cinnamyl—sesamol ethers, eg (35), are useful as insect chemosterilants (111). 3,4-Methylenedioxyphenyl-3-halo-2-propynyl ethers (36, X = halogen) are synergists for carbamate insecticides (112). HaloaLkyl or haloalkenyl ethers, eg (37), show acaricidal and insect juvenile hormone activity (113). The first total synthesis of gibbereUic acid was from 2-methoxy-6-aLkoxyethyl-l,4-benzoquinone, a derivative of hydroxyhydroquinone (114). 

In 1976 scientists at the Merck Corporation discovered a complex of eight closely related natural products, subsequently named avermectins A through in a culture of Streptomjces avermitilis MA-4680 (NRRL8165) originating from a soil sample collected at Kawana, Ito City, Shizuoka Prefecture, Japan and isolated by the Kitasato Institute. Their stmctures are shown in Figure 1 (1 6). They are among the most potent anthelmintic, insecticidal, and acaricidal compounds known. 

Pesticides (includes acaricides, avicides, bactericides, insecticides, molluskicides, nematocides, piscicides, rodenticides) Pharmaceuticals... 

The compounds represented by general formula 117 are useful as a insecticides, acaricides, and bactericides (99INP9946247). 

Akajou, m. acajou (either cashew or mahogany tree), -harz, n. acajou resin, -nuss, /. cashew nut, -31, n. cashew (nut) oil. Akaridentod, m. acaricide. 

Most analytical work on sulphones has naturally been concerned with the compounds synthesized for special purposes, e.g. sulphonal, trional and tetronal as sedatives and hypnotics Sulphenone (4-chlorodiphenyl sulphone) and Tedion (2,4,4, 5 -tetrachlorodiphenyl sulphone) as acaricides 4,4 -diaminodiphenyl sulphone as an antileprotic. In choosing examples preference has been given to methods devoted to more than a single sulphone. 

Detection in HPLC by ultraviolet absorption is commonplace and does not merit special mention here (see Section F.l below). There appear to be only few quantitative procedures for sulphones which are based on measurements of UV absorption. The final stage in a determination of the acaricide Sulphenone by Shuman29 was differential measurement of the absorption at 230,240 and 250 nm in isooctane solution. Kashiwa and... 

The rapid rise in the industrial (catalyst in PVC and foam production), agricultural (fungicides and acaricides), and biological applications (wood, stone, and glass preservatives) of organotin(IV) compounds during the last few decades has led to their accumulation in the environment and, consequently, in biological systems. 

The next major discovery in this field, which was the result of a joint research effort in 1968 between M and T Chemicals, Inc., and the Dow Chemical Company in the United States (475, 524), was that tricyclo-hexyltin hydroxide ("Plictran ) possesses a very high activity against certain types of mites, and this compound was subsequently introduced by Dow as an acaricide for use on apple, pear, and citrus-fruit trees. A second triorganotin acaricide, bis(trineophyltin) oxide ("Vendex or "Torque ), has recently been introduced by Shell Chemical Company (476). Two other tricyclohexyltin compounds are currently under de-... 

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