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Acaricidal properties of di-(p-chlorophenyl)-trifluoromethylcarbinol
Year:
1961
Source of publication :
Nature
Authors :
Ascher, K. R. Simon
;
.
Volume :
191
Co-Authors:
Ascher, K.R.S., Department of Toxicology, National and University Institute of Agriculture, Beit-Dagan, Rehovot, Israel
Cwilich, R., Department of Toxicology, National and University Institute of Agriculture, Beit-Dagan, Rehovot, Israel
Facilitators :
From page:
1322
To page:
1323
(
Total pages:
2
)
Abstract:
Di-(p-chlorophenyl)-trifluoromethylcarbinol, (Cl.C 6H 4) 2C(OH).CF 3 1,2, has several interesting biological properties : it is a synergist for DDT in the house-fly 1,3-5 and inhibits oviposition, on tarsal contact, in house-flies 6 and mosquitoes 7. Since it is the fluorine analogue of two acaricides, namely DMC [di-(p-chlorophenyl)-methylcarbinol] and 'Kelthane' [di-(p-chlorophenyl)-trichloromethylcarbinol], it seemed interesting to assay also its acaricidal properties. The compound was tested against adult females of the red spider mite Tetranychus telarius L. on beans, by a method described recently 8, and was compared with the commercial acaricides 'Kelthane' and chlorobenzilate (ethyl p,p′-dichlorobenzilate). The activity of the fluorine compound was intermediate between those of 'Kelthane' and chlorobenzilate (Table 1). © 1961 Nature Publishing Group.
Note:
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DOI :
10.1038/1911322b0
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
19801
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:31
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Scientific Publication
Acaricidal properties of di-(p-chlorophenyl)-trifluoromethylcarbinol
191
Ascher, K.R.S., Department of Toxicology, National and University Institute of Agriculture, Beit-Dagan, Rehovot, Israel
Cwilich, R., Department of Toxicology, National and University Institute of Agriculture, Beit-Dagan, Rehovot, Israel
Acaricidal properties of di-(p-chlorophenyl)-trifluoromethylcarbinol
Di-(p-chlorophenyl)-trifluoromethylcarbinol, (Cl.C 6H 4) 2C(OH).CF 3 1,2, has several interesting biological properties : it is a synergist for DDT in the house-fly 1,3-5 and inhibits oviposition, on tarsal contact, in house-flies 6 and mosquitoes 7. Since it is the fluorine analogue of two acaricides, namely DMC [di-(p-chlorophenyl)-methylcarbinol] and 'Kelthane' [di-(p-chlorophenyl)-trichloromethylcarbinol], it seemed interesting to assay also its acaricidal properties. The compound was tested against adult females of the red spider mite Tetranychus telarius L. on beans, by a method described recently 8, and was compared with the commercial acaricides 'Kelthane' and chlorobenzilate (ethyl p,p′-dichlorobenzilate). The activity of the fluorine compound was intermediate between those of 'Kelthane' and chlorobenzilate (Table 1). © 1961 Nature Publishing Group.
Scientific Publication
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