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Plant growth regulators
captan
Chemical Identification
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General Product Information
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Physical & Safety Data
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Shared Information
Chemical Identification
Edit
Common Name
captan
中文通用名
克菌丹
IUPAC
N-(trichloromethylthio)cyclohex-4-ene-1,2-dicarboximide
CAS
3a,4,7,7a-tetrahydro-2-[(trichloromethyl)thio]-1H-isoindole-1,3(2H)-dione
CAS No.
133-06-2
Molecular Formula
C
9
H
8
Cl
3
NO
2
S
Molecular Structure
General Product Information
Edit
Category
Fungicides > Dicarboximide fungicides
Activity
Captan provides consistent control of the most damaging diseases that attack apple, almond, stone fruit and berry. Along with superior efficacy against primary and secondary scab, captan delivers broad-spectrum control of many other diseases such as black rot (frogeye), sooty blotch, fly speck, black rot, Botryosphaeria rot, bull's eye rot, Botrytis rot and bitter rot.
Premix
imidacloprid+captan+carboxin
Dust, flowable, wettable powder. Premix Parters: lindane;
Physical & Safety Data
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Physical Properties
Molecular weight:300.6; Physical form: Colourless crystals; (tech. is a colourless to beige amorphous solid, with a pungent odour). Density:1.74 (26 °C); Composition:Tech. is 90-95% pure. Melting point:178 °C (tech., 175-178 °C); Vapour pressure:<1.3 mPa(25 °C); Henry constant:<1.18×10-1 Pa m3 mol-1 (calc.); Partition coefficient(n-octanol and water):logP = 2.8 (25 °C); Solubility:In water 3.3 mg/l (25 °C). In xylene 20, chloroform 70, acetone 21, cyclohexanone 23, dioxane 47, benzene 21, toluene 6.9, isopropanol 1.7, ethanol 2.9, diethyl ether 2.5 (all in g/kg, 26 °C). Insoluble in petroleum oils.; Stability:Hydrolysed slowly at neutral pH, rapidly in alkali. Thermal DT50 >4 y (80 °C), 14.2 d (120 °C). Very low solubility in organic solvents. Insoluble in petroleum oils. Solubility at 25°C: in xylene 20 g/kg; chloroform 70 g/kg; acetone 20 g/kg; cyclohexanone 20 g/kg; 2-propanol 1 g/kg.
Toxicology
Oral:Acute oral LD
50
for rats 9000 mg/kg. Percutaneous:Acute percutaneous LD
50
for rabbits >4500 mg/kg. Corrosive to eyes; mild skin irritant (rabbits). Inhalation:LC
50
for male rats >0.72, female rats 0.87 mg/l (tech.). Dust may cause respiratory irritation. Phytotoxicity:Non-phytotoxic if used as directed, but some varieties of apple (e.g. Red Delicious, Winesap) and pear (e.g. D'Anjou, Bosc) may be injured, as also may lettuce seeds and, at higher dosage
Environmental Profile
Ecotoxicology: Bees:ED
50
(oral) 91; (contact) 788
mg/bee.Birds:Acute oral LD
50
for mallard ducks and pheasants >5000, bobwhite quail 2000-4000 mg/kg. Not toxic to starlings or red-winged blackbirds at 100 mg/kg.Daphnia: LC
50
(48 h) 7-10 ppm.Fish:LC
50
(96 h) for bluegill sunfish 0.047-0.111 ppm,rainbow 0.066-0.080 ppm (96 h), trout harlequin fish 0.3 mg/l, brook trout 0.034 mg/l.Other aquatic spp.:Moderately toxic to aquatic invertebrates. Environmental fate: Animals:In mammals, the three chlorine atoms are cleaved under the influence of cellular sulfhydryl compounds. Trithiocarbamate, thiophosgene, and tetrahydrophthalimide are formed (R. G. Owens,
Ann. New York Acad. Sci
., 1969,
160
, 114-13Soil:Soil K
d
3-8 (pH 4.5-7.2, o.m. 2.2-6.7%); DT
50
c.
1 d (25 °C, pH 7.2, o.m. 1.2%). WATER SOLUBILITY: <5 mg/l at room temperature.
Transport Information
Signal Word:DANGER; Hazard Class:Ib (Highly hazardous)
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captan
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