|
| | Cyproconazole Chemical Properties |
| Melting point | 108℃ | | Boiling point | >250℃ | | density | 1.32 | | vapor pressure | 3.46 x l0-5 Pa (20 °C) | | refractive index | 1.6330 (estimate) | | Fp | >100 °C | | storage temp. | Store at -20°C | | solubility | Soluble in acetone, ethanol, xylene, and dimethyl sulfoxide. | | form | neat | | Water Solubility | 140 mg l-1(25 °C) | | pka | 12.59±0.29(Predicted) | | BRN | 8396421 | | Stability: | Hygroscopic | | LogP | 3.1 at 25℃ and pH7.2 | | CAS DataBase Reference | 94361-06-5(CAS DataBase Reference) | | EPA Substance Registry System | Cyproconazole (94361-06-5) |
| Hazard Codes | Xn,N | | Risk Statements | 22-50/53-63 | | Safety Statements | 36/37-60-61-36 | | RIDADR | UN3077 9/PG 3 | | WGK Germany | 3 | | RTECS | XZ4803250 | | HazardClass | 9 | | Hazardous Substances Data | 94361-06-5(Hazardous Substances Data) | | Toxicity | LD50 in male and female rats (mg/kg): 1020, 1330 orally; in rats: 2000 dermally; LD50 in carp: 18.9 mg/l; in trout 7.2 mg/l; in bluegill sunfish 6.0 mg/l in water; LD50 in bobwhite quail (mg/kg): 150 orally; LD50 (8 day dietary) in bobwhite quail, mallard duck: 816, 1197 mg/kg (Gisi, 1986) |
| | Cyproconazole Usage And Synthesis |
| Physical and chemical properties | It appears as colorless crystals with the melting point of 106 to 109 °C, the boiling point of> 250 °C and the vapor pressure at 20 ° C of 0.03470 mPa. It has a relative density of 1.259 with water solubility at 25 ℃ of 1.4g/kg, acetone> 2300g/kg, dimethyl sulfoxide> 180g/kg, ethanol> 230g/kg and xylene: 1200g/kg. It has a Ko819 (±195) (pH 7). Under 70 °C, it can be stable up to 15 days. The DT50 of the soil surface was 21 days under the sunlight; pH value is at the range of 3~9. It is stable under 59 ℃. The soil adsorption coefficient K was 4.1 (loam, pH 6.4, organic matter content: 2.3%), 16 (soil sandy soil, pH 5.1, organic matter content: 3.9%). | | Fungicide | Cyproconazole is a kind of triazole agricultural fungicide with the mechanism of action being inhibition of sterol demethylation with prevention and treatment effect. Currently it has been widely used in pesticides, being effective in the treatment of powdery mildew, rust fungi, Rhizopus, Cercospora, Acipenseris and Scleroderma in cereal crops, coffee, sugar beet and fruit trees. It is effective in the treatment of following plant diseases such as the rust diseases of cereals and coffee, powdery mildew diseases of cereals, fruit trees and grape, leaf spot of peanuts and beet, apple scab and white rot disease cereal eye spot, leaf spot and reticulosis of peanuts.
Its persistence in the treatment of wheat rust disease is about 4 to 6 weeks and of powdery mildew is 3 to 4 weeks. The spraying method is as follows: spray, the dosage is 80g/ha for cereal crops, 20-50g/ha for coffee, 40-60g/ha for beets and 10 g/ha for fruit tree. For example, we can apply 40~100g/ha for prevention of cereals and coffee rust, cereal, fruit powdery mildew and so on. Cyproconazole can be mixed with other fungicides for better control of cereal eye disease, leaf spot and leaf net blotch disease.
Analytical method: The product was analyzed by GLC or HPLC. The residue was assayed by GLC.
Allowable residue: The residual amount of the parent compound in the cereal crop is 0.03 mg/kg. | | Toxicity | Male rats had acute oral LD50 of 1020 mg/kg, female rats of 1333 mg/kg; male mice of 200 mg/kg and female mice of 218 mg/kg. Rats, rabbits acute percutaneous LD50> 2g/kg; rats acute inhalation LC50 (4 hours)> 5.65mg/L • air. (1 year) and 1 mg/(kg • d) in rats (2 years). No irritation to rabbit skin and eyes, no mutagenic effect, no skin allergies to guinea pigs. Low toxicity to birds, quail acute oral LD50 of 150mg/kg; LC50 of duck in 8 days feeding test is 1197mg/kg, while the value for quail is 816mg/kg. Fish poisoning LC50 (96 hours): carp 18.9mg/L, rainbow trout 19mg/L, blue gills 21mg/L. Bees LD50> 0.1mg/bee (contact),> 1mg/kg (oral). Daphnia LC50 (48 hours) was 26 mg/L. | | Preparation | 1-(4-chlorophenyl)-2-cyclopropyl-1-propanone was reacted with sodium hydride and methyl iodide to give 1-(4-chlorophenyl)-2-cyclopropyl-1-acetone, followed by reaction with CH3(CH2) 11S + (CH3)2CH3SO3-to produce ethylene oxide derivatives, and finally condensed with 1H-1, 2, 4-triazole, leading to the formation of Cyproconazole. | | Chemical Properties | Colorless, crystalline solid. Odorless. | | Uses | Cyproconazole is a fungicide treatment for wood preservative that prevents decay from fungi in above-ground applications. | | Uses | Cyproconazole is used to inhibit demeythylation in fungal sterol synthesis. And it is used on greenhouse and field-grown roses and as a wood preservative, surface application or pressure treatment of wood for above-ground uses, including siding, plywood, millwork, shingles, lumber. | | Uses | Cyproconazole is used as a systemic fungicide to control cereal
and sugar beet foliar diseases: Septoria, rust, powdery mildew, Rhyncosporium,
Cercospora and Ramularia. It is also used in fruit trees, vines,
coffee, banana, turf, and vegetables to control Venturia, powdery mildew,
rust, Mycosphaerela, Monilia, Mycena, Sclerotinia and Rhizoctonia. | | Definition | ChEBI: 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol is a tertiary alcohol that is butan-2-ol substituted by a 4-chlorophenyl group at position 2, a cyclopropyl group at position 3 and a 1H-1,2,4-triazol-1-yl group at position 1. It is a member of monochlorobenzenes, a tertiary alcohol, a member of triazoles and a member of cyclopropanes. | | Agricultural Uses | Fungicide: Used to control fungus on cereals, coffee beans; anthracnose and other diseases on turfgrass; used against rust and leaf spot disease. | | Trade name | ALTO®; ALTO®, ELITE; ATEMI®; ATEMI-50-SL®;EVIPOL®; FLINT®; NOAH GOLD®; SAN-619 F®; SENTINEL®; SN 108266® | | Potential Exposure | Triazole fungicide used to control fun-
gus on cereals, coffee beans; anthracnose and other diseases
on turfgrass; used against rust and leaf spot disease. | | Metabolic pathway | Cyproconazole is a mixture of diastereiosomers and the preferential
mammalian metabolism of one isomer has been observed. Pathways
of metabolism in plants and mammals are quite similar. Metabolism
primarily involves oxidation of the terminal methyl group to alcohols
and carboxylic acids and/or hydroxylation at the 3-position. Loss of the
alkyl cyclopropyl moiety or the triazolyl ring also occurs. | | Shipping | UN3082 Environmentally hazardous substances,
liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous haz-
ardous material, Technical Name Required | | Degradation | Cyproconazole is stable and decomposition was <5% after 2 years. It
was stable in aqueous solutions (at pH 1-9) for 35 days (50 °C) or 14
days (80 °C). It is slowly hydrolysed in hydrochloric acid or sodium
hydroxide.
14C-Labelled cyproconazole was applied at a rate equivalent to
100 g ha-1 to the surface of a 2 mm layer of loam soil. The samples were
exposed to natural sunlight for up to 72 days on open dishes or in flasks
fitted with plugs to trap volatile products. Samples were extracted at
intervals and analysed. After 37 days exposure on dishes, 50% of the
applied cyproconazole remained whereas 85% remained after 72 days in
the flasks. In the dishes, unextractable residues amounted to 13-20% of
the applied radiolabel after 20 days or more exposure, whereas in the
flasks it reached a maximum of 6% after 15 days. The products identified
in the dishes were: 1-(4-chlorophenyl)-2-(1H -1,2,4-triazol-l-yl)-
ethanone (2, 5%), 3-cyclopropyl-1-(1H-1,2,4-triazol-l-yl)butanone(4,4%),
2-(2- or 3-hydroxy-4-chlorophenyl)-3-cyclopropyl-1-(1H -1,2,4-triazol-1-yl)-
butan-2-ol (3 4%), and 4-chlorobenzoic acid 5 (Scheme 1) (PSD, 1991).
Degradation in the flasks was similar but occurred to a lesser extent. No
volatde products were trapped and recoveries of radiolabel were 94-
102%. | | Incompatibilities | The triazoles are sensitive to heat, fric-
tion, and impact. Sensitivity varies with the type substitu-
tion to the triazole ring. Metal chelated and halogen
substitution of the triazol ring make for a particularly heat
sensitive material. Azido and nitro derivatives have been
employed as high explosives. No matter the derivative
these materials should be treated as explosives
. | | Waste Disposal | Consult with environmental
regulatory agencies for guidance on acceptable disposal
practices. Contact a licensed disposal facility about surplus
and nonrecyclable solutions. Burn in a chemical incinerator
equipped with an afterburner and scrubber. Extra care must
be exercised as the material in an organic solvent is highly
flammable. In accordance with 40CFR165, follow recom-
mendations for the disposal of pesticides and pesticide con-
tainers. Containers must be disposed of properly by
following package label directions or by contacting your
local or federal environmental control agency, or by con-
tacting your regional EPA office. Incineration or permanga-
nate oxidation. |
| | Cyproconazole Preparation Products And Raw materials |
|
