Enilconazole (CAS 35554-44-0) — formula C14H14Cl2N2O, molecular weight 297.2.
| CAS Number | 35554-44-0 |
|---|---|
| Molecular Formula | C14H14Cl2N2O |
| Molecular Weight | 297.2 |
| Melting Point | 52.7 °C |
| Boiling Point | 347 °C |
| LogP | 3.8 |
| Applications | Uses: Broad spectrum antimycotic used to disinfect stable and kennel equipment and to treat fungal infections in humans and animals, [Merck Index] Used to protect fruit, vegetables, and ornamentals, as seed dressing for cereals, as post-harvest treatment for citrus fruit, pome fruit, bananas, and seed potatoes, to treat equipment and egg storage areas in chicken hatcheries, [HSDB], Using Disinfectants or Biocides [Category: Clean], Farming (Pesticides) [Category: Industry], For Imazalil (USEPA, OPP Pesticide Code: 111901) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Mesh Heading: fungicides, industrial, Systemic fungicide used to control a wide range of fungal diseases on fruit, Fungicide, Wheat and barley seed treatment for common (dryland) root rot (Fusarium, Helminthosporium) and associated seedling diseases. For control of seedborne leaf stripe, net blotch, and Septoria nodorum. Prevents post-harvest decay of citrus, banana, and pome fruit. Active against benzimidazole-resistant strains of plant pathogenic fungi., For more Uses (Complete) data for IMAZALIL (7 total), please visit the HSDB record page., This is a man-made compound that is used as a pesticide., Use Classification: Fungicides, Environmental transformation -> Pesticides (parent, predecessor), Methods of Manufacturing: E. F. Godefroi et al., German patent 2, 063, 857 corresponds to US patent 3, 658, 813 (1971, 1972 both to Janssen), alpha, 2, 4-Trichloroacetophenone + imidazole + allyl chloride (amine formation, carbonyl reduction, ether formation)., By bromination of 2', 4'-dichloroacetophenone, followed by reduction with sodium borohydride to form an epoxide intermediate. The epoxide is opened with imidazole, and the resulting alcohol is then etherified., Formulations, Preparations: Emulsifiable concentrate, water soluble powder, soluble liquid., Trade Names: Fungaflor, Fungazil, Deccozil, Nuzone, Freshguard., Technical is > or =95% pure., Selected products: Deccozil, Flo-Pro, Freshgard, Magnate, Mazal. Mixtures: Baytan Combi (+fuberidazole +triadimenol) (fuberidazole not present in some formulations), Baytan Universal (+fuberidazole +triadimenol) (seed treatment), Vincit (+flutriafol +thiabendazole). Other products: Florasan, Sphinx, Stryper. Mixtures: Nectec (+azaconazole), Baytan IM (+fuberidazole +triadimenol), Citrocil (+2-phenylphenol), Extratect (+thiabendazole) (seed), Manta Plus (+fuberidazole +imidacloprid +triadimenol) (Germany), Panoctine Plus (+guazatine), Raxil (+tebuconazole) (seed treatment, East Europe), Raxil Complex Liquido (+tebuconazole) (seed treatment, Italy), Raxil IM (+tebuconazole) (seed treatment), Raxil MD Extra (+metalaxyl +tebuconazole), Robust (+triticonazole), Vincit FS (+flutriafol +thiabendazole), Vitaflo Extra (+carboxin +thiabendazole), Vitavax Extra (+carboxin +thiabendazole). Discontinued products: mixtures: Larin (+fenpiclonil +tebuconazole) (seed treatment, Germany), Raxil WS (+tebuconazole) (seed treatment, E Europe)., General Manufacturing Information: Control powdery mildews on cucurbits and ornamentals, powdery mildew on roses, storage diseases (particularly Penicillium, Gloeosporium, Phomopsis spp., etc.) of citrus fruit, and seed potatoes. Also used as a seed dressing, for control of diseases (particularly Fuasrium and Helminthosporium spp.) of cereals. It is particularly active against benzimidazole-resistant strains of plant-pathogenic fungi. |
Documented applications: Uses: Broad spectrum antimycotic used to disinfect stable and kennel equipment and to treat fungal infections in humans and animals, [Merck Index] Used to protect fruit, vegetables, and ornamentals, as seed dressing for cereals, as post-harvest treatment for citrus fruit, pome fruit, bananas, and seed potatoes, to treat equipment and egg storage areas in chicken hatcheries, [HSDB], Using Disinfectants or Biocides [Category: Clean], Farming (Pesticides) [Category: Industry], For Imazalil (USEPA, OPP Pesticide Code: 111901) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Mesh Heading: fungicides, industrial, Systemic fungicide used to control a wide range of fungal diseases on fruit, Fungicide, Wheat and barley seed treatment for common (dryland) root rot (Fusarium, Helminthosporium) and associated seedling diseases. For control of seedborne leaf stripe, net blotch, and Septoria nodorum. Prevents post-harvest decay of citrus, banana, and pome fruit. Active against benzimidazole-resistant strains of plant pathogenic fungi., For more Uses (Complete) data for IMAZALIL (7 total), please visit the HSDB record page., This is a man-made compound that is used as a pesticide., Use Classification: Fungicides, Environmental transformation -> Pesticides (parent, predecessor), Methods of Manufacturing: E. F. Godefroi et al., German patent 2, 063, 857 corresponds to US patent 3, 658, 813 (1971, 1972 both to Janssen), alpha, 2, 4-Trichloroacetophenone + imidazole + allyl chloride (amine formation, carbonyl reduction, ether formation)., By bromination of 2', 4'-dichloroacetophenone, followed by reduction with sodium borohydride to form an epoxide intermediate. The epoxide is opened with imidazole, and the resulting alcohol is then etherified., Formulations, Preparations: Emulsifiable concentrate, water soluble powder, soluble liquid., Trade Names: Fungaflor, Fungazil, Deccozil, Nuzone, Freshguard., Technical is > or =95% pure., Selected products: Deccozil, Flo-Pro, Freshgard, Magnate, Mazal. Mixtures: Baytan Combi (+fuberidazole +triadimenol) (fuberidazole not present in some formulations), Baytan Universal (+fuberidazole +triadimenol) (seed treatment), Vincit (+flutriafol +thiabendazole). Other products: Florasan, Sphinx, Stryper. Mixtures: Nectec (+azaconazole), Baytan IM (+fuberidazole +triadimenol), Citrocil (+2-phenylphenol), Extratect (+thiabendazole) (seed), Manta Plus (+fuberidazole +imidacloprid +triadimenol) (Germany), Panoctine Plus (+guazatine), Raxil (+tebuconazole) (seed treatment, East Europe), Raxil Complex Liquido (+tebuconazole) (seed treatment, Italy), Raxil IM (+tebuconazole) (seed treatment), Raxil MD Extra (+metalaxyl +tebuconazole), Robust (+triticonazole), Vincit FS (+flutriafol +thiabendazole), Vitaflo Extra (+carboxin +thiabendazole), Vitavax Extra (+carboxin +thiabendazole). Discontinued products: mixtures: Larin (+fenpiclonil +tebuconazole) (seed treatment, Germany), Raxil WS (+tebuconazole) (seed treatment, E Europe)., General Manufacturing Information: Control powdery mildews on cucurbits and ornamentals, powdery mildew on roses, storage diseases (particularly Penicillium, Gloeosporium, Phomopsis spp., etc.) of citrus fruit, and seed potatoes. Also used as a seed dressing, for control of diseases (particularly Fuasrium and Helminthosporium spp.) of cereals. It is particularly active against benzimidazole-resistant strains of plant-pathogenic fungi..
Enilconazole is a chemical compound with CAS registry number 35554-44-0 and molecular formula C14H14Cl2N2O (molecular weight 297.2).
CAS number: 35554-44-0
Its molecular formula C14H14Cl2N2O comprises 14 C, 14 H, 2 Cl, 2 N, 1 O atoms.
Also known as: Enilconazole · 烯菌灵;依灭利;1-[2-(烯丙氧基)-2-(2,4-二氯苯基)乙基]-1H-咪唑 · IMAZALIL
The CAS registry number of Enilconazole is 35554-44-0.
Molecular formula C14H14Cl2N2O, molecular weight 297.2.
It is also registered under: Enilconazole, 烯菌灵;依灭利;1-[2-(烯丙氧基)-2-(2,4-二氯苯基)乙基]-1H-咪唑, IMAZALIL.
Recorded applications: Uses: Broad spectrum antimycotic used to disinfect stable and kennel equipment and to treat fungal infections in humans and animals, [Merck Index] Used to protect fruit, vegetables, and ornamentals, as seed dressing for cereals, as post-harvest treatment for citrus fruit, pome fruit, bananas, and seed potatoes, to treat equipment and egg storage areas in chicken hatcheries, [HSDB], Using Disinfectants or Biocides [Category: Clean], Farming (Pesticides) [Category: Industry], For Imazalil (USEPA, OPP Pesticide Code: 111901) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Mesh Heading: fungicides, industrial, Systemic fungicide used to control a wide range of fungal diseases on fruit, Fungicide, Wheat and barley seed treatment for common (dryland) root rot (Fusarium, Helminthosporium) and associated seedling diseases. For control of seedborne leaf stripe, net blotch, and Septoria nodorum. Prevents post-harvest decay of citrus, banana, and pome fruit. Active against benzimidazole-resistant strains of plant pathogenic fungi., For more Uses (Complete) data for IMAZALIL (7 total), please visit the HSDB record page., This is a man-made compound that is used as a pesticide., Use Classification: Fungicides, Environmental transformation -> Pesticides (parent, predecessor), Methods of Manufacturing: E. F. Godefroi et al., German patent 2, 063, 857 corresponds to US patent 3, 658, 813 (1971, 1972 both to Janssen), alpha, 2, 4-Trichloroacetophenone + imidazole + allyl chloride (amine formation, carbonyl reduction, ether formation)., By bromination of 2', 4'-dichloroacetophenone, followed by reduction with sodium borohydride to form an epoxide intermediate. The epoxide is opened with imidazole, and the resulting alcohol is then etherified., Formulations, Preparations: Emulsifiable concentrate, water soluble powder, soluble liquid., Trade Names: Fungaflor, Fungazil, Deccozil, Nuzone, Freshguard., Technical is > or =95% pure., Selected products: Deccozil, Flo-Pro, Freshgard, Magnate, Mazal. Mixtures: Baytan Combi (+fuberidazole +triadimenol) (fuberidazole not present in some formulations), Baytan Universal (+fuberidazole +triadimenol) (seed treatment), Vincit (+flutriafol +thiabendazole). Other products: Florasan, Sphinx, Stryper. Mixtures: Nectec (+azaconazole), Baytan IM (+fuberidazole +triadimenol), Citrocil (+2-phenylphenol), Extratect (+thiabendazole) (seed), Manta Plus (+fuberidazole +imidacloprid +triadimenol) (Germany), Panoctine Plus (+guazatine), Raxil (+tebuconazole) (seed treatment, East Europe), Raxil Complex Liquido (+tebuconazole) (seed treatment, Italy), Raxil IM (+tebuconazole) (seed treatment), Raxil MD Extra (+metalaxyl +tebuconazole), Robust (+triticonazole), Vincit FS (+flutriafol +thiabendazole), Vitaflo Extra (+carboxin +thiabendazole), Vitavax Extra (+carboxin +thiabendazole). Discontinued products: mixtures: Larin (+fenpiclonil +tebuconazole) (seed treatment, Germany), Raxil WS (+tebuconazole) (seed treatment, E Europe)., General Manufacturing Information: Control powdery mildews on cucurbits and ornamentals, powdery mildew on roses, storage diseases (particularly Penicillium, Gloeosporium, Phomopsis spp., etc.) of citrus fruit, and seed potatoes. Also used as a seed dressing, for control of diseases (particularly Fuasrium and Helminthosporium spp.) of cereals. It is particularly active against benzimidazole-resistant strains of plant-pathogenic fungi..
Independent reference data for Enilconazole (CAS 35554-44-0), compiled from public chemistry databases.
| CAS 号 | 35554-44-0 |
|---|---|
| PubChem CID | 37175 |
| 分子式 | C14H14Cl2N2O |
| IUPAC 名称 | 1-[2-(2,4-dichlorophenyl)-2-prop-2-enoxyethyl]imidazole |
| UNII（FDA） | 6K0NOF3XQ6 |
| Molecular Weight | 297.2 |
|---|---|
| XLogP3 | 3.8 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Exact Mass | 296.0483185 |
| Monoisotopic Mass | 296.0483185 |
| Topological Polar Surface Area | 27.1 |
| Heavy Atom Count | 19 |
| Boiling Point | 347 °C |
|---|---|
| Boiling Point | 347.00 °C. @ 760.00 mm Hg |
| Boiling Point | 319-347 °C (estimated) |
| Melting Point | 52.7 °C |
| Melting Point | 50 °C |
| Flash Point | 192 °C |
| Solubility | In water, 0.18 g/L at pH 7.6, 20 °C |
| Solubility | 180 mg/L @ 20 °C (exp) |
| Density | 1.348 g/ml at 26 °C |
| Vapor Pressure | 0.00000119 [mmHg] |
IMAZALIL; Enilconazole; 35554-44-0; Deccozil; Fungaflor; Imaverol; Clinafarm; Fungazil; Chloramizol; Florasan; Magnate; Eniloconazol (SP); Deccozil S 75; NuZone; Deccosil; Enilconazol
| GHS 通报统计 | 100% (3 / 3) |
|---|
| GHS 通报统计 | 100% (3 / 3) |
|---|---|
| 已通报的危害声明 | H301, H318, H332, H351, H410, H302 (28.8%), H373 (19.8%), H400 (53.1%) |
烯菌灵;依灭利;1-[2-(烯丙氧基)-2-(2,4-二氯苯基)乙基]-1H-咪唑 · CAS 35554-44-0 · C14H14Cl2N2O. UNII 6K0NOF3XQ6. Boiling Point: 347 °C; Boiling Point: 347.00 °C. @ 760.00 mm Hg; Boiling Point: 319-347 °C (estimated).
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.