Fungicide Pesticide & Repellent Carbendazim 15% + Thiram 35% WP
CarbendazimCarbendazim is a fungicide that is not approved for use in the EU. It has a low aqueous solubility, is volatile and moderately mobile. It is moderately persistent in soil and can be very persistent in water systems under certain conditions. Carbendazim has a low mammalian toxicity and is not expected to bioaccumulate. It is, however, reported as a reproduction/developmental toxicant. It is moderately toxic to honeybees and most aquatic organisms. It is highly toxic to earthworms but non-toxic to birds.
Description: A fungicide used to control a a range of diseases including Septoria, Fusarium and Sclerotina. Can also be a pesticide transformation product
Example pests controlled: Husk spot; Chocolate spot; Grey mould; Green mould; Crown rot
Example applications: Beans; Macademia nuts; Lentils; Chickpeas; Strawberries; Sugarcane; Cereals
Chemical structure: | Isomerism | None |
| Chemical formula | C9H9N3O2 |
| Canonical SMILES | COC(=O)NC1=NC2=CC=CC=C2N1 |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | TWFZGCMQGLPBSX-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C9H9N3O2/c1-14-9(13)12-8-10-6-4-2-3-5-7(6)11-8/h2-5H,1H3,(H2,10,11,12,13) |
| Pesticide type | Fungicide, Metabolite |
| Metabolite Type | Soil |
| Substance group | Benzimidazole |
| Minimum active substance purity | 960 g/kg |
| Known relevant impurities | EU dossier - 3-amino-2-hydroxyphenazine 0.0005 g/kg; 2,3-diamino-phenazine 0.0006 g/kg |
| Substance origin | Synthetic |
| Mode of action | Systemic with curative and protectant activity. Inhibition of mitosis and cell division (Beta-tubulin assembly in mitosis). |
| CAS RN | 10605-21-7 |
| EC number | 234-323-0 |
| CIPAC number | 263 |
| US EPA chemical code | 115001/128872 |
| PubChem CID | 25429 |
| CLP index number | 613-048-00-8 |
| Molecular mass (g mol-1) | 191.21 |
| PIN (Preferred Identification Name) | methyl 1H-1,3-benzimidazol-2-ylcarbamate |
| IUPAC name | methyl benzimidazol-2-ylcarbamate |
| CAS name | methyl 1H-benzimidazol-2-ylcarbamate |
| Other status information | Marine Pollutant |
| Relevant Environmental Water Quality Standards | Environment Agency UK non-statutory standard for the protection of aquatic life: freshwater and saltwater annual average 0.1 ug/L; max acceptable conc: 1.0 ug/L |
Example pests controlled: As a fungicide: Seed decay; Seedling blight; Damping-off; Kernal smut; Smuts; Bunts. As a repellent: Rabbits; Deer
Example applications: Cereals including barley, millet, oats, rye, triticale; Beans and peas; Brassicas; Beet crops; Aubergines; Flax; Onions; Soybean; Sunflowers; Tomatoes; Fruit including apples, pear, cherry, strawberry
Chemical structure: | Isomerism | None |
| Chemical formula | C6H12N2S4 |
| Canonical SMILES | CN(C)C(=S)SSC(=S)N(C)C |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | KUAZQDVKQLNFPE-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C6H12N2S4/c1-7(2)5(9)11-12-6(10)8(3)4/h1-4H3 |
| Pesticide type | Fungicide, Repellent, Metabolite |
| Metabolite Type | Soil, Water, Animal |
| Substance group | Carbamate |
| Minimum active substance purity | 980 g/kg |
| Known relevant impurities | EU dossier - None declared |
| Substance origin | Synthetic |
| Mode of action | Contact action with protective properties, acts by inhibiting spore germination and mycelial growth. Repellent properties caused by aversion to its taste. Multi-site activity. |
| CAS RN | 137-26-8 |
| EC number | 205-286-2 |
| CIPAC number | 24 |
| US EPA chemical code | 079801 |
| PubChem CID | 5455 |
| Molecular mass (g mol-1) | 240.43 |
| PIN (Preferred Identification Name) | N1,N1,N3,N3-tetramethyl-2-dithioperoxy-1,3-dithiodicarbonic diamide |
| IUPAC name | tetramethylthiuram disulfide |
| CAS name | tetramethylthioperoxydicarbonic diamide |
| Other status information | Chemical subject to PIC regulations (some formulations) |