Imidacloprid 20% + Metalaxyl-M 20% + Tebuconazole 2% WS
Imidacloprid
Imidacloprid is an insecticide approved for use in the EU with certain restrictions for flowering crops. It is highly soluble, non-volatile and persistent in soil. It is moderately mobile. It has a low risk of bioaccumulating. It is highly toxic to birds and honeybees. Moderately toxic to mammals and earthworms. It is non-toxic to fish.
Description: A chloronicotine insecticide used to control sucking and soil insects. Also used as a flea treatment for domestic pets.
Example pests controlled: Plant hoppers, Aphids, Termites, Colorado bettle, Fleas, White grups, Craneflies; Crickets, Ants
Example applications: Lawns and turf; Domestic pets; Rice, Cereals; Maize; Potatoes; Sugar beet
Chemical structure:
| Isomerism |
Isomeric - existing as both the E- and Z- forms however many commerical products are comprised of almost entirely the (E)-isomer |
| Chemical formula |
C9H10ClN5O2 |
| Canonical SMILES |
C1CN(C(=N1)N[N+](=O)[O-])CC2=CN=C(C=C2)Cl |
| Isomeric SMILES |
No data |
| International Chemical Identifier key (InChIKey) |
YWTYJOPNNQFBPC-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) |
InChI=1S/C9H10ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-2, 5H, 3-4, 6H2, (H, 11, 13) |
General status:
| Pesticide type |
Insecticide, Veterinary substance |
| Substance group |
Neonicotinoid |
| Minimum active substance purity |
970 g/kg |
| Known relevant impurities |
EU dossier - None declared |
| Substance origin |
Synthetic |
| Mode of action |
Systemic with contact and stomach action. Acetylcholine receptor (nAChR) agonist. |
| CAS RN |
138261-41-3 |
| EC number |
- |
| CIPAC number |
582 |
| US EPA chemical code |
129099 |
| PubChem CID |
86418 |
| Molecular mass (g mol-1) |
255.66 |
| PIN (Preferred Identification Name) |
- |
| IUPAC name |
(E)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine |
| CAS name |
(2E)-1-((6-chloro-3-pyridinyl)methyl)-N-nitro-2-imidazolidinimine |
| Other status information |
NOTE ban or usage restriction may be in place for use on flowering crops in some Member States |
Metalaxyl-M
Description: A fungicide used to control diseases caused by air- and soil-borne pathogens
Example pests controlled: Foliar and tuber blight; Downey mildews; Pseudoperonospora humuli; Phytophthora infestans; Peronospora tabacina
Example applications: Potatoes; Tomatoes; Hops; Lettuce; Vegetables; Tobacco
Chemical structure:
| Isomerism |
Metalaxyl-M is the biologically active enantiomer (R-form) of the isomeric compound metalaxyl |
| Chemical formula |
C15H21NO4 |
| Canonical SMILES |
CC1=C(C(=CC=C1)C)N(C(C)C(=O)OC)C(=O)COC |
| Isomeric SMILES |
No data |
| International Chemical Identifier key (InChIKey) |
ZQEIXNIJLIKNTD-GFCCVEGCSA-N |
| International Chemical Identifier (InChI) |
InChI=1S/C15H21NO4/c1-10-7-6-8-11(2)14(10)16(13(17)9-19-4)12(3)15(18)20-5/h6-8, 12H, 9H2, 1-5H3/t12-/m1/s1 |
General status:
| Pesticide type |
Fungicide |
| Substance group |
Phenylamide |
| Minimum active substance purity |
910 g/kg |
| Known relevant impurities |
EU dossier - 2, 6-dimethyl-phenylamine; 4-methoxy-5-methyl-5H-(1, 2)oxathiole 2, 2-dioxide; 1-methoxy-1-oxopropan-2-yl N-(2, 6-dimethylphenyl)-N-(methoxyacetyl)alaninate |
| Substance origin |
Synthetic |
| Mode of action |
Systemic with curative and protective action. Disrupts fungal nucleic acid synthesis - RNA ploymerase 1. |
| CAS RN |
70630-17-0 |
| EC number |
- |
| CIPAC number |
580 |
| US EPA chemical code |
- |
| PubChem CID |
11150163 |
| Molecular mass (g mol-1) |
279.33 |
| PIN (Preferred Identification Name) |
- |
| IUPAC name |
Methyl N-(methoxyacetyl)-N-(2, 6-xylyl)-D-alaninate |
| CAS name |
Methyl N-(2, 6-dimethylphenyl)-N-(methoxyacetyl)-D-alaninate |
Tebuconazole
Description: A fungicide effective against various foliar diseases in cereals and other field crops
Example pests controlled: Smut; Bunt; Stripe rust; Yellow leaf spot; Powdery mildew; Scelerotinia rot; Black spot; Net blotch
Example applications: Cereals including wheat, barley, oat, rye; Grapes; Peanuts; Vegetables including onions, peas, pepper; Bananas; Sugarcane
Chemical structure:
| Isomerism |
A chiral molecule. The technical material is an isomeric mixture of the (S-) and (R-) isomers. The R-form is more biologically active than the S-form. |
| Chemical formula |
C16H22ClN3O |
| Canonical SMILES |
CC(C)(C)C(CCC1=CC=C(C=C1)Cl)(CN2C=NC=N2)O |
| Isomeric SMILES |
No data |
| International Chemical Identifier key (InChIKey) |
PXMNMQRDXWABCY-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) |
InChI=1S/C16H22ClN3O/c1-15(2, 3)16(21, 10-20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7, 11-12, 21H, 8-10H2, 1-3H3 |
General status:
| Pesticide type |
Fungicide, Plant growth regulator |
| Substance group |
Triazole |
| Minimum active substance purity |
950 g/kg |
| Known relevant impurities |
EU dossier - None declared |
| Substance origin |
Synthetic |
| Mode of action |
Systemic with protective, curative and eradicant action. Disrupts membrane function. Sterol biosynthesis inhibitor. |
| CAS RN |
107534-96-3 |
| EC number |
403-640-2 |
| CIPAC number |
494 |
| US EPA chemical code |
128997 |
| PubChem CID |
86102 |
| Molecular mass (g mol-1) |
307.82 |
| PIN (Preferred Identification Name) |
Rac-(3R)-1-(4-chlorophenyl)-4, 4-dimethyl-3-(1H-1, 2, 4-triazol-1-ylmethyl)pentan-3-ol |
| IUPAC name |
(RS)-1-p-chlorophenyl-4, 4-dimethyl-3-(1H-1, 2, 4-triazol-1-ylmethyl)pentan-3-ol |
| CAS name |
Α-(2-(4-chlorophenyl)ethyl)-α-(1, 1-dimethylethyl)-1H-1, 2, 4-triazole-1-ethanol |
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