Audited Supplier
SC
137512-74-4
C49h77no13
Powder
Organic Synthesis
Highly Toxic and High Toxic Drugs
Systemic Insecticide
Nerve Poison
MOLOTUS
25kg Drum
TC SC
China
3808
Product Description
Spirotetramat 11% + Buprofezin 22% SC Acaricide & Molluscicide (Insecticide) Pesticide
Spirotetramat
Description: New insecticide for the control of a wide range of sucking insects on crops such as fruit and potatoes
Example pests controlled: Scale insects; Aphids; Mealybugs; Mites; Whiteflies; Psyllids; Thrips; Spider mites; Leafhoppers
Example applications: Fruit including citrus, mango, apples, pears; Lettuce; Potatoes; Cotton; Vegetables (fruiting, leafy, brassica, tuberous, and corm); Christmas tree plantations
Efficacy & activity: -
Availability status: Current
Chemical structure:
| Isomerism | Spirotetramat is a chiral molecule. The technical material is a mixture of two stereoisomers cis-spirotetramat and trans-spirotetramat. It is the cis-isomer that is the active substance. |
| Chemical formula | C21H27NO5 |
| Canonical SMILES | CCOC(=O)OC1=C(C(=O)NC12CCC(CC2)OC)C3=C(C=CC(=C3)C)C |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | CLSVJBIHYWPGQY-GGYDESQDSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C21H27NO5/c1-5-26-20(24)27-18-17(16-12-13(2)6-7-14(16)3)19(23)22-21(18)10-8-15(25-4)9-11-21/h6-7,12,15H,5,8-11H2,1-4H3,(H,22,23)/t15-,21+/f/h22H |
General status:
| Pesticide type | Insecticide |
| Substance group | Tetramic acid |
| Minimum active substance purity | 960 g/kg |
| Known relevant impurities | EU dossier - none declared |
| Substance origin | Synthetic |
| Mode of action | Stomach acting, broad spectrum, long acting insecticide that is rapidly translocated, inhibition of lipogenesis in treated insects |
| CAS RN | 203313-25-1 |
| EC number | - |
| CIPAC number | 795 |
| US EPA chemical code | 392201 |
| PubChem CID | 9969573 |
| Molecular mass (g mol-1) | 373.48 |
| PIN (Preferred Identification Name) | (5s,8s)-3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-yl ethyl carbonate |
| IUPAC name | cis-4-(ethoxycarbonyloxy)-8-methoxy-3-(2,5-xylyl)-1-azaspiro[4.5]dec-3-en-2-one |
| CAS name | cis-3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro(4.5)dec-3-en-4-yl ethyl carbonate |
Buprofezin
Description: A moulting inhibitor, thiadiazine insecticide for whitefly and other insect control
Example pests controlled: Whitefiles, Leaf- and plant-hoppers, Scale insects, Lady beetles, Mealybugs
Example applications: Citrus crops; Top fruit; Cucumbers; Tomatoes; Sweet potatoes; Rice; Cotton
Chemical structure:
| Isomerism | Theoretically can exists in both the Z- and E- form, but X-ray analysis indicates that buprofezin consists of the Z-isomer exclusively (both in solid and in dissolved state). |
| Chemical formula | C16H23N3OS |
| Canonical SMILES | CC(C)N1C(=NC(C)(C)C)SCN(C1=O)C2=CC=CC=C2 |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | PRLVTUNWOQKEAI-VKAVYKQESA-N |
| International Chemical Identifier (InChI) | InChI=1S/C16H23N3OS/c1-12(2)19-14(17-16(3,4)5)21-11-18(15(19)20)13-9-7-6-8-10-13/h6-10,12H,11H2,1-5H3/b17-14- |
General status:
| Pesticide type | Insecticide, Acaricide |
| Substance group | Unclassified |
| Minimum active substance purity | 985 g/kg |
| Known relevant impurities | EU dossier - None declared |
| Substance origin | Synthetic |
| Mode of action | Contact and stomach action. Inhibitors of chitin biosynthesis. |
| CAS RN | 69327-76-0 |
| EC number | - |
| CIPAC number | 681 |
| US EPA chemical code | 275100 |
| PubChem CID | 50367 |
| Molecular mass (g mol-1) | 305.44 |
| PIN (Preferred Identification Name) | (2Z)-2-(tert-butylimino)-5-phenyl-3-(propan-2-yl)-1,3,5-thiadiazinan-4-one |
| IUPAC name | (Z)-2-tert-butylimino-3-isopropyl-5-phenyl-1,3,5-thiadiazinan-4-one |
| CAS name | 2-((1,1-dimethylethyl)imino)tetrahydro-3-(1-methylethyl)-5-phenyl-4H-1,3,5-thiadiazin-4-one |
