| CAS No.: | 107534-96-3 |
|---|---|
| Formula: | C16h22cln3o |
| EINECS: | 403-640-2 |
| Appearance: | Liquid |
| Application: | Fungicide |
| Usage Mode: | Protective Agent |
| Samples: |
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| Customization: |
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Tebuconazole 98% TC, 430g/L SC, 80% WDG, 75% WP, 60g/L Fs
| 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 |
| 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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