TEBUCONAZOLE 6.7% + CAPTAN 26.9% SC

CAS Number: 107534-96-3

Molecular Formula: C16H22ClN3O, C9H8Cl3NO2S

About TEBUCONAZOLE 6.7% + CAPTAN 26.9% SC

Tebuconazole (CAS 107534-96-3) functions as a critical systemic triazole fungicide within the US agricultural sector, where 98% purity technical grade material is increasingly sought by formulators to develop high-efficiency SC and WG products that manage foliar and soil-borne pathogens. Alpha-[2-(4-chlorophenyl)ethyl]...

Variants

Tebuconazole Technical

CAS: 107534-96-3

Tebuconazole 2% DS

CAS: 107534-96-3

Tebuconazole 10% + Sulphur 65% WG

CAS: 107534-96-3

TEBUCONAZOLE 6.7% + CAPTAN 26.9% SC Specifications

CAS Number

107534-96-3

Molecular Formula

C16H22ClN3O, C9H8Cl3NO2S

Molecular Weight

307.82 g/mol (Tebuconazole), 300.61 g/mol (Captan)

IUPAC Name

Tebuconazole: (RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol; Captan: (3aR,7aS)-2-[(trichloromethyl)sulfanyl]-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione

Canonical SMILES

CC(C)(C)C(CCC1=CC=C(C=C1)Cl)(CN2C=NC=N2)O. C1C=CCC2C1C(=O)N(C2=O)SC(Cl)(Cl)Cl

CAS Number

107534-96-3

Molecular Formula

C16H22ClN3O, C9H8Cl3NO2S

Molecular Weight

307.82 g/mol (Tebuconazole), 300.61 g/mol (Captan)

IUPAC Name

Tebuconazole: (RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol; Captan: (3aR,7aS)-2-[(trichloromethyl)sulfanyl]-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione

Canonical SMILES

CC(C)(C)C(CCC1=CC=C(C=C1)Cl)(CN2C=NC=N2)O. C1C=CCC2C1C(=O)N(C2=O)SC(Cl)(Cl)Cl

Molecular Weight

307.82 g/mol (Tebuconazole), 300.61 g/mol (Captan)

Broad-spectrum Fungicide

A systemic and contact suspension concentrate formulation combining Tebuconazole and Captan used for the preventive and curative management of fungal diseases such as powdery mildew, anthracnose, scab, and blights in various agricultural crops including apple, chilli, tomato, and grapes

Agricultural Chemical

A high-purity chemical reagent employed in integrated crop protection practices to inhibit ergosterol biosynthesis and deactivate fungal enzymes through multi-site action