2,6 – Dichlorotoluene Intermediates Pesticide Fungicides
| CAS Number | 118-69-4 |
| Chemical Name | 2,6-Dichlorotoluene |
| Molecular Weight | 161.03 |
| Molecular Formula | C7H6CI2 |
| Synonyms | 2,6-DCT 2,6-Dichloro-Toluen |
| EINECS | 204-269-7 |
| Appearance | Colorless transparent liquid |
| Storage conditions | Store in a cool, ventilated warehouse and keep the container sealed. |
| CAS Number | 118-69-4 |
| Chemical Name | 2,6-Dichlorotoluene |
| Molecular Weight | 161.03 |
| Molecular Formula | C7H6CI2 |
| Synonyms | 2,6-DCT 2,6-Dichloro-Toluen |
| EINECS | 204-269-7 |
| Appearance | Colorless transparent liquid |
| Storage conditions | Store in a cool, ventilated warehouse and keep the container sealed. |
Core mechanism of action
The essence of 2,6-Dichlorotoluene is to provide "active structural units" for downstream pesticide molecules through aromatic ring functional group transformation and side chain modification. Its reaction logic fully serves the "target action requirements" of pesticides (such as inhibiting weed enzyme activity, destroying pathogen cell membranes, and blocking pest nerve conduction).
Core Advantages in the Agricultural Sector
2,6-Dichlorotoluene is High selectivity enables targeted construction of pesticide active cores, reducing the risk of pesticide damage. Mature synthesis processes ensure cost-effectiveness and large-scale pesticide supply. Compatibility with a variety of reaction systems enables flexible production of diverse pesticide types. High purity reduces impurities, helping downstream pesticides achieve low residues and meeting the needs of green agriculture.
Typical usage scenarios focus on pesticide production
first, the synthesis of herbicides such as nicosulfuron to control weeds in corn and rice fields; second, the preparation of fungicides such as metalaxyl to control downy mildew and powdery mildew; and third, the production of insecticides such as hexaflumuron, which are highly effective and low-toxic against cotton bollworms and aphids.











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