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Atomfair Dichlorprop C9H8Cl2O3
Description Dichlorprop (CAS No. 120-36-5), with the molecular formula C9H8Cl2O3and IUPAC name 2-(2,4-dichlorophenoxy)propanoic acid , is a selective systemic phenoxy herbicide widely used in agricultural and horticultural applications. This white to light brown crystalline solid is highly effective against broadleaf weeds in cereal crops, grasslands, and non-crop areas. With a purity level of ??98%, our Dichlorprop is rigorously tested to meet industry standards, ensuring optimal performance in research and commercial formulations. The product is supplied in sealed containers to maintain stability and prevent degradation. Suitable for laboratory analysis, field studies, and formulation development, this compound is a critical tool for…
Description
Description
Dichlorprop (CAS No. 120-36-5), with the molecular formula C9H8Cl2O3 and IUPAC name 2-(2,4-dichlorophenoxy)propanoic acid, is a selective systemic phenoxy herbicide widely used in agricultural and horticultural applications. This white to light brown crystalline solid is highly effective against broadleaf weeds in cereal crops, grasslands, and non-crop areas. With a purity level of ??98%, our Dichlorprop is rigorously tested to meet industry standards, ensuring optimal performance in research and commercial formulations. The product is supplied in sealed containers to maintain stability and prevent degradation. Suitable for laboratory analysis, field studies, and formulation development, this compound is a critical tool for plant scientists and agrochemical researchers.
- CAS No: 120-36-5
- Molecular Formula: C9H8Cl2O3
- Molecular Weight: 235.06
- Exact Mass: 233.9850495
- Monoisotopic Mass: 233.9850495
- IUPAC Name: 2-(2,4-dichlorophenoxy)propanoic acid
- SMILES: CC(C(=O)O)OC1=C(C=C(C=C1)Cl)Cl
- Synonyms: Dichlorprop, 120-36-5, 2-(2,4-Dichlorophenoxy)propanoic acid, 2-(2,4-Dichlorophenoxy)propionic acid, DICHLOROPROP
Application
Dichlorprop is primarily used as a post-emergence herbicide for controlling broadleaf weeds in wheat, barley, oats, and other cereal crops. It functions as a synthetic auxin, disrupting normal plant growth and leading to uncontrolled cell division and vascular tissue damage. Researchers also utilize Dichlorprop in studies investigating herbicide resistance mechanisms and environmental fate. Its selective action makes it valuable for integrated weed management systems.
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