Overview
2,3-Dichlorophenoxyacetic acid is a chlorinated derivative of phenoxyacetic acid developed as part of the phenoxy herbicide family. First introduced in the mid-20th century, it belongs to the same chemical class as the more widely known 2,4-D herbicide. The compound functions as a plant growth regulator, specifically targeting broadleaf weeds through its auxin-like activity. This herbicide is particularly valued in agricultural settings for its selective action, allowing effective weed control without damaging grass crops. Its molecular structure features two chlorine atoms at the 2 and 3 positions of the phenoxy ring, which contributes to its specific herbicidal properties and differentiates it from other phenoxy herbicides.
Physical and Chemical Properties
2,3-D presents as a crystalline solid at room temperature with limited water solubility (approximately 500 mg/L at 20°C). The compound demonstrates greater solubility in organic solvents such as acetone, ethanol, and ether. Its melting point range of 140-142°C indicates moderate thermal stability under normal storage conditions. Chemically, 2,3-D is a weak organic acid with a pKa of approximately 2.73. The presence of chlorine atoms increases its lipophilicity compared to non-chlorinated phenoxy acids. The compound shows stability in acidic conditions but may degrade under alkaline environments or when exposed to UV radiation over extended periods.
Main Applications
The primary application of 2,3-D is as a selective herbicide in agriculture, particularly for cereal crops where broadleaf weed control is required. It finds use in wheat, barley, and oat fields, as well as in turf management for golf courses and sports fields. The herbicide is often formulated as water-soluble salts or ester derivatives to enhance application properties. In industrial settings, 2,3-D serves in right-of-way vegetation management along railways and power lines. Some specialized applications include its use in forestry and pasture management, though these are less common than agricultural uses. The compound is typically applied as a foliar spray during active weed growth periods.
Safety and Storage
2,3-D requires careful handling due to its moderate toxicity (oral LD50 in rats approximately 500-1000 mg/kg). Appropriate personal protective equipment including gloves, goggles, and respiratory protection should be used during handling. The compound may cause eye irritation and skin sensitization upon repeated exposure. Storage should be in original, tightly sealed containers away from food and feedstuffs. Ideal storage conditions include a cool, dry environment with temperatures below 30°C. Special attention must be given to preventing contamination of water sources, as the compound is toxic to aquatic organisms even at low concentrations.
B2B Procurement Guide
When procuring 2,3-D, buyers should verify the technical grade purity (typically 95-98%) and request certificates of analysis. Important considerations include the formulation type (acid, salt, or ester) and compatibility with existing application equipment. Regulatory compliance documents should accompany all shipments. Bulk purchasers should evaluate suppliers based on consistent quality, packaging integrity, and technical support capabilities. Price negotiations should consider volume discounts, with typical commercial quantities ranging from 25kg drums to metric ton shipments. Lead times may vary seasonally due to agricultural demand patterns.
Related Manufacturers
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