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15146-99-3

15146-99-3 Structure

15146-99-3 Structure
IdentificationBack Directory
[Name]

tetrahydrofurfuryl 2,4-dichlorophenoxyacetate
[CAS]

15146-99-3
[Synonyms]

tetrahydrofurfuryl 2,4-dichlorophenoxyacetate
Oxolan-2-ylmethyl 2-(2,4-dichlorophenoxy)acetate
2,4-Dichlorophenoxyacetic acid (tetrahydrofuran-2-yl)methyl ester
Acetic acid, 2-(2,4-dichlorophenoxy)-, (tetrahydro-2-furanyl)methyl ester
[EINECS(EC#)]

239-207-8
[Molecular Formula]

C13H14Cl2O4
[MOL File]

15146-99-3.mol
[Molecular Weight]

305.154
Chemical PropertiesBack Directory
[EPA Substance Registry System]

2,4-D tetrahydrofurfuryl ester (15146-99-3)
Hazard InformationBack Directory
[Production Methods]

2,4-D-tefuryl is produced via a process that begins with technical grade 2,4-D acid, obtained through the standard phenoxyacetic acid route involving chlorination of phenol and etherification with monochloroacetic acid. Once purified, the acid is converted to its acid chloride or another activated intermediate, which is then reacted with tefuryl alcohol to form the corresponding ester under controlled, non aqueous conditions. After the esterification step, the crude product is purified, solvents are removed, and the material is crystallised or distilled to yield technical grade 2,4-D-tefuryl suitable for formulation.
[Mechanism of action]

Selective, systemic, absorbed through roots and increases biosynthesis and production of ethylene causing uncontrolled cell division and so damages vascular tissue. Synthetic auxin.
[Pesticide Type]

Herbicide
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