| Identification | Back Directory | [Name]
(2,4-DICHLOROPHENOXY)ACETIC ACID-BUTOXY POLYPROPYLENE GLYCOL ESTER | [CAS]
1928-45-6 | [Synonyms]
2,4-D PGBE
dowweedkillerx[qr]
2,4-d,butoxypropylester
2,4-dbutoxypropylester[qr]
2,4-D-Butoxypolypropyleneester
2,4-DPROPYLENEGLYCOLBUTYLETHER
3-butoxypropyl2,4-dichlorophenoxyacetate
3-butoxypropyl 2-(2,4-dichlorophenoxy)ethanoate
2,4-dichlorophenoxy-aceticaci3-butoxypropylester
2,4-dichlorophenoxyacetic acid butoxypropyl ester
(2,4-Dichlorophenoxy)acetic acid 3-butoxypropyl ester
(2,4-dichlorophenoxy)-aceticaci3-butoxypropylester[qr]
2-(2,4-dichlorophenoxy)acetic acid 3-butoxypropyl ester
aceticacid,(2,4-dichlorophenoxy),2-butoxymethylethylester[qr]
(±)-(2,4-dichloro-phenoxy)-aceticacid2-butoxy-1-methyl-ethylester
(2,4-DICHLOROPHENOXY)ACETIC ACID-BUTOXY POLYPROPYLENE GLYCOL ESTER | [Molecular Formula]
C15H20Cl2O4 | [MDL Number]
MFCD03265586 | [MOL File]
1928-45-6.mol | [Molecular Weight]
335.22 |
| Hazard Information | Back Directory | [Production Methods]
2,4-D-terboxyl is produced through a straightforward process that begins with technical grade 2,4 D acid, obtained after the standard phenol chlorination and etherification steps used to make the parent phenoxyacetic acid. The purified acid is then dissolved in water or a mixed solvent and neutralised with the proprietary “terboxyl” amine, forming the corresponding amine salt under controlled pH and temperature to avoid excess free acid or unreacted amine. | [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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