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25537-26-2

25537-26-2 Structure

25537-26-2 Structure
IdentificationBack Directory
[Name]

KURON
[CAS]

25537-26-2
[Synonyms]

BUTOXYPROPYL SILVEX
2-(2,4,5-trichlorophenoxy)propionic acid butoxypropylester
[Molecular Formula]

C16H21Cl3O4
[MOL File]

25537-26-2.mol
[Molecular Weight]

383.69
Chemical PropertiesBack Directory
[Boiling point ]

452.7±45.0 °C(Predicted)
[density ]

1.245±0.06 g/cm3(Predicted)
[EPA Substance Registry System]

Silvex 3-butoxypropyl ester (25537-26-2)
Safety DataBack Directory
[RIDADR ]

2902
[HazardClass ]

6.1(b)
[PackingGroup ]

III
Hazard InformationBack Directory
[Production Methods]

Fenoprop-terboxyl was produced through a classic “ester of an ester” route that mirrored other phenoxy herbicide derivatives of its era. Manufacturers began with technical-grade fenoprop, itself obtained by chlorinating and then etherifying the appropriate phenolic precursor to install the 2-propyl side chain. Once purified, this phenoxy acid was esterified with the chosen terboxyl alcohol under controlled, typically acid-catalysed conditions, using heat and continuous removal of water to drive the reaction to completion while preventing degradation of the phenoxy structure.
[Mechanism of action]

Synthetic auxin affecting nucleic acid biosynthesis and cell elongation. Systemic, selective.
[Pesticide Type]

Herbicide; Plant Growth Regulator
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