ChemicalBook--->CAS DataBase List--->1713-15-1

1713-15-1

1713-15-1 Structure

1713-15-1 Structure
IdentificationMore
[Name]

Isobutyl 2,4-dichlorophenoxyacetate
[CAS]

1713-15-1
[Synonyms]

2,4-Dichlorophenoxy acetic acid isobutyl ester
2,4-D ISOBUTYL ESTER
isobutyl 2,4-d
Isobutyl 2,4-dichlorophenoxyacetate
(2,4-dichlorophenoxy)-aceticaci2-methylpropylester
(2,4-dichlorophenoxy)-aceticaciisobutylester
Acetic acid, (2,4-dichlorophenoxy)-, isobutyl ester
2.4-d-iso-butyl glycol ester (technical)
2-Methylpropyl 2-(2,4-dichlorophenoxy)acetate
Acetic acid, (2,4-dichlorophenoxy)-, 2-methylpropyl ester
2,4-D isobutyl
[EINECS(EC#)]

216-992-5
[Molecular Formula]

C12H14Cl2O3
[MDL Number]

MFCD00072476
[Molecular Weight]

277.14
[MOL File]

1713-15-1.mol
Chemical PropertiesBack Directory
[Boiling point ]

133-134 °C(Press: 1 Torr)
[density ]

1.238±0.06 g/cm3(Predicted)
[CAS DataBase Reference]

1713-15-1(CAS DataBase Reference)
[NIST Chemistry Reference]

Acetic acid, (2,4-dichlorophenoxy)-, 2-methylpropyl ester(1713-15-1)
[EPA Substance Registry System]

1713-15-1(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302-H317-H410
[Precautionary statements ]

P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P264-P270-P301+P312-P330-P501-P273-P391-P501
[RIDADR ]

3348
[HazardClass ]

6.1(b)
[PackingGroup ]

III
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2,4-Dichlorophenoxy acetic acid isobutyl ester(1713-15-1).msds
Hazard InformationBack Directory
[Production Methods]

Commercial production of 2,4-D-butyl would have followed the same industrial pathway used for other ester derivatives of 2,4-D, although specific data for this variant are limited. Production begins with large scale synthesis of 2,4-D acid, which is then esterified with isobutanol under controlled temperature and solvent conditions to form the isobutyl ester.
[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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