ChemicalBook--->CAS DataBase List--->19480-43-4

19480-43-4

19480-43-4 Structure

19480-43-4 Structure
IdentificationBack Directory
[Name]

MCPA-BUTOXYETHYL ESTER
[CAS]

19480-43-4
[Synonyms]

MCPA-butotyl
Adrenaline Impurity 69
MCPA-BUTOXYETHYL ESTER
mcpa,butoxyethanolester
MCPA-butoxyethylester solution
MCPA-butoxyethyl ester in Acetonitrile
2-Butoxyethyl-4-chlor-o-tolyloxyacetat
MCPA butoxyethyl ester Solution, 100ppm
2-butoxyethyl4-chloro-o-tolyloxyacetate
BUTOXYETHYL2-METHYL-4-CHLOROPHENOXYACETATE
MCPA-butoxyethyl ester 100 μg/ml Acetonitrile
2-methyl-4-chlorophenoxyaceticacid,butoxyethylester
2-methyl-4-chlorophenoxyaceticacid,2-butoxyethylester
MCPA-butoxyethyl ester Solution in Toluene, 1000μg/mL
(4-chloro-2-methylphenoxy)-aceticaci2-butoxyethylester
4-Chloro-2-methylphenoxyacetic acid 2-butoxyethyl ester
Acetic acid, 2-(4-chloro-2-methylphenoxy)-, 2-butoxyethyl ester
[EINECS(EC#)]

243-103-8
[Molecular Formula]

C15H21ClO4
[MDL Number]

MFCD00144730
[MOL File]

19480-43-4.mol
[Molecular Weight]

300.78
Chemical PropertiesBack Directory
[Boiling point ]

398.0±32.0 °C(Predicted)
[density ]

1.126±0.06 g/cm3(Predicted)
[Fp ]

4 °C
[storage temp. ]

APPROX 4°C
[EPA Substance Registry System]

MCPA-butotyl (19480-43-4)
Safety DataBack Directory
[Symbol(GHS) ]

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

Warning
[Hazard statements ]

H319-H410-H302+H312+H332
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P273-P391-P501
[Hazard Codes ]

F,Xn,N
[Risk Statements ]

11-38-50/53-65-67-20/21/22
[Safety Statements ]

16-29-33-60-61-62-13
[RIDADR ]

UN 1262 3/PG 2
[TSCA ]

TSCA listed
Hazard InformationBack Directory
[Production Methods]

MCPA-butotyl is produced by first manufacturing and purifying technical-grade MCPA acid through the standard industrial sequence of para-cresol chlorination followed by carboxylation to form the phenoxyacetic acid. The purified acid is then esterified with the branched C4 alcohol sec-butanol (the “butotyl” alcohol) in the presence of an acid catalyst, with the reaction run under conditions that continuously remove water so the equilibrium favours ester formation. After the desired conversion is reached, the reaction mixture is neutralised and washed to remove residual catalyst and unreacted alcohol, and the crude ester is refined, often by vacuum distillation, before being formulated.
[Mechanism of action]

Selective, systemic with translocation. Synthetic auxin.
[Pesticide Type]

Herbicide
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