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Merck
CN

45732

Supelco

2,4-D 1-butyl ester

PESTANAL®, analytical standard

Synonym(s):

2,4-D 1-butyl ester, Butyl 2,4-dichlorophenoxyacetate

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About This Item

Empirical Formula (Hill Notation):
C12H14Cl2O3
CAS Number:
94-80-4
Molecular Weight:
277.14
Beilstein:
2056085
EC Number:
202-364-8
MDL number:
MFCD00126845
UNSPSC Code:
41116107
PubChem Substance ID:
329756927
NACRES:
NA.24

Key Documents

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grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCCCOC(=O)COc1ccc(Cl)cc1Cl

InChI

1S/C12H14Cl2O3/c1-2-3-6-16-12(15)8-17-11-5-4-9(13)7-10(11)14/h4-5,7H,2-3,6,8H2,1H3

InChI key

UQMRAFJOBWOFNS-UHFFFAOYSA-N

General description

2,4-D-1-butyl ester is a chlorophenoxy acid herbicide primarily used to control the growth of broad-leaved weeds.

Application

2,4-D-1-butyl ester may be used as a reference standard for the determination of 2,4-D-1-butyl ester in soil samples by capillary high performance liquid chromatography with ultraviolet detection.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H317,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF1180
BCBT9593
BCBT0935V

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A M de Duffard et al.
Toxicology, 64(3), 265-270 (1990-12-03)
Brain concentrations of Serotonin (5-HT) and 5-hydroxyindolacetic acid (5-HIAA) were determined in male, mother and virgin female adult rats after exposure to 69 mg/kg body weight/day of 2,4-dichlorophenoxyacetic butyl ester (2,4-Dbe) during 15 or 45 consecutive days. Both 5-HT and
G B Mori de Moro et al.
Neurotoxicology, 6(3), 133-137 (1985-01-01)
Fertilized hens' eggs were externally treated with 2,4-dichlorophenoxyacetic (2,4-D) butyl ester (2.4 mg/egg) before starting incubation. The specific activity of 2',3'-cyclic nucleotide 3'-phosphohydrolase (CNPase) was diminished in the whole brain of animals born from treated eggs, as compared with controls.
J M Argüello et al.
Biochemical pharmacology, 40(11), 2441-2448 (1990-12-01)
Fertilized hen eggs were treated externally with 2,4-dichlorophenoxyacetic butyl ester (2,4-D b.e.) (3.1 mg/egg) before the start of the incubation. Actomyosin and sarcoplasmic reticulum adenosine triphosphatase (ATPase) activities from leg and complexus muscles of chicks hatched from treated eggs were
G E Schulze
Neurotoxicology and teratology, 9(5), 363-367 (1987-09-01)
The herbicide 2,4-Dichlorophenoxyacetic acid (2,4-D) is a commonly used herbicide and one component of Agent Orange. The herbicide is commonly formulated as the butyl ester. The effects of a 50:50 mixture of n-butyl and iso-butyl esters of 2,4-D (2,4-D mixed
S M Castro de Cantarini et al.
Drug and chemical toxicology, 12(2), 137-146 (1989-06-01)
Fertilized hen eggs were topically applied with 2,4-Dichlorophenoxyacetic acid butyl ester (3.1 mg/egg) before starting incubation. During the incubation time 20% of the compound applied on eggs was lost by volatilization. At different incubation times (0, 1, 5, 10 and
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