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D7299

Sigma-Aldrich

2,4-Dichlorophenoxyacetic acid

≥95%, crystalline

Synonym(s):

2,4-D

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About This Item

Linear Formula:
Cl2C6H3OCH2CO2H
CAS Number:
94-75-7
Molecular Weight:
221.04
Beilstein:
1214242
EC Number:
202-361-1
MDL number:
MFCD00004300
UNSPSC Code:
12352207
PubChem Substance ID:
24894121
NACRES:
NA.71

vapor pressure

0.4 mmHg ( 160 °C)

Quality Level

200

Assay

≥95%

form

crystalline

mp

136-140 °C (lit.)

application(s)

agriculture

SMILES string

OC(=O)COc1ccc(Cl)cc1Cl

InChI

1S/C8H6Cl2O3/c9-5-1-2-7(6(10)3-5)13-4-8(11)12/h1-3H,4H2,(H,11,12)

InChI key

OVSKIKFHRZPJSS-UHFFFAOYSA-N

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General description

2,4-Dichlorophenoxyacetic acid is a synthetic auxin and an analogue of indole-3-acetic acid.

Application

2,4-Dichlorophenoxyacetic acid has been used as a supplement in:
  • Murashige and Tucker medium for thin cell layer explant culture
  • Murashige and Skoog medium media to initiate callus
  • N6-basal medium for immature zygotic embryo culture

Signal Word

Danger

Hazard Statements

H302,H317,H318,H335,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Callus induction and organogenesis in soybean [Glycine max (L.) Merr.] cv. Pyramid from mature cotyledons and embryos
Joyner EY, et al.
The Open Plant Science Journal, 4(1), 57-63 (2010)
Leandro O Conte et al.
Journal of hazardous materials, 372, 113-120 (2018-04-22)
The effects of four inorganic anions (Cl-, SO42-, HCO3-, NO3-) usually present in groundwater were investigated on the photo-Fenton degradation of 2,4-dichlorophenoxyacetic acid (2,4-D). A kinetic model derived from a reaction sequence is proposed using the ferrioxalate complex as iron
A small acidic protein 1 (SMAP1) mediates responses of the Arabidopsis root to the synthetic auxin 2, 4-dichlorophenoxyacetic acid
Rahman A, et al.
The Plant Journal, 47(5), 788-801 (2006)
Effect of 2, 4-D and 4-CPPU on somatic embryogenesis from stigma and style transverse thin cell layers of Citrus
Fiore S, et al.
Plant Cell, Tissue and Organ Culture, 68(1), 57-63 (2002)
Sze Chieh Tan et al.
Talanta, 216, 120962-120962 (2020-05-28)
Two miniaturized sample preparation techniques, ultrasound-assisted emulsification microextraction (USAEME) and micro-solid-phase extraction (μ-SPE) have been integrated for the pre-concentration of four polar chlorophenoxy acid (CPA) herbicides from environmental aqueous samples. An metal-organic framework, MIL-101(Cr), characterized by its high porosity and
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