Online Database of Chemicals from Around the World

2,4-Dichlorophenoxyacetic acid
[CAS# 94-75-7]

List of Suppliers
Jiahua Import & Export Co., Ltd. China Inquire  
+86 (573) 8280-7222
Pesticide@jiahuachemical.com
Chemical distributor
chemBlink standard supplier since 2006
Nanjing Source Chemical Co., Ltd. China Inquire  
+86 (25) 8457-4770
njagrochem@gmail.com
Chemical manufacturer
chemBlink standard supplier since 2007
Zhengzhou Zhengshi Chemical Co., Ltd. China Inquire  
+86 (371) 6381-7136
zhengshichem@126.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2008
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
Ring Specialty Chemicals Inc. Canada Inquire  
+1 (416) 493-6870
info@ringchemicals.com
Chemical distributor
chemBlink standard supplier since 2010
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
Ecosfarm(Guangzhou) Bio-technologies Co., Ltd. China Inquire  
+86 (20) 8398-2853
millyhuang@ecosfarm.com
Chemical manufacturer since 2003
chemBlink standard supplier since 2015
Complete supplier list of 2,4-Dichlorophenoxyacetic acid
Identification
Classification Biochemical >> Amino acids and their derivatives >> Threonine derivative
Name 2,4-Dichlorophenoxyacetic acid
Synonyms Amidox; B-Selektonon; U-5043; Crotilin; Decamine; Dicopur; Dicotox; Ipaner; Netagrone; Pennamine; Weedone-2,4-DP; Helena 2,4-D; 2,4-D LV6; Weedar 64A; Chloroxone; BH 2,4-D; Agrotect; Amoxone; Weed Tox; Weedtrol; Emulsamine BK; Envert DT; Dormone
Molecular Structure CAS # 94-75-7, 2,4-Dichlorophenoxyacetic acid, Amidox, B-Selektonon, U-5043, Crotilin, Decamine, Dicopur, Dicotox, Ipaner, Netagrone, Pennamine, Weedone-2,4-DP, Helena 2,4-D, 2,4-D LV6, Weedar 64A, Chloroxone, BH 2,4-D, Agrotect, Amoxone, Weed Tox, Weedtrol, Emulsamine BK, Envert DT, Dormone
Molecular Formula C8H6Cl2O3
Molecular Weight 221.04
CAS Registry Number 94-75-7
EC Number 202-361-1
SMILES C1=CC(=C(C=C1Cl)Cl)OCC(=O)O
Properties
Density 1.563 g/cm3
Melting point 137-141 ºC
Boiling point 160 ºC (0.4 torr)
Water solubility Slightly soluble. Decomposes. 0.0890 g/100 mL
Safety Data
Hazard Symbols symbol symbol   GHS05;GHS07 Danger    Details
Hazard Statements H302:-H317:-H318:-H335:-H412:    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P272-P273-P280-P301+P317-P302+P352-P304+P340-P305+P354+P338-P317-P319-P321-P330-P333+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Skin sensitizationSkin Sens.1H317
Serious eye damageEye Dam.1H318
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Specific target organ toxicity - single exposureSTOT SE3H335
Acute hazardous to the aquatic environmentAquatic Acute1H400
Acute toxicityAcute Tox.4H312
Respiratory sensitizationResp. Sens.1H334
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.4H332
CarcinogenicityCarc.2H351
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
Transport Information UN 2765
SDS Available
up Discovory and Applicatios
2,4-Dichlorophenoxyacetic acid, commonly abbreviated as 2,4-D, is one of the most extensively used synthetic auxins and herbicides in agricultural history. It was first developed in the 1940s, during the period of intense research on plant growth regulators and chemical weed control. The chemical structure of 2,4-D mimics that of natural auxins, particularly indole-3-acetic acid, allowing it to selectively disrupt normal plant growth processes. When applied to broadleaf weeds, it induces uncontrolled cell division and elongation, ultimately causing the plant's death while leaving monocot crops like wheat, corn, and rice relatively unharmed.

The initial discovery and testing of 2,4-D were driven by the need to increase crop productivity by eliminating competition from unwanted vegetation. During World War II, its potential for large-scale application in food production gained strategic importance. After the war, it quickly became commercialized and was one of the first herbicides to be produced in large quantities for agricultural use. Its success helped usher in the era of modern chemical weed management, shaping weed control practices for decades to follow.

2,4-D has been applied in various agricultural systems, including cereal grains, maize, sugarcane, and pasture management. Its ability to control a wide range of broadleaf weeds at relatively low application rates made it highly popular. In turf management and lawn care, it has also been widely used to maintain weed-free grass areas. In forest management, it serves as a tool for controlling brush and invasive species. Additionally, 2,4-D has played a role in no-till and conservation tillage systems by allowing weed control without disrupting the soil.

Several forms of 2,4-D are commercially available, including acid, ester, and salt derivatives, which vary in volatility, solubility, and persistence. This flexibility allows for tailored application methods depending on crop type, climate, and environmental conditions. Formulations have been designed to improve efficacy while minimizing environmental impact, and many are compatible with tank mixes for integrated weed control strategies.

Despite its widespread use, 2,4-D has also been the subject of regulatory review and public scrutiny due to concerns about its ecological and human health effects. Environmental fate studies have shown that it can leach into groundwater and affect non-target species if not used properly. Regulatory agencies around the world have established guidelines and safety thresholds for its use, including buffer zones and application timing restrictions, to reduce the risk of drift and contamination. As part of sustainable agriculture, there is ongoing research into improving application technologies and resistance management strategies to maintain the long-term utility of 2,4-D.

The legacy of 2,4-D is significant in both agronomic and scientific contexts. It was instrumental in demonstrating the feasibility of chemical weed control on a global scale and continues to be an important tool in integrated weed management. Advances in biotechnology, including genetically modified crops tolerant to 2,4-D, have extended its utility and opened new avenues for its application.

References

1984. A gas chromatographic method for determination of 2,4-D residues in urine after occupational exposure. Bulletin of Environmental Contamination and Toxicology, 33(6).
DOI: 10.1007/bf01625578

1979. Oxygen consumption in Lepomis machrochirus exposed to 2,4-D or 2,4,5-T. Bulletin of Environmental Contamination and Toxicology, 22(1).
DOI: 10.1007/bf01685512

1971. Pesticide effect on growth and 14 C assimilation in a freshwater alga. Bulletin of Environmental Contamination and Toxicology, 6(1).
DOI: 10.1007/bf01559063
Market Analysis Reports
List of Reports Available for 2,4-Dichlorophenoxyacetic acid
Related Products
2,4-Dichlorophenethyl alcohol  2,4-Dichlorophenethylamine  2,3-Dichlorophenethylamine  2,6-Dichlorophenethylamine  2,3-Dichlorophenol  3,4-Dichlorophenol  2,6-Dichlorophenol  2,4-Dichlorophenol  2,5-Dichlorophenol  3,5-Dichlorophenol  2,4-Dichlorophenoxyacetic acid diethanolamine salt  3,5-Dichlorophenoxyacetone  (2R,4'R,8'aR)-1-[2-[4-[[2-(2,4-Dichlorophenoxy)acetyl]amino]phenyl]acetyl]tetrahydro-6'-oxospiro[pyrrolidine-2,7'(6'H)-[2H]pyrrolo[2,1-b][1,3]thiazine]-4'-carboxamide  2,5-Dichloro-4-nitropyridine 1-oxide  2,6-Dichloro-4-nitropyridine N-oxide  4,6-Dichloro-5-nitro-2-pyrimidinamine  2,4-Dichloro-5-nitropyrimidine  4,6-Dichloro-5-nitropyrimidine  2,4-Dichloro-6-(nitro)pyrrolo[2,1-f][1,2,4]triazine  2,4-Dichloro-6-nitroquinazoline