Record Information |
---|
Version | 2.0 |
---|
Creation Date | 2009-06-02 22:18:41 UTC |
---|
Update Date | 2014-12-24 20:22:50 UTC |
---|
Accession Number | T3D0802 |
---|
Identification |
---|
Common Name | 2,4-Dichlorophenoxybutyric acid |
---|
Class | Small Molecule |
---|
Description | 2,4-DB or 4-(2,4-dichlorophenoxy)butyric acid is a selective systemic phenoxy herbicide used to control many annual and perennial broadleaf weeds in alfalfa, peanuts, soybeans, and other crops. Its active metabolite, 2,4-D, inhibits growth at the tips of stems and roots. It is classified in toxicity class III. |
---|
Compound Type | - Aromatic Hydrocarbon
- Ether
- Organic Compound
- Organochloride
- Pesticide
- Synthetic Compound
|
---|
Chemical Structure | |
---|
Synonyms | Synonym | (2,4-Dichlorophenoxy)butyric acid | 2,4-(Dichlorophenoxy)butyric acid | 2,4-D Butyric | 2,4-D Butyric acid | 2,4-DB | 2,4-Dichlorophenoxybutyrate | 4-(2, 4-Dichlorophenoxy)butyric acid | 4-(2,4-DB) | 4-(2,4-Dichlorophenoxy)butanoic acid | 4-(2,4-Dichlorophenoxy)butyric acid | Butirex | Butormone | Butoxon | Butoxone | Butoxone amine | Butoxone ester | Butyrac | Butyrac 118 | Butyrac 200 | Butyrac ester | Campbell's DB straight | Caswell No. 316 | Dichlorophenoxy)butyric acid | Embutone | Embutox | Embutox e | Embutox klean-up | gamma-(2,4-Dichlorophenoxy)-butanoic acid | gamma-(2,4-Dichlorophenoxy)-butyric acid | gamma-(2,4-Dichlorophenoxy)butanoic acid | gamma-(2,4-Dichlorophenoxy)butyric acid | Legumex | Legumex d | Sys 67 Buratal | Venceweed |
|
---|
Chemical Formula | C10H10Cl2O3 |
---|
Average Molecular Mass | 249.091 g/mol |
---|
Monoisotopic Mass | 248.001 g/mol |
---|
CAS Registry Number | 94-82-6 |
---|
IUPAC Name | 4-(2,4-dichlorophenoxy)butanoic acid |
---|
Traditional Name | butyrac |
---|
SMILES | OC(=O)CCCOC1=CC=C(Cl)C=C1Cl |
---|
InChI Identifier | InChI=1S/C10H10Cl2O3/c11-7-3-4-9(8(12)6-7)15-5-1-2-10(13)14/h3-4,6H,1-2,5H2,(H,13,14) |
---|
InChI Key | InChIKey=YIVXMZJTEQBPQO-UHFFFAOYSA-N |
---|
Chemical Taxonomy |
---|
Description | belongs to the class of organic compounds known as dichlorobenzenes. Dichlorobenzenes are compounds containing a benzene with exactly two chlorine atoms attached to it. |
---|
Kingdom | Organic compounds |
---|
Super Class | Benzenoids |
---|
Class | Benzene and substituted derivatives |
---|
Sub Class | Halobenzenes |
---|
Direct Parent | Dichlorobenzenes |
---|
Alternative Parents | |
---|
Substituents | - Phenoxy compound
- Phenol ether
- 1,3-dichlorobenzene
- Alkyl aryl ether
- Aryl chloride
- Aryl halide
- Carboxylic acid derivative
- Carboxylic acid
- Ether
- Monocarboxylic acid or derivatives
- Organooxygen compound
- Organic oxygen compound
- Carbonyl group
- Organic oxide
- Hydrocarbon derivative
- Organohalogen compound
- Organochloride
- Aromatic homomonocyclic compound
|
---|
Molecular Framework | Aromatic homomonocyclic compounds |
---|
External Descriptors | |
---|
Biological Properties |
---|
Status | Detected and Not Quantified |
---|
Origin | Exogenous |
---|
Cellular Locations | |
---|
Biofluid Locations | Not Available |
---|
Tissue Locations | Not Available |
---|
Pathways | Not Available |
---|
Applications | |
---|
Biological Roles | |
---|
Chemical Roles | Not Available |
---|
Physical Properties |
---|
State | Solid |
---|
Appearance | White powder. |
---|
Experimental Properties | Property | Value |
---|
Melting Point | 118°C | Boiling Point | Not Available | Solubility | 0.046 mg/mL at 25°C [TOMLIN,C (1994)] | LogP | Not Available |
|
---|
Predicted Properties | |
---|
Spectra |
---|
Spectra | Spectrum Type | Description | Splash Key | Deposition Date | View |
---|
Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-000t-1090000000-de21dab06a16d9dd594d | 2016-08-03 | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-0f79-5980000000-d0e043f212807520d758 | 2016-08-03 | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-0006-9500000000-4b1c202a64296810a0bb | 2016-08-03 | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-0002-0390000000-bd4c785c99731f0c92b6 | 2016-08-04 | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-03di-0950000000-b1a394053669af6dae72 | 2016-08-04 | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-03di-1900000000-728872f0231b0d0a25fe | 2016-08-04 | View Spectrum | MS | Mass Spectrum (Electron Ionization) | splash10-03di-7900000000-5d6f201d2468101b3001 | 2014-09-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 25.16 MHz, CDCl3, experimental) | Not Available | 2014-09-23 | View Spectrum |
|
---|
Toxicity Profile |
---|
Route of Exposure | Not Available |
---|
Mechanism of Toxicity | Some of the endocrine effects of 2,4-DB may be mediated by the 2,4-D mediated displacement of sex hormones from the sex hormone binding globulin or the 2,4-D mediated blocking or OAT6 transport proteins that are needed for the transport of functional organic ions and dicarboxylates (including estrone sulfate).
|
---|
Metabolism | CDDs are absorbed through oral, inhalation, and dermal routes of exposure. CDDs are carried in the plasma by serum lipids and lipoproteins, distributing mainly to the liver and adipose tissue. CDDs are very slowly metabolized by the microsomal monooxygenase system to polar metabolites that can undergo conjugation with glucuronic acid and glutathione. They may increase the rate of their own metabolism by inducing CDDs induce both phase I and phase II enzymes. The major routes of excretion of CDDs are the bile and the feces, though smaller amounts are excreted in the urine and via lactation. (2) |
---|
Toxicity Values | LD50: 370-700 mg/kg (Oral, Rat); LD50: 2000 mg/kg (Dermal, Rabbit) (5) |
---|
Lethal Dose | Not Available |
---|
Carcinogenicity (IARC Classification) | 2B, possibly carcinogenic to humans. (6) |
---|
Uses/Sources | Broadleaf herbicide, widely used in agriculture, functions as a synthetic auxin. (2, 3)
|
---|
Minimum Risk Level | Not Available |
---|
Health Effects | All forms of 2,4-DB are considered low in toxicity when absorbed via skin or via inhalation. Female rats fed moderate doses of 75 mg/kg of 2,4-DB, experienced a number of chronic effects including lower ovarian weights, fewer offspring born and lower overall body weight. In addition, numerous offspring (pups) died during lactation.
|
---|
Symptoms | Symptoms of acute oral exposure include vomiting, diarrhea, headache, confusion, renal failure, aggressive or bizarre behavior, hypotension and muscle twitching. Skeletal muscle injury and renal failure may also occur. Prolonged dermal exposure may include skin irritation, whereas prolonged inhalation exposure may lead to coughing and burning sensations in the upper respiratory tract and chest. (2) |
---|
Treatment | The general treatment of acute chlorophenoxy herbicide poisoning consists of decontamination of the gastrointestinal tract, resuscitation and supportive care. For severe, acute oral poisoning by 2,4-DB or 2,4-D, forced alkaline diuresis appears to be most effective (1). Forced alkaline diuresis is often used to increase the excretion of acidic drugs like salicylates and phenobarbitone. For forced alkaline diuresis, a diuretic like furosemide is given intravenously and sodium bicarbonate is added to the infusion fluid to make blood and, in turn, urine alkaline. Potassium replacement becomes of utmost importance during the process because potassium is usually lost in urine. If blood levels of potassium are depleted below normal levels, then hypokalemia occurs, which promotes bicarbonate ion retention and prevents bicarbonate excretion, thus interfering with the alkalinization of the urine. |
---|
Normal Concentrations |
---|
| Not Available |
---|
Abnormal Concentrations |
---|
| Not Available |
---|
External Links |
---|
DrugBank ID | Not Available |
---|
HMDB ID | Not Available |
---|
PubChem Compound ID | 1489 |
---|
ChEMBL ID | CHEMBL1892377 |
---|
ChemSpider ID | 1444 |
---|
KEGG ID | C14404 |
---|
UniProt ID | Not Available |
---|
OMIM ID | |
---|
ChEBI ID | 73173 |
---|
BioCyc ID | CPD-335 |
---|
CTD ID | C004764 |
---|
Stitch ID | 2,4-Dichlorophenoxybutyric acid |
---|
PDB ID | Not Available |
---|
ACToR ID | 6426 |
---|
Wikipedia Link | Not Available |
---|
References |
---|
Synthesis Reference | Not Available |
---|
MSDS | T3D0802.pdf |
---|
General References | - Wells WD, Wright N, Yeoman WB: Clinical features and management of poisoning with 2,4-D and mecoprop. Clin Toxicol. 1981 Mar;18(3):273-6. [7237959 ]
- ATSDR - Agency for Toxic Substances and Disease Registry (1998). Toxicological profile for chlorinated dibenzo-p-dioxins (CDDs). U.S. Public Health Service in collaboration with U.S. Environmental Protection Agency (EPA). [Link]
- Wikipedia. Polychlorinated dibenzodioxins. Last Updated 19 May 2009. [Link]
- US Environmental Protection Agency (2009). Recognition and Management of Pesticide Poisonings. [Link]
- 2,4-DB [Link]
- International Agency for Research on Cancer (2014). IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. [Link]
|
---|
Gene Regulation |
---|
Up-Regulated Genes | Not Available |
---|
Down-Regulated Genes | Not Available |
---|