 | |
 | |
| Names | |
|---|---|
| Preferred IUPAC name
(2,4-Dichlorophenoxy)acetic acid | |
| Other names
2,4-D | |
| Identifiers | |
3D model (JSmol) |
|
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.147 |
| KEGG | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C8H6Cl2O3 | |
| Molar mass | 221.04 g/mol |
| Appearance | white to yellow powder |
| Melting point | 140.5 °C (284.9 °F; 413.6 K) |
| Boiling point | 160 °C (320 °F; 433 K) 0.4 mm Hg |
| 900 mg/L | |
| Hazards | |
| GHS labelling:[1] | |
  | |
| H302, H317, H318, H335, H412 | |
| P261, P273, P280, P305+P351+P338 | |
| Flash point | nonflammable[2] |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
500 mg/kg (oral, hamster) 100 mg/kg (oral, dog) |
| NIOSH (US health exposure limits): | |
PEL (Permissible) |
TWA 10 mg/m3[2] |
REL (Recommended) |
TWA 10 mg/m3[2] |
IDLH (Immediate danger) |
100 mg/m3[2] |
| Safety data sheet (SDS) | ICSC 0033 |
| Related compounds | |
Related compounds |
2,4,5-T, Dichlorprop |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
2,4-Dichlorophenoxyacetic acid is an organic compound with the chemical formula C8H6Cl2O3. It is usually referred to by its ISO common name 2,4-D.[4] It is a systemic herbicide that kills most broadleaf weeds by causing uncontrolled growth, but most grasses such as cereals, lawn turf, and grassland are relatively unaffected.
2,4-D is one of the oldest and most widely available herbicides and defoliants in the world, having been commercially available since 1945, and is now produced by many chemical companies since the patent on it has long since expired. It can be found in numerous commercial lawn herbicide mixtures, and is widely used as a weedkiller on cereal crops, pastures, and orchards. Over 1,500 herbicide products contain 2,4-D as an active ingredient.
History
2,4-D was first reported in 1944 by Franklin D. Jones at the C. B. Dolge Company in Connecticut.[5] The biological activity of 2,4-D as well as the similar hormone herbicides 2,4,5-T, and MCPA were discovered during World War II, a case of multiple discovery by four groups working independently under wartime secrecy in the United Kingdom and the United States: William G. Templeman and associates at Imperial Chemical Industries (ICI) in the UK; Philip S. Nutman and associates at Rothamsted Research in the UK; Franklin D. Jones and associates at the American Chemical Paint Company; and Ezra Kraus, John W. Mitchell, and associates at the University of Chicago and the United States Department of Agriculture. All four groups were subject to wartime secrecy laws and did not follow the usual procedures of publication and patent disclosure. In December 1942, following a meeting at the Ministry of Agriculture the Rothamsted and ICI workers pooled resources and Nutman moved to Jealott's Hill to join the ICI effort.[6] The first scientific publication describing the 2,4-D structure and plant growth regulating activity was by Percy Zimmerman and Albert Hitchcock at the Boyce Thompson Institute,[7] who were not the original inventors. The precise sequence of early 2,4-D discovery events and publications has been discussed.[8]
William Templeman found that when indole-3-acetic acid (IAA), a naturally occurring auxin, was used at high concentrations, it could stop plant growth. In 1940, he published his finding that IAA killed broadleaf plants within a cereal field.[9] MCPA was discovered at about that time by his ICI group.[6][10]: Sec 7.1
In the United States, a similar search for an acid with a longer half life, i.e., a metabolically and environmentally more stable compound, led to 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), both phenoxy herbicides and analogs of IAA. Robert Pokorny, an industrial chemist for the C.B. Dolge Company in Westport, Connecticut, published their synthesis in 1941.[5]
2,4-D was not used as a chemical warfare agent during World War II.[10]: Sec 7.1 The Allies of World War II were looking for a chemical to starve Nazi Germany and Japan into submission by killing their potato and rice crops, but 2,4-D was found to be ineffective for that purpose, because both crops tolerate it. Within a year after the war ended, 2,4-D was commercially released as an herbicide to control broadleaf weeds in grain crops such as rice and wheat,[11] and in the 1950s it was registered in the United States to control size and enhance skin color in potatoes without affecting yields.[12]
The first publication of 2,4-D's use as a selective herbicide came in 1944.[13][14] The ability of 2,4-D to control broadleaf weeds in turf was documented soon thereafter, in 1944.[15] Starting in 1945, the American Chemical Paint Company brought 2,4-D to market as an herbicide called "Weedone". It revolutionized weed control, as it was the first compound that, at low doses, could selectively control dicotyledons (broadleaf plants), but not most monocotyledons — narrowleaf crops, such as wheat, maize (corn), rice, and similar cereal grass crops.[10] At a time when labor was scarce and the need for increased food production was large, it literally "replaced the hoe".[10]: Sec 7.1 Its effectiveness, together with its non-corrosive, non-explosive and seemingly non-irritating or poisonous qualities, led to it being considered the best all-around herbicide by 1946.[16]
2,4-D is one of the ingredients in Agent Orange, an herbicide that was widely used during the Malayan Emergency and the Vietnam War.[17] However, 2,3,7,8-tetrachlorodibenzodioxin (TCDD), a contaminant in the production of another ingredient in Agent Orange, 2,4,5-T, was the cause of the adverse health effects associated with Agent Orange.[18][19]
In the 2000s, Dow AgroSciences developed a new choline salt version of 2,4-D (2,4-D choline) that Dow included in its "Enlist Duo" herbicide along with glyphosate and an agent that reduces drift; the choline salt form of 2,4-D is less volatile than 2,4-D.[20][21][22]
Manufacture
2,4-D is a member of the phenoxy family of herbicides.[18] It is manufactured from chloroacetic acid and 2,4-dichlorophenol, which is itself produced by chlorination of phenol. Alternatively, it is produced by the chlorination of phenoxyacetic acid. The production processes may create several contaminants including di-, tri-, and tetrachlorodibenzo-p-dioxin isomers and N-nitrosamines, as well as monochlorophenol.[23]
Mode of action
2,4-D is a synthetic auxin that induces uncontrolled growth and eventually death in susceptible plants.[24][25][26] It is absorbed through the leaves and is translocated to the meristems of the plant. Uncontrolled, unsustainable growth ensues, causing stem curl-over, leaf withering, and eventual plant death. 2,4-D is typically applied as an amine salt, but more potent ester versions exist, as well.[25]
Applications
2,4-D is primarily used as a selective herbicide that kills many terrestrial and aquatic broadleaf weeds, but not grasses. 2,4-D can be found in commercial lawn herbicide mixtures, which often contain other active ingredients including mecoprop and dicamba. Over 1,500 herbicide products contain 2,4-D as an active ingredient.[27]
A variety of sectors use products containing 2,4-D to kill weeds and unwanted vegetation. In agriculture, it was the first herbicide for selective killing of weeds but not crops. It has been used since 1945[28] to control broad-leafed weeds in pastures, orchards, and cereal crops such as corn, oats, rice, and wheat.[29] Cereals, in particular, have excellent tolerance to 2,4-D when it is applied before planting. 2,4-D is the cheapest way for farmers to control winter annual weeds by spraying in the fall, often at the lowest recommended rate. This is particularly effective before planting beans, peas, lentils, and chickpeas.[30] The estimated use of 2,4-D in US agriculture is mapped by the US Geological Survey. In 2019, the latest date for which figures are available, this reached 45,000,000 pounds (20,000,000 kg) annually.[31]
In domestic lawn and garden maintenance, 2,4-D is commonly used. In forestry, it is used for stump treatment, trunk injection, and selective control of brush in conifer forests. Along roadways, railways, and power lines, it is used to control weeds and brush which might interfere with safe operation and damage equipment. Along waterways, it is used to control aquatic weeds that might interfere with boating, fishing, and swimming or clog irrigation and hydroelectric equipment. It is often used by government agencies to control the spread of invasive, noxious, and non-native weed species and prevent them from crowding out native species, and also to control many poisonous weeds such as poison ivy and poison oak.[32]: 35–36 [33]
A 2010 monitoring study conducted in the US and Canada found that "current exposures to 2,4-D are below applicable exposure guidance values."[34]
2,4-D has been used in laboratories for plant research as a supplement in plant cell culture media such as MS medium since at least 1962.[35] 2,4-D is used in plant cell cultures as a dedifferentiation (callus induction) hormone. It is classified as an auxin plant hormone derivative.[36]
Health effects
Men who work with 2,4-D are at risk for abnormally shaped sperm and thus fertility problems; the risk depends on the amount and duration of exposure and other personal factors.[37]
Acute toxicity
According to the U.S. Environmental Protection Agency, "The toxicity of 2,4-D depends on its chemical forms, including salts, esters, and an acid form. 2,4-D generally has low toxicity for humans, except certain acid and salt forms can cause eye irritation. Swimming is restricted for 24 hours after application of certain 2,4-D products applied to control aquatic weeds to avoid eye irritation."[19] As of 2005[update] the median lethal dose or LD50 determined in acute toxicity rat studies was 639 mg/kg.[38]
Urinary alkalinisation has been used in acute poisoning, but evidence to support its use is poor.[39]
Cancer risk
The International Agency for Research on Cancer classifies 2,4-D as a possible carcinogen to humans while the United States Environmental Protection Agency does not.[40][41] The International Agency for Research on Cancer (IARC), said 2,4-D was classified as "possibly carcinogenic to humans (Group 2B), based on inadequate evidence in humans and limited evidence in experimental animals".[42]
In June 2015 the World Health Organization's International Agency for Research on Cancer confirmed its 1987 classification of 2,4-D as a possible carcinogen.[43][44]
On August 8, 2007, the EPA issued a ruling that existing data do not support a link between human cancer and 2,4-D exposure.[45]
A 1995 panel of 13 scientists reviewing studies on the carcinogenicity of 2,4-D had divided opinions. None of the scientists thought the weight of the evidence indicated that 2,4-D was a "known" or "probable" cause of human cancer. The predominant opinion indicated that it is possible that 2,4-D can cause cancer in humans, although not all of the panelists believed the possibility was equally likely: one thought the possibility was strong, leaning toward probable, and five thought the possibility was remote, leaning toward unlikely. Two panelists believed it unlikely that 2,4-D can cause cancer in humans.[46]
In a prior 1987 report the IARC classified some chlorphenoxy herbicides including 2,4-D, MCPA and 2,4,5-T as a group as class 2B carcinogens - "possibly carcinogenic to humans".[47]
2,4-D has been linked to lymphoma and bladder cancer in dogs.[48]
Contaminants
A July 2013 Four Corners investigation found elevated levels of dioxins in a generic version of 2,4-D, one of Australia's most widely used herbicides. Samples imported from China had "one of the highest dioxin readings for 2,4-D in the last 10 to 20 years, and could pose potential health risks."[49]
Metabolism
When radioactively labeled 2,4-D was fed to livestock, 90% or more of the total radioactive residue (TRR) was shed in urine unchanged or as conjugated forms of 2,4-D. A relatively small portion of 2,4-D was metabolized into dichlorophenol, dichloroanisole, 4-chlorophenoxyacetic acid (6.9% of the TRR in milk), and 2,4-dichlorophenol (5% of the TRR in milk; 7.3% of the TRR in eggs and 4% of the TRR in chicken liver). Residue levels in kidney were the highest.[32]: 21
Environmental behavior
Owing to the longevity and extent of use, 2,4-D has been evaluated several times by regulators and review committees.[50][51][52]
2,4-D amine salts and esters are not persistent under most environmental conditions.[18] The degradation of 2,4-D is rapid (half life of 6.2 days) in aerobic mineral soils.[38]: 54 2,4-D is broken down by microbes in soil, in processes that involve hydroxylation, cleavage of the acid side-chain, decarboxylation, and ring opening. The ethyl hexyl form of the compound is rapidly hydrolyzed in soil and water to form the 2,4-D acid.[18] 2,4-D has a low binding affinity in mineral soils and sediment, and in those conditions is considered intermediately to highly mobile, and therefore likely to leach if not degraded.[18]
In aerobic aquatic environments, the half life is 15 days. In anaerobic aquatic environments 2,4-D is more persistent, with a half life of 41 to 333 days.[53] 2,4-D has been detected in streams and shallow groundwater at low concentrations, in both rural and urban areas. Breakdown is pH dependent.[18] Some ester forms are highly toxic to fish and other aquatic life.[17]
"The ester forms of 2,4-D can be highly toxic to fish and other aquatic life. 2,4-D generally has moderate toxicity to birds and mammals, is slightly toxic to fish and aquatic invertebrates, and is practically nontoxic to honeybees" per EPA.[19][date missing]
Microbial breakdown
A number of 2,4-D-degrading bacteria have been isolated and characterized from a variety of environmental habitats.[54][55] Metabolic pathways for the compound's degradation have been available for many years, and genes encoding 2,4-D catabolism have been identified for several organisms. As a result of the extensive metadata on environmental behavior, physiology, and genetics, 2,4-D was the first herbicide for which the bacteria actively responsible for in situ degradation were demonstrated.[56] This was accomplished using the technique of DNA-based stable isotope probing, which enables a microbial function (activity), such as degrading a chemical, to be linked with the organism's identity without the need to culture the organism involved.[57]
Regulation
Maximum residue limits were first set in the EU in 2002 and re-evaluated in 2011 by the European Food Safety Authority, which concluded that the codex maximum residue limits were "not expected to be of concern for European consumers".[32]: 26 The total chronic exposure represented less than 10% of the acceptable daily intake (ADI).[32]: 28 2,4-D is currently not approved for use on lawns and gardens in Denmark, Norway, Kuwait, and the Canadian provinces of Québec[58] and Ontario.[59][failed verification] 2,4-D use is severely restricted in the country of Belize. In 2008, Dow AgroScience, LLC, sued the Canadian government for allowing Quebec to ban 2,4-D, but settled in 2011.[60]
In 2012, EPA denied the petition filed November 6, 2008, by the Natural Resources Defense Council to revoke all tolerances and to cancel all registrations of 2,4-D. EPA stated that new study and EPA's comprehensive review confirmed EPA's previous finding that the 2,4-D tolerances are safe at anticipated exposure.[52][61][62] The estimated annual use of 2,4-D in US agriculture is mapped by the US Geological Service.[63]
In October 2014, the US EPA registered Enlist Duo, an herbicide containing the less volatile 2,4-D choline salt, glyphosate, and an antidrift agent, for use in six states: Illinois, Indiana, Iowa, Ohio, South Dakota, and Wisconsin.[20] In November 2015, the EPA attempted to withdraw its own approval of Enlist Duo, as a result of legal actions against both the agency and Dow by two U.S. groups. However, while it was implied that the approval was "gone" because of the action, in fact, Enlist Duo was still approved pending a decision by the courts. On January 25, 2016, the US Ninth Circuit Court of Appeals denied EPA's motion to vacate its Enlist Duo registration. Dow stated the product would be available in 15 US states and Canada for the 2016 crop season.[64][65]
On August 21, 2013, the Australian Pesticides and Veterinary Medicines Authority (APVMA) banned selected 2,4-D high volatile ester (HVE) products due to their environmental hazards. HVE 2,4-D products had already been banned in Europe and North America for 20 years; low volatile ester products continue to be available in Australia and worldwide.[66] In July 2013 APVMA published their report findings.[67]
Genetically modified crops
In 2010, Dow published that it had created genetically modified soybeans made resistant to 2,4-D by insertion of a bacterial aryloxyalkanoate dioxygenase gene, aad1.[68][69][70]: 1 Dow intended it to be used as an alternative or complement to Roundup Ready crops due to the increasing prevalence of glyphosate-resistant weeds.[71]
As of April 2014, genetically modified maize and soybeans resistant to 2,4-D and glyphosate have been approved in Canada.[21] In September 2014, the USDA also approved Dow's maize and soybeans, and in October, the EPA registered the "Enlist Duo" herbicide containing 2,4-D and glyphosate.[20][69][72]
See also
References
- ↑ Sigma-Aldrich Co., 2,4-D. Retrieved on March 17, 2022.
- 1 2 3 4 NIOSH Pocket Guide to Chemical Hazards. "#0173". National Institute for Occupational Safety and Health (NIOSH).
- ↑ "2,4-D". National Institute for Occupational Safety and Health. December 4, 2014. Retrieved February 26, 2015.
- ↑ "Compendium of Pesticide Common Names".
- 1 2 Pokorny R (1941). "New Compounds. Some Chlorophenoxyacetic Acids". Journal of the American Chemical Society. 63 (6): 1768. Bibcode:1941JAChS..63.1768P. doi:10.1021/ja01851a601.
- 1 2 Allen H, et al. (1978). "Chapter 5: Selective herbicides". In Peacock F (ed.). Jealott's Hill: Fifty years of Agricultural Research 1928-1978. Imperial Chemical Industries Ltd. pp. 35–41. ISBN 0-901747-01-7.
- ↑ Zimmerman PW, Hitchcock AE (1942). "Substituted phenoxy and benzoic acid growth substances and the relation of structure to physiological activity". Contrib. Boyce Thompson Institute. 12: 321–343.
- ↑ Troyer J (2001). "In the beginning: the multiple discovery of the first hormone herbicides". Weed Science. 49 (2): 290–297. doi:10.1614/0043-1745(2001)049[0290:ITBTMD]2.0.CO;2. S2CID 85637273.
- ↑ Templeman WG, Marmoy CJ (November 1940). "The effect upon the growth of plants of watering with solutions of plant-growth substances and of seed dressings containing these materials". Annals of Applied Biology. 27 (4): 453–471. doi:10.1111/j.1744-7348.1940.tb07517.x.
- 1 2 3 4 Cobb AH, Reade JP (June 9, 2011). Herbicides and Plant Physiology. John Wiley & Sons. ISBN 978-1-4443-2249-1.Andrew H. Cobb, John P. H. Reade. Herbicides and Plant Physiology. Wiley-Blackwell; 2nd edition (October 25, 2010) ISBN 978-1405129350
- ↑ "The weed-crop connection". University of California at Davis. Archived from the original on December 7, 2011. Retrieved November 23, 2015.
- ↑ Waterer D (September 1, 2010). "Influence of growth regulators on skin colour and scab diseases of red-skinned potatoes". Canadian Journal of Plant Science. 90 (5): 745–753. doi:10.4141/CJPS10055.
- ↑ Quastel JH (1950). "2,4-Dichlorophenoxyacetic Acid (2,4-D) as a Selective Herbicide". Agricultural Control Chemicals. Advances in Chemistry. Vol. 1. pp. 244–249. doi:10.1021/ba-1950-0001.ch045. ISBN 9780598202970.
{{cite book}}: ISBN / Date incompatibility (help) - ↑ Hamner CL, Tukey HB (1944). "The Herbicidal Action of 2,4 Dichlorophenoxyacetic and 2,4,5 Trichlorophenoxyacetic Acid on Bindweed". Science. 100 (2590): 154–155. Bibcode:1944Sci...100..154H. doi:10.1126/science.100.2590.154. PMID 17778584.
- ↑ Mitchell JW, Davis FF and Marth PC (1944) Turf and weed control with plant growth regulators. Golfdom 18:34-38.
- ↑ Consumer Reports 1947. Consumers Union of U.S., Inc. 1947. p. 375.https://archive.org/details/sim_consumer-reports_1947/page/374/mode/2up?q=Fertilizer Consumer Reports 1947 Buying Guide, p. 375.
- 1 2 "2,4-D General Fact Sheet". National Pesticide Information Center. Retrieved October 7, 2015.
- 1 2 3 4 5 6 National Pesticide Information Center NPIC 2,4-D Technical Fact Sheet
- 1 2 3 "Ingredients Used in Pesticide Products 2,4-D". www2.epa.gov. EPA. September 22, 2014. Archived from the original on April 26, 2022. Retrieved November 6, 2014.
- 1 2 3 EPA Press Release. October 15, 2014 EPA Announces Final Decision to Register Enlist Duo, Herbicide Containing 2, 4-D and Glyphosate/Risk assessment ensures protection of human health, including infants, children EPA Documents: Registration of Enlist Duo
- 1 2 Fleury D (April 2014). "Enlist weed control system in Canada. A new tool for managing hard to control and resistant weeds". AG Annex. Archived from the original on May 3, 2014. Retrieved May 3, 2014.
- ↑ Flint J (August 31, 2011). "Dow AgroSciences Names Its Newest Herbicide Offering Enlist Duo". Prairie Farmer. Archived from the original on May 4, 2014.
- ↑ International Programme on Chemical Safety (1984). "2,4-Dichlorophenoxyacetic Acid (2,4-D)". UNEP, WHO ILO. Retrieved February 2, 2020.
- ↑ "Synthetic Auxins - MSU Extension | Montana State University". www.montana.edu. Montana State University Extension. Archived from the original on December 29, 2023. Retrieved December 29, 2023.
- 1 2 Song Y (2014). "Insight into the mode of action of 2,4-dichlorophenoxyacetic acid (2,4-D) as an herbicide". Journal of Integrative Plant Biology. 56 (2): 106–113. Bibcode:2014JIPB...56..106S. doi:10.1111/jipb.12131. PMID 24237670.
- ↑ "Weed Control Methods Handbook: 2,4-D" (PDF). invasive.org. University of Georgia Center for Invasive Species and Ecosystem Health. April 2001. Archived (PDF) from the original on March 4, 2016. Retrieved November 1, 2015.
- ↑ "EPA Chemical Summary: 2,4-Dichlorophenoxyacetic Acid (2,4-D)" (PDF). Archived from the original (PDF) on September 10, 2015.
- ↑ Ganzel B. "Herbicides – 2,4-D & Its Cousins". Wessels Living History Farm. Archived from the original on November 12, 2015. Retrieved November 12, 2015.
- ↑ Harvey W, Robblns W (February 1947). "2,4-D as a Weed Killer". University of California at Berkeley. Archived from the original on December 8, 2015. Retrieved November 12, 2015.
- ↑ "Fall Weed Control - FAQs" (PDF). Saskatchewan Ministry of Agriculture. September 2008. Archived from the original (PDF) on December 8, 2015. Retrieved November 12, 2015.
- ↑ US Geological Survey (October 12, 2021). "Estimated Agricultural Use for 2,4-D, 2019". Retrieved December 27, 2021.
- 1 2 3 4 European Food Safety Authority (November 2011). "Review of the existing maximum residue levels (MRLs) for 2,4-D according to Article 12 of Regulation (EC) No 396/2005". EFSA Journal. 9 (11): 2431. doi:10.2903/j.efsa.2011.2431.
- ↑ "2,4-D Benefits". The Industry Task Force II on 2,4-D Research Data. 2015. Archived from the original on November 2, 2015. Retrieved November 6, 2015.
- ↑ Aylward LL, Morgan MK, Arbuckle TE, Barr DB, Burns CJ, Alexander BH, Hays SM (February 2010). "Biomonitoring data for 2,4-dichlorophenoxyacetic acid in the United States and Canada: interpretation in a public health risk assessment context using Biomonitoring Equivalents". Environmental Health Perspectives. 118 (2): 177–81. Bibcode:2010EnvHP.118..177A. doi:10.1289/ehp.0900970. PMC 2831914. PMID 20123603.
- ↑ Murashige, T. and F. Skoog. A revised medium for rapid growth and bioassays with tobaccotissue cultures. Physiol. Plantarum 1962. 15:473-97. in: Sharp WR, Gunckel JE (July 1969). "Physiological Comparisons of Pith Callus With Crown-Gall and Genetic Tumors of Nicotiana glauca, N. langsdorffii, and N. glauca-langsdorffii Grown in Vitro. II. Nutritional Physiology". Plant Physiology. 44 (7): 1073–9. doi:10.1104/pp.44.7.1073. PMC 396217. PMID 16657160.
- ↑ Endreb R (1994). Plant Cell Biotechnology. Germany: Springer. pp. 17, 18. ISBN 978-0-387-56947-5.
- ↑ "The Effects of Workplace Hazards on Male Reproductive Health". NIOSH. Archived from the original on May 6, 2017.
- 1 2 US EPA 2,4-D Reregistration Eligibility Decision, 2005. Associated RED Fact sheet Archived May 17, 2008, at the Wayback Machine EPA
- ↑ Roberts DM, Buckley NA (2007). Roberts DM (ed.). "Urinary alkalinisation for acute chlorophenoxy herbicide poisoning". Cochrane Database Syst Rev (1) CD005488. doi:10.1002/14651858.CD005488.pub2. PMID 17253558.
- ↑ Pubchem. "2,4-Dichlorophenoxyacetic acid". pubchem.ncbi.nlm.nih.gov. Archived from the original on May 29, 2015.
- ↑ Loomis D (June 22, 2015). "Carcinogenicity of lindane, DDT, and 2,4-dichlorophenoxyacetic acid". The Lancet Oncology. 16 (8): 891–892. doi:10.1016/s1470-2045(15)00081-9. PMID 26111929.
- ↑ "IARC Monographs evaluate DDT, lindane, and 2,4-D" (PDF). June 23, 2015. Retrieved February 14, 2016.
- ↑ Loomis D, Guyton K, Grosse Y, El Ghissasi F, Bouvard V, Benbrahim-Tallaa L, Guha N, Mattock H, Straif K (August 2015). "Carcinogenicity of lindane, DDT, and 2,4-dichlorophenoxyacetic acid". The Lancet Oncology. 16 (8): 891–892. doi:10.1016/S1470-2045(15)00081-9. PMID 26111929.
- ↑ Carey Gillam for Reuters. June 22, 2015 WHO unit finds 2,4-D herbicide 'possibly' causes cancer in humans Archived June 23, 2015, at the Wayback Machine
- ↑ "EPA: Federal Register: 2,4-D, 2,4-DP, and 2,4-DB; Decision Not to Initiate Special Review". Epa.gov. August 8, 2007. Retrieved May 3, 2014.
{{cite web}}: CS1 maint: deprecated archival service (link) - ↑ Ibrahim MA, Bond, GG, Burke, TA, Cole, P, Dost, FN, Enterline, PE, et al. (1991). "Weight of the evidence on the human carcinogenicity of 2,4-D". Environ Health Perspect. 96: 213–22. Bibcode:1991EnvHP..96..213I. doi:10.1289/ehp.9196213. PMC 1568222. PMID 1820267.
- ↑ Chlorphenoxy Herbicides (Group 2B) in IARC monographs on the evaluation of carcinogenic risks to humans: An updating of IARC Monographs volumes 1 to 42. Supplement 7, WHO, Lyon, France 1987.
- ↑ Harveston K (March 13, 2019). "Canine Cancers Linked to Lawn Care Chemicals".
- ↑ Four Corners By Janine Cohen (July 22, 2013). "Four Corners investigation finds dangerous dioxins in widely used herbicide 2,4-D". Abc.net.au. Retrieved May 3, 2014.
- ↑ Islam F, Wang J, Farooq MA, Khan MS, Xu L, Zhu J, Zhao M, Muños S, Li QX, Zhou W (2018). "Potential impact of the herbicide 2,4-dichlorophenoxyacetic acid on human and ecosystems". Environment International. 111: 332–351. Bibcode:2018EnInt.111..332I. doi:10.1016/j.envint.2017.10.020. PMID 29203058.
- ↑ von Stackelberg K. A (2013). "Systematic Review of Carcinogenic Outcomes and Potential Mechanisms from Exposure to 2,4-D and MCPA in the Environment". J Toxicol. 2013 371610. doi:10.1155/2013/371610. PMC 3600329. PMID 23533401.
- 1 2 Andrew Pollack for the New York Times. April 9, 2012 E.P.A. Denies an Environmental Group's Request to Ban a Widely Used Weed Killer Quote: "The E.P.A. has reviewed the safety of 2,4-D several times, particularly with regard to an increased risk of cancer."
- ↑ Ju Z, Liu SS, Xu YQ, Li K (2019). "Combined Toxicity of 2,4-Dichlorophenoxyacetic Acid and Its Metabolites 2,4-Dichlorophenol (2,4-DCP) on Two Nontarget Organisms". ACS Omega. 4 (1): 1669–1677. doi:10.1021/acsomega.8b02282. PMC 6648169. PMID 31459423.
- ↑ Cavalca, L., A. Hartmann, N. Rouard, and G. Soulas. 1999. Diversity of tfdC genes: distribution and polymorphism among 2,4-dichlorophenoxyacetic acid degrading soil bacteria. FEMS Microbiology Ecology 29: 45-58.
- ↑ Suwa Y., Wright A.D., Fukimori F., Nummy K.A., Hausinger R.P., Holben W.E., Forney L.J. (1996). "Characterization of a chromosomally encoded 2,4-dichlorophenoxyacetic acid alpha-ketoglutafate dioxygenase from Burkholderia sp. strain RASC". Applied and Environmental Microbiology. 62 (7): 2464–2469. Bibcode:1996ApEnM..62.2464S. doi:10.1128/AEM.62.7.2464-2469.1996. PMC 168028. PMID 8779585.
- ↑ Cupples A.M., Sims G.K. (2007). "Identification of In Situ 2,4-Dichlorophenoxyacetic Acid-Degrading Soil Microorganisms using DNA-Stable Isotope Probing". Soil Biology and Biochemistry. 39 (1): 232–238. Bibcode:2007SBiBi..39..232C. doi:10.1016/j.soilbio.2006.07.011.
- ↑ Radajewski S., Ineson P., Parekh N.R., Murrell J.C. (2000). "Stable-isotope probing as a tool in microbial ecology". Nature. 403 (6770): 646–649. Bibcode:2000Natur.403..646R. doi:10.1038/35001054. PMID 10688198. S2CID 4395764.
- ↑ "The Pesticides Management Code - Protecting the environment and health in our green spaces". Mddep.gouv.qc.ca. April 3, 2005. Retrieved May 3, 2014.
- ↑ "Ministry of the Environment | Ontario.ca". Ene.gov.on.ca. Retrieved May 3, 2014.
- ↑ McKenna B (May 27, 2011). "Deal confirms government's right to ban 'cosmetic' pesticides, minister says". The Globe and Mail. Retrieved June 26, 2015.
- ↑ "Petition to Revoke All Tolerances and Cancel All Registrations for the Pesticide 2,4-Dichlorophenoxyacetic Acid (2,4-D); Notice of Availability" (Docket Folder Summary). Docket ID: EPA-HQ-OPP-2008-0877 Agency: EPA. United States Environmental Protection Agency. April 7, 2012. Retrieved September 12, 2012.
- ↑ "2,4-D; Order Denying NRDC's Petition To Revoke Tolerances" (Order). Federal Register. 77 (75 (Wednesday, April 18, 2012)): 23135–23158. April 18, 2012. Retrieved September 12, 2012.
Petitions to Revoke Tolerances; Denials: Natural Resources Defense Council, 2,4-dichlorophenoxyacetic acid (2-4D) Document ID: EPA-HQ-OPP-2008-0877-0446 Document Type: Rule Docket ID: EPA-HQ-OPP-2008-0877
- ↑ US Geological Survey. "Estimated Agricultural Use for 2,4-D in the USA, 2016". Retrieved February 15, 2020.
- ↑ Vogt W (January 26, 2016). "Ninth Circuit Court denies move by EPA to vacate herbicide label". Farm Futures. Retrieved February 5, 2016.
- ↑ "U.S. court upholds Enlist Duo registration". AGCanada.com. January 29, 2016. Retrieved February 5, 2016.
- ↑ "APVMA 2,4-D Review webpage". APVMA. Archived from the original on June 6, 2014. Retrieved June 6, 2014.
- ↑ "Annex to the APVMA's Preliminary Review Findings (Environment) Part 1 2,4-D Esters Volume 1 Review Summary April 2006" (PDF). APVMA. July 2013. Archived from the original (PDF) on June 6, 2014. Retrieved August 25, 2016.
- ↑ Wright TR, Shan G, Walsh TA, Lira JM, Cui C, Song P, Zhuang M, Arnold NL, Lin G, Yau K, Russell SM, Cicchillo RM, Peterson MA, Simpson DM, Zhou N, Ponsamuel J, Zhang Z (November 23, 2010). "Robust crop resistance to broadleaf and grass herbicides provided by aryloxyalkanoate dioxygenase transgenes". Proceedings of the National Academy of Sciences of the United States of America. 107 (47): 20240–5. Bibcode:2010PNAS..10720240W. doi:10.1073/pnas.1013154107. PMC 2996712. PMID 21059954.
- 1 2 ISAAA GM Approval Database GM Approval Database Genes List, Gene: aad1. International Service for the Acquisition of Agri-biotech Applications (ISAAA), n.d. accessed February 27, 2015
- ↑ Mark A. Peterson, Guomin Shan, Terence A. Walsh, and Terry R. Wright. Utility of Aryloxyalkanoate Dioxygenase Transgenes for Development of New Herbicide Resistant Crop Technologies ISB News Report,3 pages, May 2011, Research & Development, Dow AgroSciences, Indianapolis
- ↑ Pollack A (April 25, 2012). "Dow Weed Killer, Nearing Approval, Runs Into Opposition". The New York Times. Retrieved April 25, 2012.
- ↑ Keim B (September 25, 2014). "New Generation of GM Crops Puts Agriculture in a 'Crisis Situation'". Wired. Condé Nast. Retrieved April 13, 2015.
External links and further reading
- CDC - NIOSH Pocket Guide to Chemical Hazards
- Overview of the toxic effects of 2,4-D Sierra Club Canada January 2005
- "Review of 2,4-dichlorophenoxyacetic acid (2,4-D) biomonitoring and epidemiology" Review of the literature by Dow scientists Crit Rev Toxicol. Oct 2012
- PPDB Pesticides Properties database entry for 2,4-D
- 2,4-D on Pubchem
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