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| | 2-Methyl-4-chlorophenoxyacetic acid Basic information |
| | 2-Methyl-4-chlorophenoxyacetic acid Chemical Properties |
| Melting point | 114-118 °C (lit.) | | Boiling point | 288.02°C (rough estimate) | | density | 1.2799 (rough estimate) | | refractive index | 1.5230 (estimate) | | Fp | 2 °C | | storage temp. | Sealed in dry,Room Temperature | | solubility | water: insoluble(lit.) | | form | Solid | | pka | 3.14±0.10(Predicted) | | color | White to Light yellow to Light orange | | Water Solubility | 1.174g/L(25 ºC) | | Merck | 14,5764 | | BRN | 2051752 | | CAS DataBase Reference | 94-74-6(CAS DataBase Reference) | | NIST Chemistry Reference | [(4-Chloro-o-tolyl)oxy]acetic acid(94-74-6) | | EPA Substance Registry System | MCPA (94-74-6) |
| | 2-Methyl-4-chlorophenoxyacetic acid Usage And Synthesis |
| Chemical Properties | MCPA is a colorless crystalline solid | | Chemical Properties | White, crystalline solid.
Free acid insoluble in water but sodium and amine
salts are soluble. | | Uses | Labelled MCPA (C369470). Herbicide. | | Uses | (4-Chloro-2-methylphenoxy)acetic Acid is a herbicide.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list. | | Uses | Systemic postemergence herbicide used to control annual and perennial weeds in
cereals, rice, flax, vines, peas, potatoes, asparagus, grassland and turf. | | Definition | ChEBI: A chlorophenoxyacetic acid that is (4-chlorophenoxy)acetic acid substituted by a methyl group at position 2. | | General Description | Colorless plates. Corrosive. Practically insoluble in water. Used as an herbicide. | | Air & Water Reactions | Insoluble in water. | | Reactivity Profile | 2-Methyl-4-chlorophenoxyacetic acid is a chlorinated benzoic acid derivative. Reacts as a weak acid to neutralize bases, both organic (for example, the amines) and inorganic. May corrode iron, steel, and aluminum parts and containers if moist. Reacts with cyanide salts in the presence of moisture to generate gaseous hydrogen cyanide. May react if moist with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A variety of products is possible. Like other acids, may initiate polymerization reactions or catalyze other reactions. is a chlorinated carboxylic acid herbicide. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in 2-Methyl-4-chlorophenoxyacetic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. | | Agricultural Uses | Herbicide: A U.S. EPA restricted Use Pesticide (RUP) as MCPA,
sodium salt. MCPA is a systemic post-emergence phenoxy
herbicide used to control broadleaf annual and perennial
weeds (including thistle and dock) in cereals, flax, rice,
vines, peas, potatoes, grasslands, forestry applications,
and on rights-of-way. It is very compatible with many
other compounds and may be used in formulation with
many other products, including bentazone, bromoxynil,
2,4-D, dicamba, fenoxaprop, MCPB, mecoprop, thifensulfuron,
and tribenuron. | | Trade name | ACME MCPA AMINE 4®; AGRITOX®;
AGROXONE®; AGROZONE®; AGSCO®; ANICON
KOMBI®; ANICON M®; BANLENE®; BLESEL MC®;
BORDERMASTER®; BROMINAL M & PLUS®;
CAMBILENE®; CHEYENNE®; CHIMAC OXY®;
CHIPTOX®; CHWASTOX®; CORNOX M®; DAKOTA®;
DED WEED®; DICOPUR-M®; DICOTEX®; DOW
MCP AMINE WEED KILLER®; DYVEL®; EH1356
HERBICIDE®; EMCEPAN®; EMPAL®; ENVOY®;
HEDAPUR M 52®; HEDAREX M®; HEDONAL M®;
HERBICIDE M®; HORMOTUHO®; HORNOTUHO®;
KILSEM®; 4 K-2 M®; KVK®; LEGUMEX DB®;
LEUNA M®; LEYSPRAY®; LINORMONE®;
M 40®; 2 M-4C®; 2 M-4KH®; MALERBANE®;
MAYCLENE®; MEPHANAC®; MIDOX®; MXL®;
OKULTIN®; PHENOXYLENE 50®; PHENOXYLENE
PLUS®; PHENOXYLENE SUPER®; RAZOL DOCK
KILLER®; RHOMENE®; RHONOX®; SHAMOX®;
B-SELEKTONON M®; SEPPIC MMD®; TILLER®;
TRIMEC®; U 46®; VACATE®; VESAKONTUHO®;
WEEDAR®; WEEDAR MCPA CONCENTRATE®;
WEEDONE MCPA ESTER®; WEED RHAP®; ZELAN® | | Safety Profile | Suspected carcinogen.
Poison by subcutaneous and intravenous
routes. Moderately toxic by ingestion.
Human systemic effects by ingestion: blood
pressure decrease and coma. Experimental
teratogenic and reproductive effects.
Mutation data reported. An herbicide. When
heated to decomposition it emits toxic
fumes of Cl-. | | Potential Exposure | A potential danger to those involved
in the manufacture, formulation, and application of this
postemergence herbicide, used for control of broadleaf
weeds in agricultural applications. | | Environmental Fate | Biological. Cell-free extracts isolated from Pseudomonas sp. in a basal salt medium
degraded MCPA to 4-chloro-o-cresol and glyoxylic acid (Gamar and Gaunt, 1971).
Soil. Residual activity in soil is limited to approximately 3–4 months (Hartley and
Kidd, 1987).
Plant. The penetration, translocation and metabolism of radiolabeled MCPA in a
cornland weed (Galium aparine) was studied by Leafe (1962). Carbon dioxide was identified
as a metabolite but this could only account 7% of the applied MCPA. Though no
Photolytic. When MCPA in dilute aqueous solution was exposed to summer sunlight
or an indoor photoreactor (l >290 nm), 2-methyl-4-chlorophenol formed as the major
product as well as o-cresol and 4-chloro-2-formylphenol (Soderquist and Crosby, 1975).
Clapés et al. (1986) studied the photodecomposition of aqueous solution of MCPA (120
ppm, pH 5.4, 25°C) in a photoreactor equipped with a high pressure mercury lamp. After three minutes of irradiation, 4-chloro-2-methylphenol formed as an intermediate which
degraded to 2-methylphenol. Both compounds were not detected after 6 minutes of irradiation;
however, 1,4-dihydroxy-2-methylbenzene and 2-methyl-2,5-cyclohexadiene-1,4-
dione formed as major and minor photodecomposition products, respectively. The same
experiment was conducted using simulated sunlight (l <300 nm) in the presence of
riboflavin, a known photosensitizer. 4-Chloro-2-methylphenol and 4-chloro-2-methylbenzyl
formate formed as major and minor photoproducts, respectively (Clapés et al., 1986).
Ozone degraded MCPA in dilute aqueous solution with and without UV light (l >300
nm) (Benoit-Guyod et al., 1986).
Chemical/Physical. Reacts with alkalies forming water soluble salts (Hartley and Kidd,
1987). Ozonolysis of MCPA in the dark yielded the following benzenoid intermediates:
4-chloro-2-methylphenol, its formate ester, 5-chlorosalicyaldehyde, 5-chlo | | Shipping | UN3345 Phenoxyacetic acid derivative pesticide,
solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3077 Environmentally hazardous substances, solid,
n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous
material, Technical Name Required | | Purification Methods | It is insoluble in H2O (solubility is 0.55g/L at 20o) and recrystallises from *C6H6 or chlorobenzene as plates [J.nsson et al. Acta Chem Scand 6 993 1952]. The S-benzylisothiouronium salt has m 164-165o, and the Cu2+ salt has m 247-249o(dec) [Armarego et al. Nature 183 1176 1959, UV: Duvaux & Grabe Acta Chem Scand 4 806 1950, IR: J.berg Acta Chem Scand 4 798 1950]. [Beilstein 6 IV 1991.] It is a plant growth substance and a herbicide. | | Incompatibilities | A weak acid. Compounds of the carboxyl group react with all bases, both inorganic and
organic (i.e., amines) releasing substantial heat, water and a
salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds,
dithiocarbamates, isocyanates, mercaptans, nitrides, and
sulfides (releasing heat, toxic, and possibly flammable
gases), thiosulfates and dithionites (releasing hydrogen
sulfate and oxides of sulfur). Incompatible with alkalis. | | Waste Disposal | Incineration with added flammable solvent; incinerator equipped with fume scrubber.
In accordance with 40CFR165, follow recommendations
for the disposal of pesticides and pesticide containers.
Must be disposed properly by following package label
directions or by contacting your local or federal environmental control agency, or by contacting your regional
EPA office |
| | 2-Methyl-4-chlorophenoxyacetic acid Preparation Products And Raw materials |
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