64902-72-3 Usage
Chemical Properties
Different sources of media describe the Chemical Properties of 64902-72-3 differently. You can refer to the following data:
1. Pure products are white crystal, odorless. m.p.174 ~ 178℃, decomposition temperature 192℃, vapor pressure 6.133x10-4Pa (25℃). Solubility in organic solvents: dichloromethane 102g/L, acetone 57g/L, methanol 14g/L, toluene 3g/L, hexane 10mg/L. Solubility in water at 25℃: 100~125mg/L (pH=4.1) and 27.9g/L (pH=7). Unstable in the acid condition, the circulating half-life of hydrolysis is 4~8 weeks when pH is 5.7～7 but 1 week when pH is 4. Under dry conditions, the photolysis of chlorsulfuron on plant surfaces is 30% within 30 days, and the photolysis of chlorsulfuron on soil surface is 15%. The circulating half-life in the soil is 4~6 weeks.
2. Colorless, odorless crystals
Uses
Different sources of media describe the Uses of 64902-72-3 differently. You can refer to the following data:
1. Intrinsic and super-efficient sulfonylurea herbicide. When absorbed by surfaces or roots of weeds, the agent is conducted to the whole plant. It inhibits the synthesis of branched chain amino acids, valine and leucine by inhibiting the activity of acetyl lactase, thereby stopping cell division, producing chlorosis and withering away to death. It is used to control broadleaf weeds and grass weeds in cereal crop fields, such as goosefoot, polygonum, amaranth, cleaver, piemarker, field bindweed, cirsium arvense, black bindweed, german camomile, setaria viridis, ryegrass, bluegrass, allium macrostemon bunge and so on. Not effective for avena fatua and solanum nigrum. It is used early before or after germination and usually administered after autumn crops are sowed but before germination or after germination of spring weeds. It is more suitable to provide leaf surface treatments after germination. Mix 0.15~0.6 grams of active ingredient per 100m2 with water to spray. It has good effects when mixed with chlortoluron and isoproteron. The crops such as corn, rape and so on are sensitive to the second stubble. It has little effect on the following rice when the dosage exceeds 0.6g.
Chlorsulfuron is a new type of sulfonylurea herbicide developed by DuPont Company of America in 1978. DuPont has turned it into a commercial product from 1981. The product is a super-efficient herbicide with low toxicity characterized by high activity, broad spectrum, selective safety of wheat seedlings.
2. Triazine urea herbicide used to control broad-leaved weeds and some annual grass
weeds.
3. Chlorsulfuron is used as a postemergence herbicide for the
control of dicotyledonous weeds, with excellent safety for
wheat and other cereals crops. While chlorsulfuron is primarily
used to control weeds in cereals, it can also be used in range
and pasture applications. It is currently only used to a minor
extent for nonfood industrial applications and right-of-way
purposes.
Production
Preparation of 2-mino-4-methyl-6-methoxy symtriazine
The craft process of isourea salt method is as followed: Mix 4.7g cyanamide (90%) with 4g water, add razoxane ethyl ethylimidoote hydrochloride(90%) at 10℃ and stir for 1h. Then use sodium hydroxide to adjust the pH value between 5 to 6 and stir for 1h at 5~10℃. Add 10ml water, stir to layer and obtain N-cyano ethyl ethylimidoote by reduced pressure distillation in oil layer with a yield of 91%. Mix 50g carbamide, 100g dimethyl sulfate and 32g methanol together, heat up it to 55℃slowly, turn off the heat, automatically reach to 60℃, cool it at 68℃ appropriately ,stop cooling at 83℃, continue to heat up to 113℃, then reduce to 105℃automatically and cool to 50℃ to obtain methyl isoureas aimethyl sulfate slat with a yield of 93%. Add 1.4g sodium in 25ml methanol, cool it to -10℃, add 11.2g methyl isoureas aimethyl sulfate slat(90%), drop 5.6g N-cyano ethyl ethylimidoote at a temperature within the range of 0℃ to 14℃, heat it up to 20℃, stir for 20h to obtain 2-mino-4-methyl-6-methoxy symtriazine by post-processing with a yield of 69.3%.
Other synthetic methods can be found in the preparation of metsulfuron-methyl.
The preparation of N-chlorophenylsulfonyl isocyanate
Mix 230ml concentrated hydrochloric acid, 70ml water and 121g o-chloroaniline together, and cool the mixture to -5℃. Add sodium nitrite solution(40%), keep the reaction temperature below 3℃, add excessive nitrite acid. At the end of the reaction, use a little urea to destroy the excess nitrite, and then remove the solid impurities to complete the diazotization of o-chloroaniline.
Dissolve 198g sodium bisulfite in 350mL water, then divide the solution into 2 parts. One part is put into the reaction flask containing 770ml concentrated hydrochloric acid and 24g anhydrous copper sulfate. Add the other part and diazonium salt solution into the solution above at the same time under the conditions of mixed cooling. Keep the reaction temperature at 0℃, isolate the oil layer at the end of the reaction, wash with water to obtain o-chlorobenzenesulfonyl chloride. The conversion rate of the above two steps is 88.7%. Drop the o-chlorobenzenesulfonyl chloride into a reaction bottle containing 430ml concentrated ammonia water, control the bath temperature at 60℃ and keep the temperature for for 4h. After the filtration, water-dioxane(5:1) mixtures are used to recrystallize, and o-chlorobenzenesulfonamide is obtained after decolorizing with a yield of 63%.
Mix 19.2g o-chlorobenzenesulfonamide, 150ml o-dichlorobenzene and 63.5g oxalyl chloride together, react for 9h to evaporate excess oxalyl chloride. Until the reaction temperature reaches 18℃, the o-dichlorobenzene is evaporated and N-chlorophenylsulfonyl is obtained by reduced pressure distillation with a yield of 57.3%. Phosgene can also be used to replace oxalyl chloride to synthesize cyanate ester in the presence of tertiary amine.
Synthesis of chlorsulfuron
Mix 0.02mol 2-mino-4-methyl-6-methoxy symtriazine and 40ml anhydrous acetonitrile together, drop 0.02mol N-chlorophenylsulfonyl isocyanate acetonitrile solution into the mixture and then continue to stir at the room temperature for 24h. Sniff out white powders, wash with acetonitrile, dry to obtain chlorsulfuron products with a yield of 70%. Chlorsulfonide can also be prepared by the addition reaction of o-chlorobenzenesulfonamide with 4-methyl-6-methoxy symtriazine-2-isocyanate prepared by the reaction of 2-mino-4-methyl-6-methoxy symtriazine and phosgene.
Description
Chlorsulfuron is one of the first sulfonylurea herbicides
developed and commercialized by DuPont. Dr George Levitt
and his team at DuPont first synthesized chlorsulfuron in 1976,
and it was commercialized for use as a herbicide in 1981. It is
currently registered by DuPont in the United States, Canada,
the European Union, Russia, the Ukraine, Australia, New
Zealand, South Africa, Saudi Arabia, and in several countries of
South America.
Compared with many other herbicides that are applied at
levels of pounds per acre (or kilograms per acre), sulfonylureas
are highly effective at use rates of less than an ounce per acre
(approximately 6 g per acre for chlorsulfuron).
General Description
Colorless crystals. Non corrosive. Insoluble in water. Used as an herbicide.
Air & Water Reactions
Insoluble in water. Reacts slowly with water. The reaction is promoted by acid such that the pH is less than 5.0 (1/2 life of 24-48 hrs.). Reaction is also promoted by polar organic solvents such as methanol and acetone.
Agricultural Uses
Herbicide: A selective systemic herbicide used to control most
broadleaf weeds and some annual grasses in wheat, barley,
oats, duram, rye, triticale and flax. Applied to non-crop
sites such as rights-of-way, fence rows and roadsides.
Trade name
DPX 4189?; FINESSE?; GLEAN?;
GLEAN 20DF?; LANDMARK? MP; LASHER?;
RIVERDALE CORSAIR?; TELAR? DF
Potential Exposure
A selective systemic sulfonylurea herbicide used to control most broadleaf weeds and some annual grasses in wheat, barley, oats, duram, rye, triticale, and flax. Applied to noncrop sites such as rights-of-way, fence rows, and roadsides.
Environmental Fate
Soil. Degrades in soil via hydrolysis followed by microbial degradation forming low
molecular weight, inactive compounds. The estimated half-life was reported to range from
4 to 6 weeks (Hartley and Kidd, 1987; Cremlyn, 1991). Microorganisms capable of
degrading chlorsulfuron are Aspergillis niger, Streptomyces griseolus and Penicillium sp.
(Humburg et al., 1989). One transformation product reported in field soils is 2-chlorobenzenesulfonamide (Smith, 1988)The reported dissipation rate of chlorsulfuron in surface soil is 0.024/day (Walker and
Brown, 1983). The persistence of chlorsulfuron decreased when soil temperature and
moisture were increased (Walker and Brown, 1983; Thirunarayanan et al., 1985)Plant. Chlorsulfuron is metabolized by plants to hydroxylated, nonphytotoxic compounds including 2-chloro-N-(((4-methoxy-6-methyl-1,3,5-triazin-2-yl)-amino)carbonyl)benzenesulfonamide (Duke et al., 1991). Devine and Born (1985) and Peterson andPhotolytic. The reported photolysis half-lives of chlorsulfuron in distilled water, methanol and natural creek water at λ >290 nm were 18, 92 and 18 hours, respectively. In all
cases, 2-chlorobenzene sulfonamide, 2-methoxy-4-methyl-6-amino-1,3,5-triazine and
trace amounts of the tentatively identified compound nitroso-2-chlorophenylsulfone
formed as photoproducts (Herrmann et al., 1985).
Metabolic pathway
Chlorsulfuron is metabolized in wheat and in tolerant
broadleaves via different pathways where
hydroxylation occurs on the methyl group of the
triazine ring and at the phenyl ring of the chlorsulfuron
in respective plants. With chemical degradation of
chlorsulfuron on dry minerals (Syst.), two pathways of
degradation are observed, one of which is direct
Toxicity evaluation
Chlorsulfuron has a moderate to short-lived fate in the environment.
It does not bioaccumulate and is not volatile. In the
environment, chlorsulfuron degrades via a combination of
biotic and abiotic processes. Chlorsulfuron degrades in acidic
solutions and soil by cleavage of the sulfonylurea bridge, Odemethylation,
and hydroxylation. Chlorsulfuron is metabolized
by soil microbes to numerous minor degradation products, is mineralized to CO2, and sequestered as nonextractable
residues. Photodegradation is not a significant
pathway of dissipation for chlorsulfuron in the environment.
Hydrolytic processes are not expected to be a major contributing
factor in the environmental degradation of chlorsulfuron,
and would only be significant at acidic pH.
Incompatibilities
Slowly hydrolyzes in water, releasing ammonia and forming acetate salts. May bencompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.
Waste Disposal
It is the responsibility of chemical waste generators to determine the toxicity and physical properties and of a discarded chemical and to properly identify its classification and certification as a hazardous waste and to determine the disposal method. United States Environmental Protection Agency guidelines for the classification determination are listed in 40 CFR Parts 261.3. In addition, waste generators must consult and follow all regional, national, state, and local hazardous waste laws to ensure complete and accurate classification and disposal methods. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material’s impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations
Check Digit Verification of cas no
The CAS Registry Mumber 64902-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,0 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64902-72:
(7*6)+(6*4)+(5*9)+(4*0)+(3*2)+(2*7)+(1*2)=133
133 % 10 = 3
So 64902-72-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H12ClN5O4S/c1-7-14-10(17-12(15-7)22-2)16-11(19)18-23(20,21)9-6-4-3-5-8(9)13/h3-6H,1-2H3,(H2,14,15,16,17,18,19)
64902-72-3Relevant articles and documents
Research on controllable degradation of sulfonylurea herbicides
Hua, Xue-Wen,Chen, Ming-Gui,Zhou, Shaa,Zhang, Dong-Kai,Liu, Ming,Zhou, Sha,Liu, Jing-Bo,Lei, Kang,Song, Hai-Bin,Li, Yong-Hong,Gu, Yu-Cheng,Li, Zheng-Ming
, p. 23038 - 23047 (2016/03/12)
In order to seek ecologically safer and environmentally benign sulfonylurea herbicides (SU), insight into the structure/bioassay/soil degradation tri-factor relationship was first established. With the introduction of various groups (alkyl, nitro, halogen, cyano etc.) at the 5th position of its benzene ring, structural derivatives of chlorsulfuron were designed, synthesized, and evaluated for their herbicidal activity. The structures of the title compounds were confirmed by infrared spectroscopy, ultraviolet spectroscopy, 1H and 13C NMR, mass spectrometry, elemental analysis and X-ray diffraction. Bioassay results confirmed that most derivatives retained their superior herbicidal activities in comparison with chlorsulfuron. After investigating the soil degradation behavior of each molecule under set conditions, it was found that structures with electron-withdrawing substituents at the 5th position of the benzene ring retained their long degradation half-lives, yet the introduction of electron-donating substituents accelerated the degradation rate. These results will provide a valuable clue to further explore the potential controllable degradation of SU and other herbicides, and to discover novel herbicides that are favorable for environmentally and ecologically sustainable development.
Herbicidal heterocyclic sulfonylurea compositions safened by herbicidal acids such as 2,4-D below a pH of 5
-
, (2008/06/13)
Disclosed are herbicidal concentrate formulation compositions having reduced grass crop plant phytotoxicity comprising certain sulfonamide or sulfonylurea herbicides in admixture with a herbicidal organic acid from the group consisting of clopyralid, 2,4-D, 2,4-DP, dicamba, dichlorprop-P, fluroxypyr MCPA, MCPP, mecoprop-P, picloram, triclopyr or mixtures of said acids; also disclosed is the preparation of said compositions and the pre- and post-emergent agricultural uses thereof in water diluted form.
N-phenylpyrrolidines
-
, (2008/06/13)
The 1-(3,5-bis-trifluoromethylphenyl)-2-thioxopyrrolidine-4-carboxylic acid derivatives of the formula I below are suitable for protecting crop plants against the phytotoxic action of herbicides and for regulating the plant growth. The 1-(3,5-bis-trifluoromethylphenyl)-2-thioxopyrrolidine-4-carboxylic acid derivatives are those of the formula I STR1 wherein A is --COOR1, --COSR1, --COO? M≈, --CONR2 R3 or --COCl; R1 is hydrogen, C1 -C4 alkyl, C2 -C6 alkenyl or C2 -C6 alkynyl; R2 and R3 independently of one another are hydrogen, C1 -C4 alkyl or C3 -C7 cycloalkyl; or R2 and R3 together with the nitrogen atom to which they are bonded are a saturated 3- to 7-membered heterocycle which can contain an additional hetero atom selected from the group comprising O, N and S and which is unsubstituted or up to trisubstituted by C1 14 C4 alkyl; and M≈ is the equivalent of an alkali metal cation or an alkaline earth metal cation or HN≈ (R2)3, and their isomers in optically pure or enriched form.
