hysical & Chemical Properties:
Appearance: White to brown powder. Melting Point: 76-77° CVapour
Pressure: 0.000011MPa at 20° C.
Stability: Solubility in water 0.4mg/L at 20° C, solubility in acetone 200g/l, methanol 50 g/l, benzene 2.5 g/l.
Toxicity Oral LD50 (rat) 1210 to 1670 mg/kg, dermal LD50 (rat) is greater than 2000 mg/kg, Inhal. LC50 rat without effect 5.8mg/L.
Applicationï¼?
It is is a selective, postemergence phenoxy herbicide. It is used to control annual and perennial grass weeds in potatoes, soybeans, sugar beets, peanuts, vegetables, cotton and flax, as well as other crops.
Application 1,It is a broad-spectrum contact herbicide and is used to control a wide range of weeds after the crop emerges or for total vegetation control on land not used for cultivation. Glufosinate herbicides are also used to desiccate (dry off) crops before harvest.
2,It is used to kill agricultural herbicide, and it is easy to be decompound in oil. It has very low poison and high activery, it is used to kill many kinds of weed. And it is easy to be decompound in soil, so it is safe to crops and entironment. Controlling spectrum
3,It can be used to kill gramineous weed which grow one year or many years in mealie, paddy, orchard, grapery, potato field, nursery, foresr, rangeland, ornamental and so on.
Target crops Orchards, vineyards, potato fields, non-arable land
Composition Methomyl is a mixture of (Z)- and (E)- isomers, the former predominating. Mol. wt. 162.2 M.f. C5H10N2O2S Form Colourless crystals, with a slight sulfurous odour. M.p. 78-79 V.p. 0.72 mPa (25 ) KOW logP = 0.093 Henry 2.13 ?10-6 Pa m3 mol-1 S.g./density 1.2946 (25 ) Solubility In water 57.9 g/l (25 ). In methanol 1000, acetone 730, ethanol 420, isopropanol 220, toluene 30 (all in g/kg, 25 ). Sparingly soluble in hydrocarbons. Stability Stable in water for 30 d (pH 5 and 7); DT50 c. 30 d (pH 9). Stable up to 140 . Stable to sunlight when exposed for 120 d.
NOMENCLATURE
Common name chlorfenapyr (BSI, pa ISO, ANSI)
IUPAC name 4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile
Chemical Abstracts name 4-bromo-2-(4-chlorophenyl)-1-(ethoxymethyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile
CAS RN [122453-73-0] Development codes AC 303,630; CL 303,630 (both Cyanamid); MK-242 (Mitsubishi Chemical)
NOMENCLATURE Common name pyrazosulfuron-ethyl
IUPAC name ethyl 5-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl)-1-methylpyrazole-4-carboxylate
Chemical Abstracts name ethyl 5-[[[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrazole-4-carboxylate
CAS RN [93697-74-6] Development codes NC-311 (Nissan)
PHYSICAL CHEMISTRY Mol. wt. 414.4 M.f. C14H18N6O7S Form Colourless crystals. M.p. 177.8-179.5 V.p. 4.2 ?10-5 mPa (25 ) KOW logP = 3.16 (hplc method) S.g./density 1.46 (20 ) Solubility In water 9.76 mg/l (20 ). In methanol 4.32, hexane 0.0185, benzene 15.6, 200, acetone 33.7 (all in g/l, 20 ). Stability Stable at 50 for 6 months. Relatively stable at pH 7. Unstable in acidic or alkaline media. pKa 3.7
NOMENCLATURE
Common name thiamethoxam (ATXht98120 BSIATXht0 , pa ATXht98195 ISOATXht0 )
IUPAC name 3-(2-chloro-1,3-thiazol-5-ylmethyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene(nitro)amine
Chemical Abstracts name 3-[(2-chloro-5-thiazolyl)methyl]tetrahydro-5-methyl-N-nitro-4H-1,3,5-oxadiazin-4-imine
CAS RN [153719-23-4] Development codes CGA 293343 (Ciba-Geigy)
Mol. wt. 242.1 M.f. C10H5Cl2NO2 Form Colourless crystals. M.p. 274 V.p.
Composition Tech. is 95% pure. Mol. wt. 304.3 M.f. C12H21N2O3PS Form Clear colourless liquid; (tech., yellow liquid). B.p. 83-84 /0.0002 mmHg; 125 /1 mmHg V.p. 1.2 101 mPa (25 ) (OECD 104) KOW logP = 3.30 (OECD 107) Henry 6.09 ?10-2 Pa m3 mol-1 (calc.) S.g./density 1.11 (20) Solubility In water 60 mg/l (20 ). Completely miscible with common organic solvents, e.g. ethers, alcohols, benzene, toluene, hexane, cyclohexane, dichloromethane, acetone, petroleum oils. Stability Susceptible to oxidation above 100 â??. Stable in neutral media, but slowly hydrolysed in alkaline media, and more rapidly in acidic media; DT50 (20 ) 11.77 h (pH 3.1), 185 d (pH 7.4), 6.0 d (pH 10.4). Decomposes above 120 . pKa 2.6 (OECD 112) F.p. 2
Mol. wt. 221.0 M.f. C4H7Cl2O4P Form Colourless liquid; (ATXht981180 tech.ATXht0 , colourless-to-amber liquid, with an aromatic odour). M.p. 100 (DIN 51758); 172 (Pensky-Martens closed cup, 1 105 Pa)
PHYSICAL CHEMISTRY
Composition A mixture of emamectin B1a (90%) and emamectin B1b (10%), as their benzoate salts. Mol. wt. 1008.3 (B1a); 994.2 (B1b) M.f. C56H81NO15 (B1a); C55H79NO15 (B1b) Form White to off-white powder. M.p. 141-146 V.p. 4 10-3 ATXht981131 mPaATXht0 (21 ) KOW logP = 5.0 (ATXht981151 pHATXht0 7) S.g./density 1.20 (23 ) Solubility In water 0.024 g/l (ATXht981151 pHATXht0 7, 25).
NOMENCLATURE
Common name amitraz (BSI, E-ISO, ANSI, ESA, BAN, JMAF); amitraze ((m) F-ISO)
IUPAC name N-methylbis(2,4-xylyliminomethyl)amine
Chemical Abstracts name N'-(2,4-dimethylphenyl)-N-[[(2,4-dimethylphenyl)imino]methyl]-N-methylmethanimidamide
Other names N,N-bis(2,4-xylyliminomethyl)methylamine; N-methyl-N'-2,4-xylyl-N-(N-2,4-xylylformimidoyl)formamidine; 1,5-di-(2,4-dimethylphenyl)-3-methyl-1,3,5-triazapenta-1,4-diene CAS RN [33089-61-1] EEC no. 251-375-4 Development codes BTS 27 419 (Boots) Official codes OMS 1820; ENT 27 967
NOMENCLATURE : Common name paraquat (ATXht98120 BSIATXht0 , ATXht98155 E-ISOATXht0 , (m) ATXht98167 F-ISOATXht0 , ATXht98111 ANSIATXht0 , ATXht981193 WSSAATXht0 , ATXht981100 JMAFATXht0 ); no name (Germany)
IUPAC name 1,1'-dimethyl-4,4'-bipyridinediium; 1,1'-dimethyl-4,4'-bipyridinium; 1,1'-dimethyl-4,4'-bipyridylium
Chemical Abstracts name 1,1'-dimethyl-4,4'-bipyridinium
CAS RN [4685-14-7] EEC no. 225-141-7
NOMENCLATURE: Common name pyrazosulfuron-ethyl
IUPAC name ethyl 5-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl)-1-methylpyrazole-4-carboxylate
Chemical Abstracts name ethyl 5-[[[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrazole-4-carboxylate
CAS RN [93697-74-6] Development codes NC-311 (Nissan)
NOMENCLATUR Common name paraquat (ATXht98120 BSIATXht0 , ATXht98155 E-ISOATXht0 , (m) ATXht98167 F-ISOATXht0 , ATXht98111 ANSIATXht0 , ATXht981193 WSSAATXht0 , ATXht981100 JMAFATXht0 ); no name (Germany)
IUPAC name 1,1'-dimethyl-4,4'-bipyridinediium; 1,1'-dimethyl-4,4'-bipyridinium; 1,1'-dimethyl-4,4'-bipyridylium
Chemical Abstracts name 1,1'-dimethyl-4,4'-bipyridinium
CAS RN [4685-14-7] EEC no. 225-141-7
NOMENCLATURE
Common name dimethomorph (BSI, draft E-ISO); dimé? homorphe ((m) draft F-ISO)
IUPAC name (E,Z)-4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl]morpholine
Chemical Abstracts name (E,Z)-4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-oxo-2-propenyl]morpholine
CAS RN [110488-70-5] EEC no. 404-200-2 Development codes CME 151 (Celamerck); SAG 151; WL 127 294 (Shell); AC 336379; CL 183776; CL 336379 (all Cyanamid); BAS 550F
Composition Tech. is >85% pure. Mol. wt. 314.2 M.f. C14H17Cl2N3O Form White, crystalline solid. M.p. 110-112 V.p. 0.018 mPa (20 ) KOW logP = 3.9 (20 ) Henry 3.33 10-4 Pa m3 mol-1 (calc.) S.g./density 1.29 g/cm3 (25 ) Solubility In water 0.017 g/l (20 ). In dichloromethane 336, methanol 246, acetone 164, ethyl acetate 120, toluene 59, hexane 0.8 (all in g/l, 20 ). Stability Stable for at least 6 years at ambient temperatures. Stable to hydrolysis and photolysis in water. Formulations stable in sales containers for 6 months at 50, and 2 years at ambient temperature
NOMENCLATURE:
Common name hexaconazole (BSI, ANSI, draft E-ISO, (m) draft F-ISO)
IUPAC name (RS)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol
Chemical Abstracts name (-a-butyl-a-(2,4-dichlorophenyl)-1H-1,2,4-triazole-1-ethanol
CAS RN [79983-71-4] Development codes PP523; ICIA0523 (both ICI)
PHYSICAL CHEMISTRY:
Composition Tech. is >85% pure. Mol. wt. 314.2 M.f. C14H17Cl2N3O Form White, crystalline solid. M.p. 110-112 â?? V.p. 0.018 mPa (20 â??) KOW logP = 3.9 (20 â??) Henry 3.33 ?10-4 Pa m3 mol-1 (calc.) S.g./density 1.29 g/cm3 (25 â??) Solubility In water 0.017 g/l (20 â??). In dichloromethane 336, methanol 246, acetone 164, ethyl acetate 120, toluene 59, hexane 0.8 (all in g/l, 20 ). Stability Stable for at least 6 years at ambient temperatures. Stable to hydrolysis and photolysis in water. Formulations stable in sales containers for 6 months at 50 â??, and 2 years at ambient temperature.
Mol. wt. 387.8 M.f. C19H18ClN3O4 Form White or light beige crystalline solid. M.p. 63.7-65.2 V.p. 2.6 ?10-5 mPa (20 ) KOW logP = 3.99 (22 ) Henry 5.3 10-6 Pa m3 mol-1 (calc.) Solubility In water 1.9 mg/l (20 ). Stability Stable >30 d (pH 5-7, 25 ). Photolysis DT50 in water
Application
Thiamethoxam can effectively prevent and cure various aphid, leafhopper, planthopper, whitefly, beetle larvae and potato beetles, worms, ground beetle, leafminer, insect pests. It can be used in stem and leaf treatment, seed treatment and soil treatment. suitable crops are: rice crops, sugar beet, rape, potato, cotton, beans, fruit, peanut, sunflower, soybean, tobacco and citrus.
Target crops Rice, Chrysanthemum, sugar beet, rape, potato, cotton, beans, fruit, peanut, sunflower, soybean and citrus.
Description:
Azoxystrobin difenoconazole is a broad spectrum fungicide with activity against several diseases on many edible crops and ornamental plants. Some diseases controlled or prevented are rice blast, rusts, downy mildew, powdery mildew, late blight, apple scab, and Septoria etc. The substance is used as an active agent protecting plants and fruit/vegetables from fungal diseases.
Product uses :
Cucumberã??Grapeã??Rice
Mode of Action:
1.Fungicide with protectant, curative, eradicant, translaminar and systemic properties.
2.Inhibits spore germination and mycelial growth, and also shows antisporulant activity.
The prevention and therapy of rice leaf blast.Using the tricyclazole during 3-4 leaf period.
Mode of action Systemic foliar fungicide with protective and curative action, with translocation acropetally in the xylem. Uses Systemic foliar fungicide with a broad range of activity, at 100-150 g/ha. On cereals, it controls diseases caused by Cochliobolus sativus, Erysiphe graminis,Leptosphaeria nodorum, Puccinia spp., Pyrenophora teres,Pyrenophora tritici-repentis, Rhynchosporium secalis, and Septoriaspp. In bananas, control of Mycosphaerella musicola andMycosphaerella fijiensis var. difformis. Other uses are in turf againstSclerotinia homoeocarpa, Rhizoctonia solani, Puccinia spp. andErysiphe graminis; in rice against Rhizoctonia solani,Helminthosporium oryzae, and dirty panicle complex; in coffee againstHemileia vastatrix; in peanuts against Cercospora spp.; in stone fruit against Monilinia spp., Podosphaera spp., Sphaerotheca spp. andTranzschelia spp.; in maize against Helminthosporium spp.
Mode of action Systemic foliar fungicide with protective and curative action, with translocation acropetally in the xylem. Uses Systemic foliar fungicide with a broad range of activity, at 100-150 g/ha. On cereals, it controls diseases caused by Cochliobolus sativus, Erysiphe graminis,Leptosphaeria nodorum, Puccinia spp., Pyrenophora teres,Pyrenophora tritici-repentis, Rhynchosporium secalis, and Septoriaspp. In bananas, control of Mycosphaerella musicola andMycosphaerella fijiensis var. difformis. Other uses are in turf againstSclerotinia homoeocarpa, Rhizoctonia solani, Puccinia spp. andErysiphe graminis; in rice against Rhizoctonia solani,Helminthosporium oryzae, and dirty panicle complex; in coffee againstHemileia vastatrix; in peanuts against Cercospora spp.; in stone fruit against Monilinia spp., Podosphaera spp., Sphaerotheca spp. andTranzschelia spp.; in maize against Helminthosporium spp.
Chlorothalonil is a broad spectrum, protective fungicide. The mechanism of action is that it can interact with glyceraldehyde triphosphate dehydrogenase in fungal cells and combine with proteins containing cysteine in the enzyme, thus destroying the activity of the enzyme and making the metabolism of fungal cells destroyed and thus losing vitality.
Composition Racemate (i.e. 1:1 mixture of (1R)- and (1S)- enantiomers). Mol. wt. 293.8 M.f. C14H16ClN3O2 Form Colourless crystals, with a weak characteristic odour. M.p. 82.3 V.p. 0.02 mPa (20 ); 0.06 mPa (25 ) KOW logP = 3.11 Henry 9 ?10-5 Pa m3 mol-1 (20 â?? ) S.g./density 1.22 (20 â?? ) Solubility In water 64 mg/l (20 ). Moderately soluble in most organic solvents except aliphatics. In dichloromethane, toluene >200, isopropanol 99, hexane 6.3 (all in g/l, 20 ). Stability Stable to hydrolysis; DT50 (22 ) >1 y (pH 3, 6, and 9).
Mode of action Systemic foliar fungicide with protective and curative action, with translocation acropetally in the xylem. Uses Systemic foliar fungicide with a broad range of activity, at 100-150 g/ha. On cereals, it controls diseases caused by Cochliobolus sativus, Erysiphe graminis,Leptosphaeria nodorum, Puccinia spp., Pyrenophora teres,Pyrenophora tritici-repentis, Rhynchosporium secalis, and Septoriaspp. In bananas, control of Mycosphaerella musicola andMycosphaerella fijiensis var. difformis. Other uses are in turf againstSclerotinia homoeocarpa, Rhizoctonia solani, Puccinia spp. andErysiphe graminis; in rice against Rhizoctonia solani,Helminthosporium oryzae, and dirty panicle complex; in coffee againstHemileia vastatrix; in peanuts against Cercospora spp.; in stone fruit against Monilinia spp., Podosphaera spp., Sphaerotheca spp. andTranzschelia spp.; in maize against Helminthosporium spp.
Glyphosate Mode of action: Non-selective systemic herbicide, absorbed by the foliage, with rapid translocation throughout the plant. Inactivated on contact with soil.
Glyphosate Uses: Control of annual and perennial grasses and broad-leaved weeds, pre-harvest, in cereals, peas, beans, oilseed rape, flax and mustard, at c. 1.5-2 kg/ha; Glyphosate control of annual and perennial grasses and broad-leaved weeds in stubble and post-planting/pre-emergence of many crops; as a directed spray in vines and olives, at up to 4.3 kg/ha; in orchards, pasture, forestry and industrial weed control, at up to 4.3 kg/ha. As an aquatic herbicide, at c. 2 kg/ha.
PHYSICAL CHEMISTRY: Mol. wt. 239.7 M.f. C12H14ClNO2 Form Clear, colourless to light brown, viscous liquid. M.p. 25 B.p. 275 V.p. 19.2 mPa (25 ) KOW logP = 2.5 Henry 4.19 10-3 Pa m3 mol-1 S.g./density 1.192 (20 ) Solubility In water 1.1 g/l. Miscible with acetone, acetonitrile, chloroform, cyclohexanone, dichloromethane, methanol, toluene, heptane, dimethylformamide. Stability Stable at ambient temperatures for at least 2 y; stable at 50 for at least 3 mo. In sunlight, DT50 >30 d in aqueous solution. F.p. 70-75 (closed cup)
Emamectin benzoate�Biochemistry:
Acts by stimulating the release of γ-aminobutyric acid, an inhibitory neurotransmitter, thus finally activating chloride channels.
Emamectin benzoate�Mode of action:
Non-systemic insecticide which penetrates leaf tissues by translaminar movement. Paralyses the Lepidoptera, which stop feeding within hours of ingestion, and die 2-4 dat.
Use:
Control of sucking insects, including rice-, leaf- and plan thoppers, aphids, thrips, whitefly and lepidoptera on vegetables, brassicas, cotton. rice, cereals, maize, sugar beet, potatoes, citrus fruit, pome fruit and stone fruit.
Product Description:
Polyazole is a plant growth regulator with effects of delaying plant growth, inhibiting stem elongation, shortening internodes, promoting plant tillering, increasing plant stress resistance and increasing yield.
Product uses:
This product is suitable for rice, wheat, peanut, fruit tree, , rape, soybean, flower and grass etc
Product Description:
Pyridaben is a�broad spectrum, acaricidal agent, can be used to control a�variety of plant eating pests.It has good effect on ovum, ovum, Verna and adult mite in the whole growth period of the mite, and it also has obvious quick killing effect on the adult mite in mobile period.The drug is not affected by temperature changes, whether early spring or autumn use, can achieve full effect.
Product uses:
The mite has obvious control effect on the phytophagous pests . Suitable for citrus, apples, pears, hawthorn, cotton, tobacco, vegetables (except eggplant) and ornamental plants.
Application:
Novel structure of pyrrolidones and mites. It has excellent prevention effect on drilling, sucking and chewing pests and mites.
It is�broad-spectrum insecticidal and anti-killing agents; both stomach and touch-killing functions; no interaction resistance with other insecticides; moderate residual activity on the crops; and selective internal absorption activity in the nutrient solution through the absorption of the roots; and the oral toxicity to the mammal is moderate, and the percutaneous toxicity is low; And the effective pesticide application amount is low (100 g of effective component/ hm2).
Applicable crops:
It can be used in vegetables, fruit trees, ornamental plants, etc., and can be widely used to control pests and mites in cotton, vegetables, citrus, grapes, soybeans and other crops. Acephate and other conventional agents were 4 times higher than 16 times higher. It can also be used to control termites.
Composition Tech. is 95% pure. Mol. wt. 304.3 M.f. C12H21N2O3PS Form Clear colourless liquid; (tech., yellow liquid). B.p. 83-84 /0.0002 mmHg; 125 /1 mmHg V.p. 1.2 101 mPa (25 ) (OECD 104) KOW logP = 3.30 (OECD 107) Henry 6.09 ?10-2 Pa m3 mol-1 (calc.) S.g./density 1.11 (20 ) Solubility In water 60 mg/l (20 ). Completely miscible with common organic solvents, e.g. ethers, alcohols, benzene, toluene, hexane, cyclohexane, dichloromethane, acetone, petroleum oils. Stability Susceptible to oxidation above 100 Stable in neutral media, but slowly hydrolysed in alkaline media, and more rapidly in acidic media; DT50 (20 ) 11.77 h (pH 3.1), 185 d (pH 7.4), 6.0 d (pH 10.4). Decomposes above 120 . pKa 2.6 (OECD 112) F.p. 2
NOMENCLATURE
Common name emamectin (BSI, pa E-ISO, ANSI); emamectine ((f) pa F-ISO)
IUPAC name A mixture containing 90% of (10E,14E,16E,22Z)-(1R,4S,5'S,6S,6'R,8R,12S,13S,20R,21R,24S)-6'-[(S)-sec-butyl]-21,24-dihydroxy-5',11,13,22-tetramethyl-2-oxo-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6-spiro-2'-(5',6'-dihydro-2'H-pyran)-12-yl 2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-a-L-lyxo-hexopyranosyl)-a-L-arabino-hexopyranoside and 10% of (10E,14E,16E,22Z)-(1R,4S,5'S,6S,6'R,8R,12S,13S,20R,21R,24S)-21,24-dihydroxy-6'-isopropyl-5',11,13,22-tetramethyl-2-oxo-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6-spiro-2'-(5',6'-dihydro-2'H-pyran)-12-yl 2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-a-L-lyxo-hexopyranosyl)-a-L-arabino-hexopyranoside
Emamectin Benzoate
NOMENCLATURE
Common name emamectin (BSI, pa E-ISO, ANSI); emamectine ((f) pa F-ISO)
IUPAC name A mixture containing 90% of (10E,14E,16E,22Z)-(1R,4S,5'S,6S,6'R,8R,12S,13S,20R,21R,24S)-6'-[(S)-sec-butyl]-21,24-dihydroxy-5',11,13,22-tetramethyl-2-oxo-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6-spiro-2'-(5',6'-dihydro-2'H-pyran)-12-yl 2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-a-L-lyxo-hexopyranosyl)-a-L-arabino-hexopyranoside and 10% of (10E,14E,16E,22Z)-(1R,4S,5'S,6S,6'R,8R,12S,13S,20R,21R,24S)-21,24-dihydroxy-6'-isopropyl-5',11,13,22-tetramethyl-2-oxo-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6-spiro-2'-(5',6'-dihydro-2'H-pyran)-12-yl 2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-a-L-lyxo-hexopyranosyl)-a-L-arabino-hexopyranoside
NOMENCLATURE :CAS RN [40465-66-5] monoammonium salt; [69254-40-6] diammonium salt; [114370-14-8] unspecified ammonium salt Development codes MON 8750 (Monsanto)
NOMENCLATURE: Common name glyphosate (BSI, E-ISO, (m) F-ISO, ANSI, WSSA, JMAF)
IUPAC name N-(phosphonomethyl)glycine
Chemical Abstracts name N-(phosphonomethyl)glycine
CAS RN [1071-83-6] EEC no. 213-997-4 Development codes MON-0573 (Monsanto); CP 67573 (Monsanto)
NOMENCLATURE :Common name pyridaben (ATXht98120 BSIATXht0 , draft ATXht98155 E-ISOATXht0 )
IUPAC name 2-tert-butyl-5-(4-tert-butylbenzylthio)-4-chloropyridazin-3(2H)-one
Chemical Abstracts name 4-chloro-2-(1,1-dimethylethyl)-5-[[[4-(1,1-dimethylethyl)phenyl]methyl]thio]-3(2H)-pyridazinone
CAS RN [96489-71-3] EEC no. 405-700-3 Development codes NC-129; NCI-129 (both Nissan); BAS-300I (BASF)
Composition Tech. is 95% pure. Mol. wt. 354.1 M.f. C6H18AlO9P3 Form Colourless powder; (ATXht981180 tech.ATXht0 is a white to yellowish powder). M.p. 215 V.p.
Composition Purity 96.5% nominal. Material is the resolved (R)- isomer. Mol. wt. 357.4 M.f. C20H20FNO4 Form White crystalline solid. M.p. 49.5 B.p. decomp.ATXht0 >270 V.p. 5.3 Â 10-2 ATXht981131 mPaATXht0 (25 ) KOW logP = 3.31 (25 ) Henry 9.51 10-4 Pa m3 mol-1 (ATXht98124 calc.ATXht0 ) S.g./density 1.172 (20 ) Solubility In water 0.44 (unbuffered), 0.46 (ATXht981151 pHATXht0 5), 0.44 (ATXht981151 pHATXht0 7.0) (all ATXht981123 mgATXht0 /l, 20 ). In acetonitrile >250, n-heptane 6.06, n-octanol 16.0, dichloroethane >250, methanol >250, acetone >250, ethyl acetate >250 (all in g/l, 20 ). Stability Stable at ATXht981151 pHATXht0 4, hydrolysed slowly at ATXht981151 pHATXht0 7. At ATXht981151 pHATXht0 1.2 or ATXht981151 pHATXht0 9, decomposition is rapid.
Composition Purity 96.5% nominal. Material is the resolved (R)- isomer. Mol. wt. 357.4 M.f. C20H20FNO4 Form White crystalline solid. M.p. 49.5 B.p. decomp.ATXht0 >270 V.p. 5.3 10-2 ATXht981131 mPaATXht0 (25 ) KOW logP = 3.31 (25 ) Henry 9.51 10-4 Pa m3 mol-1 (ATXht98124 calc.ATXht0 ) S.g./density 1.172 (20) Solubility In water 0.44 (unbuffered), 0.46 (ATXht981151 pHATXht0 5), 0.44 (ATXht981151 pHATXht0 7.0) (all ATXht981123 mgATXht0 /l, 20 ). In acetonitrile >250, n-heptane 6.06, n-octanol 16.0, dichloroethane >250, methanol >250, acetone >250, ethyl acetate >250 (all in g/l, 20 â??). Stability Stable at ATXht981151 pHATXht0 4, hydrolysed slowly at ATXht981151 pHATXht0 7. At ATXht981151 pHATXht0 1.2 or ATXht981151 pHATXht0 9, decomposition is rapid.
Composition Tech. is 95.2% pure. Mol. wt. 186.1 M.f. C3H11N2O5P Form Odourless, white powder. M.p. Decomp. >190, without melting V.p. 9 ?10-3 mPa (25) KOW logP
Composition Tech. is 95.2% pure. Mol. wt. 186.1 M.f. C3H11N2O5P Form Odourless, white powder. M.p. Decomp. >190 , without melting V.p. 9 10-3 mPa (25) KOW logP
Mol. wt. 364.9 M.f. C19H25ClN2OS Form Colourless crystals. M.p. 111-112 â?? V.p.
Emamectin benzoate Biochemistry
Acts by stimulating the release of γ-aminobutyric acid, an inhibitory neurotransmitter, thus finally activating chloride channels.
Use
Control of sucking insects, including rice-, leaf- and plan thoppers, aphids, thrips, whitefly and lepidoptera on vegetables, brassicas, cotton. rice, cereals, maize, sugar beet, potatoes, citrus fruit, pome fruit and stone fruit.
Emamectin benzoate Biochemistry
Acts by stimulating the release of γ-aminobutyric acid, an inhibitory neurotransmitter, thus finally activating chloride channels.
Use
Control of sucking insects, including rice-, leaf- and plan thoppers, aphids, thrips, whitefly and lepidoptera on vegetables, brassicas, cotton. rice, cereals, maize, sugar beet, potatoes, citrus fruit, pome fruit and stone fruit.
Introduction:
A broad spectrum carbamate pesticide, fast acting anti-cholinesterase agent with effective contact and stomach action. Also as a nematicide against roundworms. Works by blocking the normal functioning of cholinesterase.Effective systemic and excellent knowdown properties but poor lasting action.
Usage:
Mainly used to control citrus, cotton, ornamental Aphididae crops, potatoes, soybeans, tobacco, fruit and vegetables on the CICADELLIDAE, Lepidoptera, leafminer genus TETRANYCHIDAE, Thysanoptera, such as root-knot.
Emamectin benzoate Biochemistry
Acts by stimulating the release of γ-aminobutyric acid, an inhibitory neurotransmitter, thus finally activating chloride channels.
Use
Control of sucking insects, including rice-, leaf- and plan thoppers, aphids, thrips, whitefly and lepidoptera on vegetables, brassicas, cotton. rice, cereals, maize, sugar beet, potatoes, citrus fruit, pome fruit and stone fruit.
Product Description:
Pyridaben is a broad spectrum, acaricidal agent, can be used to control a variety of plant eating pests.It has good effect on ovum, ovum, Verna and adult mite in the whole growth period of the mite, and it also has obvious quick killing effect on the adult mite in mobile period.The drug is not affected by temperature changes, whether early spring or autumn use, can achieve full effect.
Product uses:
The mite has obvious control effect on the phytophagous pests . Suitable for citrus, apples, pears, hawthorn, cotton, tobacco, vegetables (except eggplant) and ornamental plants.
Product Description:
Abamectin is an effective and broad - spectrum antibiotic and mite - killing agent.It is composed of a group of macrolides, the active material is AVERMECTIN, and has the function of stomach toxicity and palming to mites and insects.The surface of the sprayed leaves can rapidly decompose and dissipate, and the active ingredients which infiltrate into the plant parenchyma can exist in the tissue for a long time and have a conducting effect, and have long residual effect on the insects that are harmful to mite and food intake in the plant tissue.
Product uses:
Uses Control of motile stages of mites, leaf miners, suckers, Colorado beetles, etc. on ornamentals, cotton, citrus fruit, pome fruit, nut crops, vegetables, potatoes, and other crops. Application rates are 5.6 to 28 g/ha for mite control, 11 to 22 g/ha for control of leaf miners. Also used for control of nematodes by seed treatment, and of fire ants.
Mode of Action:
Tolfenpyrad prevent Mitochondrial Electron Transfer Inhibitor, (METI) in cell.
Application:
Broad-spectrum insecticidal for Lepidoptera, Hemiptera, Beetles, Hymenoptera, Diptera pests and Mites.
1. Broad-spectrum insecticidal. Have good effect on egg, larva, and imago.
2. Quick acting. Pests will die immediately once processed.
3. Effect lasting longer with about 10days.
4. No interactive resistance.
5. Resistance to rain. Almost not affected by the rainfall.
Emamectin benzoate Biochemistry:
Acts by stimulating the release of γ-aminobutyric acid, an inhibitory neurotransmitter, thus finally activating chloride channels.
Emamectin benzoate Mode of action:
Non-systemic insecticide which penetrates leaf tissues by translaminar movement. Paralyses the Lepidoptera, which stop feeding within hours of ingestion, and die 2-4 dat.
Use:
Control of sucking insects, including rice-, leaf- and plan thoppers, aphids, thrips, whitefly and lepidoptera on vegetables, brassicas, cotton. rice, cereals, maize, sugar beet, potatoes, citrus fruit, pome fruit and stone fruit.
Application:
Mode of action Insecticide active by contact and ingestion. Affected insects cease feeding, with poor co-ordination, paralysis and ultimately death. Uses DPX-MP062 is used for broad-spectrum control of Lepidoptera in cotton, vegetables and fruit, at 12.5-125 g/ha.
Target crops:
Cabbage, broccoli, kale, tomatoes, peppers, cucumbers, zucchini, eggplant, lettuce, apple, pear, peach, apricot, tea, cotton, potato, grapes
Application:
Novel structure of pyrrolidones and mites. It has excellent prevention effect on drilling, sucking and chewing pests and mites.
It is broad-spectrum insecticidal and anti-killing agents; both stomach and touch-killing functions; no interaction resistance with other insecticides; moderate residual activity on the crops; and selective internal absorption activity in the nutrient solution through the absorption of the roots; and the oral toxicity to the mammal is moderate, and the percutaneous toxicity is low; And the effective pesticide application amount is low (100 g of effective component/ hm2).
Applicable crops:
It can be used in vegetables, fruit trees, ornamental plants, etc., and can be widely used to control pests and mites in cotton, vegetables, citrus, grapes, soybeans and other crops. Acephate and other conventional agents were 4 times higher than 16 times higher. It can also be used to control termites.
Application:
1. Fosthiazate belongs to a broad-spectrum organothiophosphate nematicide, acaricide and soil insecticide.
2. Fosthiazate has properties of strong contact action, significant systemic activity to many kinds of nematode, insects and mites.
3. Fosthiazate has a good effect on the pests which have become resistant to traditional pesticide.
To prevent ground thysanoptera, lepidoptera, coleoptera, diptera and many pests, also have effect to underground root pests, and many mites.
Applicable crops:
Soybean, Vegetables and Fruit trees etc.
Introduction:
A broad spectrum carbamate pesticide, fast acting anti-cholinesterase agent with effective contact and stomach action. Also as a nematicide against roundworms. Works by blocking the normal functioning of cholinesterase.Effective systemic and excellent knowdown properties but poor lasting action.
Usage:
Mainly used to control citrus, cotton, ornamental Aphididae crops, potatoes, soybeans, fruit and vegetables on the CICADELLIDAE, Lepidoptera, leafminer genus TETRANYCHIDAE, Thysanoptera, such as root-knot.
Introduction: A broad spectrum carbamate pesticide, fast acting anti-cholinesterase agent with effective contact and stomach action. Also as a nematicide against roundworms. Works by blocking the normal functioning of cholinesterase.Effective systemic and excellent knowdown properties but poor lasting action. Usage: Mainly used to control citrus, cotton, ornamental Aphididae crops, potatoes, soybeans, fruit and vegetables on the CICADELLIDAE, Lepidoptera, leafminer genus TETRANYCHIDAE, Thysanoptera, such as root-knot.
Product Description:
Polyazole is a plant growth regulator with effects of delaying plant growth, inhibiting stem elongation, shortening internodes, promoting plant tillering, increasing plant stress resistance and increasing yield.
Product uses:
This product is suitable for rice, wheat, peanut, fruit tree, rape, soybean, flower and grass etc
Description:
Azoxystrobin difenoconazole is a�broad spectrum fungicide with activity against several diseases on many edible crops and ornamental plants. Some diseases controlled or prevented are rice blast, rusts, downy mildew, powdery mildew, late blight, apple scab, and Septoria etc. The substance is used as an active agent protecting plants and fruit/vegetables from fungal diseases.
Product uses :
Cucumber?Grape?Rice
Mode of Action:
1.Fungicide with protectant, curative, eradicant, translaminar and systemic properties.
2.Inhibits spore germination and mycelial growth, and also shows antisporulant activity.
Product Description:
Buprofezin is a insecticide which works as a chitin synthesis inhibitor. Buprofezin is used to control stubborn rice pests and is effective in controlling green leaf hoppers and white back plant hoppers for long durations.
Product uses:
It has special effects on the leaf hopper of planthopper, and also has good effects on some scale insects such as the paracoccus, which is mainly used for the prevention and treatment of rice leaf hoppers and planthopper, potato leaf hoppers, citrus cotton and vegetable pink louse, citrus shield scale and mealybug
Applicationï¼?
Buprofezin is insecticide with persistent larvicidal action against Homoptera, some Coleoptera and also Acarina. Effective against Cicadellidae, Deltocephalinae (leafhoppers) and Delphacidae (planthoppers) in rice, at 50-250 g/ha; Cicadellidae (lady beetle) in potatoes; Aleyrodidae (whitefly) in citrus, cotton and vegetables, at 0.025-0.075 g/ha; Coccidae, Diaspididae (scale insects) and Pseudococcidae (mealybugs) in citrus and top fruit, at 25-50 g/hl; Tarsonemidae in vegetables, at 250-500 g/ha. Suitable for IPM programmes.
Target cropsï¼?
Rice, fruit trees, tea tree potatoses, citrus, cotton, vegetables
