Related Searches : Carbendazim 50%SCBuprofezin/InsecticideNicosulfuron SC2SC2694MANCOZEB 43 scNicosulfuron 4%SC

Buprofezin 50% SC

  • 1 Ton/Tons
  • Jiangsu China (Mainland)
  • C16H23N3OS
  • insecticide
  • Powder
  • Buprofezin, insecticide,pesticide
  • Supplier - Zhenjiang Agreen Co., Ltd.
  • China (Mainland)China (Mainland)
  • US$10 Million - US$50 Million
  • 301 - 500 People
  • Manufacturer, Trading Company
  • North America,South America,Eastern Europe,Southeast Asia,Mid East,Eastern Asia,Western Europe
  •   
  • Mr.steven
  • 86-511-85210316
Post Date : August 30
Product Details
Company Profile

Item specifics

Jiangsu China (Mainland)
C16H23N3OS
insecticide
Powder
Shanghai or any ports
95%TC, 98%TC
2-tert-butylimino-3-isopropyl-5-p...
20days
L/C,T/T
5 Ton/Tons per Day
Acaricide, Insecticide
69327-76-0

Specifications

Formulation:
Buprofezin 95%TC, 98%TC
Buprofezin 50% SC
Buprofezin 10%WP, 25%WP,75%WP
Buprofezin 70WDG

NOMENCLATURE
Common name buprofezin (BSI, draft E-ISO); buprofine ((f) draft F-ISO)
IUPAC name 2-tert-butylimino-3-isopropyl-5-phenyl-1,3,5-thiadiazinan-4-one 
Chemical Abstracts name 2-[(1,1-dimethylethyl)imino]tetrahydro-3-(1-methylethyl)-5-phenyl-4H-1,3,5-thiadiazin-4-one 
CAS RN [69327-76-0]  Development codes NNI-750 (Nihon Nohyaku); PP618 (ICI) 

PHYSICAL CHEMISTRY
Composition Tech. is 99.1%.  Mol. wt. 305.4  M.f. C16H23N3OS  Form White crystals; (tech., white or pale yellow crystalline powder).  M.p. 104.5-105.5   V.p. 1.25 mPa (25 )  KOW logP = 4.3  Henry 4.24 ?10-1 Pa m3 mol-1 (calc.)  S.g./density 1.18 (20 )  Solubility In water 0.9 mg/l (25 ). In chloroform 520, benzene 370, toluene 320, acetone 240, ethanol 80, hexane 20 (all in g/l, 25 ).  Stability Stable in acidic and alkaline media. Stable to heat and light. 

COMMERCIALISATION
History Insecticide reported by H. Kanno et al. (Proc. Br. Crop Prot. Conf. - Pests Dis., 1981, 1, 59). Introduced by Nihon Nohyaku Co., Ltd.  Manufacturers Nihon Nohyaku

APPLICATIONS
Biochemistry Probable chitin synthesis and prostaglandin inhibitor. Hormone disturbing effect, leading to suppression of ecdysis.  Mode of action Persistent insecticide and acaricide with contact and stomach action; not translocated in the plant. Inhibits moulting of nymphs and larvae, leading to death. Also suppresses oviposition by adults; treated insects lay sterile eggs.  Uses 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.  Phytotoxicity Slightly phytotoxic to Chinese cabbage.  Formulation types DP; GR; SC; WP.  Selected tradenames: 'Applaud' (Nihon Nohyaku)

OTHER TRADENAMES
'Accolade' (Aventis); 'Viappla' (Vipesco) mixtures: 'Dadeci' (+ deltamethrin) (Aventis); 'Karapp' (+ lambda-cyhalothrin) (Syngenta)

ANALYSIS
Product by gc. Residues in soil and rice plants and water, by gc with ECD (M. Uchida et al., J. Pestic. Sci., 7, 397 (1982)); in crops, by gc with NPD (H. Nishizawa et al., J. AOAC International, 77, 1631 (1994)). Details from Nihon Nohyaku. 

MAMMALIAN TOXICOLOGY
Reviews FAO/WHO 86 (see part 2 of the Bibliography).  Oral Acute oral LD50 for male rats 2198, female rats 2355, male and female mice >10 000 mg/kg.  Skin and eye Acute percutaneous LD50 for rats >5000 mg/kg. Mild skin irritant (guinea pigs); not irritating to skin and eyes (rabbits).  Inhalation LC50 (4 h) for rats >4.57 mg/l air.  NOEL for male rats 0.90, female rats 1.12 mg/kg daily.  ADI (JMPR) 0.01 mg/kg [1999].  Other Non-carcinogenic, non-mutagenic.  Toxicity class WHO (a.i.) III (Table 5); EPA (formulation) III 

ECOTOXICOLOGY
Fish LC50 (48 h) for carp 2.7, rainbow trout >1.4 mg/l.  Daphnia LC50 (3 h) for D. pulex 50.6 mg/l.  Bees No direct effect at 2000 mg/l (WP formulation).  Other beneficial spp. No effect on various predators (Euseius stipulatus 250 mg/l; Phytoseiulus persimilis 500 mg/l; Cyrtorhinus lividipennis, Microvelia atrolineata 250 mg/l; Lycosa pseudoannulata 2000 mg/l) or parasites (Aphytis linganensis 125 mg/l; Cales noacki, Encarsia formosa, Paracentrobia andoi 250 mg/l; Ephedrus japonicus 1000 mg/l). 

ENVIRONMENTAL FATE
Animals Low residues were found in nearly all ruminant and poultry tissues. Extensive metabolism was observed, with a large number of minor metabolites being produced  Plants Limited metabolism in most plant species; minor metabolites indicate a pathway involving hydroxylation or oxidative loss of the tert-butyl group, followed by opening of the heterocyclic ring.  Soil/Environment DT50 (25 ) 104 d (flooded conditions, silty clay loam, o.c. 3.8%, pH >6.4), 80 d (upland conditions, sandy loam, o.c. 2.4%, pH 7.0) (J. Pestic. Sci., 11, 605-610 (1986)). 

Company Related ProductsView the Seller's Products
Dichlorvos

Dichlorvos

Dichlorvos

1)Dichlorvos 95% 98%TC10%25%75%WP 50%SC 70%WDG
2)Quality Certificate by SGS
3)Fine packet
4)Competitive price

Dichlorvos

 

NOMENCLATURE
Common name dichlorvos (BSI, E-ISO, (m) F-ISO, BAN, ESA); DDVP (JMAF); dichlorfos (USSR); DDVF* (former exception, USSR)
IUPAC name 2,2-dichlorovinyl dimethyl phosphate 
Chemical Abstracts name 2,2-dichloroethenyl dimethyl phosphate 
CAS RN [62-73-7]  EEC no. 200-547-7  Development codes Bayer 19 149; C 177 (Ciba)  Official codes OMS 14; ENT 20 738 

PHYSICAL CHEMISTRY
Mol. wt. 221.0  M.f. C4H7Cl2O4P  Form Colourless liquid; (tech., colourless-to-amber liquid, with an aromatic odour).  B.p. 234.1 /1 ?105 Pa (OECD 103); 74 /1.3 ?102 Pa  V.p. 2.1 ?103 mPa (25 ) (OECD 104)  KOW logP = 1.9 (OECD 117); 1.42 (separate study)  Henry 2.58 ?10-2 Pa m3 mol-1  S.g./density 1.425 (20 ) (OECD 109)  Solubility In water c. 18 g/l (25 ). Completely miscible with aromatic hydrocarbons, chlorinated hydrocarbons and alcohols; moderately soluble in diesel oil, kerosene, isoparaffinic hydrocarbons, and mineral oils.  Stability Stable to heat. Slowly hydrolysed in water and in acidic media, and rapidly hydrolysed by alkalis, to dimethyl hydrogen phosphate and dichloroacetaldehyde; DT50 (est.) 31.9 d (pH 4), 2.9 d (pH 7), 2.0 d (pH 9) (22 ).  F.p. >100 (DIN 51758); 172 (Pensky-Martens closed cup, 1 ?105 Pa) 

COMMERCIALISATION
History Insecticide described by Ciba AG (now Syngenta AG) (GB 775085), but an incorrect structure given to the compound; later reported by A. M. Martson et al. (J. Agric. Food Chem., 1955, 3, 319) as an insecticidal impurity in trichlorfon. Introduced by Ciba AG, Shell Chemical Co. (now BASF AG), and Bayer AG.  First marketed by Ciba in 1959.  Patents GB 775085 to Ciba-Geigy; US 2956073 to Shell  Manufacturers Aimco; Amvac; Denka; DE-NOCIL; Hindustan; Jin Hung; Lucava; Makhteshim-Agan; Nagarjuna Agrichem; New Chemi; Nippon Soda; Q.E.A.C.A.; Rallis; Reposo; Sanonda; Shenzhen Jiangshan; Sudarshan; Syngenta; United Phosphorus

APPLICATIONS
Biochemistry Cholinesterase inhibitor.  Mode of action Insecticide and acaricide with respiratory, contact, and stomach action. Gives rapid knockdown.  Uses Control of household and public health insect pests, e.g. flies, mosquitoes, cockroaches, bedbugs, ants, etc.; stored-product pests in warehouses, storerooms, etc.; flies and midges in animal houses; sciarid and phorid flies in mushrooms; sucking and chewing insects, and spider mites in a wide range of crops, including fruit, vines, vegetables, ornamentals, tea, rice, cotton, hops, glasshouse crops, etc. Also used as a veterinary anthelmintic.  Phytotoxicity Non-phytotoxic when used as directed, except to some varieties of chrysanthemum.  Formulation types AE; EC; GR; HN; KN; OL; SL; Impregnated strip.  Compatibility Incompatible with alkaline materials, chinomethionat, and dichlofluanid.  Selected tradenames: 'Dedevap' (Bayer); 'Nuvan' (Syngenta); 'Vapona' (agronomic uses only) (BASF); 'Amidos' (Aimco); 'Charge' (Sanonda); 'Dash' (Nagarjuna Agrichem); 'Denkavepon' (Denka); 'Divipan' (Makhteshim-Agan); 'Doom' (United Phosphorus); 'Hilvos' (Hindustan); 'Lucaphos' (Lucava); 'Phosvit' (Nippon Soda); 'Rupini' (Ramcides); 'Swing' (Caffaro); 'Uniphos' (Florin); 'Vantaf' (Rallis)

OTHER TRADENAMES
'Equigard' (BASF); 'Nogos' (Syngenta); 'Aimdos' (Aimco); 'Didivane' (Diachem); 'Divap' (Pesticides India); 'Nuchlor' (BEC); 'Saviour' (Crop Health); 'Szklarniak' (Azot); 'Tazusa' (Vipesco); 'Vaportape' (Hercon); 'Winylofos' (Azot) Discontinued names: 'Benfos' * (Q.E.A.C.A.)

ANALYSIS
Product analysis by reaction with excess of iodine, which is estimated by titration (CIPAC Handbook, 1980, 1A, 1214) or by glc (CIPAC Proc., 1981, 3, 173). Residues determined by glc (Pestic. Anal. Man., 1979, I, 201-H, 201-I; Analyst (London), 1973, 98, 19; 1977, 102, 858; 1980, 105, 515; Man. Pestic. Residue Anal., 1987, I, 3, 6, S13, S17, S19; Anal. Methods Residues Pestic., 1988, Part I, M2, M5). Sampling of atmospheres (Anal. Methods Pestic. Plant Growth Regul., 1972, 6, 529). In drinking water, by gc with FID (AOAC Methods, 1995, 991.07). Methods for the determination of residues are available from Bayer. 

MAMMALIAN TOXICOLOGY
Reviews FAO/WHO 68, 70 (see part 2 of the Bibliography). Food Cosmet. Toxicol., 1974, 28, 765-772; and A. S. Wright et al., Arch. Toxikol., 1979, 42, 1-18.  IARC ref. 53  class 2B  Oral Acute oral LD50 for rats c. 50 mg/kg.  Skin and eye Acute percutaneous LD50 for rats c. 90 mg/kg. Slight skin and eye irritant (rabbits).  Inhalation LC50 (4 h) for rats 340 mg/m3; (1 h) for rats 455 mg/m3.  NOEL (2 y) for rats 10 mg/kg diet.  ADI (JMPR) 0.004 mg/kg b.w. [1993].  Toxicity class WHO (a.i.) Ib; EPA (formulation) I  EC hazard T R24/25 

ECOTOXICOLOGY
Birds Acute oral LD50 for bobwhite quail 24 mg/kg. Sub-acute oral LD50 (8 d) for Japanese quail 300 mg/kg.  Fish LC50 (96 h) for rainbow trout 200, golden orfe 450 mg/l (both 500 EC).  Daphnia LC50 (48 h) 0.19 mg/l.  Algae EC50 (5 d) for Scenedesmus subspicatus 52.8 mg/l.  Bees Acute oral LD50 0.29 mg/bee. 

ENVIRONMENTAL FATE
EHC 79 (WHO, 1989), 63 (WHO, 1986; a general review of organophosphorus insecticides).  EHC review concludes that, with the exception of gross spillage, recommended use does not constitute a hazard for aquatic or terrestrial organisms. The high toxicity to birds and bees necessitates caution in use.  Animals In mammals, following oral administration, rapidly degraded in the liver by hydrolysis and O-demethylation, with a half-life of c. 25 minutes (D. L. Bull & R. L. Ridgway, J. Agric. Food Chem., 1969, 17, 837; D. H. Hutson & E. C. Hoadley, Arch. Toxikol., 1972, 30, 9-18; A. S. Wright et al., Arch. Toxikol., 1979, 42, 1-18).  Plants Rapidly decomposed in plants (D. L. Bull & R. L. Ridgway, J. Agric. Food Chem., 1969, 17, 837).  Soil/Environment Non-persistent in the environment, with rapid decomposition in the atmosphere. Undergoes hydrolysis in damp media, with the formation of phosphoric acid and CO2. But G. Keller et al. (Proc. 9th IUPAC Int. Congr. Pestic. Chem., London, 1998, 2, 7C-005) say soil metabolites are dichloroethanol, dichloroacetic acid and dichloroacetaldehyde; DT50 c. 10 h. Half-lives <1 d in biologically active soils and water systems. 

Detail more >>
Dimethoate

Dimethoate

Dimethoate

1)Dimethoate 98%Tech 40%EC
2)Quality Certificate by SGS
3)Fine packet or as per requirement
4)Competitive price

Dimethoate

NOMENCLATURE
Common name dimethoate (BSI, E-ISO, (m) F-ISO, ANSI, ESA, JMAF); fosfamid (USSR)
IUPAC name O,O-dimethyl S-methylcarbamoylmethyl phosphorodithioate; 2-dimethoxyphosphinothioylthio-N-methylacetamide 
Chemical Abstracts name O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] phosphorodithioate 
CAS RN [60-51-5]  EEC no. 200-480-3  Development codes EI 12 880 (Cyanamid); L 395 (Montedison); BAS 152J (BASF)  Official codes OMS 94; OMS 111; ENT 24 650 

PHYSICAL CHEMISTRY
Composition Tech. grade is 95% pure.  Mol. wt. 229.3  M.f. C5H12NO3PS2  Form Colourless crystals; (tech., white to greyish crystals).  M.p. 49 ; (tech., 43-45 )  B.p. 117 /0.1 mmHg  V.p. 0.25 mPa (25 )  KOW logP = 0.704  Henry 1.2 ?10-6 Pa m3 mol-1  S.g./density 1.277 at 65   Solubility In water 23.3 (pH 5), 23.8 (pH 7), 25.0 (pH 9) (all in g/l, 20 ). Readily soluble in most organic solvents, e.g. in alcohols, ketones, benzene, toluene, chloroform, dichloromethane >300, carbon tetrachloride, saturated hydrocarbons, n-octanol >50 (all in g/kg, 20 ).  Stability Relatively stable in aqueous media at pH 2-7. Hydrolysed in alkaline solutions; DT50 12 d (pH 9). Decomposes on heating, forming the O,S-dimethyl analogue. 

COMMERCIALISATION
History Insecticide reported by E. I. Hoegberg & J. T. Cassaday (J. Am. Chem. Soc., 1951, 73, 557; Ital. Agric., 1955, 92, 747). Introduced by American Cyanamid Co. (who sold rights to Wilbur Ellis), by BASF AG, by Boehringer Sohn (now BASF AG), and by Montecatini S.p.A. (now Isagro S.p.A).  Patents US 2494283 to Cyanamid; DE 1076662 to Celamerck; GB 791824 to Montedison  Manufacturers Cheminova; Mico; Rallis; Shaw Wallace; Sinon

APPLICATIONS
Biochemistry Cholinesterase inhibitor.  Mode of action Systemic insecticide and acaricide with contact and stomach action.  Uses Control of a wide range of Acari, Aphididae, Aleyrodidae, Coccidae, Coleoptera, Collembola, Diptera, Lepidoptera, Pseudococcidae and Thysanoptera in cereals, citrus, coffee, cotton, fruit, grapes, olives, pastures, beetroot, potatoes, pulses, tea, tobacco, and vegetables. Also used for control of flies in animal houses.  Phytotoxicity Non-phytotoxic when used as directed, except to some varieties of lemon, peach, fig, olive, walnut, hop, tomato, bean, cotton, and pine. Russetting is possible with Red Delicious and Golden Delicious apples, and with some ornamentals.  Formulation types EC; GR; UL; WP; Aerosol.  Compatibility Incompatible with alkaline materials and with sulfur-based formulations.  Selected tradenames: 'Perfekthion' (BASF); 'Rogor' (Isagro); 'Afidox' (Lucava); 'Cekutoate' (Cequisa); 'Danadim' (Cheminova); 'Diadhan' (Dhanuka); 'Dicentra' (Sanonda); 'Dimezyl' (Agriphar); 'Efdacon' (Efthymiadis); 'Hilthioate' (Hindustan); 'Robgor' (Ramcides); 'Romethoate' (Rotam); 'Tara 909' (Shaw Wallace); 'Teeka' (Nagarjuna Agrichem)

OTHER TRADENAMES
'Dygon' (Wilbur-Ellis); 'Rebelate' (BASF); 'Agrothoate' (Agrochem); 'Barclay Dimethosect' (Barclay); 'Chimigor' (Diachem); 'Cropgor' (Crop Health); 'Dimeton' (AgroSan); 'Oligor' (Papaeconomou); 'Parrydimate' (Parry); 'Pelethon' (GreenCrop); 'Portman Sysdim 40' (Portman); 'Rogor Dragon' (Agricultura Nacional); 'Rogor L' (Chemiplant); 'Vidithoate' (Vipesco) mixtures: 'Rogodial' (+ phenthoate) (Isagro); 'Salut' (+ chlorpyrifos) (BASF); 'Decis D' (+ deltamethrin) (Aventis); 'Maktion' (+ methidathion) (Makhteshim-Agan); 'Vegehon' (+ fenvalerate) (Agros); 'Vibam' (+ fenobucarb) (Vipesco); 'Wing Tip' (+ chlorpyrifos) (Probelte) Discontinued names: 'Cygon' * (Wilbur-Ellis); 'Roxion' * (Wilbur-Ellis); 'Champ' * (Searle India) mixtures: 'Atlas Sheriff' * (+ chlorpyrifos) (Atlas)

ANALYSIS
Product analysis by glc (CIPAC Handbook, 1980, 1A, 1225; CIPAC Proc., 1981, 3, 204, 211; CIPAC Handbook, 1992, E, 69-72). Residues determined by glc (Analyst (London), 1977, 102, 858; 1980, 105, 515; 1985, 110, 765; J. E. Boyd, Anal. Methods Pestic. Plant Growth Regul., 1972, 6, 357; Man. Pestic. Residue Anal., 1987, I, 3, 6, S8, S13, S17, S19; Anal. Methods Residues Pestic., 1988, Part I, M5, M12). 

MAMMALIAN TOXICOLOGY
Reviews FAO/WHO 77, 79 (see part 2 of the Bibliography).  Oral Acute oral LD50 for rats 387, mice 160, rabbits 300, guinea pigs 350 mg/kg.  Skin and eye Acute percutaneous LD50 for rats >2000 mg/kg. Non-irritating to skin (rabbits).  Inhalation LC50 (4 h) for rats >1.6 mg/l air.  NOEL (2 y) for rats 5.0 mg/kg diet (0.2 mg/kg daily).  ADI (JMPR) 0.002 mg/kg b.w. (sum of dimethoate and omethoate, expressed as dimethoate) [1996].  Toxicity class WHO (a.i.) II; EPA (formulation) II  EC hazard Xn; R21/22 

ECOTOXICOLOGY
Birds Acute oral LD50 for male pheasants 15, quail 84, chickens 108, female mallard ducks 40 mg/kg.  Fish LC50 (96 h) for mosquito fish 40-60, rainbow trout 6.2, bluegill sunfish 6 mg/l.  Daphnia LC50 (24 h) 4.7 mg/l; NOEC (24 h) 1 mg/l.  Algae EC50 (72 h) for Selenastrum capricornutum 282.3 mg/l; NOEC (72 h) 30.5 mg/l.  Bees Toxic to bees. LD50 (oral and topical) 0.1-0.2 mg/bee. 

ENVIRONMENTAL FATE
EHC 90 (WHO, 1989), 63 (WHO, 1986; a general review of organophosphorus insecticides).  Dimethoate degrades with short half-life in soil, water and plants. When used correctly, exposure of the population through air, food or water is negligible.  Animals In mammals, metabolism follows the same pattern as in plants.  Plants In plants, oxidised to O,O-dimethyl-phosphorothioate and hydrolysed to O,O-dimethyl-phosphorodithioate, -phosphorothioate, and -phosphate. The ester group is demethylated and the methylamino group is hydrolytically cleaved. Oxidation of dimethoate gives the corresponding oxone (omethoate q.v.), which is classified as toxic and a strong cholinesterase inhibitor, and which appears to show similar rapid degradation in environmental compartments as dimethoate.  Soil/Environment Adsorption and desorption constants have been shown to be a linear function of soil silt content. Koc ranges from 16.25 (sandy loam) to 51.88 (sand/loamy sand). Aerobic DT50 2-4.1 d. Photolytic DT50 on soil surface 7-16 d. Low potential for leaching to groundwater because of rapid degradation in soil. 

Detail more >>
You may also be interested in:AN2135SC2SC23952SC26522SC3074SC-SC Patch CableFCA50CC50sc adapterSC AttenuatorSC Adaptor
Talk with SupplierX
yan steven:
Can I help you?
Contact Supplier

Selected(1/4)Contact or Compare