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Thiabendazole 2.5%+Flutriafol 2.5% SC

  • 1000 Liter/Liters
  • Jiangsu China (Mainland)
  • C10H7N3S/C16H13F2N3O
  • Fungicide
  • Liquid
  • Tag:thiabendazole flutriafol,fungicide thiabendazole,fungicide flutriafol
  • 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
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Item specifics


1)Thiabendazole2.5%+Flutriafol2.5% SC
2)Quality Certificate by SGS
3)Fine packet or as per requirement
4)Competitive price.


Common name: thiabendazole (BSI, E-ISO, (m) F-ISO, BAN, JMAF)
IUPAC name: 2-(thiazol-4-yl)benzimidazole; 2-(1,3-thiazol-4-yl)benzimidazole
Chemical Abstracts name: 2-(4-thiazolyl)-1H-benzimidazole
CAS RN: [148-79-8]

EEC no.: 205-725-8

Development codes: MK 360 (Merck)

Applications:Biochemistry Inhibits mitosis by binding to tubuline and thus severely impairs fungal growth and development Mode of action Systemic fungicide with protective and curative action. Thiabendazole forms a protective deposit on the treated surface of fruit and tubers. Uses As a mainly post-harvest fungicide for the control of Aspergillus, Botrytis, Ceratocystis, Cercospora, Cladosporium, Colletotrichum, Corticium, Diaporthe, Diplodia, Fusarium, Gibberella, Gloeosporium, Oospora, Penicillium, Phoma, Rhizoctonia, Sclerotinia, Septoria, Thielaviopsis, Verticillium spp., etc., in avocados, bananas, chicory, citrus fruit, some cucurbits, mangoes, mushrooms, ornamentals, pome fruit, potatoes, strawberries and other crops. Also used for foliar application (on fruits and vegetables), seed treatment and stem injection application. Formulation types SC; SL; TB; WP. Compatibility Incompatible with copper products and oxidising agents such as chlorates and nitrates.


Common name: flutriafol (BSI, ANSI, draft E-ISO, (m) draft F-ISO)
IUPAC name: (RS)-2,4'-difluoro-a-(1H-1,2,4-triazol-1-ylmethyl)benzhydryl alcohol
Chemical Abstracts name: (?-a-(2-fluorophenyl)-a-(4-fluorophenyl)-1H-1,2,4-triazole-1-ethanol
CAS RN: [76674-21-0]

Development codes: PP450 (ICI)

Applications: Biochemistry Inhibits ergo sterol biosynthesis (steroid demethylation inhibitor), causing fungal cell wall collapse and inhibition of hyphal growth. Mode of action Contact and systemic fungicide with eradicant and protective action. Absorbed by the foliage, with translocation acropetally in the xylem. Uses Control of a broad spectrum of leaf and ear diseases (including Erysiphe graminis, Rhynchosporium secalis, and Septoria, Puccinia, and Helminthosporium spp.) in cereals, at 125 g a.i./ha. Also used in non-mercurial seed treatment formulations to control the major soil-borne and seed-borne diseases of cereals. Formulation types SC. Selected tradenames: 'Impact' (Cheminova); mixtures: 'Vincit' (+ imazalil+ thiabendazole) (Cheminova)

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Carbendazim5%+Carbofuran10% FS

Carbendazim5%+Carbofuran10% FS

Carbendazim5%+Carbofuran10% FS

1)Carbendazim5%+ Carbofuran10% FS
2)Quality Certificate by SGS
3)Fine packet or as per requirement
4)Competitive price


Common name: carbendazim (BSI, E-ISO); carbendazime ((f) F-ISO); carbendazol (JMAF)
IUPAC name: methyl benzimidazol-2-ylcarbamate
Chemical Abstracts name: methyl 1H-benzimidazol-2-ylcarbamate
Other names: MBC; BMC

CAS RN: [10605-21-7]

EEC no.: 234-232-0

Development codes: BAS 346F (BASF); Hoe 017411 (Hoechst); DPX-E 965 (Du Pont)

Biochemistry: Reported to inhibit beta-tubulin synthesis.

Mode of action: Systemic fungicide with protective and curative action. Absorbed through the roots and green tissues, with translocation acropetally. Acts by inhibiting development of the germ tubes, the formation of appressoria, and the growth of mycelia. Uses: Control of Septoria, Fusarium, Erysiphe and Pseudocercosporella in cereals; Sclerotinia, Alternaria and Cylindrosporium in oilseed rape; Cercospora and Erysiphe in sugar beet; Uncinula and Botrytis in grapes; Cladosporium and Botrytis in tomatoes; Venturia and Podosphaera in pome fruit and Monilia and Sclerotinia in stone fruit. Application rates vary from 120-600 g/ha, depending on crop. A seed treatment (0.6-0.8 g/kg) will control Tilletia, Ustilago, Fusarium and Septoria in cereals, and Rhizoctonia in cotton. Also shows activity against storage diseases of fruit as a dip (0.3-0.5 g/l).

Compatibility: Incompatible with alkaline materials.


Common name: carbofuran (BSI, E-ISO, (m) F-ISO, ANSI, ESA)
IUPAC name: 2,3-dihydro-2,2-dimethylbenzofuran-7-yl methylcarbamate
Chemical Abstracts name: 2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate
CAS RN: [1563-66-2]; (carbofuran phenol [1563-38-8]; 3-ketocarbofuran phenol [17781-16-7])

EEC no.: 216-353-0

Development codes: FMC 10 242; BAY 70 143 (Bayer); D 1221 Official codes OMS 864; ENT 27 164

Biochemistry Cholinesterase inhibitor.

Mode of action: Systemic, with predominantly contact and stomach action.

Uses: Control of soil-dwelling and foliar-feeding insects (including wireworms, white grubs, millipedes, symphylids, frit flies, bean seed flies, root flies, flea beetles, weevils, sciarid flies, aphids, thrips, etc.) and nematodes in vegetables, ornamentals, beet, maize, sorghum, sunflowers, oilseed rape, potatoes, alfalfa, peanuts, soya beans, sugar cane, rice, cotton, coffee, cucurbits, tobacco, lavender, citrus, vines, strawberries, bananas, mushrooms, and other crops.

Compatibility: Incompatible with alkaline materials.

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Emamectin benzoate 5%+Deltamethrin10% WP

Emamectin benzoate 5%+Deltamethrin10% WP

Emamectin benzoate 5%+Deltamethrin10% WP

2)Quality Certificate by SGS
3)Fine packet or as per requirement
4)Competitive price.

Emamectin benzoate

CAS RN: [155569-91-8]; formerly [137512-74-4] and [179607-18-2]

Development codes: MK 244 (Merck)

Composition: A mixture of emamectin B1a (?0%) and emamectin B1b (?0%), as their benzoate salts.

Mode of action: Non-systemic insecticide which penetrates leaf tissues by translaminar movement.

Uses: For control of Lepidoptera on vegetables, brassicas and cotton, at up to 16 g/ha, and in pine trees, at 5-25 g/ha.

IUPAC name:
(S)-a-cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate
Roth: (S)-a-cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate
Chemical Abstracts name: [1R-[1a(S*),3a]]-cyano(3-phenoxyphenyl)methyl 3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropanecarboxylate
CAS RN: [52918-63-5]; [52820-00-5] ((RS)- (1R)-cis- isomer pair)

EEC no.: 258-256-6

Development codes: NRDC 161; RU 22 974 (Roussel Uclaf); AE F032640 (AgrEvo) Official codes OMS 1998

Composition: Tech. produced industrially by Aventis contains ?8% deltamethrin (i.e. the single isomer).

Mode of action: Non-systemic insecticide with contact and stomach action. Fast-acting.

Uses: A potent insecticide, effective by contact and ingestion against a wide range of pests. Crop protection uses include: Coleoptera (2.5-7.5 g/ha), Heteroptera (5.0-7.5 g/ha), Homoptera (6.2-12.5 g/ha), Lepidoptera (5.0-21 g/ha) and Thysanoptera (5-10 g/ha) in cereals, citrus, cotton, grapes, maize, oilseed rape, soya beans, top fruit and vegetables. It controls Acrididae (5.0-12.5 g/ha), and is recommended against locusts. Soil surface sprays (2.5-5.0 g/ha) control Noctuidae. It is used against indoor crawling and flying insects (12.5 mg/m2) and pests of stored grain (0.25-0.5 g/t) and timber (Blattodea, Culicidae, Muscidae). Dip or spray (12.5-75 mg/l), and pour-on (0.75 mg/kg b.w.) applications give good control of Muscidae, Tabanidae, Ixodidae and other Acari on cattle, sheep and pigs, etc.

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