Florasulam 97%TC & 5%SC

IUPAC name: 2′,6′,8-trifluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonanilide
Chemical Abstracts name: N-(2,6-difluorophenyl)-8-fluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide
CAS RN: [145701-23-1]
Biochemistry: Branched chain amino acid (leucine, isoleucine and valine) synthesis (ALS or AHAS) inhibitor. Selectivity in wheat is due to differential metabolism.
Mode of action: Taken up by root and shoots, and translocated in both xylem and phloem.
Uses: Herbicide for post-emergence control of broad-leaved weeds, especially Galium aparine, Stellaria media, Polygonum convolvulus, Matricaria spp., and various cruciferae, in cereals and maize, at rates up to 7.5 g/ha.
Packing *: 25kg drum (TC), 1L bottle (SC)
* (NOTE: Upon request we provide customized packing)

Trinexapac-ethyl 96%TC & 25% EC

IUPAC name: ethyl 4-cyclopropyl(hydroxy)methylene-3,5-dioxocyclohexanecarboxylate
Chemical Abstracts name: ethyl 4-(cyclopropylhydroxymethylene)-3,5-dioxocyclohexanecarboxylate
CAS RN: 95266-40-3
Biochemistry: Inhibits 3b-hydroxylation of GA20 to GA3 in gibberellin biosynthesis. The reduced level of gibberellins leads to growth retardation of plants.
Mode of action: Plant growth regulator and retardant, which reduces stem growth by inhibition of internode elongation. Absorbed by the foliage, with translocation to the growing shoot.
Uses: Used for the prevention of lodging in cereals and in winter oilseed rape, at 0.1-0.3 kg/ha. Also used in turf, at 0.15-0.5 kg/ha, to reduce mowing; and as a maturation promoter in sugar cane at 0.1-0.25 kg/ha.
Packing *: 25kg drum (TC), 1L bottle (EC)
* (NOTE: Upon request we provide customized packing)

Gibberellic acid 90%TC & 10%SP & 4% EC

IUPAC name: (3S,3aR,4S,4aS,7S,9aR,9bR,12S)-7,12-dihydroxy-3-methyl-6-methylene-2-oxoperhydro-4a,7-methano-9b,3-propeno[1,2-b]furan-4-carboxylic acid
Alt: (3S,3aR,4S,4aS,6S,8aR,8bR,11S)-6,11-dihydroxy-3-methyl-12-methylene-2-oxo-4a,6-ethano-3,8b-prop-1-enoperhydroindeno[1,2-b]furan-4-carboxylic acid
Chemical Abstracts name: (1a,2b,4aa,4bb,10b)-2,4a,7-trihydroxy-1-methyl-8-methylenegibb-3-ene-1,10-dicarboxylic acid 1,4a-lactone
Other names: gibberellin A3; GA3 (ambiguous)
CAS RN: 77-06-5
Mode of action: Acts as a plant growth regulator on account of its physiological and morphological effects in extremely low concentrations. Translocated. Generally affects only the plant parts above the soil surface.
Uses: Has a variety of applications, e.g. to improve fruit setting of clementines and pears (especially William pears); to loosen and elongate clusters and increase berry size in grapes; to control fruit maturity by delaying development of the yellow colour in lemons; to reduce rind stain and retard rind ageing in navel oranges; to counteract the effects of cherry yellows virus diseases in sour cherries; to produce uniform seedling growth in rice; to promote elongation of winter celery crop; to induce uniform bolting and increase seed production in lettuce for seed; to break dormancy and stimulate sprouting in seed potatoes; to extend the picking season by hastening maturity in artichokes; to increase the yield in forced rhubarb; to increase the malting quality of barley; to produce brighter-coloured, firmer fruit, and to increase the size of sweet cherries; to increase yields and aid harvesting of hops; to reduce internal browning and increase yields of Italian prunes; to increase fruit set and yields of tangelos and tangerines; to improve fruit setting in blueberries; to advance flowering and increase the yield of strawberries; and also a variety of applications on ornamentals. Application rates up to 80 g/a per application, depending on desired effect.
Packing *: 25kg drum (TC), 1L bottle (EC), 500g Aluminum bag (SP)
* (NOTE: Upon request we provide customized packing)

Trifloxystrobin 96%TC & 50%SC & 50%WG & 75%WG

IUPAC name: methyl (E)-methoxyimino-{(E)-a-[1-(a,a,a-trifluoro-m-tolyl)ethylideneaminooxy]-o-tolyl}acetate
Chemical Abstracts name: methyl (aE)-a-(methoxyimino)-2-[[[(E)-[1-[3-(trifluoromethyl)phenyl]ethylidene]amino]oxy]methyl]benzeneacetate
CAS RN: [141517-21-7]; [221007-60-9] former number
Biochemistry: Inhibits mitochondrial respiration by blocking electron transfer at the Qo centre of cytochrome bc1.
Mode of action: Mesostemic, broad-spectrum fungicide with preventative and specific curative activity and displaying rain-fastness. Redistributed by superficial vapour movement and also has translaminar activity.
Uses: Broad spectrum fungicide for foliar use on a wide range of agricultural and horticultural crops in temperate, sub-tropical and tropical climates in open fields or protected under glass and plastic. In Europe its uses will be focussed on cereals (at 50 g/ha), grapes (at 187.5 g/ha), pome fruit (at 75 g/ha), and cucurbit crops (at 187.5 g/ha).Trifloxystrobin is active against fungi in all four classes – Ascomycetes, Deuteromycetes, Basidiomycetes and Oomycetes.
Packing *: 25kg drum (TC), 1L bottle (SC), 500 g Aluminum Bag (WG)
* (NOTE: Upon request we provide customized packing)

Tridemorph 99%TC & 75% EC & 86%OL

IUPAC name: 4-alkyl-2,6-dimethylmorpholine; for original definition, 2,6-dimethyl-4-tridecylmorpholine
Chemical Abstracts name: for original structure/main component, 2,6-dimethyl-4-tridecylmorpholine
CAS RN: [81412-43-3] new definition; [24602-86-6] 4-tridecyl- component
Biochemistry: Ergosterol biosynthesis inhibitor, by inhibition of steroid reduction (sterol-D14-reductase) and isomerisation (D8 to D7-isomerase).
Mode of action: Systemic fungicide with eradicant action. Absorbed by the leaves and roots, giving some protective action.
Uses: Control of Erysiphe graminis in cereals, Mycosphaerella spp. in bananas, Corticium salmonicolor and Exobasidium vexans in tea, and Oidium heveae in hevea. Mixed with carbendazim to extend spectrum of cereal diseases controlled.
Packing *: 25kg drum (TC), 1L bottle (EC & OL)
* (NOTE: Upon request we provide customized packing)

Tricyclazole 95%TC & 75%WP

IUPAC name: 5-methyl-1,2,4-triazolo[3,4-b][1,3]benzothiazole
Chemical Abstracts name: 5-methyl-1,2,4-triazolo[3,4-b]benzothiazole
CAS RN: [41814-78-2]
Biochemistry: Melanin biosynthesis inhibitor (reduction of 1,3,8-trihydroxynaphthalene and vermelone).
Mode of action: Systemic fungicide, absorbed rapidly by the roots, with translocation through the plant.
Uses: Control of rice blast (Pyricularia oryzae) in transplanted and direct-seeded rice at 100 g/ha. Can be applied as a flat drench, transplant root soak, or foliar application. One or two applications by one or more of these methods give a season-long control of the disease.
Packing *: 25kg drum (TC), 500g Aluminum bag (WP)
* (NOTE: Upon request we provide customized packing)

Thiabendazole 99%TC & 45%SC

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]
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, Podosphaera leucotricha, Rhizoctonia, Sclerotinia, Septoria, Thielaviopsis, Venturia inaequalis, Verticillium spp., etc., in avocados (2 g/l), bananas (0.2-0.4 g/l), chicory, citrus fruit (2.2 g/l), mangoes (2 g/l), mushrooms, ornamentals, pome fruit (1.1 g/l) and potatoes (30 g/ton). Also used for seed treatment and stem injection application.
Packing *: 25kg drum (TC), 1L bottle (SC)
* (NOTE: Upon request we provide customized packing)

Tebuconazole 97%TC & 43%SC & 25%EC & 12%FS & 6%FS

IUPAC name: (RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol
Chemical Abstracts name: (?-a-[2-(4-chlorophenyl)ethyl]-a-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol
CAS RN: [107534-96-3]
Biochemistry: Steroid demethylation (ergosterol biosynthesis) inhibitor.
Mode of action: Systemic fungicide with protective, curative, and eradicant action. Rapidly absorbed into the vegetative parts of the plant, with translocation principally acropetally.
Uses: As a seed dressing, tebuconazole is effective against various smut and bunt diseases of cereals such as Tilletia spp., Ustilago spp., and Urocystis spp., also against Septoria nodorum (seed-borne), at 1-3 g/dt seed; and Sphacelotheca reiliana in maize, at 7.5 g/dt seed. As a spray, tebuconazole controls numerous pathogens in various crops including: rust species (Puccinia spp.) at 125-250 g/ha, powdery mildew (Erysiphe graminis) at 200-250 g/ha, scald (Rhynchosporium secalis) at 200-312 g/ha, Septoria spp. at 200-250 g/ha, Pyrenophora spp. at 200-312 g/ha, Cochliobolus sativus at 150-200 g/ha, and head scab (Fusarium spp.) at 188-250 g/ha, in cereals; leaf spots (Mycosphaerella spp.) at 125-250 g/ha, leaf rust (Puccinia arachidis) at 125 g/ha, and Sclerotium rolfsii at 200-250 g/ha, in peanuts; black leaf streak (Mycosphaerella fijiensis) at 100 g/ha, in bananas; stem rot (Sclerotinia sclerotiorum) at 250-375 g/ha, Alternaria spp. at 150-250 g/ha, stem canker (Leptosphaeria maculans) at 250 g/ha, and Pyrenopeziza brassicae at 125-250 g/ha, in oilseed rape; blister blight (Exobasidium vexans) at 25 g/ha, in tea; Phakopsora pachyrhizi at 100-150 g/ha, in soya beans; Monilinia spp. at 12.5-18.8 g/100 l, powdery mildew (Podosphaera leucotricha) at 10.0-12.5 g/100 l, Sphaerotheca pannosa at 12.5-18.8 g/100 l, scab (Venturia spp.) at 7.5-10.0 g/100 l, white rot in apples (Botryosphaeria dothidea) at 25 g/100 l, in pome and stone fruit; powdery mildew (Uncinula necator) at 100 g/ha, in grapevines; rust (Hemileia vastatrix) at 125-250 g/ha, berry spot disease (Cercospora coffeicola) at 188-250 g/ha, and American leaf disease (Mycena citricolor) at 125-188 g/ha, in coffee; white rot (Sclerotium cepivorum) at 250-375 g/ha, and purple blotch (Alternaria porri) at 125-250 g/ha, in bulb vegetables; leaf spot (Phaeoisariopsis griseola) at 250 g/ha, in beans; early blight (Alternaria solani) at 150-200 g/ha, in tomatoes and potatoes.
Packing *: 25kg drum (TC), 1L bottle (EC & SC & FS)
* (NOTE: Upon request we provide customized packing)

Spiroxamine 95%TC & 50% EC & 80% EC

IUPAC name: 8-tert-butyl-1,4-dioxaspiro[4.5]decan-2-ylmethyl(ethyl)(propyl)amine
Chemical Abstracts name: 8-(1,1-dimethylethyl)-N-ethyl-N-propyl-1,4-dioxaspiro[4,5]decane-2-methanamine
CAS RN: [118134-30-8]
Biochemistry: Sterol biosynthesis inhibitor, acting mainly by inhibition of D14-reductase.
Mode of action: Protective, curative and eradicative systemic fungicide. Readily penetrates into the leaf tissue, followed by acropetal translocation to the leaf tip. Uniformly distributed within the whole leaf.
Uses: Spiroxamine is control of powdery mildew in cereals (Erysiphe graminis), at 500-750 g/ha, and in grapes (Uncinula necator), at 400 g/ha. Also gives good control of rusts (Rhynchosporium and Pyrenophora teres), together with certain side-effects against Septoria diseases. Penetration studies have shown that tank mixes of spiroxamine and triazoles can positively influence the uptake of triazoles in plants.
Packing *: 25kg drum (TC), 1L bottle (EC)
* (NOTE: Upon request we provide customized packing)

Pyrimethanil 95%TC & 40%SC

IUPAC name: N-(4,6-dimethylpyrimidin-2-yl)aniline
Chemical Abstracts name: 4,6-dimethyl-N-phenyl-2-pyrimidinamine
CAS RN: [53112-28-0]
Biochemistry: Proposed inhibitor of methionine biosynthesis, leading to inhibition of the secretion of enzymes necessary for infection.
Mode of action: Protectant (in Botrytis) and both protective and curative action (in Venturia).
Uses: Pyrimethanil is control of grey mould (Botrytis cinerea) on vines, fruit, vegetables and ornamentals. Control of leaf scab (Venturia inaequalis or V. pirina) on pome fruit.
Packing *: 25kg drum (TC), 1L bottle (SC)
* (NOTE: Upon request we provide customized packing)