Herbicides Products :

Glyphosate 41% SL

Physical Chemistry:
Composition Tech. is ³95% pure. Zwitterion structure (P. Knuuttila & H. Knuuttila, Acta Chem. Scand., 1979, 33, 623). Mol. wt. 169.1 M.f. C3H8NO5P Form Colourless crystals. M.p. 189.5±0.5 °C B.p. Decomp. >200 °C V.p. 1.31 ´ 10-2 mPa (25 °C) KOW logP <-3.2 (pH 2-5, 20 °C), (OECD 107; EEC A8) Henry <2.1 ´ 10-7 Pa m3 mol-1 S.g./density 1.705 (20 °C) Solubility In water 11.6 g/l (25 ºC). Insoluble in common organic solvents, e.g. acetone, ethanol and xylene. The alkali-metal and amine salts are readily soluble in water. Stability Glyphosate and all its salts are non-volatile, do not photochemically degrade and are stable in air. Glyphosate is stable to hydrolysis at pH 3, 6 and 9 (5-35 °C). pKa 5.77±0.03, 2.18±0.02 (20±2 °C), (OECD 112) F.p. Not flammableglyphosate-isopropylammonium
Composition As a wet cake, contains c. 62% w/w isopropylamine salt, c. 35% water. Mol. wt. 228.2 M.f. C6H17N2O5P Form Odourless, white powder. M.p. Occurs in 2 steps, 143-164 °C and 189-223 °C B.p. Decomposes without boiling V.p. 2.1 ´ 10-3 mPa (25 °C) KOW logP = -5.4 Henry 4.6 ´ 10-10 Pa m3 mol-1 (25 °C, calc.) S.g./density 1.482 (20 °C) Solubility In water 1050 g/l (25 °C, pH 4.3). In dichloromethane 0.184, methanol 15.88 (both in g/l, 20 °C). pKa 5.77±0.03, 2.18±0.02 (20±2 °C), (OECD 112).
Glyphosate 71% WG

Biochemistry Inhibits 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS), an enzyme of the aromatic acid biosynthetic pathway. This prevents synthesis of essential aromatic amino acids needed for protein biosynthesis.

Mode of action Non-selective systemic herbicide, absorbed by the foliage, with rapid translocation throughout the plant. Inactivated on contact with soil. Uses Control of annual and perennial grasses and broad-leaved weeds, pre-harvest, post-planting/pre-emergence and in stubble, in cereals, peas, beans, oilseed rape, flax and mustard, at c. 1.5-2 kg/ha; as a directed spray in vines and olives, at c. 4.3 kg/ha; in orchards, pasture, forestry and industrial weed control, at c. 4.3 kg/ha. As an aquatic herbicide, at c. 2 kg/ha. Formulation types SG; SL.

Clients can avail this Bhasma 71 (Glyphosate 71% wdg) at industry leading prices from us

Paraquat Dicloride 24% SL

IUPAC name 1,1′-dimethyl-4,4′-bipyridinediium dichloride; 1,1′-dimethyl-4,4′-bipyridinium dichloride; 1,1′-dimethyl-4,4′-bipyridylium dichloride
Chemical Abstracts name 1,1′-dimethyl-4,4′-bipyridinium dichloride
Other names methyl viologen CAS RN [1910-42-5]; [2074-50-2] bis(methyl sulfate) EEC no. 217-615-7 Development codes PP148; PP910 for bis(methyl sulfate) (both ICI)

paraquat Common name paraquat (BSI, E-ISO, (m) F-ISO, ANSI, WSSA, JMAF); 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

Physical Chamistry:
Composition Not normally isolated from the tech. products, which are >95% pure. Mol. wt. 257.2 M.f. C12H14Cl2N2 Form Colourless, hygroscopic crystals. M.p. Decomposes at c. 340 ºC V.p. <1 ´ 10-2 mPa (25 °C) KOW logP = -4.5 (20 °C) Henry <4 ´ 10-9 Pa m3 mol-1 (calc.) S.g./density 1.24-1.26 (20 ºC) Solubility In water c. 620 g/l (20 ºC). Practically insoluble in most organic solvents. Stability Stable in neutral and acidic media, but readily hydrolysed in alkaline media. Photochemically decomposed by u.v. irradiation in aqueous solution.

Imazethapyr 10%SL


Common name imazethapyr (BSI, ANSI, draft E-ISO, (m) draft F-ISO)

IUPAC name(RS)-5-ethyl-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)nicotinic acid

Chemical Abstracts name(?-2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-ethyl-3-pyridinecarboxylic acid


Apply to actively growing weeds in the 2 to 4 leaf stage. Weeds may not be totally controlled but populations will be significantly reduced and surviving plants will generally be severely retarded. Good crop growth will aid weed control.

Clodinafop Propargyl 15 wp

Wettable Powder
Mode of Action:
The active ingredient clodinafop-propargyl and the safener cloquintocet-mexyl are absorbed through he leaves and shoots actively growing plants. They are rapidly translocated in the plants and accumulate in the meristematic tissues.
The achieved result is inhibition of the enzyme acetyl CoA carboxylase (ACC-ase). Within 48 hours after application, susceptible grass species cease to grow. Plant death occurs within 2-3 weeks.
Main Benefits of Using Security :
Security  gives reliable control under varying climatic conditions. The grower can be sure that the product will work even under unfavorable conditions.
Security  has an extremely broad application spectrum and a superior crop tolerance.
Security has a wide window of application for the effective control of advanced weeds allowing the grower more flexibility for time of application.
Security has no limitation for crop rotation and therefore offers greater flexibility for follow up crops.
Security has an excellent environmental profile and fits very well into an integrated crop management program. Its half-life period in the soil is only a few days, and the potential for leaching is very low.