Best Mancozeb Supplier

Best  Mancozeb  Supplier

Product Name
Mancozeb
CAS No.
8018-1-7
Categories
 Fungicides
Chemical Structure
NOMENCLATURE
Common name: mancozeb; mancoz
ébe; manzeb
IUPAC name: manganese ethylenebis(dithiocarbamate) (polymeric) complex with zinc salt
Chemical Abstracts name: [[1,2-ethanediylbis[carbamodithioato]](2-)]manganese mixture with [[1,2-ethanediylbis[carbamodithioato]](2-)]zinc
CAS RN: [8018-01-7] (formerly [8065-67-6]); [8018-01-7] is also applied to other mixed manganese and zinc ethylenebis(dithiocarbamate) complexes
PHYSICAL CHEMISTRY
Composition: The ISO definition is 'a complex of zinc and maneb containing 20% of manganese and 2.55% of zinc, the salt present being stated (for instance mancozeb chloride)'.
Form: Greyish-yellow powder.
M.p.: Decomposes at 192-204C.
V.p.: Negligible at 20C.
S.g./density: 1.92. Solubility: In water 6.2 ppm (pH 7.5, 25C). Insoluble in most organic solvents; dissolves in solutions of powerful chelating agents but cannot be recovered from them.
Stability: Stable under normal, dry storage conditions. Slowly decomposed by heat and moisture. On hydrolysis (25C), DT50 20 d (pH 5), 17 h (pH 7), 34 h (pH 9). Mancozeb a.i. is unstable and the tech. not isolated; the formulated product is produced in continuous process.
F.p.: 137.8C (Tag open cup).
APPLICATIONS
Biochemistry: Non-specific thiol reactant, inhibiting respiration.
Mode of action: Fungicide with protective action.
Uses: Control of many fungal diseases (e.g. blight, leaf spot, rust, downy mildew, scab, etc.) in field crops, fruit, nuts, vegetables, ornamentals, etc. Particular uses include control of early and late blights of potatoes and tomatoes (at 1.36 kg a.i./ha); Rhizoctonia solani and Streptomyces scabies on seed potatoes; leaf spot diseases on celery, cucurbits, beet, berries and currants; rusts on cereals, vegetables, roses, carnations, asparagus, beans, apples and plums (at 1.6 kg/ha); downy mildews on hops, vines, onions, leeks, lettuce, cucurbits, ornamentals and tobacco; Gloeodes pomigena, Glomerella cingulata, Microthyriella rubi and Physalospora obtusa on apples; scab on apples and pears (at 2.4-3.6 kg/ha); sigatoka disease (Cercospora musae) in bananas; shot-hole of stone fruit; anthracnose of beans and cucurbits; damping-off diseases of vegetables; black leg of beet; needle cast in forestry; and many seed-borne diseases of cereals. Used for foliar application or as a seed treatment.
Formulation types: DP; DS; SC; WG; WP.
MAMMALIAN TOXICOLOGY
Oral: Acute oral LD50 for rats >5000 mg/kg.
Skin and eye: Acute percutaneous LD50 for rats >10 000, rabbits >5000 mg/kg. Mild to moderate skin irritant; moderate eye irritant.
Inhalation: LC50 (4 h) for rats >5.14 mg/l.
ADI: 0.03 mg/kg b.w. (group ADI with maneb, metiram and zineb); ethylenethiourea 0.004 mg/kg b.w.
Other: At very high levels, mancozeb has caused birth defects in test animals; ethylenethiourea, a trace contaminant and breakdown product of mancozeb, has caused thyroid effects, tumours and birth defects in laboratory animals.
Toxicity class: WHO (a.i.) III (Table 5); EPA (formulation) IV
EC hazard: Xi; R37| R43
ECOTOXICOLOGY
Birds: In 10-day dietary studies, there were no mortalities in mallard ducks at 6400 mg/kg daily, and in Japanese quail at 3200 mg/kg daily.
Fish: LC50 (48 h) for goldfish 9.0, rainbow trout 2.2, catfish 5.2, carp 4.0 mg/l.
Bees: LC50 0.193 mg/bee.
ENVIRONMENTAL FATE
Plants: Extensively metabolised in plants, forming ethylenethiourea, ethylenethiuram monosulfide, ethylenethiuram disulfide, and sulfur as transitory intermediates. Terminal metabolites are natural products, especially those derived from glycine.
Soil/Environment Rapidly degraded in the environment by hydrolysis, oxidation, photolysis, and metabolism. DT50 in soil c. 6-15 d. Koc >2000.

 

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