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Sell Atrazine

Sell Atrazine

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( Negotiable )

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Minimum Order

Place of Origin:

China

Price for Minimum Order:

-

Minimum Order Quantity:

1000 Kilogram

Packaging Detail:

25kg in plastic bag lined cardboard drum

Delivery Time:

25 days

Supplying Ability:

1000000 Kilogram per Year

Payment Type:

T/T, L/C

今すぐお問い合わせください
無料会員

連絡先担当者 Elaine

Baling zhonglu, Yueyang, Hunan

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Description


PHYSICAL CHEMISTRY
Composition Tech. is ≥*5% pure.
Mol. wt. **5.7 M.f. C8H*4ClN5 Form Colourless powder. M.p. **5.8 °C B.p. **5.0 °C/**1 kPa V.p. 3.*5 × ***2 mPa (*5 °C) (OECD **4) Kow logP = 2.5 (*5 °C) Henry 1.5 × ***4 Pa m3 mol*1 (calc.) S.g./density 1.*3 (*2 °C) Solubility In water *3 mg/l (pH 7, *2 °C). In ethyl acetate *4, acetone *1, dichloromethane *8, ethanol *5, toluene 4.0, n-hexane 0.*1, n-octanol 8.7 (all in g/l, *5 °C). Stability Relatively stable in neutral, weakly acidic and weakly alkaline media. Rapidly hydrolysed to the hydroxy derivative in strong acids and alkalis, and at *0 °C in neutral media; DT*0 (pH 1) 9.5, (pH 5) *6, (pH *3) 5.0 d. pKa 1.6, v. weak base
 
APPLICATIONS
Biochemistry Photosynthetic electron transport inhibitor at the photosystem II receptor site. Maize tolerance is attributed to rapid detoxification by glutathione transferases. Mode of action Selective systemic herbicide, absorbed principally through the roots, but also through the foliage, with translocation acropetally in the xylem and accumulation in the apical meristems and leaves.
Uses Pre- and post-emergence control of annual broad-leaved weeds and annual grasses in maize, sorghum, sugar cane, pineapples, chemical fallow, grassland, macadamia nuts, conifers, and industrial weed control. In Europe, use is concentrated in maize and sorghum, at ≤1.5 kg/ha. Used also in combinations with many other herbicides. Phytotoxicity Phytotoxic to many crops, including most vegetables, potatoes, soya beans, and peanuts.
Formulation types FW; GR; SC; WG; WP.

ENVIRONMENTAL FATE
Animals In mammals, following oral administration, atrazine is rapidly and completely metabolised, primarily by oxidative dealkylation of the amino groups (R. Ikonen et al., Toxicol. Lett., ***8, *4, **9; Bull. Environ. Contam. Toxicol., ***9, *3, **9; Y. Deng et al., J. Agric. Food Chem., ***0, *8, ***1), and by reaction of the chlorine atom with endogenous thiols. Diaminochlorotriazine is the main primary metabolite, which readily conjugates with glutathione. More than *0% of the dose is eliminated in the urine and around *3% in the faeces within *4 hours. Plants In tolerant plants, atrazine is readily metabolised to hydroxyatrazine and amino acid conjugates, with further decomposition of hydroxyatrazine by degradation of the side-chains and hydrolysis of the resulting amino acids on the ring, together with evolution of CO2. In sensitive plants, unaltered atrazine accumulates, leading to chlorosis and death. Soil/Environment Major metabolites under all conditions are desethylatrazine and hydroxyatrazine. Field DT*0 *6–**7 d (median *8 d), the longer values being from cold or dry conditions. In natural waters, DT*0 *4–**5 d (mean *5 d). DT*0 under groundwater conditions **5–>**0 d, depending on test system (M. J. Wood et al. (***1) In: A Walker (ed.), Pesticides in soils and water: current perspectives, BCPC Monograph no. *7, pp. **5–**2). Kd 0.2–*8 ml/g, Koc *9–**3 ml/g; desalkylated metabolites had values similar to those of atrazine (Kd 0.2–8.6 ml/g) whereas hydroxyatrazine (Kd 1.6–**0) was much more strongly adsorbed.

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Elaine < Yueyang D.P. Chemical Engineering & Technology Co., Ltd. >

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