hexazinone herbicide 250SL in Herbicide

hexazinone herbicide 250SL in Herbicide

Negotiable /Kilogram

Min.Order:500 Kilograms

Supply Ability:
10000 Liter / Liters per Month
Port:
FOB SHANGHAI
Payment Terms:
T/T Credit Card

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Classification:
Herbicide
CAS No.:
51235-04-2
Other Names:
hexazinone
MF:
C12H20N4O2
EINECS No.:
0000
Place of Origin:
Jiangsu, China

Shenzhen Cropstar Chemical Industry Co., Ltd.

Business Type: Manufacturer,Trading Company
Shenzhen Guangdong China
Main Products: Glyphosate ,Imidacloprid ,Kresoxim-Methyl ,Metalaxyl ,Lambda-Cyhalothrin

Product Details

Specifications

hexazinone 96%TC and 75%DF/25%SL(250g/l SL)
Best quality/price/service
Professional package
FAO Standards

NOMENCLATURE

Common name: hexazinone

 

Classification: herbicide

 

IUPAC name: 3-cyclohexyl-6-dimethylamino-1-methyl-1,3,5-triazine-2,4-(1H,3H)-dione 


Chemical name: 3-cyclohexyl-6-(dimethylamino)-1-methyl-1,3,5-triazine-2,4-(1H,3H)-dione 

 
CAS RN [51235-04-2]  EEC no. 257-074-4  Development codes DPX A3674 (Du Pont) 

 

 

PHYSICAL CHEMISTRY
Mol. wt. 252.3   M.f. C12H20N4O2  Form Colourless, odourless crystals.  M.p. 115-117 ºC  B.p. Decomposes on distillation.  V.p. 0.03 mPa (extrapolated) (25 ºC); 8.5 mPa (86 ºC)  KOW logP = 1.2 (pH 7)  S.g./density 1.25  Solubility In water 33 g/kg (25 ºC). In chloroform 3880, methanol 2650, benzene 940, dimethylformamide 836, acetone 792, toluene 386, hexane 3 (all in g/kg, 25 ºC).  Stability Stable in aqueous media between pH 5 and pH 9 and below 37 ºC. Decomposed by strong acids and strong alkalis. Stable to light. 

 

APPLICATIONS
Biochemistry Photosynthetic electron transport inhibitor at the photosystem II receptor site.  Mode of action Non-selective, primarily contact herbicide, absorbed by the leaves and roots, with translocation acropetally.  Uses A post-emergence contact herbicide effective against many annual and biennial weeds and, except for Sorghum halepense, most perennial weeds, at 6-12 kg a.i./ha. Used for selective control in alfalfa, pineapples, sugar cane and in plantations of certain coniferous species; also on non-crop areas, but not on sites adjacent to deciduous trees or other desirable plants.  Phytotoxicity Should not be used for weed control in larch (Larix spp.) or in areas planted with deciduous species.  Formulation types GR; SL; SP. 

 

MAMMALIAN TOXICOLOGY
Oral Acute oral LD50 for rats 1690, guinea pigs 860 mg/kg.  Skin and eye Acute percutaneous LD50 for rabbits >5278 mg/kg. Reversible irritant to eyes (rabbits); non-irritating to skin (guinea pigs).  Inhalation LC50 (1 h) for rats >7.48 mg/l.  NOEL (2 y) for rats 200, mice 200 ppm; (1 y) for dogs 200 ppm.  Toxicity class WHO (a.i.) III; EPA (formulation) II  EC hazard Xn; R22| Xi; R36| N; R50, R53 

 

ECOTOXICOLOGY
Birds Acute oral LD50 for bobwhite quail 2258 mg/kg. Dietary LC50 (8 d) for bobwhite quail and mallard ducklings >10 000 mg/kg diet.  Fish LC50 (96 h) for rainbow trout 320-420, fathead minnow 274, bluegill sunfish 370-420 mg/l.  Daphnia LC50 (48 h) 442 mg/l.  Bees Not toxic to bees; LD50 >60 mg/bee. 

 

ENVIRONMENTAL FATE
Animals Major urinary metabolites in rats are 3-(4-hydroxycyclohexyl)-6-(dimethylamino)-1-methyl-1,3,5-triazine-2,4-(1H,3H)-dione, 3-cyclohexyl-6-(methylamino)-1-methyl-1,3,5-triazine-2,4-(1H,3H)-dione, and 3-(4-hydroxycyclohexyl)-6-(methylamino)-1-methyl-1,3,5-triazine-2,4-(1H,3H)-dione.  Soil/Environment Microbial degradation occurs in soil and natural waters. The triazine ring is broken, with the liberation of CO2. DT50 in soil c. 1-6 mo, depending on climate and soil type. 

 

Contact Supplier

Mr. David Meng Chat Now
Telephone
86-755-86317161
Fax
86-755-86069699
Address
Rm. 910-912, Block E, XihaiMingzhu Building, Taoyuan Road, Nanshan District Shenzhen,Guangdong

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