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Postion:Product Catalog >Chemical pesticides>Insecticides>Organochlorine pesticides>Triadimenol
Triadimenol
  • Triadimenol

Triadimenol

Price $1
Package 1kg
Min. Order: 1g
Supply Ability: 100KG
Update Time: 2019-07-06

Product Details

Product Name: Triadimenol CAS No.: 55219-65-3
Min. Order: 1g Purity: 99%
Supply Ability: 100KG Release date: 2019/07/06
Product:: AD68
Triadimenol Basic information
Chemical properties Uses Toxicity Preparation method
Product Name: Triadimenol
Synonyms: 2-(4-chlorophenoxy)-1-tert-butyl-2-(1h-1,2,4-triazole-1-yl)-ethano;2-(4-Chlorophenoxy)-1-tert-butyl-2-(1H-1,2,4-triazole-1-yl)ethanol;a-(4-chlorophenoxy)-b-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol;BAY KWG 0519;bayfrdanew;baykwg0519;baytan15;baytantf3479b
CAS: 55219-65-3
MF: C14H18ClN3O2
MW: 295.76
EINECS: 259-537-6
Product Categories: INSECTICIDE;Pesticide
Mol File: 55219-65-3.mol
Article illustration
 
Triadimenol Chemical Properties
Melting point  112-117°
density  1.2990 (rough estimate)
refractive index  1.5270 (estimate)
Fp  2 °C
storage temp.  2-8°C
Merck  13,9667
CAS DataBase Reference 55219-65-3(CAS DataBase Reference)
NIST Chemistry Reference Triadimenol(55219-65-3)
EPA Substance Registry System 1H-1,2,4-Triazole- 1-ethanol, .beta.-(4-chlorophenoxy)-. alpha.-(1,1-dimethylethyl)- (55219-65-3)
 
Safety Information
Hazard Codes  Xn,F,T
Risk Statements  22-52/53-36-20/21/22-11-23-20/22
Safety Statements  22-61-36-26-45
RIDADR  2588
RTECS  KK2200000
HazardClass  6.1(b)
PackingGroup  III
Toxicity LD50 in male, female rats (mg/kg): 1161, 1105 orally; >5000 dermally, 24-hr; LD50 in quail: >10000 mg/kg (Frohberger)
MSDS Information
Provider Language
alpha-tert-butyl-beta-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol English
 
Triadimenol Usage And Synthesis
Chemical properties The pure triadimenol is white, tasteless fine crystalline powder. m.p.: 112 ° C, vapor pressure: 1 × 10 -3 Pa (20 ° C). Solubility in organic solvents: cyclohexane 40%, isopropanol 15%, methylene chloride 10%, toluene 4%; Solubility in water: 0.12g / L. Stable in neutral or weak acid medium, easy to break down when boiled in strong acidic medium.
Uses It is a systemic broad-spectrum seed treatment fungicide which can kill pathogens attached to the internal and external surface of seed. It works through the inhibition of fungal ergosterol biosynthesis. It’s used on cereal grains to control powdery mildew and smut diseases such as loose smut, stinking smut and root rot on wheat, loose smut, rust, leaf stripe disease and net blotch etc on barley, and it is more than 90% effective when 100kg of seeds are treated with 30 ~ 50g of 25% DS. It is more than 90% effective when 100kg of seeds are treated with 42 ~ 75g of 25% DS to control smut on corn and sorghum head smut. If 100kg of seeds are treated with 30g of triadimenol and 5g of furidazol, it will be 92% to 100% effective for the control of loose smut, stripe disease, net blotch and root rot on spring barley , loose smut, stinking smut, snow mold on winter wheat, and leaf stripe disease, loose smut on spring oat.
Triadimenol is a broad-spectrum fungicide with high efficiency and low toxicity. It is used on wheat and rice to control rust, powdery mildew, sheath blight and other diseases, and has a significant yield increasing effect. It can be also used as a cereal seed treatment and for the control of cereal smut.
Toxicity The acute oral toxicity LD50 in rats was 1161 mg / kg (female), 1105 mg / kg (male). The acute oral toxicity LD50 in mice was 1300 mg / kg (male & female). No effect dose for dogs and rats during 90 days feeding test: 600mg / kg • d. The acute inhalation The LC50 in goldfish and rainbow trout was 10~15mg/L and 23.5mg/L respectively (both 96 hours). The LD50 in quail was > 1000mg / kg. No effect on bees.
Preparation method Mostly, using triadimefon as the starting material , triadimenol is prepared through different reduction processes.
1. Reduction by hydrogen in the presence of a catalyst and any polar solvent, or reduction by aluminum isopropoxide in the presence of a solvent:Article illustration
2. Reduction by borohydride in the presence of any polar solvent.
3. Reduction by formamidine sulfinic acid and alkali metal hydroxide in the presence of any polar solvent: Article illustration
4. Reduction by using formic acid - triethylamine adduct as a reducing agent:Article illustration
Uses β-(4-Chlorophenoxy)-α-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol is a agricultural fungicide that is systemically active against powdery mildews and rusts of grains.
Definition ChEBI: A member of the class of triazoles that is 3,3-dimethyl-1-(1,2,4-triazol-1-yl)butane-1,2-diol substituted at position O1 by a 4-chlorophenyl group. A fungicide for cereals, beet and brassicas used to control a range of diseases including powdery mildew, ru ts, bunts and smuts.
Uses Systemic agricultural fungicide; cereal seed protectant.
Agricultural Uses Fungicide: Triadimenol is used to control seed-and soil-borne diseases and to provide early season control of foliar diseases. It is applied to seeds of barley, corn, oats, rye, sorghum and wheat and also to fruits, vegetables and ornamentals. Registered for use in EU countries . Registered for use in the U.S. U.S. Maximum Allowable Residue Levels for Triadimenol
Trade name BAYFIDAN®; BAYFRDAN EW®; BAY KWG 0519®; BAYTAN® SEED TREATMENT; BAYTAN 30® FUNGICIDE; PROTEGE ALLEGIANCE BAYTAN®; SPINNAKER®; SUMMIT®; TRIADIMENOL®; TRIAFOL®; TRIAPHOL®

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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