Tribenuron methyl
- Product Name:
- Tribenuron methyl
- CAS No.
- 101200-48-0
- Chemical Name:
- Tribenuron methyl
- CBNumber:
- CB5209758
- Molecular Formula:
- C15H17N5O6S
- Formula Weight:
- 395.39
- MOL File:
- 101200-48-0.mol
Tribenuron methyl Property
- Melting point:
- 141°C
- Density
- 1.4143 (rough estimate)
- vapor pressure
- 1.24 at pH 7 (25 °C)
- refractive index
- 1.6460 (estimate)
- storage temp.
- 0-6°C
- form
- neat
- Water Solubility
- 55 g l-1(25 °C)
- pka
- 4.34±0.10(Predicted)
- CAS DataBase Reference
- 101200-48-0(CAS DataBase Reference)
- EPA Substance Registry System
- Tribenuron-methyl (101200-48-0)
Safety
- Hazard Codes
- Xi,N
- Risk Statements
- 43-50/53
- Safety Statements
- 22-24-37-61-60-46
- RIDADR
- UN 3077 9 / PGIII
- WGK Germany
- 1
- RTECS
- DH3565000
- Hazardous Substances Data
- 101200-48-0(Hazardous Substances Data)
N-Bromosuccinimide Price More Price(1)
- Product number:
- 46013
- Product name :
- Tribenuron-methyl
- Purity:
- PESTANAL?, analytical standard
- Packaging:
- 100mg
- Price:
- $63.2
- Updated:
- 2020/08/18
- Buy:
- Buy
Tribenuron methyl Chemical Properties,Usage,Production
Uses
Methomyl is a broad spectrum carbamate insecticide with both contact and oral toxicity to control chewing and sucking Lepidotera, Homoptera, Coleoptera and Hemiptera pests in vegetable, orchard, vine and field crops.
Definition
ChEBI: The methyl ester of tribenuron.
General Description
Colorless crystals. Non corrosive. Used as an herbicide.
Air & Water Reactions
Hydrolysis occurs rapidly at pH <7 or >12.
Reactivity Profile
A sulfonylurea derivative.
Agricultural Uses
Herbicide: Used to control annual grasses and broadleaf weeds on barley, blueberries, oats, wheat, flax and rape seed (canola). Registered for use in EU countries . Registered for use in the U.S. U.S. Maximum Allowable Residue Levels for the residues of the herbicide tribenuron methyl [40 CFR 180.451(a)]: in or on the following raw agricultural commodities: barley, grain 0.05 ppm; barley, straw 0.10ppm; canola, seed 0.02 ppm; cotton, gin byproducts 0.02 ppm; cotton, undelinted seed 0.02 ppm; flax, seed 0.02 ppm; oat, grain 0.05 ppm; oat, straw 0.10ppm; wheat, grain 0.05ppm; and wheat, straw 0.10 ppm. Tolerances with regional registration, as defined in 180.1(n), are established. [40 CFR 180.451(c)]: in or on the following raw agricultural commodities: grass, forage, fodder and hay, group (except Bermudagrass); forage 0.10ppm; and grass, forage, fodder and hay, group (except Bermudagrass); hay 0.10 ppm.
Trade name
ALLY®; CANVAS®; DPX-L-5300®; EXPRESS®; EXPRESS®-75 DF; HARMONY EXTRA®; INL-5300®; L 5300®; MATRIX®
Metabolic pathway
The chemical structure of tribenuron methyl possesses a mono-N-methyl group in the sulfonylurea linkage which is a unique sulfonylurea herbicide and undergoes complex degradation reactions in the environment. Tribenuron methyl degrades into many degradation products, as indicated in the pathways by photolytic and hydrolytic chemical reactions and by biological degradations by mammal, plant, and soil. It is interesting to note that photolysis in different solvents yields diverse products depending on the individual solvents.
Degradation
Methomyl (1) was hydrolysed under alkaline conditions at 25 °C (DT50
ca. 14 days) and was stable under neutral to acidic conditions [DT50 > 30
days at pH 5 and 7 (Friedman, 1983)l. Cleavage of the carbamate ester
bond is the primary degradation pathway, yielding S-methyl N-hydroxy-thioacetimidate
(2).
Irradiation of methomyl in dilute aqueous solution at 254 nrn yielded
acetonitrile (3), dimethyl disulfide, acetone, N-ethylidenethylamine and
carbon dioxide (Freeman and Ndip, 1984). Methomyl does not absorb
sunlight but underwent degradation to acetonitrile by indirect photolytic
reactions in/on soil surfaces (Swanson, 1986).
Tribenuron methyl Preparation Products And Raw materials Raw materials
Raw materials
Preparation Products
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101200-48-0, Tribenuron methylRelated Search:
- benzoicacid,2-(((((4-methoxy-6-methyl-1,3,5-triazin-2-yl)methylamino)carbonyl
- dpx-l5300
- express75df
- l5300
- matrix
- EXPRESS
- EXPRESS(R)
- TRIBENURON-METHYL
- TRIBENURON METHYL 6
- DXP-L5300
- Express TM
- POINTER
- TRIBENURON-METHYL PESTANAL, 100 MG
- methyl 2-(3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)3-methylureidosulphonyl)benzoate
- Tribenuron W.P.
- 2-methyl-[4-methoxy-6-methyl-1,3,5-triazin-2-yl (methyl) carbamoylsulfamoyl] benzoate
- Benzoic acid, 2-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)methylaminocarbonylaminosulfonyl-, methyl ester
- Tribenuron-met
- 2-[[3-(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)-3-methylureido]sulfonyl]benzoic acid methyl ester
- Tribenuron-methyl (technical)
- Methyl 2-(N-((4-Methoxy-6-Methyl-1,3,5-triazin-2-yl)(Methyl)carbaMoyl)sulfaMoyl)benzoate
- Metometuron
- methyl2-[[[[n-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)methylamino]carbonyl]ami
- no]sulfonyl]benzoate
- sulfmethmeton-methyl
- Tribenuronmethylester
- Methyl 2-[[[[N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)methylamino]carbonyl]amino]sulfonyl] benzoate
- METHYL-2-[[[[(4-METHOXY-6-METHYL-1,3,5-TRIAZIN-2-YL)METHYLAMINO]CARBONYL]-AMINO]SULFONYL]BENZOATE
- GRANSTAR
- Tribenuron-methyl Solution, 1000ppm
- Tribenuron-methyl (~90%)
- Tribenuron-methyl@100 μg/mL in Acetonitrile
- Tribenuron-methylSolution,1000mg/L,1ml
- Tribenuron-methyl@1000 μg/mL in Acetonitrile
- Tribenuron-methyl Standard
- 101200-48-0 Tribenuron Methyl Selective Herbicides For Maize , White powder
- Tribenuron / Metsulfuron methyl Selective Herbicides 101200-48-0 / 74223-64-6
- 101200-48-0
- C16H17N5O6S
- C15H17N5O6S
- NULL
- Herbicide
- Alpha sort
- Herbicides
- Pesticides&Metabolites
- Q-ZAlphabetic
- TP - TZPesticides&Metabolites
- Urea structure