Tribenuron methyl

ChemicalBook > CAS DataBase List > Tribenuron methyl

Product Name: Tribenuron methyl
CAS No.: 101200-48-0
Chemical Name: Tribenuron methyl
Synonyms: TRIBENURON-METHYL;matrix;EXPRESS;1000PPM;l5300;POINTER;GRANSTAR;dpx-l5300;DXP-L5300;Express TM
CBNumber: CB5209758
Molecular Formula: C15H17N5O6S
Formula Weight: 395.39
MOL File: 101200-48-0.mol

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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
solubility: Chloroform (Slightly), DMSO (Slightly)
Water Solubility: 55 g l^-1(25 °C)
pka: 4.34±0.10(Predicted)
Stability:: Hygroscopic, Unstable in Solution
CAS DataBase Reference: 101200-48-0(CAS DataBase Reference)
EPA Substance Registry System: Tribenuron-methyl (101200-48-0)

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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)
Toxicity: quail,LD50,oral,> 2250mg/kg (2250mg/kg),Pesticide Manual. Vol. 9, Pg. 840, 1991.

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H317May cause an allergic skin reaction

H373May cause damage to organs through prolonged or repeated exposure

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P272Contaminated work clothing should not be allowed out of the workplace.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P314Get medical advice/attention if you feel unwell.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 46013
Product name: Tribenuron-methyl
Purity: PESTANAL?, analytical standard
Packaging: 100mg
Price: $81.3
Updated: 2024/03/01

TRC

Product number: T767555
Product name: Tribenuron-methyl(~90%)
Packaging: 5g
Price: $155
Updated: 2021/12/16

AK Scientific

Product number: F021
Product name: Tribenuron-methyl
Packaging: 1g
Price: $345.24
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM0014988
Product name: TRIBENURON-METHYL
Purity: 95.00%
Packaging: 1G
Price: $1030.84
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM0014988
Product name: TRIBENURON-METHYL
Purity: 95.00%
Packaging: 5G
Price: $1612.96
Updated: 2021/12/16

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Tribenuron methyl Chemical Properties,Usage,Production

Chemical Properties

Tribenuron-methyl (TBM) is a member of the sulfonylurea herbicide family. It is a relatively polar, weak, acidic compound that is soluble in water. It can be extracted with polar organic solvent, buffer solution, or a mixture of organic solvent and water.
Tribenuron-methyl is a selective herbicide that inhibits the biosynthesis of branched amino acids in sensitive plants by competitively binding to the enzyme system which catalyzes the formation of these amino acids, the acetolactate synthase (ALS). It is used in cereals for the control of broadleaved weeds.

Uses

Tribenuron-methyl is a sulfonyl urea herbicide derivative employed for protection of crops such as corn, citrus, potatoes, tomatoes, rice and vines via inhibiting the growth of many grasses and broad-leaf weed species.Tribenuron-methyl is applied as a foliar spray and directly to the soil as it is rapidly absorbed by the foliage and the roots, and is translocated throughout the plant to the growing points.
Tribeneuron-methyl acts by inhibiting the synthesis of amino acids, specifically valine and isoleucine, which prevents cell division and cell growth. Selectivity occurs due to the differences in the metabolism of sulfonylureas between crops and weeds.
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

Triazine B Xylene Dicyandiamide BENZENESULFONYL ISOCYANATE Dimethyl ester 2-Amino-4-methoxy-6-methyl-1,3,5-triazine o-Toluic acid 2-methylamino-4-methoxy-6-methyl-s-triazine N-2,4-DIMETHYLPHENYL-N'-METHYLFORMAMIDINE Diphosgene Butyl isocyanate 2-Carbomethoxybenzenesulfonamide Methyl formate Triethylenediamine 1,3,5-Triazine METSULFURON METHYL cyanic acid

Preparation Products

Bensulfuron-methyl WP

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View Lastest Price from Tribenuron methyl manufacturers

Hebei Weibang Biotechnology Co., Ltd

Product: Tribenuron methyl 101200-48-0
Price: US $0.00-0.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 500000kg
Release date: 2024-11-05

Hebei Yanxi Chemical Co., Ltd.

Product: Tribenuron methyl 101200-48-0
Price: US $0.00/kg
Min. Order: 1kg
Purity: 99%
Supply Ability: 20tons
Release date: 2023-09-18

qingdao trust agri chemical co.,ltd

Product: Tribenuron methyl 101200-48-0
Price: US $0.00/kg
Min. Order: 100kg
Purity: 75%
Supply Ability: 20tons
Release date: 2024-07-03

101200-48-0, Tribenuron methylRelated Search:

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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

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Tribenuron-methyl@1000 μg/mL in Acetonitrile

Tribenuron-methyl Standard

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tribenuron-methy

1000PPM

high purity of Tribenuron methyl

tribenuron-methyl [ANSI]

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101200-48-0

C16H17N5O6S

C15H17N5O6S

Herbicide

Alpha sort

Herbicides

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