ChemicalBook > CAS DataBase List > Tribenuron methyl

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).

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View Lastest Price from Tribenuron methyl manufacturers

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
Hebei Guanlang 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
2023-03-30
Weifang Yuanye Biotechnology Co., Ltd
Product
Tribenuron Methyl 101200-48-0
Price
US $0.00/KG
Min. Order
25KG
Purity
95%TC,75%WDG
Supply Ability
100MT
Release date
2021-02-18

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