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Bentazone

Bentazone Structure
CAS No.
25057-89-0
Chemical Name:
Bentazone
Synonyms
BENTAZON;leader;GALAXY;Bendioxide;3-isopropyl-1h-2,1,3-benzothiadiazin-4(3h)-one-2,2-dioxide;laddok;Adagio;Thianon;bas3510;Bazargan
CBNumber:
CB7235319
Molecular Formula:
C10H12N2O3S
Molecular Weight:
240.28
MOL File:
25057-89-0.mol
Modify Date:
2024/3/14 15:18:27

Bentazone Properties

Melting point 137-139°C
Boiling point 395.7±25.0 °C(Predicted)
Density 1.3387 (rough estimate)
refractive index 1.5650 (estimate)
Flash point 2 °C
storage temp. APPROX 4°C
solubility Chloroform (Slightly), Methanol (Slightly)
pka pKa (24°): 3.3
form Solid
color White
Water Solubility 0.5g/L(20 ºC)
Merck 13,1051
BRN 530220
NIST Chemistry Reference Bentazone(25057-89-0)
EPA Substance Registry System Bentazon (25057-89-0)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H317-H319-H412
Precautionary statements  P261-P273-P280-P301+P312-P302+P352-P305+P351+P338
Hazard Codes  Xn,F
Risk Statements  22-36-43-52/53-20/21/22-11
Safety Statements  2-24-37-61-36-26-16
RIDADR  UN 1648 3/PG 2
WGK Germany  2
RTECS  DK9900000
HS Code  29349990
Toxicity LD50 in male, female rats (mg/kg): 383.2, 433.6 orally (Ugazio)
NFPA 704
0
2 0

Bentazone price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 32052 Bentazon PESTANAL?, analytical standard 25057-89-0 250MG ₹2760.38 2022-06-14 Buy
TCI Chemicals (India) B3825 Bentazon 25057-89-0 1G ₹3200 2022-05-26 Buy
TCI Chemicals (India) B3825 Bentazon 25057-89-0 5G ₹7900 2022-05-26 Buy
Product number Packaging Price Buy
32052 250MG ₹2760.38 Buy
B3825 1G ₹3200 Buy
B3825 5G ₹7900 Buy

Bentazone Chemical Properties,Uses,Production

Description

Bentazon is unique under these herbicides because it is the only compound that bears a sulfonyl group. A puzzle that is not solved yet is that bentazone is an excellent herbicide but has a very low pI50-value.

Chemical Properties

Bentazon is a colorless to white crystalline powder.

Uses

Herbicide.

Definition

ChEBI: A benzothiadiazine that is 1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide substituted by an isopropyl group at position 3.

Agricultural Uses

Selective post-emergent herbicide: A post-emergence herbicide used to control broadleaf weeds in crops such as beans, corn, mint, soybeans, rice, and peanuts. All products formerly marketed in the U.S. contain the sodium salt of bentazon as the active ingredient, referred to as sodium bentazon. Also used in selective post-emergent control of broadlelaf weeds and sedges in alfalfa, asparagus, cereals, clover, digitalis, dry peas, flax, garlic, grasses, green lima beans, mint, onions, potatoes, snap beans for seed, sorghum, soybeans and sugarcane. Not currently registered in the U.S. It is reported to be used in most European countries.

Trade name

ASAGIO®; BAS 351-H®; BASAGRAN®; BENDIOXIDE®; BENTA®; BLAST®; ENTRY®; LADDOK®; LEADER®; PLEDGE®; STORM®

Safety Profile

Moderately toxic by ingestion and skin contact. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits very toxic fumes of SO, and NOx.

Potential Exposure

A potential danger to those involved in the manufacture, formulation or application of this selective postemergent thiadiazine herbicide.

Environmental Fate

Soil. Under aerobic conditions, bentazone was reported to degrade to 6- and 8-hydrox ybentazone compounds. In addition, anthranilic acid and isopropylamide were reported as soil hydrolysis products (Otto et al., 1978). Persistence in soil is less than 6 weeks (Hartley and Kidd, 1987). Bentazone is readily adsorbed onto organic carbon and therefore, is not expected to leach to groundwater (Abernathy and Wax, 1973). The dissipation half life of bentazone in field soil is 5 days (Ross et al., 1989).
Plant. Undergoes hydroxylation of the aromatic ring and subsequent conju-gation in plants (Otto et al., 1978; Hartley and Kidd, 1987) forming 6- and 8-hydroxybentazone compounds (Otto et al., 1978). The half-life in and/or on plants is 2–3 days (
Photolytic. Humburg et al. (1989) reported that 30% degradation of bentazone on glass plates occurred when exposed to UV light (λ = 200–400 nm); however, no photoproduct(s) were reported. The natural sunlight and simulated sunlight irradiation of
Chiron et al. (1995) investigated the photodegradation of bentazone (20 μg/L) in distilled water and Ebro River water using an xenon arc irradiation. In distilled water, bentazone completely disappeared after 16 hours of irradiation. Photodegradation appeared to follow pseudo-first-order kinetics with a half-life of about 2.5 hours. The presence of humic substances (4 mg/L) increased the rate of photodegradation and the disappearance of bentazone was achieved in 8 hours. No significant breakdown photoproducts were identified.

Metabolic pathway

14C-Bentazon degrades in soils under conventional tillage and no-tillage (3-18 years) with varying histories of bentazon application. The half-life for bentazon degradation ranges from 4.6 to 49.5 days; half-lives for some no-tillage soils with the longest histories of application are lower than those of conventional tillage soils. Half-lives for soils with no bentazon history are 3-11 times higher than the half- lives of those previously exposed to bentazon. N- Methylbentazon is the most consistently observed metabolite. The other metabolites identified in soils result from hydroxylation on the phenyl ring and the cleavage of the benzothiadiazine ring, yielding 6- and 8-hydroxybentazons and anthranilic acid via 2-amino-N-isopropylbenzamide.

Shipping

UN2588 Pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1—Poisonous materials, Technical Name Required.

Incompatibilities

Keep away from flammable materials, heat and flame. Risk of fire and explosion if formulations contain flammable/explosive solvents.

Waste Disposal

In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Global( 235)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Hebei Mojin Biotechnology Co., Ltd +86 13288715578 +8613288715578 China 12459 58 Inquiry
Hebei Yanxi Chemical Co., Ltd. +86-17531190177; +8617531190177 China 6011 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21676 55 Inquiry
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Thiadiazinol 3-Isopropyl-(1H)-benzo-2,1,3-thiadiazin-4-one-2,2-dioxide,aqueous(25%) Bentazone Standard 3,4-Dihydro-3-isopropyl-1H-2,1,3-benzothiadiazin-4-one 2,2-Dioxide Basagran 480 BasaMais Bazargan Bentazone solution Basagran (BASF) Thianon BENTAZON METHYL DERIVATIVE, 50MG, NEAT BENTAZON, 250MG, NEAT BENTAZON PESTANAL, 250 MG 3-(1-METHYLETHYL)-1H-2,1,3-BENZOTHIADIAZIN-4(3H)-ONE,2-DIOXIDE bentazon (ansi,wssa,canada) bentazon solution bentazone (bsi, iso,jmaf) BENTAZONTP 3-(1-methylethyl)-1H-2,1,3-benzothiadiazin-4(3H)-ol 3-isopropyl-1h-2,1,3-benzothiaiazin-4(3h)-one-2,2-dioxide 3-isopropyl-1h-benzo-2,1,3-thiadiazin-4-one-2,2-dioxide 3-Isopropyl-2,1,3-benzothiadiazinon-(4)-2,2-dioxid 3-isopropyl-2,1,3-benzothiadiazinon-(4)-2,2-dioxid[german] BAS 3510 BAS 351-07H BAS 3510H BAS 3512H BAS 3517H bas3510 bas351-07h bas3510h bas3512h bas3517h basagrankv basagran-plus graminon-plus herbatox laddok Pentazone bentazone (ISO) 3-isopropyl-2,1,3-benzothiadiazine-4-one-2,2-dioxide Acetochlor+Metribuzin,W.P. Bentazon, Herbicide Mix Bentazone,aqueous(25%) Adagio 3-Isopropyl-2,1,3-benzothiadiazinone-(4)-2,2-dioxide 3-Isopropyl-3,4-dihydro-2,1,3-benzothiadiazin-4(1H)-one 2,2-dioxide 3-(1-METHYLETHYL)-1H-2,1,3-BENZOTHIADIAZIN-4(3H)-ONE-2,2-DIOXIDE 2-ISO-PROPYL-(1H)-BENZO-2,1,3-THIADIAZIN 4-ONE-2,2-DIOXIDE bas 351h BASAGRAN basagran 4e BASF 3510H 2,2-Dioxo-3-propan-2-yl-1H-benzo[d][1,2,6]thiadiazin-4-one Bentazon 250mg [25057-89-0] 3-(1-Methylethyl)-2,1,3-benzothiadiazin-4(3H)-one 2,2-Dioxide 1H-2,1,3-Benzothiadiazin-4(3H)-one, 3-(1-methylethyl)-, 2,2-dioxide 1H-2,1,3-Benzothiadiazin-4(3H)-one, 3-isopropyl-, 2,2-dioxide 1H-2,1,3-Benzothiadiazin-4(3H)-one,3-(1-methylethyl)-,2,2-dioxide