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BUTAMIFOS

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Products Intro: Product Name:Butamifos;Cremart;36335-67-8
CAS:36335-67-8
Purity:0.99 Package:25KG,200L
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CAS:36335-67-8
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CAS:36335-67-8
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Products Intro: Product Name:Butamifos
CAS:36335-67-8
Purity:98% Package:10mg Remarks:B67382
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Products Intro: Product Name:Butamifos
CAS:36335-67-8
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BUTAMIFOS Basic information
Product Name:BUTAMIFOS
Synonyms:(1-methylpropyl)-phosphoramidothioicacio-ethylo-(5-methyl-2-nitropheny;h26905;hercules26905;kremart;metacrefos;n-(sec-butyl)-phosphoramidothioicacio-ethylo-(6-nitro-m-tolyl)ester;o-ethylo-(3-methyl-6-nitrophenyl)n-sec-butylphosphorothioamidate;o-ethyl-o-(5-methyl-2-nitrophenyl)(1-methylpropyl)phosphoramidothioate
CAS:36335-67-8
MF:C13H21N2O4PS
MW:332.36
EINECS:
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Mol File:36335-67-8.mol
BUTAMIFOS Structure
BUTAMIFOS Chemical Properties
Melting point <25 °C
Boiling point 422.1±55.0 °C(Predicted)
density 1.223±0.06 g/cm3(Predicted)
storage temp. 0-6°C
pka-0.51±0.70(Predicted)
BRN 2165895
Henry's Law Constant3.4×101 mol/(m3Pa) at 25℃, Ebert et al. (2023)
EPA Substance Registry SystemPhosphoramidothioic acid, (1-methylpropyl)-, O-ethyl O-(5-methyl-2-nitrophenyl) ester (36335-67-8)
Safety Information
Hazard Codes Xn,N
Risk Statements 22-50/53
Safety Statements 61
RIDADR UN 3082 9 / PGIII
WGK Germany 3
HS Code 29299090
MSDS Information
BUTAMIFOS Usage And Synthesis
UsesButamifos (S-2846) is an organophosphoramidate herbicide used to control annual weeds with low toxicity to mammals. Butamifos acts on the growing points of susceptible plants, causing severe radial enlargement of the affected tissues[1].
DefinitionChEBI: Butamifos is a C-nitro compound.
Metabolic pathwayIn water, butamifos undergoes photoinduced intramolecular oxygen transfer from the nitro group to the P=S moiety, resulting in the formation of the nitrosooxon derivative. Through the successive reduction of the nitroso group to hydroxyamino and amino groups, as well as oxidation to the nitro group, the nitrosooxon derivative is finally photodegraded to various polar compounds. The isomer of butamifos is photodegraded more slowly than butamifos in air, and its main photodegradation pathway in water is oxidation of the arylmethyl group to form a corresponding carboxylic acid derivative.
References[1] SUMIDA S, et al. Chlorella as a model system to study herbicidal mode of action and its application to a new herbicide, O-ethyl-O-(3-methyl-6-nitrophenyl)-N-sec-butyl phosphorothioamidate (S-2846)[M]. 1974.
BUTAMIFOS Preparation Products And Raw materials
Tag:BUTAMIFOS(36335-67-8) Related Product Information
Phoxim Benoxacor Anilofos BROMOBUTIDE Pipemidic acid Chlorpromazine Diphenhydramine Ambroxol AMIKACIN 5-Fluorouracil Loperamide Butylamine Triadimenol Ethoprophos 5-Methyl-2-nitrophenol BUTAMIFOS O,O-Dimethyl phosphoramidothioate BUTAMIFOS OXON,BUTAMIFOS OXON STANDARD