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Oxycarboxin

CAS No.
5259-88-1
Chemical Name:
Oxycarboxin
Synonyms
Carboxin sulfone;f461;DMOCD;F 461;DCMOD;DCMOO;Rendor;Vitavex;PLANTVAX;F 461(R)
CBNumber:
CB8415020
Molecular Formula:
C12H13NO4S
Molecular Weight:
267.3
MDL Number:
MFCD00055404
MOL File:
5259-88-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:55:43

Oxycarboxin Properties

Melting point 128-130℃ (ethanol )
Boiling point 527.6±50.0 °C(Predicted)
Density 1.3431 (rough estimate)
refractive index 1.6280 (estimate)
Flash point 100 °C
storage temp. 0-6°C
pka 11.26±0.70(Predicted)
Water Solubility 1g/L(25 ºC)
Henry's Law Constant 9.3×105 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
EWG's Food Scores 1
FDA UNII NPU5GBN17X
EPA Substance Registry System Oxycarboxin (5259-88-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H412
Precautionary statements  P273
Hazard Codes  Xn
Risk Statements  22-52/53
Safety Statements  61
RIDADR  UN3077 (solid)
RTECS  RP4900000
HS Code  29349990
Hazardous Substances Data 5259-88-1(Hazardous Substances Data)
Toxicity LD50 oral in rat: 2gm/kg

Oxycarboxin price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC O870643 Oxycarboxine 5259-88-1 25mg $40 2021-12-16 Buy
TRC O870643 Oxycarboxine 5259-88-1 100mg $105 2021-12-16 Buy
TRC O870643 Oxycarboxine 5259-88-1 1g $370 2021-12-16 Buy
American Custom Chemicals Corporation AGR0000324 OXYCARBOXIN 95.00% 5259-88-1 5MG $497.88 2021-12-16 Buy
Product number Packaging Price Buy
O870643 25mg $40 Buy
O870643 100mg $105 Buy
O870643 1g $370 Buy
AGR0000324 5MG $497.88 Buy

Oxycarboxin Chemical Properties, Uses, Production

Chemical Properties

Oxydisulfoton is a white corrosive solid.

Uses

OXYCARBOXIN is effective against rust in grains and vegetables, and has both preventative and curative effects.

Production Methods

Oxycarboxin is commercially produced through a multi-step synthesis involving oxathiin ring formation and sulfone oxidation. It begins with the construction of the oxathiin ring system, which is derived from precursors such as 2-hydroxyethyl thiocarbamate and methyl-substituted aromatic compounds. These undergo cyclisation to form the dihydro-oxathiin core. The sulphur atom in the ring is then oxidized to a sulfone using oxidizing agents like hydrogen peroxide or peracids, enhancing the compound’s stability and biological activity. The final step involves acylation with phenyl isocyanate or similar reagents to introduce the carboxamide group. These reactions are typically carried out in organic solvents such as acetonitrile or toluene under controlled temperature and pH conditions to ensure high yield and purity.

Definition

ChEBI: An anilide obtained by formal condensation of the amino group of aniline with the carboxy group of 2-methyl-5,6-dihydro-4,4-dioxo-1,4-oxathiine-3-carboxylic acid. A fungicide for the control of rust diseases on ornamentals, cereals and nursery trees as wel as fairy rings on turf.

Agricultural Uses

Fungicide: Registered as a foliar systemic fungicide for use against rust on carnations and greenhouse geranium. Not approved for use in EU countries. Registered for use in the U.S. and Canada

Trade name

CARBOJECT®[C]; DYNAM®; F461®;FUNGISOL®[C]; PLANTVAX®; PLANT WAX®; VITAVEX®

Mechanism of action

Systemic with curative action. Inhibition of nucleic acid synthesis. Succinate DeHydrogenase Inhibitor.

Metabolic pathway

The oxathiin ring of the oxycarboxin undergoes a glass-catalyzed ring-opening reaction resulting in a simple step for hydrolytic removal of an acetyl group to give 2-(vinylsulfonyl)acetanilide in aqueous solution. The decomposition of oxycarboxin involves the container and is surface-type dependent.

Shipping

UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneoushazardous material, Technical Name Required. UN1596 Dinotoanilines, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Incompatibilities

May react with strong oxidizers such as chlorates, peroxides, and nitrates. Can become unstable in acidic and alkaline media. Combustible; dust may form explosive mixture with air. Corrosive, may attack some metals, rubbers, and plastics.

Waste Disposal

Do not discharge into drains or sewers. Dispose of waste material as hazardous waste using alicensed disposal contractor to an approved landfill. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. If allowed, Incineration with effluent gas scrubbing is recommended. Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Pesticide Type

Fungicide; Metabolite

Oxycarboxin Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 70)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Sichuan Kulinan Technology Co., Ltd 400-1166-196 18981987031 cdhxsj@163.com China 11674 57
Chengdu Ai Keda Chemical Technology Co., Ltd. 4008-755-333 18080918076 800078821@qq.com China 9706 55
Chengdu RunZeBenTu Chemical Co., Ltd 13096311329 028-88469284 616445927 616445927@qq.com China 2870 50
Alta Scientific Co., Ltd. 022-6537-8550 15522853686 sales@altasci.com.cn China 4508 55
Shanghai YuanYe Biotechnology Co., Ltd. 18916372613 yanzihan@shyuanye.com China 87240 60
Shandong Xiya Chemical Co., Ltd. 4009903999 13395398332 sales@xiyashiji.com China 20788 60
Hubei widely chemical technology Co., Ltd. 027-83991130 18627774460 1718093273@QQ.COM China 1615 58
Shenzhen Regent Biochemical Technology Co., Ltd. 0755-85201366 18938635012 sales@regentsciences.com China 9107 58
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 sales@rrkchem.com China 57336 58
1,4-Oxathiin, 2,3-dihydro-5-carboxanilido-6-methyl-, 4,4-dioxide 1,4-oxathiin,2,3-dihydro-5-carboxanilido-6-methyl-,4,4-dioxide 1,4-Oxathiin-3-carboxamide, 5,6-dihydro-2-methyl-N-phenyl-, 4,4-dioxide 1,4-oxathiin-3-carboxamide,5,6-dihydro-2-methyl-n-phenyl-,4,4-dioxide 1,4-Oxathiin-3-carboxanilide, 5,6-dihydro-2-methyl-, 4,4-dioxide 1,4-oxathiin-3-carboxanilide,5,6-dihydro-2-methyl-,4,4-dioxide 2,3-Dihydro-5-carboxanilido-6-methyl-1,4-oxathiin 4,4-dioxide 2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiin,4,4-dioxide LABOTEST-BB LT00134855 OXYCARBOXIN, 1GM, NEAT oxycarboxin (bsi,iso,ansi,jmaf) OXYCARBOXIN STANDARD Carboxin dioxide oxycarboxin (ISO) 2,3-dihydro-6-methyl-5-(N-phenylcarbamoyl)-1,4-oxothiine 4,4-dioxide DMOCD 2,3-dihydro-6-methyl-5-(N-phenylcarbamoyl)-1,4-oxothiine 4,4-dioxide,oxycarboxin (ISO) Dioxide of vitavax dioxideofvitavax F 461 F 461 (Pesticide) f461 f461[pesticide] methyl-6phenylcarbamoyl-5dihydro-2,3oxathiine-1,4-dioxyde-4,4 Oxathiin-3-carboxamide, 5,6-dihydro-2-methyl-N-phenyl-, 4,4-dioxide Oxathiin-3-carboxanilide, 5,6-dihydro-2-methyl-, 4,4-dioxide Oxicarboxin Oxykisvax Plant Wax Plantvax 20 Plantvax 75 plantvax20 Rendor Ringmaster Vitavax sulfone 4,4-diketo-6-methyl-N-phenyl-2,3-dihydro-1,4-oxathiine-5-carboxamide 6-methyl-4,4-dioxo-N-phenyl-2,3-dihydro-1,4-oxathiine-5-carboxamide Oxycarboxin 1g [5259-88-1] NSC 232673 PLANTVAX PLANTVAX(R) OXYCARBOXINE F 461(R) CARBOJECT 2-Methyl-N-phenyl-5,6-dihydro-1,4-oxathiine-3-carboxamide 4,4-dioxide 5,6-Dihydro-2-methyl-1,4-oxathiin-3-carboxanilide 4,4-dioxide 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide4,4-dioxide 5,6-dihydro-2-methyl-1,4-oxathi-ine-3-carboxanilide4,4-dioxide 5,6-Dihydro-2-methyl-3-carboxanilido-1,4-oxathiin-4,4-dioxid 5,6-Dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide 4,4-dioxide 5,6-dihydro-2-methyl-n-phenyl-1,4-oxathiin-3-carboxamide4,4-dioxide carboxinsulfone DCMOD DCMOO Dihydro-2-methyl-1,4-oxathiin-3-carboxanilide 4,4-dioxide vitavaxsulfone Vitavex 5,6-DIHYDRO-2-METHYL-1,4-OXATHIN-3-CARBOXANILIDE-4,4-DIOXIDE 2,3-DIHYDRO-5-CARBOXANILIDE-6-METHYL-1,4-OXATHIN-4,4-DIOXIDE