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Oxamyl

Oxamyl Structure
CAS No.
23135-22-0
Chemical Name:
Oxamyl
Synonyms
oxamil;Blade;d 1410;d-1410;VYDATE;OXAMYL;dpx1410;vydateg;vydatek;vydatel
CBNumber:
CB7311293
Molecular Formula:
C7H13N3O3S
Molecular Weight:
219.26
MOL File:
23135-22-0.mol
Modify Date:
2024/3/14 15:18:27

Oxamyl Properties

Melting point 100°C
Density 0.9700
vapor pressure 5.1×10-5Pa (25 °C)
refractive index 1.6630 (estimate)
storage temp. 0-6°C
solubility Chloroform: Slightly Soluble,Methanol: Slightly Soluble
pka 10.48±0.46(Predicted)
Water Solubility 28 g/100 mL
BRN 2212753
Stability Hygroscopic
CAS DataBase Reference 23135-22-0(CAS DataBase Reference)
NIST Chemistry Reference Oxamyl(23135-22-0)
EPA Substance Registry System Oxamyl (23135-22-0)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS09
Signal word  Danger
Hazard statements  H300+H330-H312-H411
Precautionary statements  P273-P280-P301+P310+P330-P302+P352+P312-P304+P340+P310
Hazard Codes  T+;N,N,T+
Risk Statements  21-26/28-51/53
Safety Statements  36/37-45-61
RIDADR  UN 2811
WGK Germany  3
RTECS  RP2300000
HazardClass  6.1(a)
PackingGroup  I
Toxicity LD50 orally in rats: 5 mg/kg (Fahmy)
NFPA 704
0
4 0

Oxamyl price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 36184 Oxamyl PESTANAL?, analytical standard 23135-22-0 100MG ₹8595.05 2022-06-14 Buy
Product number Packaging Price Buy
36184 100MG ₹8595.05 Buy

Oxamyl Chemical Properties,Uses,Production

Description

Oxamyl, is also called N,N-dimethyl-2-methylcarbamoyloxyimino- 2-(methylthio)acetamide (IUPAC), consists of colorless crystals, which are readily soluble in water, methanol, ethanol, acetone, and fairly soluble in toluene. Oxamyl is produced by chlorination of the oxime of methylglycolate, reaction with methanethiol and alkali, and conversion to the carbamate with methyl isocyanate.

Uses

Oxamyl is a pesticide used in the treatment and protection of crops from parasites and insects.

Agricultural Uses

Insecticide, Nematicide, Acaricide: A systemic and contact insecticide/acaricide and nematicide, oxamyl is a restricted use pesticide used on apples, bananas, carrots, celery, citrus, cotton, cucumbers, eggplants, garlic, ginger, muskmelon (including cantaloupe and honeydew melon), onion (dry bulb), peanuts, pears, peppers, peppermint, pineapples, plantains, potatoes, pumpkins, soybeans, spearmint, squash, sweet potatoes, tobacco, tomatoes, watermelons, yams. Oxamyl is also used on non-bearing apple, cherry, citrus, peach, pear, and tobacco. It is applied directly onto plants or the soilsurface. It is available in both liquid and granular form, but the granular form is banned in the U.S. It has no residential use. Registered for use in EU countries[115

Trade name

BLADE®; D-1410®; DPX 1410®; INSECTICIDE-NEMACIDE 1410®; OXAMYL CARBAMATE INSECTICIDE®; THIOXAMYL®; VYDATE®; VYDATE® 10G; VYDATE L®; VYDATE INSECTICIDE/NEMATICIDE®; VYDATE OXAMYL INSECTICIDE/NEMATOCIDE®[C]

Safety Profile

Poison by ingestion, skin contact, and inhalation. Experimental reproductive effects. Moderately toxic by skin contact. When heated to decomposition it emits very toxic fumes of NOx and SOx

Potential Exposure

Oxamyl is a white crystalline solid. Sulfur or garlic-like odor. Molecular weight=219.3

Environmental Fate

Soil. Oxamyl rapidly degraded in a loamy sand and fine sand soil at 25°C to carbon dioxide and the intermediate methyl N-hydroxy-N,N-dimethyl-1-thiooxaminidate (Rajagopol et al., 1984). The reported half-life in soil is approximately one week (Worthing and Hance, 1991). Ou and Rao (1986) reported a half-life in soil of 8–50 days. The reported half-lives of oxamyl in Pitstone, Devizes, Sutton Veany and Mepal soils at 15°C were reported to be 10.2–13.1, 6.2, 7.1 and 17.8 days, respectively (Bromilow et al., 1980). Smelt et al. (1987) reported that oxamyl degraded at a higher rate in field plots after repeated applications of this nematocide than in soils that received no treatment. The repeated applications of oxamyl to soils probably induced microbial activity, which resulted in the accelerated disappearance of this compound.
Harvey and Han (1978) reported a half-life of 8 days for oxamyl in soil.
Groundwater. According to the U.S. EPA (1986) oxamyl has a high potential to leach to groundwater.
Plant. Dislodgable residues of oxamyl on cotton leaf 0, 24, 48, 72 and 96 hours after application (0.41 kg/ha) were 1.5, 1.1, 1.2, 0.85 and 0.76 mg/m2, respectively (Buck et al., 1980).
Chemical/Physical. The hydrolysis half-lives of oxamyl in a sterile 1% ethanol/water solution at 25°C and pH values of 4.5, 6.0, 7.0 and 8.0, were 300, 17, 1.6 and 0.20 weeks, respectively (Chapman and Cole, 1982). Under alkaline conditions, oxam

Metabolic pathway

Oxamyl degrades in soils, plants and animals following common metabolic pathways. Primary degradation reactions include the hydrolysis of the carbamate ester to yield the corresponding oxyimidothioate and nitrile. Other major metabolic reactions include N-demethylation and the hydration/oxidation of the nitriles to the corresponding amides and acids. The majority of the oxamyl metabolites are recovered as conjugates in plants and animals. No metabolites containing the oxidised thiomethyl group were observed. The primary degradation/metabolic pathways of oxamyl are presented in Scheme 1.

Shipping

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN2991 Carbamate pesticides, liquid, toxic, flammable, flash point <23°C, Hazard Class: 6.1; Labels: 6.1-Poisonous material, 3-Flammable liquid.

Incompatibilities

Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water and a salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides (releasing heat, toxic, and possibly flammable gases), thiosulfates and dithionites (releasing hydrogen sulfate and oxides of sulfur).

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal 2264 Oxamyl practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Small quantities may be treated with alkali and buried in a landfill. 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.

Oxamyl Preparation Products And Raw materials

Raw materials

Preparation Products

1-(dimethylcarbamoyl)-n-((methylcarbamoyl)oxy)thio-formidicacimethyles 2-(dimethylamino)-n-(((methylamino)carbonyl)oxy)-2-oxoethanimidothioicacidm N-Methylcarbamic acid [(dimethylcarbamoyl)(methylthio)methylene]amino N-Methylcarbamic acid [(dimethylcarbamoyl)(methylthio)methylene]amino ester dpx1410 dpx1410l Du pont 1410 dupont1410 epapesticidechemicalcode103801 Ethanimidothioic acid, 2-(dimethylamino)-N-[[(methylamino)carbonyl]oxy]-2-oxo-, methyl ester ethanimidothioicacid,2-(dimethylamino)-n-(((methylamino)carbonyl)oxy)-2-oxo ethanimidothioicacid,2-(dimethylamino)-n-(((methylamino)carbonyl)oxy)-2-oxo, Insecticide-nematicide 1410 insecticide-nematicide1410 Methyl-N',N'-dimethyl-N-[[methylcarbamoyl] oxy]-1-thioocamimidate oxamil (jmaf) oxamyl (bsi,iso,ansi,esa) N′,N′-Dimethylcarbamoyl(methylthio)methylenamin-N-methylcarbamat Ethanimidothiocacid,2-(dimethylamino)-N-[[(methylamino)carbonyl]oxy]-2-oxo-,methylester N',N'-dimethylcarbamoyl(methylthio)methylenamine N-methylcarbamate oxamyl 2-(dimethylamino)-n-(((methylamino)carbonyl)oxy)-ethanimidothioicacimethy 2-(dimethylamino)-n-[[(methylamino)-carbonyl]oxy]-2-oxoethanimidothioicacidme 2-Dimethylamino-1-(methylthio)glyoxal O-methylcarbamoylmonoxime 2-dimethylamino-1-(methylthio)glyoxalo-methylcarbamoylmonoxime Blade caswellno561a d 1410 d-1410 dioxamyl Dpx 1410 Dpx 1410 l Methyl (1Z)-2-(dimethylamino)-N-([(methylamino)carbonyl]oxy)-2-oxoethanimidothioate Methyl 1-(dimethylcarbamoyl)-N-(methylcarbamoyloxy)thioformimidate Methyl 2-(dimethylamino)-N-(((methylamino)carbonyl)oxy)-2-oxoethanimidothioate methyl1-(dimethylcarbamoyl)-n-(methylcarbamoyloxy)thioformimidate methyl2-(dimethylamino)-n-(((methylamino)carbonyl)oxy)-2-oxoethanimidothioat methyl2-(dimethylamino)-n-(((methylamino)carbonyl)oxy)-2-oxoethanimidothioate N,N-Dimethyl-alpha-methylcarbamoyloxyimino-alpha-(methylthio)acetamide N',N'-Dimethyl-N-((methylcarbamoyl)oxy)-1-thiooxamimidic acid methyl ester n’,n’-dimethyl-n-((methylcarbamoyl)oxy)-1-methylthio-oxamimidicaci n’,n’-dimethyl-n-((methylcarbamoyl)oxy)-1-thiooxamimidicacidmethylester n’,n’-dimethyl-n-[(methylcarbamoyl)oxy]-1-thiooxamimidicacidmethylester n’n’-dimethyl-n-((methylcarbamoyl)oxy-1-thio-oxamimidicacimethylester Nematicide 1410 Oxamimidic acid, N',N'-dimethyl-N-((methylcarbamoyl)oxy)-1-methylthio- Oxamimidic acid, N',N'-dimethyl-N-[(methylcarbamoyl)oxy]-1-thio-, methyl ester Oxamyl (pesticide) s-methyln’n’-dimethyl-n-(methylcarbamoyloxy)-1-thio-oxamimidate Vydate L insecticide/nematicide Vydate L oxamyl insecticide/nematocide vydateg vydate-g vydatek vydatel vydatelinsecticide/nematicide vydateloxamylinsecticide/nematocide METHYL-N',N'-DIMETHYL-N-[(METHYL-CARBAMOYL)OXY]-1-THIOOXAMIMIDATE METHYL-N',N'-DIMETHYL-N-[(METHYL-CARBAMOYL)OXYL]-1-THIOOXAMIMIDATE