Product Name

  • Name

    Methomyl

  • EINECS 240-815-0
  • CAS No. 16752-77-5
  • Article Data7
  • CAS DataBase
  • Density 1.17 g/cm3
  • Solubility 5.8 g/100 mL in water
  • Melting Point 78 °C
  • Formula C5H10N2O2S
  • Boiling Point 144 °C
  • Molecular Weight 162.213
  • Flash Point
  • Transport Information UN 2757
  • Appearance white crystalline solid
  • Safety 1/2-22-36/37-60-61-45-16-36-26
  • Risk Codes 28-50/53-36-20/21/22-11-36/37/38
  • Molecular Structure Molecular Structure of 16752-77-5 (Methomyl)
  • Hazard Symbols VeryT+,DangerousN,HarmfulXn,FlammableF,IrritantXi
  • Synonyms Lanox 90;Mie Duo Wei;Du Pont 1179;Methyl N-(((methylamino)carbonyl)oxy)ethanimidothioate;Methomex;1-(Methylthio)ethylideneamino methylcarbamate;Dunet;Du Pont insecticide 1179;Lannate;S-Methyl N-(methylcarbamoyloxy)thioacetimidate;Insecticide 1,179;Methyl O-(methylcarbamoyl)thiolacetohydroxamate;Dupont 1179;Acetimidic acid, N-((methylcarbamoyl)oxy)thio-, methyl ester (8CI);Acetimidothioic acid, methyl-, N-(methylcarbamoyl) ester;
  • PSA 75.99000
  • LogP 1.42970

Methomyl Chemical Properties

Molecular Structure of Methomyl (CAS NO.16752-77-5):

IUPAC Name: Methyl (1E)-N-(methylcarbamoyloxy)ethanimidothioate 
Molecular Weight: 162.2101 g/mol
Molecular Formula: C5H10N2O2
Density: 1.17 g/cm3 
Melting Point: 78°C
Boiling Point: 144°C
Index of Refraction: 1.508
Molar Refractivity: 41.18 cm3
Molar Volume: 137.9 cm3
Surface Tension: 36.3 dyne/cm
XLogP3: 0.6
H-Bond Donor: 1
H-Bond Acceptor: 3
Rotatable Bond Count: 3
Tautomer Count: 2
Exact Mass: 162.046298
MonoIsotopic Mass: 162.046298
Topological Polar Surface Area: 50.7
Heavy Atom Count: 10 
Storage Temp.: 0-6 °C
Water Solubility: 5.8 g/100 mL
Canonical SMILES: CC(=NOC(=O)NC)SC
Isomeric SMILES: C/C(=N\OC(=O)NC)/SC
InChI: InChI=1S/C5H10N2O2S/c1-4(10-3)7-9-5(8)6-2/h1-3H3,(H,6,8)/b7-4+
InChIKey: UHXUZOCRWCRNSJ-QPJJXVBHSA-N
EINECS: 240-815-0
Product Categories: INSECTICIDE; Alpha sort; CarbamatesMethod Specific; Endocrine Disruptors (Draft)Pesticides&Metabolites; EPA; H-MAlphabetic; Insecticides; M; META - METH; Pesticides; Endocrine Disruptors (Draft)Alphabetic 

Methomyl Uses

 Methomyl (CAS NO.16752-77-5) is a carbamate insecticide. It was introduced in 1966, but its use is restricted because of its high toxicity to humans. Its current primary use is on alfalfa for forage.

Methomyl Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
bird - wild LD50 oral 10mg/kg (10mg/kg)   Toxicology and Applied Pharmacology. Vol. 21, Pg. 315, 1972.
 
chicken LD50 oral 28mg/kg (28mg/kg) SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Toxicology and Applied Pharmacology. Vol. 40, Pg. 1, 1977.
 
dog LD50 oral 20mg/kg (20mg/kg)   "Documentation of the Threshold Limit Values and Biological Exposure Indices," 5th ed., Cincinnati, OH, American Conference of Governmental Industrial Hygienists, Inc., 1986Vol. 6, Pg. 906, 1991.
duck LC50 inhalation 1890ppm (1890ppm)   Toxicology and Applied Pharmacology. Vol. 40, Pg. 1, 1977.
 
duck LD50 oral 15mg/kg (15mg/kg)   Shell Chemical Company.
guinea pig LDLo oral 15mg/kg (15mg/kg)   Toxicology and Applied Pharmacology. Vol. 40, Pg. 1, 1977.
 
monkey LDLo oral 40mg/kg (40mg/kg)   Toxicology and Applied Pharmacology. Vol. 40, Pg. 1, 1977.
 
mouse LD50 oral 10mg/kg (10mg/kg)   Journal of Agricultural and Food Chemistry. Vol. 26, Pg. 550, 1978.
 
pigeon LD50 oral 10mg/kg (10mg/kg)   ASTM Special Technical Publication. Vol. (680), Pg. 157, 1979.
quail LC50 inhalation 3680ppm (3680ppm)   Toxicology and Applied Pharmacology. Vol. 40, Pg. 1, 1977.
 
quail LD50 oral 23700ug/kg (23.7mg/kg)   ASTM Special Technical Publication. Vol. (680), Pg. 157, 1979.
rabbit LD50 skin 5880mg/kg (5880mg/kg)   Farm Chemicals Handbook. Vol. -, Pg. C199, 1991.
rat LC50 inhalation 77ppm/4H (77ppm) SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE

BEHAVIORAL: TREMOR

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Toxicology and Applied Pharmacology. Vol. 40, Pg. 1, 1977.
 
rat LD50 intraperitoneal 6290ug/kg (6.29mg/kg) BEHAVIORAL: TREMOR

BEHAVIORAL: STRAUB TAIL

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Environmental Toxicology and Pharmacology. Vol. 7, Pg. 119, 1999.
rat LD50 oral 14700ug/kg (14.7mg/kg)   Weisheng Dulixue Zazhi. Journal of Health Toxicology. Vol. 6, Pg. 37, 1992.
rat LD50 skin > 1600mg/kg (1600mg/kg)   World Review of Pest Control. Vol. 9, Pg. 119, 1970.
rat LD50 subcutaneous 9mg/kg (9mg/kg)   Toxicology and Applied Pharmacology. Vol. 25, Pg. 569, 1973.
 

Methomyl Safety Profile

Hazard Codes: VeryT+, DangerousN, HarmfulXn, FlammableF, IrritantXi
Risk Statements: 28-50/53-36-20/21/22-11-36/37/38 
R28:Very toxic if swallowed. 
R50/53:Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
R36:Irritating to eyes. 
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed. 
R11:Highly flammable. 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 1/2-22-36/37-60-61-45-16-36-26 
S1/2:Keep locked up and out of the reach of children. 
S22:Do not breathe dust. 
S36/37:Wear suitable protective clothing and gloves. 
S60:This material and its container must be disposed of as hazardous waste. 
S61:Avoid release to the environment. Refer to special instructions / safety data sheets. 
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) 
S16:Keep away from sources of ignition. 
S36:Wear suitable protective clothing. 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
RIDADR: UN 2757
RTECS: AK2975000
HazardClass: 6.1(a)
PackingGroup: II 

Methomyl Specification

 Methomyl (CAS NO.16752-77-5) is also named as 1-(Methylthio)acetaldehyde O-methylcarbamoyloxime ; 1-(Methylthio)ethylideneamino methylcarbamate ; 2-Methylthio-acetaldehyd-O-(methylcarbamoyl)-oxim ; 2-Methylthio-acetaldehyd-O-(methylcarbamoyl)-oxim [German] ; 2-Methylthio-propionaldehyd-O-(methylcarbamoyl)-oxim ; 2-Methylthio-propionaldehyd-O-(methylcarbamoyl)-oxim [German] ; 3-Thiabutan-2-one, O-(methylcarbamoyl)oxime ; AI3-27341 ; Acetimidothioic acid, methyl-, N-(methylcarbamoyl) ester ; BRN 2042050 ; Caswell No. 549C ; Du Pont insecticide 1179 ; Dupont 1179 ; ENT 27,341 ; EPA Pesticide Chemical Code 090301 ; Ethanimidothioic acid, N-(((methylamino)carbonyl)oxy)-, methyl ester (9CI) ; HSDB 1736 ; IN 1179 ; Insecticide 1,179 ; Lannate ; Lannate L ; Lannate LV ; Methyl O-(methylcarbamyl)thiolacetohydroxamate ; Metomil ; Metomil [Italian] ; N-(((Methylamino)carbonyl)oxy)ethanimidothioic acid methyl ester ; N-((Methylcarbamoyl)oxy)thioacetimidic acid methyl ester ; NU-Bait II ; Nudrin ; RCRA waste number P066 ; S-Methyl N-(methylcarbamoyloxy)thioacetimidate ; SD 14999 ; WL 18236 .  Methomyl (CAS NO.16752-77-5) is white crystalline solid with slight sulfurous smell. It is water soluble. Methomyl is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. Methomyl has high oral toxicity, moderate inhalation toxicity and low skin toxicity. When heated to decomposition, Methomyl emits very toxic fumes of nitrogen oxides and sulfur oxides.

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