Skip Navigation
ChemIDplus A TOXNET DATABASE LiteBrowseAdvanced

Substance Name: Chinomethionat [ISO]
RN: 2439-01-2
UNII: 888OQA249R
InChIKey: FBQQHUGEACOBDN-UHFFFAOYSA-N

Note

  • An ingredient of Morestan.

Molecular Formula

  • C10-H6-N2-O-S2

Molecular Weight

  • 234.302
 

Classification Codes

  • Acaricide
  • Agricultural Chemical
  • Fungicide, Bactericide, Wood Preservative
  • Fungicides, Industrial
  • Insecticide
  • Mutation Data
  • Pesticides
* denotes mobile formatted website

Links to Resources


Search for this InChIKey on the Web

Names and Synonyms

Results Name

  • Chinomethionat [ISO]

Name of Substance

  • Oxythioquinox
  • Quinomethionate

Synonyms

  • 1,3-Dithiolo(4,5-b)quinoxalin-2-one, 6-methyl-
  • 2,3-Quinoxalinedithiol, 6-methyl-, cyclic dithiocarbonate (ester)
  • 6-Methyl-1,3-dithiolo(4,5-b)quinoxalin-2-one
  • 6-Methyl-2,3-quinoxaline dithiocarbonate
  • 6-Methyl-2,3-quinoxalinedithiol cyclic dithiocarbonate
  • 6-Methyl-2,3-quinoxalinedithiol cyclic S,S-dithiocarbonate
  • 6-Methyl-2-oxo-1,3-dithio(4,5-b)quinoxaline
  • 6-Methyl-2-oxo-1,3-dithiolo(4,5-b)quinoxaline
  • 6-Methyl-chinoxalin-2,3-dithiol-cyclo-carbonat
  • 6-Methyl-chinoxalin-2,3-dithiol-cyclo-carbonat [German]
  • 6-Methyl-quinoxaline-2,3-dithiolcyclocarbonate
  • 6-Methyldithiolo(4,5-b)quinoxalin-2-one
  • AI3-25606
  • BAY 36205
  • Bayer 36205
  • Bayer 4964
  • Bayer ss2074
  • BRN 0526833
  • Carbonic acid, dithio-, cyclic S,S-(6-methyl-2,3-quinoxalinediyl) ester
  • Carbonic acid, dithio-, cyclic S,S-ester with 6-methyl-2,3-quinoxalinedithiol
  • Caswell No. 576
  • Cetactaelate
  • Chinomethionat
  • Chinomethionate
  • Chinomethionate [ISO-French]
  • Cyclic S,S-(6-methyl-2,3-quinoxalinediyl) dithiocarbonate
  • Daisonet XL 21
  • Dithiolo(4,5-b)quinoxalin-2-one, 6-methyl-
  • EINECS 219-455-3
  • ENT 25,606
  • EPA Pesticide Chemical Code 054101
  • Forstan
  • HSDB 1740
  • Joust
  • Morestan
  • Morestan 2
  • Morestane
  • MQD
  • NSC 379587
  • Oxythioquinox
  • Quinomethionate
  • Quinomethionate [BSI]
  • S,S-(6-Methylquinoxaline-2,3-diyl) dithiocarbonate (9CI)
  • SS 2074
  • UNII-888OQA249R

Systematic Names

  • 1,3-Dithiolo(4,5-b)quinoxalin-2-one, 6-methyl-
  • Carbonic acid, dithio-, cyclic S,S-(6-methyl-2,3-quinoxalinediyl) ester
  • Chinomethionate
  • Dithiolo(4,5-b)quinoxalin-2-one, 6-methyl- (9CI)

Superlist Names

  • 6-Methyl-1,3-dithiolo(4,5-b)quinoxalin-2-one
  • 6-Methyl-2,3-quinoxalinedithiol cyclic S,S-dithiocarbonate
  • Chinomethionat
  • Oxythioquinox

Registry Numbers

CAS Registry Number

  • 2439-01-2

FDA UNII

  • 888OQA249R

Other Registry Numbers

  • 113535-72-1
  • 85188-88-1

System Generated Number

  • 0002439012

Structure Descriptors

InChI

1S/C10H6N2OS2/c1-5-2-3-6-7(4-5)12-9-8(11-6)14-10(13)15-9/h2-4H,1H3

InChIKey

FBQQHUGEACOBDN-UHFFFAOYSA-N

Smiles

c12c(nc3ccc(cc3n1)C)sc(s2)=O

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
cat LD50 oral > 1gm/kg (1000mg/kg)   Pesticide Manual. Vol. 9, Pg. 133, 1991.
chicken LD50 oral 980mg/kg (980mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE)
Toxicology and Applied Pharmacology. Vol. 11, Pg. 49, 1967.
guinea pig LC inhalation > 5mg/m3/4H (5mg/m3)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A063, Pg. 1985,
guinea pig LD50 oral 1500mg/kg (1500mg/kg)   Pesticide Chemicals Official Compendium, Association of the American Pesticide Control Officials, Inc., 1966. Vol. -, Pg. 769, 1966.
mammal (species unspecified) LD50 unreported 2500mg/kg (2500mg/kg)   "Chemistry of Pesticides," Melnikov, N.N., New York, Springer-Verlag New York, Inc., 1971Vol. -, Pg. 182, 1971.
mouse LC inhalation > 5mg/m3/4H (5mg/m3)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A063, Pg. 1985,
mouse LD50 intraperitoneal 473mg/kg (473mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 173, Pg. 60, 1970.
mouse LDLo oral 1070mg/kg (1070mg/kg)   Archives of Environmental Contamination and Toxicology. Vol. 14, Pg. 111, 1985.
rabbit LC inhalation > 5mg/m3/4H (5mg/m3)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A063, Pg. 1985,
rabbit LD50 skin > 2gm/kg (2000mg/kg)   World Review of Pest Control. Vol. 9, Pg. 119, 1970.
rat LC50 inhalation 3gm/m3/4H (3000mg/m3)   Pesticide Manual. Vol. 9, Pg. 133, 1991.
rat LD50 intraperitoneal 95mg/kg (95mg/kg)   Pharmacologist. Vol. 9, Pg. 206, 1967.
rat LD50 oral 1100mg/kg (1100mg/kg)   World Review of Pest Control. Vol. 9, Pg. 119, 1970.
rat LD50 skin 500mg/kg (500mg/kg)   Guide to the Chemicals Used in Crop Protection. Vol. 6, Pg. 387, 1973.

Physical Properties

Physical Property Value Units Temp (deg C) Source
Melting Point 170 deg C   EXP
log P (octanol-water) 3.78 (none)   EXP
Water Solubility 1 mg/L 25 EXP
Vapor Pressure 2.00E-07 mm Hg 20 EXP
Henry's Law Constant 6.17E-08 atm-m3/mole 25 EST
Atmospheric OH Rate Constant 3.35E-12 cm3/molecule-sec 25 EST

Physical property data is provided to ChemIDplus by SRC, Inc.