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Substance Name: Profenofos [ANSI:BSI:ISO]
RN: 41198-08-7
UNII: 7J04O7BS4W
InChIKey: QYMMJNLHFKGANY-UHFFFAOYSA-N

Classification Codes

  • Acaricide
  • Agricultural Chemical
  • Human Data
  • Insecticide
  • Insecticides
  • Mutation Data
  • Pesticides
  • Reproductive Effect

Molecular Formula

  • C11-H15-Br-Cl-O3-P-S

Molecular Weight

  • 373.634
 

Names and Synonyms

Results Name

  • Profenofos [ANSI:BSI:ISO]

Name of Substance

  • Profenofos
  • Profenofos [ANSI:BSI:ISO]

Synonyms

  • AI3-29236
  • BRN 2150258
  • Caswell No. 266AA
  • CCRIS 9291
  • CGA 15324
  • Curacron
  • EC 255-255-2
  • EINECS 255-255-2
  • EPA Pesticide Chemical Code 111401
  • HSDB 6992
  • O-(4-Bromo-2-chlorophenyl)-O-ethyl-S-propyl phosphorothioate
  • Phosphorothioic acid, O-(4-bromo-2-chlorophenyl) O-ethyl S-propyl ester (9CI)
  • Phosphorothioic acid, O-(4-bromo-2-chlorophenyl)-O-ethyl S-propyl ester
  • Polycron
  • Profenofos
  • Selecron
  • UNII-7J04O7BS4W

Systematic Names

  • O-(4-Bromo-2-chlorophenyl) O-ethyl S-propyl phosphorothioate
  • Phosphorothioic acid, O-(4-bromo-2-chlorophenyl) O-ethyl S-propyl ester

Superlist Names

  • Curacron
  • O-(4-Bromo-2-chlorophenyl) O-ethyl S-propyl phosphorothioate
  • O-(4-Bromo-2-chlorophenyl)-O-ethyl-S-propylphosphorothioate
  • Profenofos

Registry Numbers

CAS Registry Number

  • 41198-08-7

FDA UNII

  • 7J04O7BS4W

Other Registry Numbers

  • 61230-42-0
  • 61287-51-2

System Generated Number

  • 0041198087

Structure Descriptors

InChI

1S/C11H15BrClO3PS/c1-3-7-18-17(14,15-4-2)16-11-6-5-9(12)8-10(11)13/h5-6,8H,3-4,7H2,1-2H3

InChIKey

QYMMJNLHFKGANY-UHFFFAOYSA-N

Smiles

c1(O[P@@](SCCC)(OCC)=O)c(cc(Br)cc1)Cl

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
chicken LD50 oral 1900ug/kg (1.9mg/kg) BEHAVIORAL: TREMOR

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Toxicology and Applied Pharmacology. Vol. 73, Pg. 16, 1984.
mouse LD50 intraperitoneal 116mg/kg (116mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 781, 1987.
mouse LD50 oral 162mg/kg (162mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS

BEHAVIORAL: TREMOR
Toxicology and Applied Pharmacology. Vol. 73, Pg. 16, 1984.
mouse LD50 subcutaneous 2gm/kg (2000mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 781, 1987.
rabbit LD50 oral 700mg/kg (700mg/kg)   Ciba-Geigy Toxicology Data/Indexes. Vol. -, Pg. -, 1977.
rabbit LD50 skin 192mg/kg (192mg/kg)   Farm Chemicals Handbook. Vol. -, Pg. C87, 1991.
rat LC50 inhalation 3gm/m3/4H (3000mg/m3)   Pesticide Manual. Vol. 9, Pg. 7705, 1991.
rat LD50 intraperitoneal 520mg/kg (520mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 781, 1987.
rat LD50 oral 358mg/kg (358mg/kg)   Pesticide Manual. Vol. 9, Pg. 705, 1991.
rat LD50 skin 1610mg/kg (1610mg/kg)   Ciba-Geigy Toxicology Data/Indexes. Vol. -, Pg. -, 1977.
rat LD50 subcutaneous 3200mg/kg (3200mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 781, 1987.
women LDLo oral 2240uL/kg (2.24mL/kg) SENSE ORGANS AND SPECIAL SENSES: MIOSIS (PUPILLARY CONSTRICTION): EYE

GASTROINTESTINAL: OTHER CHANGES

GASTROINTESTINAL: CHANGE IN STRUCTURE OR FUNCTION OF ESOPHAGUS
Journal of Toxicology, Clinical Toxicology. Vol. 36, Pg. 63, 1998.

Physical Properties

Physical Property Value Units Temp (deg C) Source
Melting Point < 25 deg C   EXP
log P (octanol-water) 4.68 (none)   EXP
Water Solubility 28 mg/L 25 EXP
Vapor Pressure 9.00E-07 mm Hg 25 EXP
Henry's Law Constant 2.21E-08 atm-m3/mole 25 EST
Atmospheric OH Rate Constant 4.48E-11 cm3/molecule-sec 25 EST

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