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Substance Name: Sulprofos [BSI:ISO]
RN: 35400-43-2
UNII: FUX2I5F01B
InChIKey: JXHJNEJVUNHLKO-UHFFFAOYSA-N

Molecular Formula

  • C12-H19-O2-P-S3

Molecular Weight

  • 322.452
 

Classification Codes

Classification Codes

  • Agricultural Chemical
  • Experimental Pesticide
  • Insecticide
  • Reproductive Effect

Superlist Classification Code

  • TWA 1 mg/m3; Not classifiable as a human carcinogen; BEI
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Names and Synonyms

Results Name

  • Sulprofos [BSI:ISO]

Name of Substance

  • Sulprofos
  • Sulprofos [BSI:ISO]

Synonyms

  • AI3-29149
  • BAY-NTN-9306
  • Bayer NTN 9306
  • Bolstar
  • BRN 1990231
  • Caswell No. 453AA
  • EINECS 252-545-0
  • EPA Pesticide Chemical Code 111501
  • Helothion
  • HSDB 6735
  • Mercaprofos
  • Mercaprophos
  • Merpafos
  • NTN 9306
  • O-Ethyl O-(4-(methylmercapto)phenyl)-S-n-propylphosphorothionothiolate
  • O-Ethyl O-(4-(methylthio)phenyl) S-propyl phosphorodithioate
  • O-Ethyl O-(4-(methylthio)phenyl)phosphorodithioic acid S-propyl ester
  • Sulprofos
  • UNII-FUX2I5F01B

Systematic Names

  • O-Ethyl O-(4-methylthiophenyl) S-propyl dithiophosphate
  • Phosphorodithioic acid, O-ethyl O-(4-(methylthio)phenyl) S-propyl ester

Superlist Names

  • O-Ethyl O-(4-(methylthio)phenyl)phosphorodithioic acid S-propyl ester
  • Phosphorodithioic acid, O-ethyl O-(4-(methylthio)phenyl) S-propyl ester
  • Sulprofos
  • Sulprophos

Registry Numbers

CAS Registry Number

  • 35400-43-2

FDA UNII

  • FUX2I5F01B

System Generated Number

  • 0035400432

Structure Descriptors

InChI

1S/C12H19O2PS3/c1-4-10-18-15(16,13-5-2)14-11-6-8-12(17-3)9-7-11/h6-9H,4-5,10H2,1-3H3

InChIKey

JXHJNEJVUNHLKO-UHFFFAOYSA-N

Smiles

O([P@@](SCCC)(OCC)=S)c1ccc(SC)cc1

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
chicken LD50 oral 65mg/kg (65mg/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. 1473, 1991.
mouse LD50 intraperitoneal 280mg/kg (280mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.
mouse LD50 oral 490mg/kg (490mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.
mouse LD50 skin 5gm/kg (5000mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.
mouse LD50 subcutaneous > 1gm/kg (1000mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.
rabbit LD50 skin 820mg/kg (820mg/kg)   Farm Chemicals Handbook. Vol. -, Pg. C47, 1991.
rat LC50 inhalation > 661mg/m3/4H (661mg/m3)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.
rat LD50 intraperitoneal 160mg/kg (160mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.
rat LD50 oral 65mg/kg (65mg/kg)   "Agricultural Chemicals," Thomson, W.T., 4 vols., Fresno, CA, Thomson Publications, 1976/77 revisionVol. 1, Pg. 205, 1977.
rat LD50 skin 2500mg/kg (2500mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.
rat LD50 subcutaneous 490mg/kg (490mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 12, Pg. 775, 1987.

Physical Properties

Physical Property Value Units Temp (deg C) Source
Melting Point -1.50E+01 deg C   EXP
log P (octanol-water) 5.48 (none)   EXP
Water Solubility 0.31 mg/L 20 EXP
Vapor Pressure 1.20E-06 mm Hg 25 EXP
Henry's Law Constant 1.64E-06 atm-m3/mole 25 EST
Atmospheric OH Rate Constant 1.07E-10 cm3/molecule-sec 25 EST

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