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Substance Name: Fluazifop-butyl [ISO]
RN: 69806-50-4
UNII: 12O1Z35LQA
InChIKey: VAIZTNZGPYBOGF-UHFFFAOYSA-N

Classification Codes

  • Agricultural Chemical
  • Herbicide
  • Herbicides
  • Pesticides
  • Reproductive Effect
  • Skin / Eye Irritant

Molecular Formula

  • C19-H20-F3-N-O4

Molecular Weight

  • 383.364
 
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Names and Synonyms

Results Name

  • Fluazifop-butyl [ISO]

Name of Substance

  • Fluazifop-butyl
  • Fluazifop-butyl [ISO]

Synonyms

  • (+-)-Butyl-2-(4-(((5-trifluoro-methyl)-2-pyridinyl)oxy)phenoxy)propanoate
  • BRN 1510062
  • Butyl 2-(4-(5-trifluoromethyl-2-pyridinyloxy)phenoxy)propanoate
  • Caswell No. 460C
  • EINECS 274-125-6
  • EPA Pesticide Chemical Code 122805
  • Fluazifop-butyl
  • Fusilade
  • Fusilade 4E
  • Hache uno super
  • Halokon
  • HSDB 6644
  • IH 773B
  • Onecide
  • Onecide EC
  • PP 009
  • Propionic acid, 2-(p-((5-(trifluoromethyl)-2-pyridyl)oxy)phenoxy)-, butyl ester
  • SL-236
  • TF 1169
  • TS-7236
  • UNII-12O1Z35LQA

Systematic Names

  • Butyl 2-(4-((5-(trifluoromethyl)-2-pyridyl)oxy)phenoxy)propionate
  • Propanoic acid, 2-(4-((5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-, butyl ester

Superlist Names

  • 2-(4-((5-(Trifluoromethyl)-2-pyridinyl)oxy)phenoxy)propanoic acid butyl ester
  • 2-(4-((5-(Trifluoromethyl)-2-pyridinyl)oxy)phenoxy)propanoic acid, butyl ester
  • Butyl (RS)-2-(4-((5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)propanoate
  • Fluazifop butyl

Registry Numbers

CAS Registry Number

  • 69806-50-4

FDA UNII

  • 12O1Z35LQA

System Generated Number

  • 0069806504

Structure Descriptors

InChI

1S/C19H20F3NO4/c1-3-4-11-25-18(24)13(2)26-15-6-8-16(9-7-15)27-17-10-5-14(12-23-17)19(20,21)22/h5-10,12-13H,3-4,11H2,1-2H3

InChIKey

VAIZTNZGPYBOGF-UHFFFAOYSA-N

Smiles

CCCCOC(=O)C(C)Oc1ccc(Oc2ccc(cn2)C(F)(F)F)cc1

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
duck LD50 oral 17gm/kg (17000mg/kg)   Defense des Vegetaux. Vol. 36, Pg. 251, 1982.
guinea pig LD50 oral 2659mg/kg (2659mg/kg)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A535, Pg. 1984,
mouse LD50 intraperitoneal 1240mg/kg (1240mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 15, Pg. 305, 1990.
mouse LD50 oral 1490mg/kg (1490mg/kg)   Pesticide Manual. Vol. 9, Pg. 400, 1991.
mouse LD50 subcutaneous > 2gm/kg (2000mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 15, Pg. 305, 1990.
rabbit LD50 oral 621mg/kg (621mg/kg)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A535, Pg. 1984,
rabbit LD50 skin > 2420mg/kg (2420mg/kg)   Defense des Vegetaux. Vol. 36, Pg. 251, 1982.
rat LC50 inhalation > 5240mg/m3 (5240mg/m3)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 15, Pg. 305, 1990.
rat LD50 intraperitoneal 1620mg/kg (1620mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 15, Pg. 305, 1990.
rat LD50 oral 2910mg/kg (2910mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 15, Pg. 305, 1990.
rat LD50 skin > 6050mg/kg (6050mg/kg)   Defense des Vegetaux. Vol. 36, Pg. 251, 1982.
rat LD50 subcutaneous > 5gm/kg (5000mg/kg)   Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 15, Pg. 305, 1990.

Physical Properties

Physical Property Value Units Temp (deg C) Source
Melting Point 13 deg C   EXP
log P (octanol-water) 4.5 (none)   EXP
Water Solubility 1 mg/L 25 EXP
Vapor Pressure 4.12E-07 mm Hg 20 EXP
Henry's Law Constant 2.08E-07 atm-m3/mole 25 EST
Atmospheric OH Rate Constant 3.01E-11 cm3/molecule-sec 25 EST

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