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Substance Name: Procymidone [BSI:ISO]
RN: 32809-16-8
UNII: EC2FI67U2Y
InChIKey: QXJKBPAVAHBARF-BETUJISGSA-N

Classification Codes

  • Agricultural Chemical
  • Agrochemicals
  • Fungicide, Bactericide, Wood Preservative
  • Fungicides, Industrial
  • Mutation Data
  • Pesticides
  • Reproductive Effect

Molecular Formula

  • C13-H11-Cl2-N-O2

Molecular Weight

  • 284.1409
 
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Names and Synonyms

Results Name

  • Procymidone [BSI:ISO]

Name of Substance

  • Procymidone
  • Procymidone [BSI:ISO]

Synonyms

  • 3-(3,5-Dichlorophenyl)-1,5-dimethyl-3-azabicyclo(3.1.0)hexane-2,4-dione (9CI)
  • 3-Azabicyclo(3.1.0)hexane-2,4-dione, 3-(3,5-dichlorophenyl)-1,5-dimethyl-
  • 5-21-10-00069 (Beilstein Handbook Reference)
  • BRN 1539058
  • Dicyclidine
  • EINECS 251-233-1
  • N-(3',5'-Dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide
  • Procymidone
  • S 7131
  • SP 751011
  • Sumilex
  • Sumisclex
  • UNII-EC2FI67U2Y

Systematic Names

  • 1,2-Cyclopropanedicarboximide, N-(3,5-dichlorophenyl)-1,2-dimethyl-
  • 3-(3,5-Dichlorophenyl)-1,5-dimethyl-3-azabicyclo(3.1.0)hexane-2,4-dione
  • 3-Azabicyclo(3.1.0)hexane-2,4-dione, 3-(3,5-dichlorophenyl)-1,5-dimethyl-

Superlist Name

  • Procymidone

Registry Numbers

CAS Registry Number

  • 32809-16-8

FDA UNII

  • EC2FI67U2Y

Other Registry Numbers

  • 60120-20-9
  • 68444-90-6

System Generated Number

  • 0032809168

Structure Descriptors

InChI

1S/C13H11Cl2NO2/c1-12-6-13(12,2)11(18)16(10(12)17)9-4-7(14)3-8(15)5-9/h3-5H,6H2,1-2H3/t12-,13+

InChIKey

QXJKBPAVAHBARF-BETUJISGSA-N

Smiles

C[C@@]12C[C@]1(C)C(=O)N(C2=O)c3cc(Cl)cc(Cl)c3

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
duck LD50 unreported > 4gm/kg (4000mg/kg)   Defense des Vegetaux. Vol. 32, Pg. 137, 1978.
mammal (species unspecified) LD50 oral > 10gm/kg (10000mg/kg)   Defense des Vegetaux. Vol. 44(262), Pg. 28, 1990.
mouse LD50 intraperitoneal 1560mg/kg (1560mg/kg)   Japan Pesticide Information. Vol. (29), Pg. 16, 1976.
mouse LD50 oral 7800mg/kg (7800mg/kg)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A337, Pg. 1983,
mouse LD50 skin 7800mg/kg (7800mg/kg)   "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A337, Pg. 1983,
mouse LD50 subcutaneous > 10gm/kg (10000mg/kg)   Japan Pesticide Information. Vol. (29), Pg. 16, 1976.
quail LDLo unreported > 6637mg/kg (6637mg/kg)   Defense des Vegetaux. Vol. 32, Pg. 137, 1978.
rabbit LD50 oral 10gm/kg (10000mg/kg) AUTONOMIC NERVOUS SYSTEM: OTHER (DIRECT) PARASYMPATHOMIMETIC

BEHAVIORAL: ATAXIA

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 54(5), Pg. 77, 1989.
rat LD50 intraperitoneal 730mg/kg (730mg/kg)   Japan Pesticide Information. Vol. (29), Pg. 16, 1976.
rat LD50 oral 7gm/kg (7000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)

BEHAVIORAL: ATAXIA
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 54(5), Pg. 77, 1989.
rat LD50 skin > 2500mg/kg (2500mg/kg)   Defense des Vegetaux. Vol. 32, Pg. 137, 1978.
rat LD50 subcutaneous > 10gm/kg (10000mg/kg)   Japan Pesticide Information. Vol. (29), Pg. 16, 1976.

Physical Properties

Physical Property Value Units Temp (deg C) Source
Melting Point 166 deg C   EXP
log P (octanol-water) 3.08 (none)   EXP
Water Solubility 4.5 mg/L 25 EXP
Vapor Pressure 1.40E-04 mm Hg 25 EXP
Henry's Law Constant 1.16E-05 atm-m3/mole 25 EST
Atmospheric OH Rate Constant 7.49E-12 cm3/molecule-sec 25 EST

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