72963-72-5
Product Name:
Imiprothrin
Formula:
C17H22N2O4
Synonyms:
2-Propargylsuccinimidylmethyl chrysanthemate
Inquiry
CHEMICAL AND PHYSICAL PROPERTIES
Physical Description | Viscous brown liquids or solids; [EXTOXNET] |
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Color/Form | Viscous liquid |
Flash Point | 110 °C |
Solubility | In water, 93.5 mg/l @ 25 °C |
Density | 1.1 g/cu cm |
Vapor Pressure | 0.00000001 [mmHg] |
LogP | log Kow = 2.9 |
Stability/Shelf Life | Stable to metals, metal ions, sunlight & elevated temperature. ... Stable when stored in commercial package (steel cans) for 1 yr. |
Chemical Classes | Pesticides -> Pyrethrins/Pyrethroids |
SAFETY INFORMATION
Signal word | Warning |
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Pictogram(s) |
Exclamation Mark Irritant GHS07 Health Hazard GHS08 Environment GHS09 |
GHS Hazard Statements |
H351:Carcinogenicity H371:Specific target organ toxicity, single exposure H410:Hazardous to the aquatic environment, long-term hazard |
Precautionary Statement Codes |
P202:Do not handle until all safety precautions have been read and understood. P260:Do not breathe dust/fume/gas/mist/vapours/spray. P273:Avoid release to the environment. P301+P312:IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. |
COMPUTED DESCRIPTORS
Molecular Weight | 318.4 g/mol |
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XLogP3 | 2.1 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 6 |
Exact Mass | 318.15795719 g/mol |
Monoisotopic Mass | 318.15795719 g/mol |
Topological Polar Surface Area | 66.9 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 622 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Imiprothrin is mixture of 20% (1R)-cis- (CHEBI:39372) and 80% (1R)-trans- (CHEBI:39373) isomers. It has a role as a pyrethroid ester insecticide. It is a member of cyclopropanes and an imidazolidinone. It contains a (1R)-cis-imiprothrin and a (1R)-trans-imiprothrin. It is functionally related to a chrysanthemic acid.