Fenpropathrin

• Formula: C₂₂H₂₃NO₃
• Molecular weight: 349.4229
• IUPAC Standard InChI: InChI=1S/C22H23NO3/c1-21(2)19(22(21,3)4)20(24)26-18(14-23)15-9-8-12-17(13-15)25-16-10-6-5-7-11-16/h5-13,18-19H,1-4H3 Copy

  
• IUPAC Standard InChIKey: XQUXKZZNEFRCAW-UHFFFAOYSA-N Copy
• CAS Registry Number: 39515-41-8
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Cyclopropanecarboxylic acid, 2,2,3,3-tetramethyl-, cyano(3-phenoxyphenyl)methyl ester; α-Cyano-3-phenoxybenzyl 2,2,3,3-tetramethyl-1-cyclopropanecarboxylate; Danitol; Danitrol; Fenpropanate; Herald; Meothrin; Rody; S 3206; SD 41706; WL 41706; XE-938; Cyano(3-phenoxyphenyl)methyl 2,2,3,3-tetramethylcyclopropanecarboxylate; Fenpropathrine; Kilumal; Tame; (.+/-.)-Fenpropathrin; Danimen; Danitol Fiori; Meiothrin; Miothrin; Smash; α-Cyano-3-phenoxybenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate; Ortho danitol; 2,2,3,3-Tetramethylcyclopropanecarboxylic acid, cyano(3-phenoxyphenyl)methyl ester (fenpropathrin)
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• Information on this page:
  • Phase change data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • IR Spectrum
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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Normal alkane RI, non-polar column, custom temperature program

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Tan, Xue, et al., 2000
Tan, Z.-C.; Xue, B.; Lu, S.-W.; Meng, S.-H.; Yuan, X.-H.; Song, Y.-J., Organometallics, 2000, 63, 1, 297-308, https://doi.org/10.1023/A:1010121427777 . [all data]

Xue, Tan, et al., 1999
Xue, B.; Tan, Z.-C.; Lu, S.-W.; Meng, S.-H.; Yuan, X.-H., Heat capacities and thermodynamic properties of fenpropathrin, Huaxue Xuebao, 1999, 57, 8, 881. [all data]

Li, Guan, et al., 1995
Li, L.; Guan, Y.; Zhou, L., Standard Kovats indexes of 20 pesticides and their identification in temperature-programmed capillary gas chromatography., Fenxi Huaxue, 1995, 23, 1, 14-19. [all data]

Department of Food Safety and Welfare, 2006
Department of Food Safety, Ministry of Health; Welfare, Analytical methods for residual compositional substances of agricultural chemicals, feed aadditives, and veterinary drugs in foods, 2006, retrieved from http://www.mhlw.go.jp/english/topics/foodsafety/positivelist060228/de/060526-1a.pdf. [all data]

Notes

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• Symbols used in this document:
  

  ΔfusH

  Enthalpy of fusion

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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