Difference between revisions of "Ronnel"

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[[File:ronnelir.jpg|thumb|Infrared spectrum of ronnel (gas phase)]]
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[[File:ronnelms.jpg|thumb|Mass spectrum of ronnel]]
 
== Description ==
 
== Description ==
  
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A non-US trademark for a light brown, solid [http://cameo.mfa.org/materials/fullrecord.asp?name=insecticide insecticide]. Ronnel is an organophosphate compound that works as a cholinesterase inhibitor. It has been used on livestock and dogs to kill fleas, ticks, and flies. Ronnel was formerly used in household formulations for [http://cameo.mfa.org/materials/fullrecord.asp?name=cockroach cockroaches], [http://cameo.mfa.org/materials/fullrecord.asp?name=termite termites], and ants. The crystalline powder was patented by Bayer in 1948.
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A non-US trademark for a light brown, solid [[insecticide|insecticide]]. Ronnel is an organophosphate compound that works as a cholinesterase inhibitor. It has been used on livestock and dogs to kill fleas, ticks, and flies. Ronnel was formerly used in household formulations for [[cockroach|cockroaches]], [[termite|termites]], and ants. The crystalline powder was patented by Bayer in 1948.
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[[[SliderGallery rightalign|ronnelir.jpg~FTIR|ronnelstr.jpg~Chemical structure]]]
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
 
phosphorothioic acid; O,O-dimethyl-O-(2,4,5 trichlorophenyl)phosphorothioate; fenchlorophos; fenchlorphos; dimethyl trichlorophenyl thiophosphate; trichlormetaphos
 
phosphorothioic acid; O,O-dimethyl-O-(2,4,5 trichlorophenyl)phosphorothioate; fenchlorophos; fenchlorphos; dimethyl trichlorophenyl thiophosphate; trichlormetaphos
  
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[[[SliderGallery rightalign|ronnelstr.jpg~Chemical structure]]]
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== Risks ==
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* Toxic by ingestion and inhalation.
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* Skin contact causes irritation.
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* ChemService: [http://cdn.chemservice.com/product/msdsnew/External/English/N-11952%20English%20SDS%20US.pdf SDS]
  
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== Other Properties ==
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==Physical and Chemical Properties==
  
 
Soluble in most organic solvents. Insoluble in water.
 
Soluble in most organic solvents. Insoluble in water.
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! scope="row"| Melting Point
 
! scope="row"| Melting Point
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| 41
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| 41 C
 
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! scope="row"| Density
 
! scope="row"| Density
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| 1.485
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| 1.485 g/ml
 
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|-
 
! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
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|-
 
! scope="row"| Boiling Point
 
! scope="row"| Boiling Point
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| 97
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| 97 C
 
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|}
  
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== Hazards and Safety ==
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==Resources and Citations==
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Toxic by ingestion and inhalation. Skin contact causes irritation.
 
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LINK: [http://www.cdc.gov/niosh/ipcsneng/neng0975.html International Chemical Safety Card]
 
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== Additional Images ==
 
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<gallery>
 
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File:ronnelms.jpg|Mass spectrum of ronnel
 
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</gallery>
 
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== Authority ==
 
  
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* Richard S. Lewis, Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
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* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
  
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* Pam Hatchfield, Pam Hatchfield, ''Pollutants in the Museum Environment'', Archetype Press, London, 2002
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* Pam Hatchfield, ''Pollutants in the Museum Environment'', Archetype Press, London, 2002
  
 
* ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983  Comment: entry 8415
 
* ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983  Comment: entry 8415
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* ''The American Heritage Dictionary'' or ''Encarta'', via Microsoft Bookshelf 98, Microsoft Corp., 1998
 
* ''The American Heritage Dictionary'' or ''Encarta'', via Microsoft Bookshelf 98, Microsoft Corp., 1998
  
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* Website address 1, Website address 1  Comment: Spectrum Laboratory - Chemical Fact sheet at http://www.speclab.com/compound/c299843.htm
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* Spectrum Laboratory - Chemical Fact sheet at http://www.speclab.com/compound/c299843.htm
  
  
  
 
[[Category:Materials database]]
 
[[Category:Materials database]]

Latest revision as of 14:22, 27 June 2022

Mass spectrum of ronnel

Description

A non-US trademark for a light brown, solid Insecticide. Ronnel is an organophosphate compound that works as a cholinesterase inhibitor. It has been used on livestock and dogs to kill fleas, ticks, and flies. Ronnel was formerly used in household formulations for cockroaches, termites, and ants. The crystalline powder was patented by Bayer in 1948.

FTIR

Ronnelir.jpg

Chemical structure

Ronnelstr.jpg

Synonyms and Related Terms

phosphorothioic acid; O,O-dimethyl-O-(2,4,5 trichlorophenyl)phosphorothioate; fenchlorophos; fenchlorphos; dimethyl trichlorophenyl thiophosphate; trichlormetaphos

Risks

  • Toxic by ingestion and inhalation.
  • Skin contact causes irritation.
  • ChemService: SDS

Physical and Chemical Properties

Soluble in most organic solvents. Insoluble in water.

Composition (CH3O)2P(S)OC6H2Cl3
CAS 299-84-3
Melting Point 41 C
Density 1.485 g/ml
Molecular Weight mol. wt. = 321.57
Boiling Point 97 C

Resources and Citations

  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • Pam Hatchfield, Pollutants in the Museum Environment, Archetype Press, London, 2002
  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 8415
  • The American Heritage Dictionary or Encarta, via Microsoft Bookshelf 98, Microsoft Corp., 1998

Retrieved from "https://cameo.mfa.org/index.php?title=Ronnel&oldid=88948"