Tirpate

Names
Preferred IUPAC name

N-[(2,4-Dimethyl-1,3-dithiolan-2-yl)methylidene]-N′-methylhydroxylamine-O-carboxamide

Identifiers

CAS Number

* 26419-73-8 Y

3D model (JSmol)

* Interactive image

ChemSpider |

* 30916

PubChem CID

* 33507

UNII |

* 8W03WH1E76 Y

InChI

* InChI=1S/C8H14N2O2S2/c1-6-4-13-8(2,14-6)5-10-12-7(11)9-3/h5-6H,4H2,1-3H3,(H,9,11)

Key: GHFMMRFMDHDOBP-UHFFFAOYSA-N

* InChI=1/C8H14N2O2S2/c1-6-4-13-8(2,14-6)5-10-12-7(11)9-3/h5-6H,4H2,1-3H3,(H,9,11)

Key: GHFMMRFMDHDOBP-UHFFFAOYAQ

SMILES

* O=C(ON=CC1(SCC(S1)C)C)NC

Properties

Chemical formula

| C8H14N2O2S2
Molar mass | 234.33 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Tirpate is a pesticide and nematocide. As of 1998, the United States Environmental Protection Agency listed the substance as discontinued in manufacturing. It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.[1]

Tirpate can also be used as a radiolabel in plant cultures.[2]

## References

1. ↑ 40 C.F.R.: Appendix A to Part 355—The List of Extremely Hazardous Substances and Their Threshold Planning Quantities (July 1, 2008 ed.). Government Printing Office. http://edocket.access.gpo.gov/cfr_2008/julqtr/pdf/40cfr355AppA.pdf. Retrieved October 29, 2011.
2. ↑ Hill, James E; Krieger, Robert I (1975). "Uptake, translocation, and metabolism of Tirpate in tobacco Nicotiana tabacum". Journal of Agricultural and Food Chemistry 23 (6): 1125–1129. doi:10.1021/jf60202a047. PMID 433.

* Datasheet at Cameo Chemicals

## External links

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*[CID]: Compound ID