Nithiazine

Last updated
Nithiazine.svg
Names
IUPAC name
(E/Z)-2-Nitromethylene-1,3-thiazinane
Identifiers
  • 58842-20-9 Yes check.svgY
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.107.942 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 611-751-4
PubChem CID
UNII
  • InChI=1S/C5H8N2O2S/c8-7(9)4-5-6-2-1-3-10-5/h4,6H,1-3H2/b5-4-
  • O=[N+](C=C1SCCCN1)[O-]
Properties
C5H8N2O2S
Molar mass 160.19 g·mol−1
AppearanceCrystals or brown powder
Density 1.388 g/cm3
Hazards
GHS classification and labelling:
GHS-pictogram-exclam.svg
Warning
H302, H312, H315, H319, H332, H335
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Nithiazine is a nitromethylene neonicotinoid insecticide. It is irritating to the eyes and skin, and is moderately toxic to mammals. [2]

Nithiazine does not act as an acetylcholinesterase inhibitor. [3]

Related Research Articles

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Insecticides are substances used to kill insects. They include ovicides and larvicides used against insect eggs and larvae, respectively. Insecticides are used in agriculture, medicine, industry and by consumers. Insecticides are claimed to be a major factor behind the increase in the 20th-century's agricultural productivity. Nearly all insecticides have the potential to significantly alter ecosystems; many are toxic to humans and/or animals; some become concentrated as they spread along the food chain.

Pyrethrum was a genus of several Old World plants now classified as Chrysanthemum or Tanacetum which are cultivated as ornamentals for their showy flower heads. Pyrethrum continues to be used as a common name for plants formerly included in the genus Pyrethrum. Pyrethrum is also the name of a natural insecticide made from the dried flower heads of Chrysanthemum cinerariifolium and Chrysanthemum coccineum. Its active ingredient are pyrethrins.

Pyrethrin Class of organic chemical compounds with insecticidal properties

The pyrethrins are a class of organic compounds normally derived from Chrysanthemum cinerariifolium that have potent insecticidal activity by targeting the nervous systems of insects. Pyrethrin naturally occurs in chrysanthemum flowers and is often considered an organic insecticide when it is not combined with piperonyl butoxide or other synthetic adjuvants. Their insecticidal and insect-repellent properties have been known and used for thousands of years.

Fenobucarb Chemical compound

Fenobucarb is a carbamate insecticide, also widely known as BPMC. A pale yellow or pale red liquid, insoluble in water; used as an agricultural insecticide, especially for control of Hemipteran pests, on rice and cotton and moderately toxic for humans.

Carbaryl Chemical compound

Carbaryl is a chemical in the carbamate family used chiefly as an insecticide. It is a white crystalline solid previously sold under the brand name Sevin, which was a trademark of the Bayer Company. The Sevin trademark has since been acquired by GardenTech, which has eliminated carbaryl from most Sevin formulations. Union Carbide discovered carbaryl and introduced it commercially in 1958. Bayer purchased Aventis CropScience in 2002, a company that included Union Carbide pesticide operations. Carbaryl was the third-most-used insecticide in the United States for home gardens, commercial agriculture, and forestry and rangeland protection. As a veterinary drug, it is known as carbaril (INN).

Isoxathion Chemical compound

Isoxathion is a molecular chemical with the molecular formula C13H16NO4PS. It is an insecticide, specifically an isoxazole organothiophosphate insecticide.

Mosquito net Fine net used to exclude mosquitos and other biting insects

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Tetramethrin Chemical compound

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Deltamethrin Chemical compound

Deltamethrin is a pyrethroid ester insecticide. Deltamethrin plays a key role in controlling malaria vectors, and is used in the manufacture of long-lasting insecticidal mosquito nets; however, resistance of mosquitos and bed bugs to deltamethrin is becoming widespread.

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Paraoxon

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Indoxacarb Chemical compound

Indoxacarb is an oxadiazine pesticide developed by DuPont that acts against lepidopteran larvae. It is marketed under the names Indoxacarb Technical Insecticide, Steward Insecticide and Avaunt Insecticide. It is also used as the active ingredient in Syngenta line of commercial pesticides: Advion and Arilon.

Pyriprole

Pyriprole is for veterinary use on dogs against external parasites such as fleas and ticks.

Cyphenothrin Chemical compound

Cyphenothrin is a synthetic pyrethroid insecticide. It is effective against cockroaches that have developed resistance to organophosphorous and carbamate insecticides.

Trichloronate Chemical compound

Trichloronate is a highly toxic organophosphate insecticide. It is used against vegetable fly larvae and soil pests.

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Cyantraniliprole Chemical compound

Cyantraniliprole is an insecticide of the ryanoid class, specifically a diamide insecticide. It is approved for use in the United States, Canada, China, and India. Because of its uncommon mechanism of action as a ryanoid, it has activity against pests such as Diaphorina citri that have developed resistance to other classes of insecticides. Cyantraniliprole is highly toxic to bees, which resulted in registration of its use as a pesticide being delayed in the USA.

Schradan Chemical compound

Schradan, named after Gerhard Schrader, is an obsolete organophosphate insecticide. Schradan itself is a weak cholinesterase inhibitor and requires metabolic activation to become active.

DFDT Chemical compound, insecticide

Difluorodiphenyltrichloroethane (DFDT) is a chemical compound. Its composition is the same as that of the insecticide DDT, except that two of DDT's chlorine atoms are replaced by two fluorine atoms.

R-16661 Chemical compound

R-16661 is an extremely toxic organophosphate insecticide. With an oral LD50 of 0.1 mg/kg in mice and rats, R-16661 is about 10 times more toxic than aldicarb, the most toxic carbamate insecticide.

References

  1. (Z)-nithiazine CSID:5013776, chemspider.com/Chemical-Structure (accessed 04:44, Jan 14, 2013)
  2. "nithiazine (Ref: BA 32476 )". University of Hertfordshire.
  3. Schroeder, M. E.; Flattum, R. F. (October 1984). "The Mode of Action and Neurotoxic Properties of the Nitromethylene Heterocycle Insecticides". Pesticide Biochemistry and Physiology. 22 (2): 148–160. doi:10.1016/0048-3575(84)90084-1.