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Fenoxycarb
Names
	Preferred IUPAC name Ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate
	Other names Varikill, Insegar, Logic
Identifiers
CAS Number	72490-01-8 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:5009 ;
ChEMBL	ChEMBL15780 ;
ChemSpider	46739 ;
ECHA InfoCard	100.069.702
KEGG	C11078 ;
PubChem CID	51605;
UNII	JEN0LSV1G9 ;
CompTox Dashboard (EPA)	DTXSID7032393 ;
	InChI InChI=1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19) Key: HJUFTIJOISQSKQ-UHFFFAOYSA-N ; InChI=1/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19) Key: HJUFTIJOISQSKQ-UHFFFAOYAM";
	SMILES O=C(OCC)NCCOc2ccc(Oc1ccccc1)cc2;
Properties
Chemical formula	C17H19NO4
Molar mass	301.34 g/mol
Melting point	53.5 °C (128.3 °F; 326.6 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Fenoxycarb is an insect growth regulator.^[1]^[2]^[3] It has a low toxicity for bees, birds, and humans, but is toxic to fish.^[3] The oral LD₅₀ for rats is greater than 16,800 milligrams per kilogram (0.269 oz/lb).^[4]

Fenoxycarb is non-neurotoxic and does not have the same mode of action as other carbamate insecticides. Instead, it prevents immature insects from reaching maturity by mimicking juvenile hormone (IRAC group 7B).^[5]^[6]

References

^ Cornell University site on Fenoxycarb
^ Pener, Meir Paul; Dhadialla, Tarlochan S. (2012). "An Overview of Insect Growth Disruptors; Applied Aspects". Insect Growth Disruptors. Advances in Insect Physiology. Vol. 43. Oxford: Academic Press. pp. 1–162. doi:10.1016/B978-0-12-391500-9.00001-2. ISBN 978-0-12-391500-9. ISSN 0065-2806.
^ ^a ^b Jeschke, Peter; Witschel, Matthias; Krämer, Wolfgang; Schirmer, Ulrich (2019). "Chapter 29. Insect Molting and Metamorphosis". Modern Crop Protection Compounds. Wiley. pp. 1013–1065. doi:10.1002/9783527699261.ch29. ISBN 9783527699261.
^ U.S. Environmental Protection Agency (1983-85). Chemical Information Fact Sheet. Office of Pesticides and Toxic Substances, Office of Pesticide Programs (TS-766C)
^ John Sullivan, Dept. of Pesticide Regulation, Sacramento CA 2000
^ Dhadialla, Tarlochan S.; Carlson, Glenn R.; Le, Dat P. (1998). "New insecticides with ecdysteroidal and juvenile hormone activity". Annual Review of Entomology. 43 (1). Annual Reviews: 545–569. doi:10.1146/annurev.ento.43.1.545. ISSN 0066-4170. PMID 9444757.

External links

Fenoxycarb in the Pesticide Properties DataBase (PPDB)

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[1] Cornell University site on Fenoxycarb

[:0-2] Pener, Meir Paul; Dhadialla, Tarlochan S. (2012). "An Overview of Insect Growth Disruptors; Applied Aspects". Insect Growth Disruptors. Advances in Insect Physiology. Vol. 43. Oxford: Academic Press. pp. 1–162. doi:10.1016/B978-0-12-391500-9.00001-2. ISBN 978-0-12-391500-9. ISSN 0065-2806.

[:022-3] Jeschke, Peter; Witschel, Matthias; Krämer, Wolfgang; Schirmer, Ulrich (2019). "Chapter 29. Insect Molting and Metamorphosis". Modern Crop Protection Compounds. Wiley. pp. 1013–1065. doi:10.1002/9783527699261.ch29. ISBN 9783527699261.

[4] U.S. Environmental Protection Agency (1983-85). Chemical Information Fact Sheet. Office of Pesticides and Toxic Substances, Office of Pesticide Programs (TS-766C)

[5] John Sullivan, Dept. of Pesticide Regulation, Sacramento CA 2000

[Dhadialla-et-al-1998-6] Dhadialla, Tarlochan S.; Carlson, Glenn R.; Le, Dat P. (1998). "New insecticides with ecdysteroidal and juvenile hormone activity". Annual Review of Entomology. 43 (1). Annual Reviews: 545–569. doi:10.1146/annurev.ento.43.1.545. ISSN 0066-4170. PMID 9444757.

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