SMILES string
CCN(CC)C(=O)c1cccc(C)c1
InChI key
MMOXZBCLCQITDF-UHFFFAOYSA-N
InChI
1S/C12H17NO/c1-4-13(5-2)12(14)11-8-6-7-10(3)9-11/h6-9H,4-5H2,1-3H3
grade
analytical standard
packaging
ampule of 250 mg
manufacturer/tradename
Chem Service, Inc. PS-902
P J Robbins et al.
Journal of toxicology and environmental health, 18(4), 503-525 (1986-01-01)
A review of the biodistribution and toxicity of the insect repellent N,N-diethyl-m-toluamide (DEET) is presented. Workers using repellent containing this compound may be exposed to greater than 442 g in 6 mo. In human studies, variable penetration into the skin
Daniel L Sudakin et al.
Journal of toxicology. Clinical toxicology, 41(6), 831-839 (2003-12-18)
The emergence of West Nile Virus (WNV) in North America has resulted in increased public awareness and utilization of insect repellents containing N,N-diethyl-m-toluamide (DEET) in the prevention of mosquito-borne disease. Regulatory reassessments in North American countries have recently been completed
T G Osimitz et al.
Journal of toxicology. Clinical toxicology, 35(5), 435-441 (1997-01-01)
N,N-Diethyl-m-toluamide, an effective tick repellent, when applied to the skin, is the major component of essentially all of the products marketed for this purpose. It is used by about 30% of the US population, and by 23-29% of children in
J R Clem et al.
The Annals of pharmacotherapy, 27(3), 289-293 (1993-03-01)
To describe a case of N,N-diethyl-m-toluamide (DEET)-induced cardiovascular toxicity in an adult and reviews other cases that have been reported in the published literature. Human and animal data available on DEET pharmacokinetics are reviewed and factors that predispose an individual
Pinky Kain et al.
Nature, 502(7472), 507-512 (2013-10-04)
There are major impediments to finding improved DEET alternatives because the receptors causing olfactory repellency are unknown, and new chemicals require exorbitant costs to determine safety for human use. Here we identify DEET-sensitive neurons in a pit-like structure in the
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