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The agency recommended that DEET-based products be used on children between the ages of 2 and 12 only if the concentration of DEET is 10% or less and that repellents be applied no more than 3 times a day, children under 2 should not receive more than 1 application of repellent in a day and DEET-based products of any concentration should not be ...
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
Little is known about the chronic toxicity of diethyl phthalate, but existing information suggests only a low toxic potential. [6] Studies suggest that some phthalates affect male reproductive development via inhibition of androgen biosynthesis.
Two possible lab syntheses of 1-octen-3-ol are: [12] by the Grignard reaction of acrolein and amyl iodide; by the selective reduction of 1-octen-3-one; Biochemically, 1-octen-3-ol is generated from the peroxidation of linoleic acid, catalyzed by a lipoxygenase, followed by cleavage of the resulting hydroperoxide with the help of a hydroperoxide lyase.
Ethyl butylacetylaminopropionate is an insect repellent whose trade name is IR3535 and was developed and commercialized by Merck KGaA (Germany). It is a colorless and odorless oil with a good skin feel in final products, and it is biodegradable.
Molar mass: 136.15 g/mol Density: 1.05 g/cm 3, solid Melting point: 111 to 113 °C (232 to 235 °F; 384 to 386 K) Boiling point: 263 °C (505 °F; 536 K) Acidity (pK a) 4.27 (in water) [2] Hazards Safety data sheet (SDS) External MSDS: Related compounds
Diethylenetriamine (abbreviated Dien or DETA) and also known as 2,2’-Iminodi(ethylamine) [2]) is an organic compound with the formula HN(CH 2 CH 2 NH 2) 2.This colourless hygroscopic liquid is soluble in water and polar organic solvents, but not simple hydrocarbons.
2,5-Dimethylfuran serves as a scavenger for singlet oxygen, a property which has been exploited for the determination of singlet oxygen in natural waters.The mechanism involves a Diels-Alder reaction followed by hydrolysis, ultimately leading to diacetylethylene and hydrogen peroxide as products.