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2. How to clean your dog’s ears - AOL

   www.aol.com/news/clean-dog-ears-192622604.html

   Vets explain the best way to clean your dog or cat’s ears, plus recommend the best pet ear cleaning solutions to use. ... The cleanser can be used on dogs or cats and is free of harsh chemicals ...

3. Quenching (fluorescence) - Wikipedia

   en.wikipedia.org/wiki/Quenching_(fluorescence)

   Dexter (also known as Dexter exchange or collisional energy transfer, colloquially known as Dexter Energy Transfer) is another dynamic quenching mechanism. [12] Dexter electron transfer is a short-range phenomenon that falls off exponentially with distance (proportional to e −kR where k is a constant that depends on the inverse of the van der Waals radius of the atom [citation needed]) and ...

4. Otitis externa in animals - Wikipedia

   en.wikipedia.org/wiki/Otitis_externa_in_animals

   Signs of ear infection include shaking of the head, and scratching at or under the ear. Some animals may also paw the ear or try to rub it on other objects to relieve pain and discomfort. Ear infections often result in a darker red ear, dirt in the ear, or a general inflamed appearance. Chronic allergic otitis externa in a dog with atopic ...

5. Quenching - Wikipedia

   en.wikipedia.org/wiki/Quenching

   Quenching can also be accomplished using inert gases, such as nitrogen and noble gases. Nitrogen is commonly used at greater than atmospheric pressure ranging up to 20 bar absolute. Helium is also used because its thermal capacity is greater than nitrogen.

6. Burow's solution - Wikipedia

   en.wikipedia.org/wiki/Burow's_solution

   The preparation has astringent and antibacterial properties and may be used to treat a number of skin conditions, including insect bites and stings, rashes caused by poison ivy and poison sumac, swelling, allergies, and bruises. However, its main use is for treatment of otitis (ear infection), including otomycosis (fungal ear infection). [2]

7. Methyl chloroformate - Wikipedia

   en.wikipedia.org/wiki/Methyl_chloroformate

   Methyl chloroformate is used in organic synthesis for the introduction of the methoxycarbonyl functionality to a suitable nucleophile (i.e. carbomethoxylation). [5]