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  2. Maropitant - Wikipedia

    en.wikipedia.org/wiki/Maropitant

    Side effects in dogs and cats include hypersalivation, diarrhea, loss of appetite, and vomiting. [12] [16] Eight percent of dogs taking maropitant at doses meant to prevent motion sickness vomited right after, likely due to the local effects maropitant had on the gastrointestinal tract. Small amounts of food beforehand can prevent such post ...

  3. FDA Issues Urgent Warning on Dangers of Common Dog Medication

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    The United States Food and Drugs Administration is warning pet owners about a common medication given to pets to treat arthritis. The F.D.A. now says that the drug Librela may be associated with ...

  4. Benadryl for Dogs? A Vet Explains How Much You Should Give - AOL

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    Related: Benadryl for Dogs: Side Effects of Long-Term Use. Signs of Benadryl Overdose in Dogs. At normal doses, Benadryl is quite safe, but a survey of over 600 dogs (1) found the following signs ...

  5. Cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin

    In the laboratory, this liquid serves as a source of HCN, which is inconveniently volatile. [4] Thus, acetone cyanohydrin can be used for the preparation of other cyanohydrins, for the transformation of HCN to Michael acceptors, and for the formylation of arenes. Treatment of this cyanohydrin with lithium hydride affords anhydrous lithium cyanide:

  6. Acetone cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Acetone_cyanohydrin

    Acetone cyanohydrin is an intermediate en route to methyl methacrylate. [6] Treatment with sulfuric acid gives the sulfate ester of the methacrylamide, [clarification needed] methanolysis of which gives ammonium bisulfate and methyl methacrylate. [7] It is used as a surrogate in place of HCN, as illustrated by its use as a precursor to lithium ...

  7. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    In transhydrocyanation, an equivalent of HCN is transferred from a cyanohydrin, e.g. acetone cyanohydrin, to another HCN acceptor. The transfer is an equilibrium process, initiated by base. The reaction can be driven by trapping reactions or by the use of a superior HCN acceptor, such as an aldehyde. [6]

  8. An experimental drug drove people to lose 23% of their body ...

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    CagriSema’s side effects appeared to be similar to other drugs in the GLP-1 class; the company said the most common ones were gastrointestinal, with the “vast majority” mild to moderate and ...

  9. Glycolonitrile - Wikipedia

    en.wikipedia.org/wiki/Glycolonitrile

    Glycolonitrile polymerizes under alkaline conditions above pH 7.0. As the product of polymerization is an amine with a basic character, the reaction is self-catalysed, gaining in speed with ongoing conversion. Glycolonitrile can react with ammonia to give aminoacetonitrile, which can be hydrolysed to give glycine:

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