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  2. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).

  3. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  4. Peroxide process - Wikipedia

    en.wikipedia.org/wiki/Peroxide_process

    The main advantage of the peroxide process to hydrazine relative to the traditional Olin Raschig process is that it does not coproduce salt. In this respect, the peroxide process is an example of green chemistry. Since many millions of kilograms of hydrazine are produced annually, this method is of both commercial and environmental significance ...

  5. It's Time to Ditch These 10 Cleaning Tips From Grandma - AOL

    www.aol.com/lifestyle/time-ditch-10-cleaning...

    Soaking your shower head in vinegar overnight. Grandma isn't completely wrong here. However, we'd like to offer a modification to the process of cleaning your shower head with vinegar.

  6. Using Minoxidil for Hair Loss? Know About These ... - AOL

    www.aol.com/using-minoxidil-hair-loss-know...

    Both over-the-counter (OTC) and prescription medications have the potential to interact with other substances, including supplements. Thankfully, minoxidil comes with a minimal risk of harmful ...

  7. Wharton reaction - Wikipedia

    en.wikipedia.org/wiki/Wharton_reaction

    An α,β-epoxyketone reacts with hydrazine hydrate to yield an allylic alcohol. [7] In the synthesis of warburganal, a bioactive natural product, the α,β-epoxyketone is formed from a cyclic α,β-unsaturated ketone and in a separate step reacts under the classical Wharton olefin synthesis conditions to yield an allylic diol. [8]

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