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  2. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    Formaldehyde (/ f ɔːr ˈ m æ l d ɪ h aɪ d / ⓘ for-MAL-di-hide, US also / f ə r-/ ⓘ fər-) (systematic name methanal) is an organic compound with the chemical formula CH 2 O and structure H−CHO, more precisely H 2 C=O.

  3. Embalming chemicals - Wikipedia

    en.wikipedia.org/wiki/Embalming_chemicals

    Formaldehyde works to fixate the tissue of the deceased. This is the characteristic that also makes concentrated formaldehyde hazardous when not handled using appropriate personal protective equipment. The carbon atom in formaldehyde, CH 2 O, carries a slight positive charge due to the high electronegativity of the oxygen double bonded with the ...

  4. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...

  5. EPA determines formaldehyde poses an ‘unreasonable risk’ to ...

    www.aol.com/epa-determines-formaldehyde-poses...

    The Biden administration has officially determined the chemical formaldehyde poses an “unreasonable” risk to human health and should be regulated. The Environmental Protection Agency (EPA ...

  6. Bromide - Wikipedia

    en.wikipedia.org/wiki/Bromide

    A bromide ion is the negatively charged form (Br −) of the element bromine, a member of the halogens group on the periodic table.Most bromides are colorless. Bromides have many practical roles, being found in anticonvulsants, flame-retardant materials, and cell stains. [3]

  7. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.

  8. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of an acidic proton next to a carbonyl (C=O) functional group by formaldehyde (H−CHO) and a primary or secondary amine (−NH 2) or ammonia (NH 3). [1]

  9. Formaldehyde releaser - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde_releaser

    Formaldehyde-releasers are added to prevent microbial growth and extend shelf life. [1] The intent of these compounds is that they release formaldehyde at levels that suppress microbial growth but sufficiently low to not threaten humans. The use of these chemicals in cosmetics has elicited controversy.