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  2. Methoxymethanol - Wikipedia

    en.wikipedia.org/wiki/Methoxymethanol

    Methoxymethanol forms spontaneously when a water solution of formaldehyde and methanol are mixed. [3] [1] or when formaldehyde is bubbled through methanol. [4] In space methoxymethanol can form when methanol radicals (CH 2 OH or CH 3 O) react. These are radiolysis products derived when ultraviolet light or cosmic rays hit frozen methanol. [3]

  3. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    In some places, such as China, manufacturers still use formaldehyde illegally as a preservative in foods, which exposes people to formaldehyde ingestion. [115] In the early 1900s, it was frequently added by US milk plants to milk bottles as a method of pasteurization due to the lack of knowledge and concern [ 116 ] regarding formaldehyde's ...

  4. Polyoxymethylene - Wikipedia

    en.wikipedia.org/wiki/Polyoxymethylene

    To make polyoxymethylene homopolymer, anhydrous formaldehyde must be generated. The principal method is by reaction of the aqueous formaldehyde with an alcohol to create a hemiformal, dehydration of the hemiformal/water mixture (either by extraction or vacuum distillation) and release of the formaldehyde by heating the hemiformal.

  5. Methanediol - Wikipedia

    en.wikipedia.org/wiki/Methanediol

    Methanediol, also known as formaldehyde monohydrate or methylene glycol, is an organic compound with chemical formula CH 2 (OH) 2. It is the simplest geminal diol . In aqueous solutions it coexists with oligomers (short polymers).

  6. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    Cyclic hemiacetals often form readily, especially when they are 5- and 6-membered rings. In this case, a hydroxy group reacts with a carbonyl group within the same molecule to undergo an intramolecular cyclization reaction. [6] Formation of a general cyclic hemiacetal Structures of some readily isolable hemiacetals and hemiketals.

  7. Methanol - Wikipedia

    en.wikipedia.org/wiki/Methanol

    Methanol and its vapours are flammable. Moderately toxic for small animals – Highly toxic to large animals and humans (in high concentrations) – May be fatal/lethal or cause blindness and damage to the liver, kidneys, and heart if swallowed – Toxicity effects from repeated over exposure have an accumulative effect on the central nervous system, especially the optic nerve – Symptoms may ...

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  9. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    As they are present in food consumed in human diets and in plants used in traditional medicine of several cultures, their role in human health and disease is a subject of research. [ 1 ] [ 5 ] [ 6 ] [ 7 ] : 104 Some phenols are germicidal and are used in formulating disinfectants.