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  2. Furfural - Wikipedia

    en.wikipedia.org/wiki/Furfural

    Furfural is used to make other furan derivatives, such as furoic acid, via oxidation, [30] and furan itself via palladium catalyzed vapor phase decarbonylation. [ 4 ] There is a good market for value added chemicals that can be obtained from furfural.

  3. Methoxymethylfurfural - Wikipedia

    en.wikipedia.org/wiki/Methoxymethylfurfural

    Methoxymethylfurfural (MMF or 5-methoxymethylfuran-2-carbaldehyde) is an organic compound derived from dehydration of sugars and subsequent etherification with methanol. [1] This colorless liquid is soluble in a wide range of solvents including lower alcohols.

  4. Hydroxymethylfurfural - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethylfurfural

    Hydroxymethylfurfural (HMF), also known as 5-(hydroxymethyl)furfural, is an organic compound formed by the dehydration of reducing sugars. [4] [5] It is a white low-melting solid (although commercial samples are often yellow) which is highly soluble in both water and organic solvents.

  5. 2-Furoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Furoic_acid

    It is a flavoring ingredient and achieved a generally recognized as safe (GRAS) status in 1995 by the Flavor and Extract Manufacturers Association (FEMA). 2-Furoic acid has a distinct odor described as sweet, oily, herbaceous, and earthy. [3] 2-Furoic acid helps sterilize and pasteurize many foods. It forms in situ from 2-furfural.

  6. Furfuryl alcohol - Wikipedia

    en.wikipedia.org/wiki/Furfuryl_alcohol

    Furfuryl alcohol is an organic compound containing a furan substituted with a hydroxymethyl group. It is a colorless liquid, but aged samples appear amber. It possesses a faint odor of burning and a bitter taste. It is miscible with but unstable in water. It is soluble in common organic solvents. [4]

  7. 2,5-Furandicarboxaldehyde - Wikipedia

    en.wikipedia.org/wiki/2,5-Furandicarboxaldehyde

    2,5-Furandicarboxaldehyde (FDC) is an organic compound with the molecular formula C 4 H 2 O(CHO) 2. It consists of a furan ring with aldehyde groups on the 2 and 5 position. It is therefore classified as a dialdehyde .

  8. Scented Wax Melts Create Particles in Indoor Air That ‘You ...

    www.aol.com/scented-wax-melts-create-particles...

    The particles eminating from burning scented wax melts indoors can create a “tremendous amount” of indoor air pollution — similar to pollution caused by diesel engines.

  9. Furan fatty acids - Wikipedia

    en.wikipedia.org/wiki/Furan_fatty_acids

    Furan fatty acids in animals are based on the uptake and accumulation of furan fatty acids from plant constituents. [6] In human blood, the total furan fatty acid content is about 50 ng/ml. Per day, a person separates between 0.5 and 3 mg of urofuran acids - the metabolic product of the furans acids.