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1 See also  





2 References  














Pyridoxal






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From Wikipedia, the free encyclopedia
 


Pyridoxal
Skeletal formula of pyridoxal

Idealised skeletal formula

Ball-and-stick model of pyridoxal

Ball-and-stick model based on the crystal structure.[1][2] Note that the acidic phenol group has donated a proton to the basic pyridine group to form a zwitterion, and the hydroxymethyl group has reacted with the aldehyde group to form a hemiacetal.

Names
Preferred IUPAC name

3-Hydroxy-5-(hydroxymethyl)-2-methylpyridine-4-carbaldehyde

Identifiers

CAS Number

  • 65-22-5 (hydrochloride) checkY
  • 3D model (JSmol)

    ChEBI
    ChEMBL
    ChemSpider
    DrugBank
    ECHA InfoCard 100.000.573 Edit this at Wikidata
    KEGG

    PubChem CID

    UNII
  • 1416KF0QBC (hydrochloride) checkY
  • CompTox Dashboard (EPA)

    • InChI=1S/C8H9NO3/c1-5-8(12)7(4-11)6(3-10)2-9-5/h2,4,10,12H,3H2,1H3 checkY

      Key: RADKZDMFGJYCBB-UHFFFAOYSA-N checkY

    • InChI=1/C8H9NO3/c1-5-8(12)7(4-11)6(3-10)2-9-5/h2,4,10,12H,3H2,1H3

      Key: RADKZDMFGJYCBB-UHFFFAOYAP

    • O=Cc1c(O)c(C)ncc1CO

    Properties

    Chemical formula

    C8H9NO3
    Molar mass 167.16 g/mol
    Melting point 165 °C (329 °F; 438 K) (decomposes)
    Related compounds

    Related arylformaldehydes

    Damnacanthal

    Gossypol

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Pyridoxal is one form of vitamin B6.

    Some medically relevant bacteria, such as those in the genera Granulicatella and Abiotrophia, require pyridoxal for growth. This nutritional requirement can lead to the culture phenomenon of satellite growth. In in vitro culture, these pyridoxal-dependent bacteria may only grow in areas surrounding colonies of bacteria from other genera ("satellitism") that are capable of producing pyridoxal.

    Pyridoxal is involved in what is believed to be the most ancient reaction of aerobic metabolism on Earth, about 2.9 billion years ago, a forerunner of the Great Oxidation Event.[3]

    See also[edit]

    References[edit]

    1. ^ "CSD Entry: BIHKEI01". Cambridge Structural Database: Access Structures. Cambridge Crystallographic Data Centre. 1985. Archived from the original on 2023-11-04. Retrieved 2023-11-04.
  • ^ MacLaurin, C. L.; Richardson, M. F. (1985). "Pyridoxal, C8H9NO3, and pyridoxamine dihydrate, C8H12N2O2.2H2O". Acta Crystallogr. C. 41 (2): 261–263. Bibcode:1985AcCrC..41..261M. doi:10.1107/S0108270185003547.
  • ^ "Protein Domain Structure Uncovers the Origin of Aerobic Metabolism and the Rise of Planetary Oxygen", Gustavo Caetano-Anolles et al., published in Structure; paper available from University of Illinois News Bureau, 2012.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Pyridoxal&oldid=1214622113"

    Categories: 
    Vitamins
    Hydroxypyridines
    Aldehydes
    3-Hydroxypropenals
    Aromatic ketones
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