Vanillin is an organic compound with the molecular formula C8H8O3. It is a phenolic aldehyde. Its functional groups include aldehyde, hydroxyl, and ether. It is the primary component of the ethanolic extract of the vanilla bean. Synthetic vanillin is now used more often than natural vanilla extract as a flavoring in foods, beverages, and pharmaceuticals.
Vanillin and ethylvanillin are used by the food industry; ethylvanillin is more expensive, but has a stronger note. It differs from vanillin by having an ethoxy group (−O−CH2CH3) instead of a methoxy group (−O−CH3).
Natural vanilla extract is a mixture of several hundred different compounds in addition to vanillin. Artificial vanilla flavoring is often a solution of pure vanillin, usually of synthetic origin. Because of the scarcity and expense of natural vanilla extract, synthetic preparation of its predominant component has long been of interest. The first commercial synthesis of vanillin began with the more readily available natural compound eugenol (4-allyl-2-methoxyphenol). Today, artificial vanillin is made either from guaiacol or lignin.
Lignin-based artificial vanilla flavoring is alleged to have a richer flavor profile than that from guaiacol-based artificial vanilla; the difference is due to the presence of acetovanillone, a minor component in the lignin-derived product that is not found in vanillin synthesized from guaiacol. |
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InChI=1S/C5H5N5O/c6-5-9-3-2(4(11)10-5)7-1-8-3/h1H,(H4,6,7,8,9,10,11) |
UYTPUPDQBNUYGX-UHFFFAOYSA-N |
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Mus musculus
(NCBI:txid10090)
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Source: BioModels - MODEL1507180067
See:
PubMed
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Saccharomyces cerevisiae
(NCBI:txid4932)
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Source: yeast.sf.net
See:
PubMed
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Escherichia coli
(NCBI:txid562)
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See:
PubMed
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Homo sapiens
(NCBI:txid9606)
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See:
DOI
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Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
algal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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View more via ChEBI Ontology
Outgoing
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guanine
(CHEBI:16235)
has parent hydride
9H-purine
(CHEBI:35589)
guanine
(CHEBI:16235)
has role
Escherichia coli metabolite
(CHEBI:76971)
guanine
(CHEBI:16235)
has role
Saccharomyces cerevisiae metabolite
(CHEBI:75772)
guanine
(CHEBI:16235)
has role
algal metabolite
(CHEBI:84735)
guanine
(CHEBI:16235)
has role
human metabolite
(CHEBI:77746)
guanine
(CHEBI:16235)
has role
mouse metabolite
(CHEBI:75771)
guanine
(CHEBI:16235)
is a
2-aminopurines
(CHEBI:20702)
guanine
(CHEBI:16235)
is a
oxopurine
(CHEBI:25810)
guanine
(CHEBI:16235)
is a
purine nucleobase
(CHEBI:26386)
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Incoming
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1,N2-ethenoguanine
(CHEBI:134096)
has functional parent
guanine
(CHEBI:16235)
1H,3H,5H-pyrimido[1,2-α]purin-2,6,10-trione
(CHEBI:233252)
has functional parent
guanine
(CHEBI:16235)
2-oxo-ethenoguanine
(CHEBI:233226)
has functional parent
guanine
(CHEBI:16235)
3H,5H-pyrimido[1,2-α]purin-6,10-dione
(CHEBI:233251)
has functional parent
guanine
(CHEBI:16235)
7,8-dihydro-8-oxoguanine
(CHEBI:52617)
has functional parent
guanine
(CHEBI:16235)
7-(2'-oxo-heptyl)-1,N2-ethenoguanine
(CHEBI:233227)
has functional parent
guanine
(CHEBI:16235)
7-(2'-oxo-heptyl)-2-oxo-ethenoguanine
(CHEBI:233228)
has functional parent
guanine
(CHEBI:16235)
8-hydroxy-7-methylguanine
(CHEBI:74064)
has functional parent
guanine
(CHEBI:16235)
8-oxoguanine
(CHEBI:44605)
has functional parent
guanine
(CHEBI:16235)
9-(2-deoxy-2-fluoro-5-O-phosphono-β-D-arabinofuranosyl)guanine
(CHEBI:42701)
has functional parent
guanine
(CHEBI:16235)
9-[2-(phosphonomethoxy)ethyl]guanine
(CHEBI:7880)
has functional parent
guanine
(CHEBI:16235)
N2,3-ethenoguanine
(CHEBI:134095)
has functional parent
guanine
(CHEBI:16235)
N2-carboxyethylguanine
(CHEBI:62032)
has functional parent
guanine
(CHEBI:16235)
O6-methyl-2'-deoxyguanosine
(CHEBI:27549)
has functional parent
guanine
(CHEBI:16235)
acyclovir
(CHEBI:2453)
has functional parent
guanine
(CHEBI:16235)
ganciclovir
(CHEBI:465284)
has functional parent
guanine
(CHEBI:16235)
guanosine
(CHEBI:16750)
has functional parent
guanine
(CHEBI:16235)
guanosines
(CHEBI:24458)
has functional parent
guanine
(CHEBI:16235)
guanyl deoxyribonucleotide residue
(CHEBI:60801)
has functional parent
guanine
(CHEBI:16235)
guanyl nucleotide
(CHEBI:61292)
has functional parent
guanine
(CHEBI:16235)
methylguanine
(CHEBI:25305)
has functional parent
guanine
(CHEBI:16235)
N2-(ADP-D-ribosyl)-guanine(2−)
(CHEBI:142716)
has functional parent
guanine
(CHEBI:16235)
nelarabine
(CHEBI:63612)
has functional parent
guanine
(CHEBI:16235)
penciclovir
(CHEBI:7956)
has functional parent
guanine
(CHEBI:16235)
pyrimido[1,2-α]purin-10(3H)-one
(CHEBI:233250)
has functional parent
guanine
(CHEBI:16235)
valacyclovir
(CHEBI:35854)
has functional parent
guanine
(CHEBI:16235)
valganciclovir
(CHEBI:63635)
has functional parent
guanine
(CHEBI:16235)
xanthine
(CHEBI:15318)
has functional parent
guanine
(CHEBI:16235)
guanin-9-yl group
(CHEBI:30755)
is substituent group from
guanine
(CHEBI:16235)
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2-amino-1,9-dihydro-6H-purin-6-one
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2-Amino-6-hydroxypurine
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KEGG COMPOUND
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2-amino-6-oxopurine
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ChEBI
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G
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ChEBI
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Gua
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CBN
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Guanine
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KEGG COMPOUND
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GUANINE
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PDBeChem
|
guanine
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UniProt
|
147911
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Reaxys Registry Number
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Reaxys
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431879
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Gmelin Registry Number
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Gmelin
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73-40-5
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CAS Registry Number
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KEGG COMPOUND
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73-40-5
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CAS Registry Number
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ChemIDplus
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73-40-5
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CAS Registry Number
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NIST Chemistry WebBook
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22770225
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PubMed citation
|
Europe PMC
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8070089
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PubMed citation
|
Europe PMC
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