Compound NJ2 (original) (raw)
Compound NJ2 is a xanthylium yellowish pigment found in wine. In model solutions, colorless compounds, such as catechin, can give rise to new types of pigments. The first step is the formation of colorless dimeric compounds consisting of two flavanol units linked by carboxy-methine bridge. This is followed by the formation of xanthylium salt yellowish pigments and their , resulting from the dehydration of the colorless dimers, followed by an oxidation process. The loss of a water molecule takes place between two A ring hydroxyl groups of the colorless dimers.
| Property | Value |
|---|---|
| dbo:abstract | Compound NJ2 is a xanthylium yellowish pigment found in wine. In model solutions, colorless compounds, such as catechin, can give rise to new types of pigments. The first step is the formation of colorless dimeric compounds consisting of two flavanol units linked by carboxy-methine bridge. This is followed by the formation of xanthylium salt yellowish pigments and their , resulting from the dehydration of the colorless dimers, followed by an oxidation process. The loss of a water molecule takes place between two A ring hydroxyl groups of the colorless dimers. (en) |
| dbo:iupacName | 6,20-bis(3,4-dihydroxyphenyl)-7,10,16,19-tetrahydroxy-5,21-dioxa-13-oxoniapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1,3(12),4(9),10,13,15,17(22)-heptaene-2-carboxylic acid (en) |
| dbo:thumbnail | wiki-commons:Special:FilePath/NJ_2.svg?width=300 |
| dbo:wikiPageID | 39723018 (xsd:integer) |
| dbo:wikiPageLength | 2170 (xsd:nonNegativeInteger) |
| dbo:wikiPageRevisionID | 1085887195 (xsd:integer) |
| dbo:wikiPageWikiLink | dbr:Catechin dbr:Phenolic_content_in_wine dbr:Wine_color dbr:Dimer_(chemistry) dbc:Polyphenols dbr:Methine dbr:Flavanol dbr:Hydroxyl_group dbr:Xanthylium dbr:Ethylester |
| dbp:imagealt | Structure of compound NJ2, a xanthylium pigment found in wine. (en) |
| dbp:imagefile | NJ 2.svg (en) |
| dbp:imagesize | 250 (xsd:integer) |
| dbp:iupacname | 620 (xsd:integer) |
| dbp:wikiPageUsesTemplate | dbt:Aromatic-stub dbt:Chembox dbt:Chembox_Hazards dbt:Chembox_Identifiers dbt:Chembox_Properties dbt:Reflist |
| dcterms:subject | dbc:Polyphenols |
| gold:hypernym | dbr:Pigment |
| rdf:type | owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q11173 yago:WikicatMolecularFormulas yago:WikicatNaturalPhenols yago:Abstraction100002137 yago:Chemical114806838 yago:Communication100033020 yago:Compound114818238 yago:Formula106816935 yago:Material114580897 yago:Matter100020827 yago:Message106598915 yago:MolecularFormula106817173 yago:OrganicCompound114727670 yago:Part113809207 yago:Phenol114989545 yago:PhysicalEntity100001930 yago:Relation100031921 dbo:ChemicalCompound yago:Statement106722453 yago:Substance100019613 |
| rdfs:comment | Compound NJ2 is a xanthylium yellowish pigment found in wine. In model solutions, colorless compounds, such as catechin, can give rise to new types of pigments. The first step is the formation of colorless dimeric compounds consisting of two flavanol units linked by carboxy-methine bridge. This is followed by the formation of xanthylium salt yellowish pigments and their , resulting from the dehydration of the colorless dimers, followed by an oxidation process. The loss of a water molecule takes place between two A ring hydroxyl groups of the colorless dimers. (en) |
| rdfs:label | Compound NJ2 (en) |
| owl:sameAs | freebase:Compound NJ2 wikidata:Compound NJ2 dbpedia-sh:Compound NJ2 dbpedia-sr:Compound NJ2 https://global.dbpedia.org/id/XuE1 yago-res:Compound NJ2 |
| prov:wasDerivedFrom | wikipedia-en:Compound_NJ2?oldid=1085887195&ns=0 |
| foaf:depiction | wiki-commons:Special:FilePath/NJ_2.svg |
| foaf:isPrimaryTopicOf | wikipedia-en:Compound_NJ2 |
| is dbo:wikiPageRedirects of | dbr:C32H25O13 dbr:Xanthylium |
| is dbo:wikiPageWikiLink of | dbr:Phenolic_content_in_wine dbr:C32H25O13 dbr:NJ2 dbr:Xanthylium |
| is foaf:primaryTopic of | wikipedia-en:Compound_NJ2 |
