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delphinidin 3-glucoside chloride

chemical compound
ChemicalSubstance type_of_chemical_entity Q945655
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delphinidin 3-glucoside chloride

Summary

delphinidin 3-glucoside chloride is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2]

Key Facts

  • delphinidin 3-glucoside chloride's instance of is recorded as type of chemical entity[3].
  • delphinidin 3-glucoside chloride's chemical structure is recorded as Mirtillin.svg[4].
  • delphinidin 3-glucoside chloride's CAS Registry Number is recorded as 6906-38-3[5].
  • delphinidin 3-glucoside chloride's canonical SMILES is recorded as C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)O)OC4C(C(C(C(O4)CO)O)O)O.[Cl-][6].
  • delphinidin 3-glucoside chloride's InChI is recorded as InChI=1S/C21H20O12.ClH/c22-6-15-17(28)18(29)19(30)21(33-15)32-14-5-9-10(24)3-8(23)4-13(9)31-20(14)7-1-11(25)16(27)12(26)2-7;/h1-5,15,17-19,21-22,28-30H,6H2,(H4-,23,24,25,26,27);1H/t15-,17-,18+,19-,21-;/m1./s1[7].
  • delphinidin 3-glucoside chloride's InChIKey is recorded as ZJWIIMLSNZOCBP-BTTVDUMLSA-N[8].
  • delphinidin 3-glucoside chloride's chemical formula is recorded as C₂₁H₂₁ClO₁₂[9].
  • delphinidin 3-glucoside chloride's subclass of is recorded as chemical compound[10].
  • delphinidin 3-glucoside chloride's Freebase ID is recorded as /m/07s4xkz[11].
  • delphinidin 3-glucoside chloride's UNII is recorded as 474A9U89JS[12].
  • delphinidin 3-glucoside chloride's ChemSpider ID is recorded as 145096[13].
  • delphinidin 3-glucoside chloride's PubChem CID is recorded as 165558[14].
  • delphinidin 3-glucoside chloride's ChEBI ID is recorded as 189576[15].
  • delphinidin 3-glucoside chloride's isomeric SMILES is recorded as C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)O)O[C@H]4C@@HO.[Cl-]C@@HO.[Cl-]">[16].
  • delphinidin 3-glucoside chloride's mass is recorded as {'unit': 'Q483261', 'amount': '+500.072'}[17].
  • delphinidin 3-glucoside chloride's SureChEMBL ID is recorded as 675415[18].
  • delphinidin 3-glucoside chloride's DSSTox substance ID is recorded as DTXSID901028800[19].
  • delphinidin 3-glucoside chloride's stereoisomer of is recorded as delphinidin 3-galactoside[20].
  • delphinidin 3-glucoside chloride's Microsoft Academic ID is recorded as 2776431911[21].
  • delphinidin 3-glucoside chloride's UniChem compound ID is recorded as 1077006[22].
  • delphinidin 3-glucoside chloride's Probes And Drugs ID is recorded as PD018053[23].

Why It Matters

delphinidin 3-glucoside chloride ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[24]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Freebase Data Dumps. wikidata.org.
  10. [12] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  11. [13] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [14] ↑ . PubChem. Retrieved . wikidata.org.
  13. [15] ↑ . ChEBI release 2022-06-13. wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . UniChem. wikidata.org.
  21. [23] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [24] ↑ . Wikidata sitelinks. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). delphinidin 3-glucoside chloride. Retrieved May 3, 2026, from https://4ort.xyz/entity/delphinidin-3-glucoside-chloride
MLA “delphinidin 3-glucoside chloride.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/delphinidin-3-glucoside-chloride.
BibTeX @misc{4ortxyz_delphinidin-3-glucoside-chloride_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{delphinidin 3-glucoside chloride}}, year = {2026}, url = {https://4ort.xyz/entity/delphinidin-3-glucoside-chloride}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): delphinidin 3-glucoside chloride — https://4ort.xyz/entity/delphinidin-3-glucoside-chloride (retrieved 2026-05-03)

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