Cyanidin

Base Information

• Chemical Name: Cyanidin
• CAS No.: 13306-05-3
• Molecular Formula: C15H11O6
• Molecular Weight: 287.249
• Hs Code.: 2907299090
• UNII: 7732ZHU564
• DSSTox Substance ID: DTXSID10157933
• Nikkaji Number: J69.705B
• Wikipedia: Cyanidin
• Wikidata: Q417606
• NCI Thesaurus Code: C68445
• Pharos Ligand ID: H3ADKSH2DAFP
• ChEMBL ID: CHEMBL404515
• Mol file: 13306-05-3.mol

Synonyms:1-benzopyrylium, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride;1-benzopyrylium, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride (1:1);2-(3,4-dihydroxyphenyl) chromenylium-3,5,7-triol;2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-1-benzopyrylium chloride;3,3',4',5,7-pentahydroxy-2-phenylbenzopyrylium chloride;3,5,7,3',4'-pentahydroxyflavylium;cyanidin;cyanidin cation;cyanidin chloride;cyanidin ion;cyanidine;cyanidol;cyanidol chloride;flavylium, 3,3',4',5,7-pentahydroxy-;flavylium, 3,3',4',5,7-pentahydroxy-, chloride;IdB 1027;IdB-1027

Chemical Property of Cyanidin

Chemical Property:

• PSA: 114.29000
• LogP: 2.90890
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 287.05556307
• Heavy Atom Count: 21
• Complexity: 364

Purity/Quality:

99% ^*data from raw suppliers

Cyanidin ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O

Technology Process of Cyanidin

There total 38 articles about Cyanidin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

PZ-5 → pelargonidin (7690-51-9) + cyanidin (13306-05-3) + delphinidin (13270-61-6) + catechin (154-23-4)

Guidance literature:

Acid hydrolysis;

DOI:10.1023/A:1015773513717

Reference yield:

cyanidin 3-β-D-xylopyranosyl-(1→2)-β-D-galactopyranoside (142506-19-2) → D-xylose (58-86-6) + cyanidin (13306-05-3) + D-Galactose (59-23-4)

Guidance literature:

With hydrogenchloride; water; at 95 ℃; for 2h;

DOI:10.1016/j.phytochem.2008.03.014

Reference yield:

cyanidin 3,5-O-diglucopyranoside (20905-74-2) → cyanidin (13306-05-3) + D-glucose (50-99-7)

Guidance literature:

Acidic aq. solution;

DOI:10.1007/s10600-009-9287-0

upstream raw materials:

procyanidin B₁

(2R,3R,4S)-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',5,7-pentaol

catechin-(4α->2)-phloroglucinol

procyanidin B₇

Downstream raw materials:

(-)-catechin

(2R,3R)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-1[2H]-benzopyran-3,5,7-triol

catechin

(+)-epicatechin

Refernces

• 1、 Li, Jian-Bin,Hashimoto, Fumio,Shimizu, Keiichi,Sakata, Yusuke. "Anthocyanins from red flowers of Camellia cultivar 'Dalicha'". . p. 3166 - 3171. Retrieved 2008.
• 2、 Qin, Chuanguang,Li, Yang,Zhang, Ruijie,Niu, Weining,Ding, Yan. "Separation and elucidation of anthocyanins in the fruit of mockstrawberry (Duchesnea indica Focke)". . p. 1589 - 1598. Retrieved 2009.
• 3、 Zhang, Yan,Sun, Jianxia,Hu, Xiaosong,Liao, Xiaojun. "Spectral alteration and degradation of cyanidin-3-glucoside exposed to pulsed electric field". . p. 3524 - 3531. Retrieved 2010.
• 4、 Ghissing, Upashana,Goswami, Ambika,Mitra, Adinpunya. "Temporal accumulation of pigments during colour transformation from white to red in Combretum indicum (L.) DeFilipps (syn. Quisqualis indica L.) flowers". supporting information. . Retrieved 2021/10/02.
• 5、 Zhang, Jia-Rong,Trossat-Magnin, Claudine,Bathany, Katell,Delrot, Serge,Chaudière, Jean. "Oxidative Transformation of Leucocyanidin by Anthocyanidin Synthase from Vitis vinifera Leads only to Quercetin". . p. 3595 - 3604. Retrieved 2019/03/29.