Product Name

  • Name

    Cyanidin chloride

  • EINECS 208-438-6
  • CAS No. 528-58-5
  • Article Data28
  • CAS DataBase
  • Density 1.2843 (rough estimate)
  • Solubility
  • Melting Point >300 °C
  • Formula C15H11ClO6
  • Boiling Point 349.55°C (rough estimate)
  • Molecular Weight 322.702
  • Flash Point
  • Transport Information
  • Appearance COA
  • Safety 22-24/25
  • Risk Codes
  • Molecular Structure Molecular Structure of 528-58-5 (Cyanidin chloride)
  • Hazard Symbols
  • Synonyms 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-benzopyrylium chloride;3,3',4',5,7-Pentahydroxy-2-phenylbenzopyrylium chloride;3,3',4',5,7-Pentahydroxyflavylium chloride;Cyanidol chloride;IdB 1027;1-Benzopyrylium,2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride (9CI);Cyanidol (6CI);Flavylium, 3,3',4',5,7-pentahydroxy-, chloride (8CI);1-Benzopyrylium,2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride (1:1);
  • PSA 114.29000
  • LogP -0.08710

Synthetic route

tetrachloromethane
56-23-5

tetrachloromethane

N-Bromosuccinimide
128-08-5

N-Bromosuccinimide

dibenzoyl peroxide
94-36-0

dibenzoyl peroxide

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
Erwaermen mit Chlorwasserstoff enthaltendem Aethanol oder mit wss. Natriumacetat-Loesung und Zinkchlorid in Cyanidin-chlorid;
quercetol
117-39-5

quercetol

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogenchloride; magnesium at 35℃;
With hydrogenchloride; sodium amalgam
2-(3,4-dimethoxy-phenyl)-5,7-dihydroxy-3-methoxy-chromenylium; chloride

2-(3,4-dimethoxy-phenyl)-5,7-dihydroxy-3-methoxy-chromenylium; chloride

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogen iodide; phenol Umsetzen des entstandenen Jodids mit Silberchlorid und Salzsaeure;
(2R,3S)-(+)-catechin 3',4',5,7-tetramethyl ether
51079-25-5

(2R,3S)-(+)-catechin 3',4',5,7-tetramethyl ether

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With 1,4-dioxane; bromine Erwaermen des jeweiligen Reaktionsprodukts mit wss. Jodwasserstoffsaeure, Phenol und Phosphor unter Kohlendioxid; Behandeln des erhaltenen Jodids mit Silberchlorid in wss.-aethanol. Salzsaeure;
(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol
69082-77-5

(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol

A

cyanidin chloride
528-58-5

cyanidin chloride

B

fisetinidin chloride
2948-76-7

fisetinidin chloride

Conditions
ConditionsYield
With hydrogenchloride In isopropyl alcohol at 97℃;
(2S,3S,4S)-4-(2,4-Dihydroxy-phenyl)-2-(3,4-dihydroxy-phenyl)-chroman-3,5,7-triol
65052-93-9, 94942-00-4, 125136-15-4, 125136-16-5, 125136-17-6, 125136-18-7

(2S,3S,4S)-4-(2,4-Dihydroxy-phenyl)-2-(3,4-dihydroxy-phenyl)-chroman-3,5,7-triol

A

cyanidin chloride
528-58-5

cyanidin chloride

B

fisetinidin chloride
2948-76-7

fisetinidin chloride

Conditions
ConditionsYield
With hydrogenchloride In isopropyl alcohol at 97℃;
hydrogenchloride
7647-01-0

hydrogenchloride

2-(3,4-dihydroxy-phenyl)-2,5,7-trihydroxy-chroman-3-one

2-(3,4-dihydroxy-phenyl)-2,5,7-trihydroxy-chroman-3-one

cyanidin chloride
528-58-5

cyanidin chloride

hydrogenchloride
7647-01-0

hydrogenchloride

2,3,5,7-tetraacetoxy-2-(3,4-diacetoxy-phenyl)-2H-chromene
96069-12-4

2,3,5,7-tetraacetoxy-2-(3,4-diacetoxy-phenyl)-2H-chromene

acetic acid
64-19-7

acetic acid

cyanidin chloride
528-58-5

cyanidin chloride

hydrogenchloride
7647-01-0

hydrogenchloride

quercetol
117-39-5

quercetol

magnesium

magnesium

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
at 35℃;
(-)-penta-O-acetyl-epicatechol

(-)-penta-O-acetyl-epicatechol

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With tetrachloromethane; N-Bromosuccinimide; dibenzoyl peroxide Erwaermen des Reaktionsprodukts mit Chlorwasserstoff enthaltendem Aethanol oder mit wss. Natriumacetat-Loesung und Zinkchlorid;
(2R)-2r-<3,4-dimethoxy-phenyl>-3t,5,7-trimethoxy-chroman

(2R)-2r-<3,4-dimethoxy-phenyl>-3t,5,7-trimethoxy-chroman

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With 1,4-dioxane; bromine Erwaermen des jeweiligen Reaktionsprodukts mit wss. Jodwasserstoffsaeure, Phenol und Phosphor unter Kohlendioxid; Behandeln des erhaltenen Jodids mit Silberchlorid in wss.-aethanol. Salzsaeure;
1,3,5-triacetoxy-2-diacetoxymethyl-benzene
858841-91-5

1,3,5-triacetoxy-2-diacetoxymethyl-benzene

3.4.ω-triacetoxy-acetophenone

3.4.ω-triacetoxy-acetophenone

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogenchloride; acetic acid Kochen des Reaktionsprodukts mit Salzsaeure;
5-benzoyl-cyanidin chloride

5-benzoyl-cyanidin chloride

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With sodium hydroxide Erwaermen des Reaktionsgemisches mit Salzsaeure auf 60grad;
chrysanthemin chlorid

chrysanthemin chlorid

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogenchloride
cyanidin chloride pentamethyl ether

cyanidin chloride pentamethyl ether

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogen iodide; phenol Umsetzen des entstandenen Jodids mit Silberchlorid und Salzsaeure;
cyanoyne chloride

cyanoyne chloride

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With fermenting yeast
With hydrogenchloride
With aspergillus-tannase
idein chloride

idein chloride

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogenchloride
keracyanin chloride

keracyanin chloride

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogenchloride
mecocyanin chloride

mecocyanin chloride

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogenchloride
(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol
69082-77-5

(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 30 mg / 0.05M benzophenone / acetone / Irradiation
2: 3M HCl / propan-2-ol / 97 °C
View Scheme
cyanidin-3-O-β-D-rutinoside hemiacetal

cyanidin-3-O-β-D-rutinoside hemiacetal

A

L-Rhamnose
3615-41-6

L-Rhamnose

B

D-glucose
50-99-7

D-glucose

C

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
Acidic conditions;
cyanidin 3-O-[2-O-(2-O-(trans-feruloyl)-glucosyl)-6-O-(trans-p-coumaroyl)-glucoside]-5-O-[6-O-(malonyl)-glucoside]

cyanidin 3-O-[2-O-(2-O-(trans-feruloyl)-glucosyl)-6-O-(trans-p-coumaroyl)-glucoside]-5-O-[6-O-(malonyl)-glucoside]

A

D-Glucose
2280-44-6

D-Glucose

B

(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
1135-24-6

(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid

C

malonic acid
141-82-2

malonic acid

D

p-Coumaric Acid
7400-08-0

p-Coumaric Acid

E

cyanidin chloride
528-58-5

cyanidin chloride

Conditions
ConditionsYield
With hydrogenchloride; water at 100℃; for 1h;
acetic anhydride
108-24-7

acetic anhydride

cyanidin chloride
528-58-5

cyanidin chloride

A

1,3,5-triacetoxybenzene
2999-40-8

1,3,5-triacetoxybenzene

B

3,4-Diacetoxy-benzoesaeure
58534-64-8

3,4-Diacetoxy-benzoesaeure

Conditions
ConditionsYield
With ruthenium(IV) oxide; sodium periodate 1) 5 h, room temp., pyridine; 2) acetone, water, 20 min : decomposition reaction;A 32%
B 67%
With ruthenium(IV) oxide; sodium periodate 1) 5 h, room temp., pyridine; 2) water, acetone, 20 min; Yield given. Multistep reaction. Yields of byproduct given;
acetic anhydride
108-24-7

acetic anhydride

cyanidin chloride
528-58-5

cyanidin chloride

2,3,5,7-tetraacetoxy-2-(3,4-diacetoxy-phenyl)-2H-chromene
96069-12-4

2,3,5,7-tetraacetoxy-2-(3,4-diacetoxy-phenyl)-2H-chromene

Conditions
ConditionsYield
With pyridine
cyanidin chloride
528-58-5

cyanidin chloride

2-(3,4-dihydroxy-phenyl)-3,5,7-trihydroxy-chromenylium; benzopyrylium hydroxide
445-86-3

2-(3,4-dihydroxy-phenyl)-3,5,7-trihydroxy-chromenylium; benzopyrylium hydroxide

Conditions
ConditionsYield
With ethanol; water
Conditions
ConditionsYield
With hydrogenchloride; methanol; platinum Hydrogenation;
cyanidin chloride
528-58-5

cyanidin chloride

KOH-solution

KOH-solution

A

3,5-dihydroxyphenol
108-73-6

3,5-dihydroxyphenol

B

3,4-Dihydroxybenzoic acid
99-50-3

3,4-Dihydroxybenzoic acid

cyanidin chloride
528-58-5

cyanidin chloride

water containing alkali

water containing alkali

A

3,5-dihydroxyphenol
108-73-6

3,5-dihydroxyphenol

B

3,4-Dihydroxybenzoic acid
99-50-3

3,4-Dihydroxybenzoic acid

Conditions
ConditionsYield
at 210 - 250℃;
hydrogenchloride
7647-01-0

hydrogenchloride

methanol
67-56-1

methanol

cyanidin chloride
528-58-5

cyanidin chloride

platinum black

platinum black

Conditions
ConditionsYield
Hydration;

Cyanidin chloride Chemical Properties

Molecular Formula:C15H11ClO6
Formula Weight:322.7g/mol
storage temp.:-20°C 
EINECS:208-438-6
Product Categories: Anthocyanins;Flavonoids
Product Categories of  Cyanidin chloride  (528-58-5): Anthocyanins; Flavonoids
Structure of  Cyanidin chloride  (528-58-5):

Cyanidin chloride Uses

It can be used as food pigment, cosmetics, etc.

Cyanidin chloride Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Source
dog LD oral > 3gm/kg (3000mg/kg) Drugs of the Future. Vol. 14, Pg. 224, 1989.
mammal (species unspecified) LD oral > 6gm/kg (6000mg/kg) Drugs of the Future. Vol. 14, Pg. 224, 1989.
rat LD50 intraperitoneal 1500mg/kg (1500mg/kg) United States Patent Document. Vol. #4229439,

Cyanidin chloride Safety Profile

Safety Statements: 22-24/25 
S22: Do not breathe dust
S24/25: Avoid contact with skin and eyes
WGK Germany: 3
RTECS: LK9824000
F: 10-21 
F 10: Keep under argon
F 21: Sensitive to humidity

Cyanidin chloride Specification

 Cyanidin chloride (CAS NO.528-58-5) is also called as 1-Benzopyrylium, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride ; 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-benzopyrylium chloride ; 3,3',4',5,7-Pentahydroxy-2-phenylbenzopyrylium chloride ; 3,3'4',5,7-Pentahydroxyflavylium chloride ; Cyanidin chloride ; Cyanidol chloride ; Gastrotelos ; 1-Benzopyrylium, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride (9CI) ; 3,3',4',5,7-Pentahydroxyflavylium chloride Flavylium, 3,3'4',5,7-pentahydroxy-, chloride   

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