Y0001061

Cyanidin chloride

Name: Cyanidin chloride
Brand: SIAL

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

3,3′,4,5,7-Pentahydroxyflavylium chloride, Cyanidol chloride

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About This Item

Empirical Formula (Hill Notation):

C₁₅H₁₁ClO₆

CAS Number:

528-58-5

Molecular Weight:

322.70

EC Number:

208-438-6

MDL number:

MFCD00017582

UNSPSC Code:

41116107

PubChem Substance ID:

329831242

NACRES:

NA.24

Key Documents

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grade

pharmaceutical primary standard

API family

anthocyanins, cyanidin chloride

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

[Cl-].Oc1cc(O)c2cc(O)c([o+]c2c1)-c3ccc(O)c(O)c3

InChI

1S/C15H10O6.ClH/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7;/h1-6H,(H4-,16,17,18,19,20);1H

InChI key

COAWNPJQKJEHPG-UHFFFAOYSA-N

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Show Differences

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This Item	1151924	PHR2695	94099
Y0001061 Cyanidin chloride	USP 1151924 Cyanidin chloride	Supelco PHR2695 Cyanidin chloride	Supelco 94099 Cyanidin chloride
grade pharmaceutical primary standard	grade pharmaceutical primary standard	grade certified reference material, pharmaceutical secondary standard	grade analytical standard
manufacturer/tradename EDQM	manufacturer/tradename USP	manufacturer/tradename -	manufacturer/tradename -
format neat	format neat	format -	format neat
application(s) pharmaceutical (small molecule)	application(s) pharmaceutical (small molecule)	application(s) pharmaceutical small molecule	application(s) food and beverages
API family anthocyanins, cyanidin chloride	API family cyanidin chloride, anthocyanins	API family anthocyanins, cyanidin chloride	API family -
storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Cyanidin chloride EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Biochem/physiol Actions

Anthocyanidin. Pigment found in several varieties of berries. Antioxidant.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

related product

Product No.

Description

Pricing

1151935

Cyanidin 3-O-glucoside chloride, United States Pharmacopeia (USP) Reference Standard

1151924

Cyanidin chloride, United States Pharmacopeia (USP) Reference Standard

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Monte Carlo modelling of non-isothermal degradation of two cyanidin-based anthocyanins in aqueous system at high temperatures and its impact on antioxidant capacities.

Xiaonan Sui et al.

Food chemistry, 148, 342-350 (2013-11-23)

The non-isothermal degradation of two cyanidin-based anthocyanins, cyanidin-3-glucoside and cyanidin-3-rutinoside, was investigated in aqueous system within the temperature range from 100 to 165 °C, and the degradation kinetics was modelled using Monte Carlo simulation. The two anthocyanins showed different stability

Species-specific defence responses facilitate conspecifics and inhibit heterospecifics in above-belowground herbivore interactions.

Wei Huang et al.

Nature communications, 5, 4851-4851 (2014-09-23)

Conspecific and heterospecific aboveground and belowground herbivores often occur together in nature and their interactions may determine community structure. Here we show how aboveground adults and belowground larvae of the tallow tree specialist beetle Bikasha collaris and multiple heterospecific aboveground

Synergistic effects between catalase inhibitors and modulators of nitric oxide metabolism on tumor cell apoptosis.

Katrin Scheit et al.

Anticancer research, 34(10), 5337-5350 (2014-10-03)

Inhibitors of catalase (such as ascorbate, methyldopa, salicylic acid and neutralizing antibodies) synergize with modulators of nitric oxide (NO) metabolism (such as arginine, arginase inhibitor, NO synthase-inducing interferons and NO dioxygenase inhibitors) in the singlet oxygen-mediated inactivation of tumor cell

Do antioxidants inhibit oxidative-stress-induced autophagy of tenofibroblasts?

Ra-Jeong Kim et al.

Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 32(7), 937-943 (2014-03-20)

Recent research on tendinopathy has focused on its relationship to programmed cell death. Increased autophagy has been observed in ruptured rotator cuff tendon tissues, suggesting a causal relationship. We investigated whether autophagy occurs in human rotator cuff tenofibroblast death induced

Functional characterization of an anthocyanidin reductase gene from the fibers of upland cotton (Gossypium hirsutum).

Yue Zhu et al.

Planta, 241(5), 1075-1089 (2015-01-13)

Metabolic profiling, gene cloning, enzymatic analysis, ectopic expression, and gene silencing experiments demonstrate that the anthocyanidin reductase (ANR) pathway is involved in the biosynthesis of proanthocyanidins in upland cotton. Proanthocyanidins (PAs) are oligomeric or polymeric flavan-3-ols, however, the biosynthetic pathway

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