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Y0001061

Cyanidinchlorid

European Pharmacopoeia (EP) Reference Standard

Synonym(e):

3,3′,4,5,7-Pentahydroxy-flavyliumchlorid, Cyanidolchlorid

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About This Item

Empirische Formel (Hill-System):
C15H11ClO6
CAS-Nummer:
528-58-5
Molekulargewicht:
322.70
EG-Nummer:
208-438-6
MDL-Nummer:
MFCD00017582
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329831242
NACRES:
NA.24

Qualität

pharmaceutical primary standard

API-Familie

anthocyanins, cyanidin chloride

Hersteller/Markenname

EDQM

Anwendung(en)

pharmaceutical (small molecule)

Format

neat

Lagertemp.

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

InChIKey

COAWNPJQKJEHPG-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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

Biochem./physiol. Wirkung

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

Verpackung

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

Sonstige Hinweise

Sales restrictions may apply.

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Preisangaben

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

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Analysenzertifikate (COA)

Lot/Batch Number

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Delphinidinchlorid analytical standard

Supelco

43725

Delphinidinchlorid

Cyanidin-3-O-glucosidchlorid United States Pharmacopeia (USP) Reference Standard

USP

1151935

Cyanidin-3-O-glucosidchlorid

Pelargonidinchlorid

Sigma-Aldrich

P1659

Pelargonidinchlorid

Delphinidin-3-glucosidchlorid phyproof® Reference Substance

PHL89627

Delphinidin-3-glucosidchlorid

TWEEN® 80 protein grade detergent, 10% solution, sterile-filtered, for immunoprecipitation and for the solubilization of membrane-bound proteins

Millipore

655207

TWEEN® 80

Kuromaninchlorid ≥95% (HPLC)

Sigma-Aldrich

52976

Kuromaninchlorid

(+)-Catechin analytical standard

Supelco

43412

(+)-Catechin

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
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
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
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
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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