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94099

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Cyanidinchlorid

analytical 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
MDL-Nummer:
MFCD00017582
UNSPSC-Code:
85151701
PubChem Substanz-ID:
329770297
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Assay

≥98% (HPLC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

food and beverages

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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Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem./physiol. Wirkung

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCG4699
BCCF7075
BCCD6997
BCCC6646
BCBZ4598

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

USP

1151935

Cyanidin-3-O-glucosidchlorid

Malvidinchlorid phyproof® Reference Substance

PHL80083

Malvidinchlorid

Delphinidinchlorid phyproof® Reference Substance

PHL89625

Delphinidinchlorid

Malvidin-3,5-diglucosidchlorid phyproof® Reference Substance

PHL89727

Malvidin-3,5-diglucosidchlorid

Pelargoninchlorid ≥90% (HPLC)

Sigma-Aldrich

52926

Pelargoninchlorid

Pelargonidinchlorid phyproof® Reference Substance

PHL80084

Pelargonidinchlorid

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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