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Delphinidin chloride

analytical standard

Synonym(s):

3,3′,4′,5,5′,7-Hexahydroxyflavylium chloride, 3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-1-benzopyrylium chloride

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About This Item

Empirical Formula (Hill Notation):
C15H11ClO7
CAS Number:
528-53-0
Molecular Weight:
338.70
EC Number:
208-437-0
MDL number:
MFCD00016663
UNSPSC Code:
41116107
PubChem Substance ID:
57650189
NACRES:
NA.24

grade

analytical standard

Quality Level

100

assay

≥95.0% (HPLC)

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

storage temp.

−20°C

SMILES string

[Cl-].Oc1cc(O)c2cc(O)c([o+]c2c1)-c3cc(O)c(O)c(O)c3

InChI

1S/C15H10O7.ClH/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6;/h1-5H,(H5-,16,17,18,19,20,21);1H

InChI key

FFNDMZIBVDSQFI-UHFFFAOYSA-N

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General description

Delphinidin chloride is commonly found in delphinium flowers. It can be obtained, via hydrolysis of delphinin chloride.

Application

Delphinidin chloride is an anthocyanin standard, which has been used in the identification and quantification of crude anthocyanin extract from Hibiscus sabdariffa, using high performance liquid chromatography coupled with diode array detector (HPLC-DAD).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem/physiol Actions

Anthocyanidin. Antioxidant. Pigment in grapes, cranberries, and pomegranates.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

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Sigma-Aldrich

52976

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Malvidin chloride phyproof® Reference Substance

PHL80083

Malvidin chloride

Cyanidin 3-glucoside chloride phyproof® Reference Substance

PHL89616

Cyanidin 3-glucoside chloride

Cyanidin chloride United States Pharmacopeia (USP) Reference Standard

USP

1151924

Cyanidin chloride

H Matsumoto et al.
Journal of agricultural and food chemistry, 49(3), 1546-1551 (2001-04-21)
Four components of black currant anthocyanins (BCA), delphinidin 3-O-beta-rutinoside (D3R), cyanidin 3-O-beta-rutinoside (C3R), delphinidin 3-O-beta-glucoside (D3G), and cyanidin 3-O-beta-glucoside (C3G), were found to be directly absorbed and distributed to the blood and excreted into urine as the glycosylated forms. In
Lee Hua Long et al.
Archives of biochemistry and biophysics, 501(1), 162-169 (2010-06-19)
Many papers in the literature have described complex effects of flavonoids and other polyphenols on cells in culture. In this paper we show that hydroxytyrosol, delphinidin chloride and rosmarinic acid are unstable in three commonly-used cell culture media (Dulbecco's modified
Silvia Vignolini et al.
The New phytologist, 196(4), 1038-1047 (2012-10-10)
The Mediterranean orchid genus Ophrys is remarkable for its pseudocopulatory pollination mechanism; naïve male pollinators are attracted to the flowers by olfactory, visual and tactile cues. The most striking visual cue is a highly reflective, blue speculum region at the
Stability and degradation kinetics of crude anthocyanin extracts from H. sabdariffa
Sipahli S, et al.
Food Sci. Technol., 37, 209-215 (2017)
The Anthocyanin Pigments of Plants (2014)
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