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43725

Supelco

Delphinidin chloride

analytical standard

Sinónimos:

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

Fórmula empírica (notación de Hill):
C15H11ClO7
Número de CAS:
528-53-0
Peso molecular:
338.70
Número CE:
208-437-0
Número MDL:
MFCD00016663
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
57650189
NACRES:
NA.24

grado

analytical standard

Ensayo

≥95.0% (HPLC)

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

food and beverages

Formato

neat

temp. de almacenamiento

−20°C

cadena SMILES

[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

Clave InChI

FFNDMZIBVDSQFI-UHFFFAOYSA-N

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Descripción general

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

Aplicación

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.

Acciones bioquímicas o fisiológicas

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

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
BCCL4744
BCCM5795
BCCK6380
BCCJ3866
BCCG3872

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Sigma-Aldrich

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Sigma-Aldrich

52976

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Malvidin chloride phyproof® Reference Substance

PHL80083

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PHL89616

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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
XianLin Zhang et al.
Journal of the science of food and agriculture, 92(7), 1533-1539 (2011-12-17)
Flavan-3-ols, which account for approximately 700-800 g kg(-1) of tea polyphenols, exert many health-promoting effects. Anthocyanidin reductase (ANR) is an important enzyme involved in the biosynthesis of flavan-3-ols in the tea plant. The purpose of this study was to establish
Yoosoo Yang et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(51), 22145-22150 (2010-12-08)
Neuronal SNARE proteins mediate neurotransmitter release at the synapse by facilitating the fusion of vesicles to the presynaptic plasma membrane. Cognate v-SNAREs and t-SNAREs from the vesicle and the plasma membrane, respectively, zip up and bring about the apposition of
A J Kortstee et al.
Transgenic research, 20(6), 1253-1264 (2011-02-23)
A mutant allele of the transcription factor gene MYB10 from apple induces anthocyanin production throughout the plant. This gene, including its upstream promoter, gene coding region and terminator sequence, was introduced into apple, strawberry and potato plants to determine whether
Hirofumi Inoue et al.
Nutrition research (New York, N.Y.), 32(5), 357-364 (2012-06-02)
Delphinidin-3-O-galactoside (D3G) is a water-soluble anthocyanin with antioxidant activity. (-)-Epigallocatechin-3-gallate (EGCG) is also known as a powerful antioxidant but concomitantly possesses a prooxidative property. We hypothesized that D3G is capable of protecting the EGCG-induced cytotoxicity and endoplasmic reticulum (ER) stress
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