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79311

Supelco

Malvidin-3-galactoside chloride

analytical standard

Sinonimo/i:

Arthanitin chloride, Primulin

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About This Item

Formula empirica (notazione di Hill):
C23H25ClO12
Numero CAS:
30113-37-2
Peso molecolare:
528.89
Numero CE:
250-055-1
Numero MDL:
MFCD00185577
Codice UNSPSC:
12000000
ID PubChem:
329768395
NACRES:
NA.25

Grado

analytical standard

Livello qualitativo

100

Saggio

≥95% (HPLC)

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

[Cl-].COc1cc(cc(OC)c1O)-c2[o+]c3cc(O)cc(O)c3cc2O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O

InChI

1S/C23H24O12.ClH/c1-31-14-3-9(4-15(32-2)18(14)27)22-16(7-11-12(26)5-10(25)6-13(11)33-22)34-23-21(30)20(29)19(28)17(8-24)35-23;/h3-7,17,19-21,23-24,28-30H,8H2,1-2H3,(H2-,25,26,27);1H/t17-,19+,20+,21-,23-;/m1./s1
YDIKCZBMBPOGFT-PWUSVEHZSA-N

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Categorie correlate

Descrizione generale

Malvidin-3-galactoside chloride is an anthocyanin pigment found in magenta and dark red flowers of Primula polyanthus.

Applicazioni

Malvidin-3-galactoside chloride is a type of fluorescent dye commonly used to identify glycerides and free fatty acids.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCL8198
BCCK5125
BCCF4290
BCBZ9203
BCBX5356

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Sigma-Aldrich

72815

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Supelco

43725

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V A Otellin et al.
Arkhiv anatomii, gistologii i embriologii, 80(1), 26-29 (1981-01-01)
A possibility to study associative and projective connections of the optic cortical fields by the method of luminescent revealing of primuline retrograde transport has been demonstrated in the experiments with cats. Initial neurons of the connective systems have been revealed
P V Sarthy et al.
Neuroscience letters, 25(3), 205-208 (1981-09-25)
Mouse retinal ganglion cells were labeled by retrograde axonal transport of the fluorescent dyes, DAPI and Primulin. The labeled retinae were dispersed by papain treatment and mechanical dissociation. Among the cells in the suspension, the ganglion cells could be unequivocally
Rose Scott-Moncrieff and the dawn of (bio)chemical genetics.
Martin C.
The Biochemical Journal, 38(2), 48-53 (2016)
[Role of membrane damage in the inactivation of yeast cells by visible light].
M E Pospelov et al.
Mikrobiologiia, 56(5), 882-885 (1987-09-01)
G Mazza et al.
Journal of agricultural and food chemistry, 50(26), 7731-7737 (2002-12-12)
In recent years, numerous studies have shown that the polyphenolics present in fruit and vegetable products exhibit a wide range of biological effects. However, there is little reliable information on the absorption of glycosylated and acylated anthocyanins in humans. In
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