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Theaflavin monogallate

analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C36H28O16
Número de CAS:
Peso molecular:
716.60
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

Quality Level

description

Mixture of Theaflavin 3-gallate and Theaflavin 3′-gallate

assay

≥80% (HPLC)

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

storage temp.

−20°C

InChI

1S/C36H28O16/c37-14-5-20(39)18-10-25(44)33(50-28(18)7-14)12-1-16-17(34-26(45)11-19-21(40)6-15(38)8-29(19)51-34)9-27(46)35(30(16)32(48)24(43)2-12)52-36(49)13-3-22(41)31(47)23(42)4-13/h1-9,25-26,33-34,37-42,44-47H,10-11H2,(H,43,48)/t25-,26?,33-,34?/m1/s1

InChI key

CKDOBTPKUHSESZ-MALJIYBWSA-N

General description

Theaflavin monogallate is a polyphenol,[1] and a naturally available antioxidant belonging to the group of theaflavins.[2]

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Theaflavin monogallate may be used as a reference standard in the determination of theaflavin monogallate in tea using reversed-phase high-performance liquid chromatography (RP-HPLC) and capillary electrophoresis (CE).[1]

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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)


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Mario A Vermeer et al.
Journal of agricultural and food chemistry, 56(24), 12031-12036 (2008-12-04)
Tea is one of the most widely consumed beverages in the world and may be associated with reduced heart disease rates. Theaflavins, which are formed in the production of black tea, have been suggested being responsible for the blood-cholesterol-lowering (BCL)
Toshiro Matsui et al.
Journal of agricultural and food chemistry, 55(1), 99-105 (2007-01-04)
To clarify the postprandial glucose suppression effect of flavonoids, the inhibitory effects of catechins and theaflavins against alpha-glucosidase (AGH) were examined in this study. It was initially demonstrated that theaflavins and catechins preferentially inhibited maltase rather than sucrase in an
G Y Yang et al.
Carcinogenesis, 21(11), 2035-2039 (2000-11-04)
The biological activities of theaflavin (TF), theaflavin gallate (TFG) and theaflavin digallate (TFdiG) from black tea and (-)-epigallocatechin 3-gallate (EGCG) and (-)-epigallocatechin (EGC) from green tea were investigated using SV40-immortalized (33BES) and Ha-ras gene transformed (21BES) human bronchial epithelial cell
Changjun Yang et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 861(1), 140-144 (2007-12-08)
In order to separate the main individual theaflavin monomers from black tea, high-speed countercurrent chromatography (HSCCC) and Sephadex LH-20 column chromatography were applied. The results showed that theaflavin (TF1), theaflavin-3-gallate (TF2A), theaflavin-3'-gallate (TF2B) and theaflavin-3,3'-digallate (TF3) can be obtained by
Yalun Su et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 27(10), 732-733 (2005-04-27)
Qimen black tea has strong inhibitory activity of canola oil oxidation. Four antioxidant compounds, theaflavin (TF1), theaflavin-3-gallate (TF2A), theaflavin-3'-gallate (TF2B) and theaflavin digallate (TF3), were isolated from acetic acetate extract of black tea by silica gel and sephadex LH-20 column

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