Theaflavine Gallate

Modify Date: 2024-01-06 07:15:01

Theaflavine Gallate Structure
Theaflavine Gallate structure
Common Name Theaflavine Gallate
CAS Number 31629-79-5 Molecular Weight 716.598
Density 1.9±0.1 g/cm3 Boiling Point 1234.0±65.0 °C at 760 mmHg
Molecular Formula C36H28O16 Melting Point N/A
MSDS USA Flash Point 391.4±27.8 °C

 Names

Name Theaflavine Gallate
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.9±0.1 g/cm3
Boiling Point 1234.0±65.0 °C at 760 mmHg
Molecular Formula C36H28O16
Molecular Weight 716.598
Flash Point 391.4±27.8 °C
Exact Mass 716.137756
LogP 3.26
Vapour Pressure 0.0±0.3 mmHg at 25°C
Index of Refraction 1.898
Storage condition ?20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport

 Articles22

More Articles
Black tea polyphenols inhibit tumor proteasome activity.

In Vivo 26(2) , 197-202, (2012)

Tea is a widely consumed beverage and its constituent polyphenols have been associated with potential health benefits. Although black tea polyphenols have been reported to possess potent anticancer ac...

The microbiota is essential for the generation of black tea theaflavins-derived metabolites.

PLoS ONE 7(12) , e51001, (2012)

Theaflavins including theaflavin (TF), theaflavin-3-gallate (TF3G), theaflavin-3'-gallate (TF3'G), and theaflavin-3,3'-digallate (TFDG), are the most important bioactive polyphenols in black tea. Beca...

Theaflavin-3-gallate and theaflavin-3'-gallate, polyphenols in black tea with prooxidant properties.

Basic Clin Pharmacol Toxicol. 103(1) , 66-74, (2008)

This study compared the in vitro responses of human gingival fibroblasts and of carcinoma cells derived from the tongue to theaflavin-3-gallate (TF-2A) and theaflavin-3'-gallate (TF-2B), polyphenols i...

 Synonyms

Theaflavin gallate
Benzoic acid, 3,4,5-trihydroxy-, 1,8-bis[(2R,3R)-3,4-dihydro-3,5,7-trihydroxy-2H-1-benzopyran-2-yl]-3,4-dihydroxy-5-oxo-5H-benzocyclohepten-6-yl ester
3,4-Dihydroxy-5-oxo-1,8-bis[(2R,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]-5H-benzo[7]annulen-6-yl 3,4,5-trihydroxybenzoate