Pterostilbene Basic information |
Product Name: | Pterostilbene |
Synonyms: | AKOS 236-80;3,5-DI-4'-HYDROXYSTILBENE;3',5'-DI-4-STILBENOL;4-[(1E)-2-(3,5-DIPHENYL)NYL]PHENOL;PTEROSTILBENE;PTEROCARPUS MARSUPIUM;TRANS-3,5-DI-4'-HYDROXYSTILBENE;(E)-3,5-Di-4'-hydroxystilbene |
CAS: | 537-42-8 |
MF: | C16H16O3 |
MW: | 256.3 |
EINECS: | 611-041-4 |
Product Categories: | chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;natural product;Health supplements;Herb extract;Inhibitors |
Mol File: | 537-42-8.mol |
Pterostilbene Chemical Properties |
Melting point | 89-92 ºC |
Boiling point | 420.4±35.0 °C(Predicted) |
density | 1.169±0.06 g/cm3(Predicted) |
storage temp. | 2-8°C |
solubility | DMSO: >20mg/mL |
form | solid |
pka | 9.96±0.26(Predicted) |
λmax | 321nm(MeOH)(lit.) |
Safety Information |
Hazard Codes | Xi,N |
Risk Statements | 41-51/53 |
Safety Statements | 26-39-61 |
RIDADR | 3077 |
WGK Germany | 3 |
HazardClass | IRRITANT |
PackingGroup | Ⅲ |
HS Code | 29095000 |
Pterostilbene Usage And Synthesis |
Description |
Pterostilbene(trans-3,5-di-4-hydroxystilbene) is a stilbenoid chemically related to resveratrol.In plants, it serves a defensive phytoalexin role. |
Natural occurrence |
Pterostilbene is found in almonds,various Vaccinium berries (including blueberries), grape leaves and vines,and Pterocarpus marsupium heartwood. |
Safety information |
Pterostilbene is considered to be a corrosive substance, is dangerous upon exposure to the eyes, and is an environmental toxin, especially to aquatic life. |
Chemical Properties | White solid |
Definition | ChEBI: A stilbenol that consists of trans-stilbene bearing a hydroxy group at position 4 as well as two substituents at positions 3' and 5'. |