Catalogue Number
BD-P0198
Analysis Method
Specification
98.0%(HPLC)
Storage
-20℃
Molecular Weight
1079.2
Appearance
Powder
Botanical Source
This product is isolated and purified from the herbs of Tribulus terrestris L.
Structure Type
Category
SMILES
CC1=C(OC2C1C3(C(C2)C4CCC5CC(CCC5(C4CC3=O)C)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O
Synonyms
IUPAC Name
Density
1.5±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
Boiling Point
Melting Point
InChl
InChl Key
TVRRDUXJKROMDX-CXLJPAHDSA-N
WGK Germany
RID/ADR
HS Code Reference
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:193605-07-1) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
29019318
Addendum for Euro Surveill. 2017;22(8)
Eurosurveillance editorial team 1
2017 Oct 5
Description :
Phytochemistry (1997) 45(4) 811-817. Steroidal saponins from fruits of Tribulus terrestris.[Reference: WebLink]METHODS AND RESULTS:Further studies on the constituents of the fruits of Tribulus terrestris led to the isolation of six new furostanol saponins, 26-O-β-D-glucopyranosyl (25R)-furostane-2α,3β,22α,26-tetrol-3-O-β-D-glucopyranosyl (1-4)-β-D- galactopyranoside, 26-O-β-D-glucopyranosyl (25R,S)-5α-furostane- 2α,3β,22α,26-tetrol-3-O-β-D-galactopyranosyl(1-2)-β-D-glucopyranosyl(1- 4)-β-D-galactopyranoside, 26-O-β-D-glucopyranosyl (25R,S)-5α-furostane- 3β,22α,26-triol-3-O-β-D-galactopyranosyl(1-2)-β-D-glucopyranosyl(1-4)- β-D-galactopyranoside, 26-O-β-D-glucopyranosyl (25R,S)-5α-furostan-12- one-3β,22α,26-triol-3-O-β-D-galactopyranosyl(1-2)-β-D-glucopyranosyl(1- 4)-β-D-galactopyranoside, 26-O-β-D-glucopyranosyl (25R,S)-furost-5-ene- 3β,22α,26-triol-3-O-β-D-galactopyranosyl(1-2)-β-D-glucopyranosyl(1-4)- β-D-galactopyranoside, 26-O-β-D-glucopyranosyl (25R)-5α-furost-20(22)-en- 12-one-3β,26-diol-3-O-β-D-galactopyranosyl(1-2)-β-D-glucopyranosyl(1-4)- β-D-galactopyranoside, named terrestrosin F, terrestrosin G, terrestrosin H, terrestrosin I, terrestrosin J, Terrestrosin K, respectively. CONCLUSIONS: The structures were elucidated on the basis of spectroscopic studies of the isolated compounds and their hydrolysed products.