6-O-Feruloylglucose | CAS:137887-25-3 | Manufacturer ChemFaces

6-O-Feruloylglucose

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6-O-Feruloylglucose Description

Source:	The herbs of Catalpa fargesii f. duclouxii
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

Sci. China C. Life Sci.,1999,42(4):420-6.

Reaction of hydroxyl radical with phenylpropanoid glycoside and its derivatives by pulse radiolysis.[Pubmed: 18763133 ]

METHODS AND RESULTS:
The reaction of hydroxyl radical with 1 phenylpropanoid glycoside (PPG), cistanoside C, and its 3 derivatives: 1-0-beta-D-2-(p-hydroxyphenyl)-ethanyl-glucose, 6-O-(E)-femloyl-glucose(6-O-Feruloylglucose) and 6-O-(E)-p-hydroxy-cinnarnoylglucose isolated from folk medicinal herbs was investigated by pulse radiolysis technique respectively. The reaction rate constants were determined by analysis of built-up trace of absorption at lambda(max) of specific transient absorption spectra of PPG and its derivatives upon attacking . OH. All four compounds react with . OH at close to diffusion controlled rate (1. 03 x 10(9)-19.139 x 10(9) L . mol(-1) . s(-1)), suggesting that they are effective . OH scavengers.
CONCLUSIONS:
The results demonstrated that the numbers of phenolic hydroxyl groups of PPG and its derivatives are directly related to their scavenging activities. By comparing the reaction rates of . OH with 1-O-beta-D-2-(p-hydroxyphenyl)-ethanyl-glucose, 6-O-(E)-feruloyl-glucose (6-O-Feruloylglucose)or 6-O-(E)-p-hydroxy-cinnomoyl-glucose, it is evident that the phenylethyl group is more impofiant than phenylacryloyl group for scavenging . OH.

Product Name	6-O-Feruloylglucose
Price:
CAS No.:	137887-25-3
Catalog No.:	CFN99431
Molecular Formula:	C₁₆H₂₀O₉
Molecular Weight:	356.3 g/mol
Purity:	>=98%
Type of Compound:	Phenylpropanoids
Physical Desc.:	Powder
Source:	The herbs of Catalpa fargesii f. duclouxii
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Download:	COA MSDS SDF Manual
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Antioxidants Compound Library Phenylpropanoids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	2.8066 mL	14.0331 mL	28.0662 mL	56.1325 mL	70.1656 mL
5 mM	0.5613 mL	2.8066 mL	5.6132 mL	11.2265 mL	14.0331 mL
10 mM	0.2807 mL	1.4033 mL	2.8066 mL	5.6132 mL	7.0166 mL
50 mM	0.0561 mL	0.2807 mL	0.5613 mL	1.1226 mL	1.4033 mL
100 mM	0.0281 mL	0.1403 mL	0.2807 mL	0.5613 mL	0.7017 mL

CFN98149	Angoroside C	115909-22-3	784.75	C₃₆H₄₈O₁₉
CFN95913	Leonoside F	1360075-79-1	638.6	C₂₇H₄₂O₁₇
CFN70272	Teupolioside	143617-02-1	786.7	C₃₅H₄₆O₂₀
CFN95111	2-O-cinnamoyl-beta-D-glucose	N/A	310.3	C₁₅H₁₈O₇
CFN95105	6-O-(E)-Caffeoylglucopyranose	209797-79-5	342.3	C₁₅H₁₈O₉
CFN99431	6-O-Feruloylglucose	137887-25-3	356.3	C₁₆H₂₀O₉
CFN99432	Arillatose B	137941-45-8	518.5	C₂₂H₃₀O₁₄
CFN95596	1-O-Feruloylglucose	64625-37-2	356.3	C₁₆H₂₀O₉
CFN95302	Clemomandshuricoside B	905294-48-6	502.2	C₂₂H₃₀O₁₃
CFN95920	Peiioside A	1610618-94-4	620.6	C₂₆H₃₆O₁₇