Naringin dihydrochalcone Basic Product Information

Product Name	Naringin dihydrochalcone	CAS	18916-17-1
Synonyms	Glucopyranoside,3,5-dihydroxy-4-(p-hydroxyhydrocinnamoyl)phenyl 2-O-(6-deoxy-a-L-mannopyranosyl)-, b-D- (8CI);Phloretin, 4'-(2-O-a-L-rhamno-b-D-glucopyranoside) (6CI);1-[4-[[2-O-(6-Deoxy-L-mannopyranosyl)-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)-1-propanone;	Molecular Formula	C27H34O14
EINECS Number		Molecular Structure
Appearance	Light Yellow Powder
Purity	Enterprise technical standards
Supply Ability

Naringin dihydrochalcone Quality documents

Naringin dihydrochalcone Appearance/Package/Shipping/Storage

package

storage condition

Store in cool & dry place,Keep away from strong light and heat

Naringin dihydrochalcone Application

Naringin dihydrochalcone literature

Synthetic method for naringin dihydrochalcone

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Paragraph 0022, (2016/10/09)

The invention discloses a synthetic method for naringin dihydrochalcone. The method comprises the following steps that natural extract naringin is adopted as a raw material, alkali dissolution is performed and then filtering is performed; a polarity organic solvent is added, a catalyst is added, hydrogenation reduction is performed on the condition of the certain pressure, the catalyst is filtered away after hydrogen absorption is completed, the pH value is adjusted for crystallization, a product is obtained through filtration, and the naringin dihydrochalcone can be obtained; the liquid phase purity is 98.5% or above, and the molar yield is 96% or above.

Dihydrochalcones: Evaluation as novel radical scavenging antioxidants

Nakamura, Yoshimasa,Watanabe, Shigeo,Miyake, Nobuyuki,Kohno, Hiroyuki,Osawa, Toshihiko

, p. 3309 - 3312 (2007/10/03)

Dihydrochalcones are a family of bicyclic flavonoids, defined by the presence of two benzene rings joined by a saturated three carbon bridge. In the present study, we systematically examined the antioxidant activities of dihydrochalcones against the stable free radical (1,1-diphenyl-2-picrylhydrazyl) and lipid peroxidation in the erythrocyte membrane. All dihydrochalcones exhibited higher antioxidant activities than the corresponding flavanones. The ¹H NMR analysis indicated that the active dihydrochalcone has a time-averaged conformation in which the aromatic A ring is orthogonal to the carbonyl group, while the inactive dihydrochalcone such as 2′-O-methyl-phloretin has a strongly hydrogen-bonded phenolic hydroxyl group, suggestive of a coplanar conformation. A hydroxyl group at the 2′-position of the dihydrochalcone A ring, newly formed by reduction of the flavanone C ring, is an essential pharmacophore for its radical scavenging potential.

Naringin dihydrochalcone Upstream and downstream

18916-17-1 Upstream product

• 10236-47-2

  naringin 

• 50376-43-7

  4'-rhamnoglucosyloxy-2',4,6'-trihydroxychalcone 

• 10236-47-2

  naringin 

18916-17-1 Downstream Products

• 60-82-2

  3-(4-Hydroxy-phenyl)-1-(2,4,6-trihydroxy-phenyl)-propan-1-on 

• 4192-90-9

  4'-(β-D-glucopyranosyloxy)-2',4”,6'-trihydroxydihydrochalcone 

• 111316-17-7

  4,2′,4′-trihydroxy-6′-methoxydihydrochalcone 

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