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Rumexin

  • CasNo.:480-10-4
  • Purity:
  • Content:
  • MF:C21H20O11
  • Packing:
  • MW:448.383
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Reputable supplier selling Rumexin 480-10-4 with stock

  • Molecular Formula:C21H20O11
  • Molecular Weight:448.383
  • Vapor Pressure:1.09E-28mmHg at 25°C 
  • Melting Point:223-229 °C 
  • Refractive Index:1.774 
  • Boiling Point:823.2 °C at 760 mmHg 
  • PKA:6.20±0.40(Predicted) 
  • Flash Point:291.5 °C 
  • PSA:190.28000 
  • Density:1.79 g/cm3 
  • LogP:-0.24450 

ASTRAGALIN(Cas 480-10-4) Usage

source

Astragalin belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Astragalin exists as a solid, slightly soluble (in water), and a very weakly acidic compound (based on its pKa). Within the cell, astragalin is primarily located in the cytoplasm. Astragalin can be converted into astragalin heptaacetate and 2''-acetylastragalin. Outside of the human body, astragalin can be found in a number of food items such as tamarind, american cranberry, chickpea, and bilberry. This makes astragalin a potential biomarker for the consumption of these food products.

Overview

Astragalin is a chemical compound. It can be isolated from Phytolacca americana (the American pokeweed) or in the methanolic extract of fronds of the fern Phegopteris connectilis.t is also found in wine.

Definition

ChEBI: A kaempferol O-glucoside in which a glucosyl residue is attached at position 3 of kaempferol via a beta-glycosidic linkage.

InChI:InChI=1/C21H20O11/c22-7-13-15(26)17(28)18(29)21(31-13)32-20-16(27)14-11(25)5-10(24)6-12(14)30-19(20)8-1-3-9(23)4-2-8/h1-6,13,15,17-18,21-26,28-29H,7H2/t13-,15-,17+,18-,21+/m1/s1

480-10-4 Relevant articles

Phlomisflavosides A and B, new flavonol bisglycosides from Phlomis spinidens

Takeda, Yoshio,Isai, Natsuko,Masuda, Toshiya,Honda, Gisho,Takaishi, Yoshihisa,Ito, Michiho,Otsuka, Hideaki,Ashurmetov, Ozodbek A.,Khodzhimatov, Olimjon K.

, p. 1039 - 1041 (2001)

From the aerial parts of Phlomis spinide...

-

Isobe,T.,Ito,N.

, p. 1877 (1980)

-

STRUCTURES AND ACCUMULATION PATTERNS OF SOLUBLE AND INSOLUBLE PHENOLICS FROM NORWAY SPRUCE NEEDLES

Strack, Dieter,Heilemann, Juergen,Wray, Victor,Dirks, Herbert

, p. 2071 - 2078 (1989)

Key Word Index - Picea abies; Pinaceae; ...

An Ambidextrous Polyphenol Glycosyltransferase PaGT2 from Phytolacca americana

Fukuda, Yohta,Hamada, Hiroki,Inoue, Tsuyoshi,Kawakami, Koki,Maharjan, Rakesh,Nakayama, Taisuke,Nakayama, Toru,Okimoto, Yuta,Ozaki, Shin-Ichi,Shimomura, Naomichi

, p. 2551 - 2561 (2020)

The glycosylation of small hydrophobic c...

Functional Characterization and Protein Engineering of a Triterpene 3-/6-/2′-O-Glycosyltransferase Reveal a Conserved Residue Critical for the Regiospecificity

Bao, Yang-Oujie,Gao, Bai-Han,Li, Fu-Dong,Qiao, Xue,Shi, Xiao-Meng,Su, Hui-Fei,Wang, Hai-Dong,Ye, Min,Yi, Yang,Zhang, Meng

supporting information, (2022/01/06)

Engineering the function of triterpene g...

Highly Promiscuous Flavonoid 3- O-Glycosyltransferase from Scutellaria baicalensis

Wang, Zilong,Wang, Shuang,Xu, Zheng,Li, Mingwei,Chen, Kuan,Zhang, Yaqun,Hu, Zhimin,Zhang, Meng,Zhang, Zhiyong,Qiao, Xue,Ye, Min

supporting information, p. 2241 - 2245 (2019/03/19)

A highly regio-specific and donor-promis...

Ep7GT, a glycosyltransferase with sugar donor flexibility from: Epimedium pseudowushanense, catalyzes the 7- O -glycosylation of baohuoside

Feng, Keping,Chen, Ridao,Xie, Kebo,Chen, Dawei,Liu, Jimei,Du, Wenyu,Yang, Lin,Dai, Jungui

, p. 8106 - 8114 (2019/09/19)

Icariin (1a), a 7-O-glycosylated flavono...

480-10-4 Process route

kaempferol 3-O-[2'',6''-di-O-(trans-p-coumaroyl)]-β-D-glucopyranoside
121651-61-4

kaempferol 3-O-[2'',6''-di-O-(trans-p-coumaroyl)]-β-D-glucopyranoside

astragalin
480-10-4

astragalin

p-Coumaric Acid
7400-08-0,50940-26-6

p-Coumaric Acid

Conditions
Conditions Yield
With potassium hydroxide; In 1,4-dioxane; for 3h;
trans-tiliroside
22153-44-2,68170-52-5,72691-81-7,104641-16-9,20316-62-5,163956-16-9

trans-tiliroside

astragalin
480-10-4

astragalin

p-Coumaric Acid
7400-08-0,50940-26-6

p-Coumaric Acid

Conditions
Conditions Yield
With sodium hydroxide; for 2.5h; Product distribution; Ambient temperature; hydrolysis;
10 mg
With sodium hydroxide; at 50 - 60 ℃;

480-10-4 Upstream products

  • 133-89-1
    133-89-1

    UDP-glucose

  • 520-18-3
    520-18-3

    kaempferol

  • 67-56-1
    67-56-1

    methanol

  • 144027-78-1
    144027-78-1

    resinoside A

480-10-4 Downstream products

  • 520-18-3
    520-18-3

    kaempferol

  • 2280-44-6
    2280-44-6

    D-Glucose

  • 2636-51-3
    2636-51-3

    Astragalin-acetat

  • 492-61-5
    492-61-5

    β-D-glucose

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