Glycitin

Modify Date: 2024-01-02 18:53:40

Glycitin Structure
Glycitin structure
Common Name Glycitin
CAS Number 40246-10-4 Molecular Weight 446.404
Density 1.5±0.1 g/cm3 Boiling Point 751.1±60.0 °C at 760 mmHg
Molecular Formula C22H22O10 Melting Point 210ºC
MSDS Chinese USA Flash Point 264.1±26.4 °C

 Use of Glycitin


Glycitin is a natural isoflavone isolated from legumes; promotes the proliferation of bone marrow stromal cells and osteoblasts and suppresses bone turnover.

 Names

Name 3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 751.1±60.0 °C at 760 mmHg
Melting Point 210ºC
Molecular Formula C22H22O10
Molecular Weight 446.404
Flash Point 264.1±26.4 °C
Exact Mass 446.121307
PSA 159.05000
LogP 0.16
Vapour Pressure 0.0±2.6 mmHg at 25°C
Index of Refraction 1.675
Storage condition Store at -20

 Safety Information

Hazard Codes Xi
Safety Phrases 24/25
RIDADR NONH for all modes of transport
WGK Germany 3.0

 Synthetic Route

~6%

Glycitin Structure

Glycitin

CAS#:40246-10-4

Literature: Shimoda, Kei; Hamada, Hiroki Molecules, 2010 , vol. 15, # 8 p. 5153 - 5161

~%

Glycitin Structure

Glycitin

CAS#:40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

~68%

Glycitin Structure

Glycitin

CAS#:40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

~%

Glycitin Structure

Glycitin

CAS#:40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

~%

Glycitin Structure

Glycitin

CAS#:40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

~94%

Glycitin Structure

Glycitin

CAS#:40246-10-4

Literature: Al-Maharik, Nawaf; Botting, Nigel P. European Journal of Organic Chemistry, 2008 , # 33 p. 5622 - 5629

~%

Glycitin Structure

Glycitin

CAS#:40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

 Articles2

More Articles
Effects of naturally occurring isoflavones on prostaglandin E2 production.

Planta Med. 68 , 97-100, (2002)

Previously, we reported that the isoflavones tectorigenin and tectoridin, a glycosylated tectorigenin, isolated from the rhizomes of Belamcanda chinensis have an activity to inhibit prostaglandin (PG)...

Isoflavone glycosides from the flowers of Pueraria thunbergiana. Park HJ

Phytochemistry 51 , 147-151, (1999)

 Synonyms

BIDD:ER0468
4',7-Dihydroxy-6-methoxyisoflavone-7-D-glucoside
3-(4-Hydroxyphenyl)-6-methoxy-4-oxo-4H-chromen-7-yl b-D-glucopyranoside
MFCD00800711
Glycitein 7-O-|A-glucoside
Glycitein-7-|A-O-glucoside
Glycitein 7-O-β-D-glucoside
3-(4-Hydroxyphenyl)-6-methoxy-4-oxo-4H-chromen-7-yl β-D-glucopyranoside
4H-1-Benzopyran-4-one
4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-
Glycitin
Glycitein 7-O-glucoside
Top Suppliers:I want be here
  • BioBioPha
  • China
  • Product Name: Glycitin
  • Price: ¥Inquiry/20mg
  • Purity: 98.0%
  • Stocking Period: 1 Day
  • Contact: Xueping-Zheng




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Price: $66/10mM*1mLinDMSO

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