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Glycitein

CAS No.
40957-83-3
Chemical Name:
Glycitein
Synonyms
Gycitein;GLYCITEIN;GLYCETEIN; Glicetein;Glycitein-RM;Glycitein(SH);Glycitein, >=98%;Glycitein (15 mg);Glycitein USP/EP/BP;GLYCITEIN,FROMSOYBEAN
CBNumber:
CB7253674
Molecular Formula:
C16H12O5
Molecular Weight:
284.26
MDL Number:
MFCD00016679
MOL File:
40957-83-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-22 18:57:36
Product description Number Pack Size Price
Glycitein phyproof? Reference Substance PHL89692 10mg $361
Glycitein analytical standard 43534 10mg $350
Glycitein United States Pharmacopeia (USP) Reference Standard 1295844 15mg $1260
Glycitein G0634 25MG $182
Glycitein ≥98% 14162 5mg $49
More product size

Glycitein Properties

Melting point >300°C
Boiling point 547.4±50.0 °C(Predicted)
Density 1.420±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility Aqueous Base (Slightly), DMSO (Slightly)
pka 7.03±0.20(Predicted)
form Solid
color Light Brown
biological source synthetic (organic)
InChI InChI=1S/C16H12O5/c1-20-15-6-11-14(7-13(15)18)21-8-12(16(11)19)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3
InChIKey DXYUAIFZCFRPTH-UHFFFAOYSA-N
SMILES C1OC2=CC(O)=C(OC)C=C2C(=O)C=1C1=CC=C(O)C=C1
LogP 2.570 (est)
CAS DataBase Reference 40957-83-3(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 92M5F28TVF
UNSPSC Code 85151701
NACRES NA.51

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS06
Signal word  Danger
Hazard statements  H301-H311-H314-H331
Precautionary statements  P260-P264-P270-P271-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P403+P233-P405-P501
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
Safety Statements  24/25
WGK Germany  3
HS Code  29329990
Storage Class 11 - Combustible Solids

Glycitein price More Price(41)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHL89692 Glycitein phyproof? Reference Substance 40957-83-3 10mg $361 2026-03-19 Buy
Sigma-Aldrich 43534 Glycitein analytical standard 40957-83-3 10mg $350 2026-03-19 Buy
Sigma-Aldrich 1295844 Glycitein United States Pharmacopeia (USP) Reference Standard 40957-83-3 15mg $1260 2026-03-19 Buy
TCI Chemical G0634 Glycitein 40957-83-3 25MG $182 2026-03-19 Buy
Cayman Chemical 14162 Glycitein ≥98% 40957-83-3 5mg $49 2024-03-01 Buy
Product number Packaging Price Buy
PHL89692 10mg $361 Buy
43534 10mg $350 Buy
1295844 15mg $1260 Buy
G0634 25MG $182 Buy
14162 5mg $49 Buy

Glycitein Chemical Properties,Uses,Production

Description

Glycitein is an O-methylated isoflavone that comprises 5-10% of the total isoflavones in soy food products. This phytoestrogen is reported to have weak estrogenic activity, displacing estradiol binding at the estrogen receptor in vitro with an IC50 value of 3.94 μM. It suppresses the proliferation of osteoblasts and promotes differentiation from its progenitor. It has also been used to attenuate proliferation (10 μM) of aortic smooth muscle cells related to atherosclerotic vascular change in stroke-prone hypertensive rats and to protect against beta amyloid (Aβ)-induced toxicity and oxidative stress (100 μg/ml) in C. elegans expressing human Aβ.

Chemical Properties

Pale Orange Solid

Uses

Glycitein may be used as a reference standard in the determination of glycitein in hydrolyzed dry soya extracts using reversed-phase high-performance liquid chromatography (RP-HPLC).

Uses

Glycitein has been used as standard for the analysis of soy isoflavones and metabolites in urine. It has also been used to bind to recombinant estrogen and progesterone receptors to know the relative binding affinity (RBA) for detection of potential endocrine disruptors.

Uses

The compund shows an anti-cancer activity, plasma cholesterol reduction, reduction in postmenopausal bone loss

Definition

ChEBI: A methoxyisoflavone that is isoflavone substituted by a methoxy group at position 6 and hydroxy groups at positions 7 and 4'. It has been isolated from the mycelia of the fungus Cordyceps sinensis.

General Description

Glycitein is an isoflavone found in soy food products.

Biochem/physiol Actions

Glycitein is a soybean (yellow cultivar) isoflavonoid; its natural glycosides are synergistic with genistein in inducing specific gene expression. Glycitein may be used to study anti-oxidation processes at the level of gene transcription where it increases the binding of transcription factors [nuclear factor-E2-related factor 2 (Nrf2) and c-Jun] to the antioxidant response element (ARE) on HO-1 and NQO1 promoters. Glycitein may be used in combination with other isoflavonoids such as genistein and daidzein to study apoptosis.

Synthesis

Methanesulfonyl chloride

124-63-0

Ethanone, 1-(2,4-dihydroxy-5-methoxyphenyl)-2-(4-hydroxyphenyl)-

79744-58-4

Glycitein

40957-83-3

Under nitrogen protection, boron trifluoride ethyl ether complex (1.6 mL, 13.13 mmol) was slowly added to an anhydrous N,N-dimethylformamide (10 mL) solution of deoxybenzene coupling (0.6 g, 2.19 mmol). After 15 min of reaction, anhydrous N,N-dimethylformamide (2 mL) solution of methanesulfonyl chloride (0.84 mL, 10.95 mmol) was added dropwise. The reaction mixture was heated and stirred in an oil bath at 70°C for 5 hours. Upon completion of the reaction, the mixture was cooled to room temperature and slowly poured into ice-cooled saturated aqueous sodium acetate solution (50 mL). The precipitated solid was collected by filtration and recrystallized from 70% ethanol to afford 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-benzopyran-4-one as a yellow solid (0.53 g, 85% yield) with a melting point of 336-338°C. The product structure was determined by 1H NMR. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6) and mass spectrometry (EI, 70 eV): 1H NMR δ 10.63 (br s, 1H, 7-OH), 9.54 (br s, 1H, 4'-OH), 8.27 (s, 1H, H-2), 7.41 (s, 1H, H-5), 7.37 (d, J = 8.7 Hz. 2H, H-2', 6'), 6.92 (s, 1H, H-8), 6.79 (d, J = 8.7 Hz, 2H, H-3', 5'), 3.86 (s, 3H, OCH3); mass spectra m/z 284 (M+, 24%), 283 (100), 268 (15), 255 (20), 212 (41), 171 (15).

References

[1] Patent: US2007/203227, 2007, A1. Location in patent: Page/Page column 3

621-59-0
40957-83-3
Synthesis of Glycitein from Isovanillin
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View Lastest Price from Glycitein manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Glycitein pictures 2026-04-22 Glycitein
40957-83-3
US $50.00 / mL 99.94% 10g TargetMol Chemicals Inc.
	Glycitein pictures 2025-09-25 Glycitein
40957-83-3
US $8.00-1.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Glycitein pictures 2023-02-24 Glycitein
40957-83-3
US $0.00 / mg 5mg ≥98%(HPLC) 10 g Shanghai Standard Technology Co., Ltd.
  • Glycitein pictures
  • Glycitein
    40957-83-3
  • US $50.00 / mL
  • 99.94%
  • TargetMol Chemicals Inc.
  • 	Glycitein pictures
  • Glycitein
    40957-83-3
  • US $8.00-1.00 / KG
  • 99%
  • Henan Fengda Chemical Co., Ltd
  • Glycitein pictures
  • Glycitein
    40957-83-3
  • US $0.00 / mg
  • ≥98%(HPLC)
  • Shanghai Standard Technology Co., Ltd.

Glycitein Spectrum

GLYCETEIN GLYCITEIN 4',7-DIHYDROXY-6-METHOXYISOFLAVONE 4,7-DIHYDROXY-6-METHOXYISOFLAVONE 7,4'-DIHYDROXY-6-METHOXYISOFLAVONE Glicetein 7-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one 4H-1-Benzopyran-4-one, 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy- 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-chromen-4-one Glycitein, >=98% Glycitein, 98%, from soybean 4μ,7-Dihydroxy-6-methoxyisoflavone, Glycetein 3-(4-Hydroxyphenyl)-6-methoxy-7-hydroxy-4H-1-benzopyran-4-one Glycitein,4′,7-Dihydroxy-6-methoxyisoflavone, Glycetein Glycitein (15 mg) GLYCITEIN,FROMSOYBEAN Glycitein USP/EP/BP Gycitein Glycitein, ≥97% (HPLC) Glycitein (P) (Compendial Traceable) 4',7- Dihydroxy -6-methoxy Isoflavone (or ) GLYCITIN 7-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one GLYCITEIN (Compendial Traceable) Glycitein(SH) Glycitein-RM Coumarin Impurity 9 (Coumarin 30) Glycitein, 10 mM in DMSO 40957-83-3 40957-83-0 Nucleoside Analogs Nucleosides, Nucleotides, Oligonucleotides Biochemicals and Reagents BioChemical Intermediates & Fine Chemicals Pharmaceuticals The group of Daidzin inhibitor chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract Iso-Flavones