Glycitin

Base Information

Chemical Name:Glycitin
CAS No.:40246-10-4
Molecular Formula:C22H22O10
Molecular Weight:446.411
Hs Code.:29389090
UNII:G2S44P62XC
DSSTox Substance ID:DTXSID80193227
Nikkaji Number:J396.591K
Wikipedia:Glycitin
Wikidata:Q27149383
Metabolomics Workbench ID:22234
Mol file:40246-10-4.mol

Synonyms:glycitein 7-O-glucoside;glycitin

Suppliers and Price of Glycitin

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
Glycitin
25mg
$ 352.00

Usbiological
Glycitin
20mg
$ 280.00

TRC
Glycitin
10mg
$ 105.00

Sigma-Aldrich
Glycitin
5mg
$ 126.00

Sigma-Aldrich
Glycitin United States Pharmacopeia (USP) Reference Standard
15mg
$ 807.00

Sigma-Aldrich
Glycitin
25mg
$ 498.00

Labseeker
Glycitin 95
10mg
$ 583.00

JR MediChem
Glycitin 98%
20mg
$ 800.00

DC Chemicals
Glycitin >98%,StandardReferencesGrade
20 mg
$ 280.00

Crysdot
Glycitin 98+%
50mg
$ 144.00

Total 82 raw suppliers

Chemical Property of Glycitin

Chemical Property:

Appearance/Colour:White solid
Vapor Pressure:1.07E-23mmHg at 25°C
Melting Point:210 °C
Refractive Index:1.674
Boiling Point:751.1 °C at 760 mmHg
PKA:9.62±0.30(Predicted)
Flash Point:264.1 °C
PSA：159.05000
Density:1.545 g/cm³
LogP:0.35290
Storage Temp.:Store at -20
Solubility.:DMSO (Slightly, Sonicated), Methanol (Slightly, Heated)
XLogP3:0.6
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:5
Exact Mass:446.12129689
Heavy Atom Count:32
Complexity:690

Purity/Quality:

NLT 98% ^*data from raw suppliers

Glycitin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: Total 1 MSDS from other Authors

Useful:

Canonical SMILES:COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O
Isomeric SMILES:COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
Uses A derivative of Glycitein. Inhibitor A metabolite of isoflavone derivatives. A metabolite of isoflavone derivatives. A derivative of Glycitein. Inhibitor.

Technology Process of Glycitin

There total 11 articles about Glycitin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 94.0%

: 1105697-69-5
4'-O-hexanoylglycitein-7-yl 2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranoside

: 40246-10-4
glycitin

Guidance literature:: With water; potassium carbonate; In tetrahydrofuran; methanol; at 40 ℃; for 5h; Inert atmosphere;
DOI:10.1002/ejoc.200800803

Reference yield: 70.0%

: 182284-73-7
Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[3-(4-hydroxy-phenyl)-6-methoxy-4-oxo-4H-chromen-7-yloxy]-tetrahydro-pyran-3-yl ester

: 40246-10-4
glycitin

Guidance literature:: With sodium methylate; for 0.333333h; Heating;

Reference yield: 5.0%

: 40957-83-3
glycitein

: 50-99-7
D-glucose

: 1237605-01-4
glycitein 4'-O-β-D-glucoside

: 40246-10-4
glycitin

Guidance literature:: With Lactobacillus delbrueckii subsp. bulgaricus; In water; at 30 ℃; for 120h; Culture medium; Microbiological reaction; Enzymatic reaction;
DOI:10.3390/molecules15085153