4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-

Base Information

Chemical Name:4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-
CAS No.:28564-83-2
Molecular Formula:C6H8O4
Molecular Weight:144.127
Hs Code.:
European Community (EC) Number:821-120-7
UNII:RAE1LU40SR
DSSTox Substance ID:DTXSID00880920
Nikkaji Number:J101.368H
Mol file:28564-83-2.mol

Synonyms:2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one;DDMP-4-one

Suppliers and Price of 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-

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

American Custom Chemicals Corporation
2,3-DIHYDRO-3,5-DIHYDROXY-6-METHYL-4(H)-PYRAN-4-ONE 95.00%
5MG
$ 502.21

Total 65 raw suppliers

Chemical Property of 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-

Chemical Property:

Vapor Pressure:0.000433mmHg at 25°C
Refractive Index:1.578
Boiling Point:281.1 °C at 760 mmHg
PKA:9.30±0.40(Predicted)
Flash Point:121.7 °C
PSA：66.76000
Density:1.482 g/cm³
LogP:-0.26390
Storage Temp.:-20°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:-0.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:144.04225873
Heavy Atom Count:10
Complexity:194

Purity/Quality:

97% ^*data from raw suppliers

2,3-DIHYDRO-3,5-DIHYDROXY-6-METHYL-4(H)-PYRAN-4-ONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=O)C(CO1)O)O
General Description 2,3-Dihydro-3,5-dihydroxy-6-methyl-4(H)-pyran-4-one (DDMP) is a Maillard reaction product known for its antioxidant properties, particularly due to its hydroxyl groups, with the enol structure at the olefin position playing a critical role in scavenging free radicals such as ABTS+, DPPH, and galvinoxyl radicals. 2,3-Dihydro-3,5-dihydroxy-6-methyl-4(H)-pyran-4-one's antioxidant activity diminishes when its hydroxyl groups are protected, highlighting the importance of these functional groups in its radical-scavenging capacity. Additionally, DDMP has been identified as a pyrolysis product of proline Amadori compounds, further linking it to thermal degradation pathways in Maillard chemistry.

Technology Process of 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-

There total 30 articles about 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl- 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: 97.22%