D-sorbose

Base Information

Chemical Name:D-sorbose
CAS No.:3615-56-3
Molecular Formula:C6H12O6
Molecular Weight:180.158
Hs Code.:29400090
European Community (EC) Number:222-796-0
UNII:JJ09461NJS
DSSTox Substance ID:DTXSID101018679
Nikkaji Number:J94.872A
Wikidata:Q27108962
Metabolomics Workbench ID:50860
Mol file:3615-56-3.mol

Synonyms:D Sorbose;D-Sorbose;L Sorbose;L-Sorbose;Sorbose

Suppliers and Price of D-sorbose

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
D-Sorbose
500mg
$ 360.00

TRC
D-Sorbose
500mg
$ 175.00

TCI Chemical
D-Sorbose >98.0%(HPLC)
100mg
$ 77.00

Sigma-Aldrich
D-(+)-Sorbose ≥99%
100mg
$ 229.00

Sigma-Aldrich
D-(+)-Sorbose ≥99%
500mg
$ 936.00

Medical Isotopes, Inc.
D-Sorbose
500 mg
$ 380.00

Medical Isotopes, Inc.
D-Sorbose
2 g
$ 590.00

Chem-Impex
D-(+)-Sorbose ≥ 99% (GC)
1G
$ 75.00

Chem-Impex
D-(+)-Sorbose,99%(GC) 99%(GC)
250MG
$ 47.88

Chem-Impex
D-(+)-Sorbose,99%(GC) 99%(GC)
5G
$ 297.92

Total 35 raw suppliers

Chemical Property of D-sorbose

Chemical Property:

Vapor Pressure:4.23E-08mmHg at 25°C
Melting Point:163-165 °C
Refractive Index:1.645
Boiling Point:551.7 °C at 760 mmHg
PKA:11.86±0.20(Predicted)
Flash Point:301.5 °C
PSA：118.22000
Density:1.589 g/cm³
LogP:-3.37720
XLogP3:-3.2
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:180.06338810
Heavy Atom Count:12
Complexity:147

Purity/Quality:

≥99% ^*data from raw suppliers

D-Sorbose ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 24/25-36-26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C(C(C(C(C(=O)CO)O)O)O)O
Isomeric SMILES:C([C@H]([C@@H]([C@H](C(=O)CO)O)O)O)O

Technology Process of D-sorbose

There total 118 articles about D-sorbose 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: 92.0%

: 96-26-4,26776-70-5
dihydroxyacetone

: 56-82-6,367-47-5,26793-98-6
Glyceraldehyde

: 453-17-8,367-47-5,26793-98-6
D-Glyceraldehyde

: 57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8
L-fructose

Guidance literature:: With E_. coli BL₂₁ (DE₃) cells harboring pETDRhaD aldolase; sodium borate buffer; In water; toluene; at 37 ℃; for 16h; pH=7.6;
DOI:10.1002/adsc.200600356