1,5-Anhydro-d-mannitol

Base Information

Chemical Name:1,5-Anhydro-d-mannitol
CAS No.:492-93-3
Molecular Formula:C6H12O5
Molecular Weight:164.158
Hs Code.:29400090
UNII:6V415COZ8I
DSSTox Substance ID:DTXSID701314215
Nikkaji Number:J12.575J
Wikidata:Q27121518
Metabolomics Workbench ID:57249
ChEMBL ID:CHEMBL3800290
Mol file:492-93-3.mol

Synonyms:1,5-anhydro-D-mannitol;1,5-anhydro-mannitol;1,5-anhydromannitol

Suppliers and Price of 1,5-Anhydro-d-mannitol

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

TRC
1,5-Anhydro-D-mannitol
1g
$ 1635.00

Biosynth Carbosynth
1,5-Anhydro-D-mannitol
100 mg
$ 175.00

Biosynth Carbosynth
1,5-Anhydro-D-mannitol
50 mg
$ 95.00

Biosynth Carbosynth
1,5-Anhydro-D-mannitol
250 mg
$ 350.00

Biosynth Carbosynth
1,5-Anhydro-D-mannitol
500 mg
$ 600.00

Biosynth Carbosynth
1,5-Anhydro-D-mannitol
1 g
$ 950.00

Apolloscientific
1,5-Anhydro-D-mannitol 98%min
250mg
$ 782.00

Apolloscientific
1,5-Anhydro-D-mannitol 98%min
500mg
$ 1298.00

Apolloscientific
1,5-Anhydro-D-mannitol 98%min
100mg
$ 363.00

American Custom Chemicals Corporation
1,5-ANHYDRO-D-MANNITOL 95.00%
500MG
$ 1732.50

Total 18 raw suppliers

Chemical Property of 1,5-Anhydro-d-mannitol

Chemical Property:

Vapor Pressure:3.21E-07mmHg at 25°C
Melting Point:156-157?C
Boiling Point:376.8°Cat760mmHg
Flash Point:181.7°C
PSA：90.15000
Density:1.533g/cm³
LogP:-2.53980
Storage Temp.:-20°C Freezer, Under Inert Atmosphere
XLogP3:-2.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:164.06847348
Heavy Atom Count:11
Complexity:128

Purity/Quality:

98%Min ^*data from raw suppliers

1,5-Anhydro-D-mannitol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(C(C(O1)CO)O)O)O
Isomeric SMILES:C1[C@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
Uses A carbohydrate metabolism regulator that has been shown to inhibit gluconeogenesis from lactate plus pyruvate and from substrates that enter the gluconeogenic pathway as triose phosphate.

Technology Process of 1,5-Anhydro-d-mannitol

There total 47 articles about 1,5-Anhydro-d-mannitol 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: 100.0%

: 13121-61-4
tetra-O-acetyl-1,5-anhydro-D-mannitol

: 492-93-3,53319-04-3
1,5-anhydro-D-mannitol

Guidance literature:: With potassium carbonate; In methanol;
DOI:10.1021/ol030023t

Reference yield: 92.0%

: 1438585-76-2
1,5-anhydro-2,3,4,6-tetra-O-allyl-D-mannitol

: 492-93-3,53319-04-3
1,5-anhydro-D-mannitol

Guidance literature:: With pyrographite; copper dichloride; palladium dichloride; In methanol; at 60 ℃; for 8h;
DOI:10.2174/1570178611310020002

Reference yield: 90.0%

: N,N-dimethyl β-D-mannopyranosyl dithiocarbamate

: 492-93-3,53319-04-3
1,5-anhydro-D-mannitol

Guidance literature:: With 2,2'-azobis(isobutyronitrile); hypophosphorous acid; sodium hydrogencarbonate; In ethanol; water; at 75 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.tetlet.2018.08.005