Synonym: 1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose
CAS Number: 4163-65-9
Empirical Formula (Hill Notation): C16H22O11
Molecular Weight: 390.34
MDL Number: MFCD00069798
Linear Formula: C16H22O11
Product Type: Chemical
| assay |
≥98% (TLC) |
| biological source |
plant (ivory nut palm) |
| form |
powder |
| InChI |
1S/C16H22O11/c1-7(17)22-6-12-13(23-8(2)18)14(24-9(3)19)15(25-10(4)20)16(27-12)26-11(5)21/h12-16H,6H2,1-5H3 |
| InChI key |
LPTITAGPBXDDGR-UHFFFAOYSA-N |
| optical activity |
[α]25/D 55.0 to 55.8°, c = 2.2% (w/v) in chloroform |
| Quality Level |
200  |
| SMILES string |
CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O |
| solubility |
chloroform: 100 mg/mL, clear, colorless |
| storage temp. |
−20°C |
| technique(s) |
thin layer chromatography (TLC): suitable |
| Application: |
α-D-Mannose pentaacetate was used for glycosylation in a study that assessed novel synthetic inhibitors of selectin-mediated cell adhesion. It has also been used in a study to investigate stereospecific entry to spiroketal glycosides using alkylidenecarbene C−H insertion. |
| General description: |
Mannose is a monosaccharide. |
| Other Notes: |
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page. |
| RIDADR |
NONH for all modes of transport |
| WGK Germany |
WGK 3 |
| Flash Point(F) |
Not applicable |
| Flash Point(C) |
Not applicable |
| Purity |
≥98% (TLC) |
| Storage Temp. |
−20°C |
| UNSPSC |
12352201 |
