Skip to Content
Merck
All Photos(1)

Documents

M6633

Sigma-Aldrich

α-D-Mannose pentaacetate

Synonym(s):

1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C16H22O11
CAS Number:
4163-65-9
Molecular Weight:
390.34
MDL number:
MFCD00069798
UNSPSC Code:
12352201
PubChem Substance ID:
24897100
NACRES:
NA.25

biological source

plant (ivory nut palm)

Quality Level

200

Assay

≥98% (TLC)

form

powder

optical activity

[α]25/D 55.0 to 55.8°, c = 2.2% (w/v) in chloroform

technique(s)

thin layer chromatography (TLC): suitable

solubility

chloroform: 100 mg/mL, clear, colorless

storage temp.

−20°C

SMILES string

CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O

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

General description

Mannose is a monosaccharide.

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.

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.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

T P Kogan et al.
Journal of medicinal chemistry, 41(7), 1099-1111 (1998-04-17)
Reports of a high-affinity ligand for E-selectin, sialyl di-Lewis(x) (sLe(x)Le(x), 1), motivated us to incorporate modifications to previously reported biphenyl-based inhibitors that would provide additional interactions with the protein. These compounds were assayed for the ability to inhibit the binding
Duncan J Wardrop et al.
Organic letters, 4(4), 489-492 (2002-02-15)
[reaction: see text] A novel method for the stereospecific preparation of [4.5]spiroketal glycosides utilizing the 1,5 C-H bond insertion of alkylidenecarbenes is described. Treatment of 2-oxopropyl beta-pyranosides A with lithium (trimethylsilyl)diazomethane in THF at -78 degrees C afforded 1,6-dioxaspiro[4,5]decenes B

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service