Skip to Content
MilliporeSigma
All Photos(5)

Key Documents

A1750

Sigma-Aldrich

Acetobromo-α-D-glucose

≥95% (TLC)

Synonym(s):

1-Bromo-α-D-glucose tetraacetate, 2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl bromide

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C14H19BrO9
CAS Number:
Molecular Weight:
411.20
Beilstein/REAXYS Number:
96669
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic (organic)

Quality Level

assay

≥95% (TLC)

form

powder

optical activity

[α]25/D 188 to 202 °, c = 1 in chloroform

contains

1% CaCO3 as stabilizer

color

white to off-white

mp

88.5 °C ((191.3 °F ))

shipped in

dry ice

storage temp.

−20°C

SMILES string

CC(=O)OC[C@H]1O[C@H](Br)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI

1S/C14H19BrO9/c1-6(16)20-5-10-11(21-7(2)17)12(22-8(3)18)13(14(15)24-10)23-9(4)19/h10-14H,5H2,1-4H3/t10-,11-,12+,13-,14+/m1/s1

InChI key

CYAYKKUWALRRPA-RGDJUOJXSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Acetobromo-α-D-glucose is used as a possible poly (ethylene terephthalate) (PET) surface modification reagent to increase its blood compatibility.

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.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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

Raechelle A D'Sa et al.
Langmuir : the ACS journal of surfaces and colloids, 26(3), 1894-1903 (2009-10-03)
This article reports the use of atmospheric pressure plasma processing to induce chemical grafting of poly(ethylene glycol) methyl ether methacrylate (PEGMA) onto polystyrene (PS) and poly(methyl methacrylate) (PMMA) surfaces with the aim of attaining an adlayer conformation which is resistant
D Sakthi Kumar et al.
Journal of biomaterials applications, 24(6), 527-544 (2009-02-11)
Poly (ethylene terephthalate) (PET) was surface modified by plasma polymerization of acetobromo-alpha-D-glucose (ABG) at different radio frequency (RF) powers. Plasma polymerization was carried out by vaporizing ABG in the powder form by heating at 135 degrees C. Surface modification resulted
Preparation and characterization of nonfouling polymer brushes on poly(ethylene terephthalate) film surfaces.
Li J, Tan D, Zhang X, Tan H, Ding M, et al.
Colloids and Surfaces, B: Biointerfaces, 78, 343-350 (2010)

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