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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

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About This Item

Empirical Formula (Hill Notation):
C14H19BrO9
CAS Number:
Molecular Weight:
411.20
Beilstein:
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

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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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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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
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
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)

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