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A1750

Sigma-Aldrich

Acetobromo-α-D-glucose

≥95% (TLC)

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Synonym(s):
1-Bromo-α-D-glucose tetraacetate, 2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl bromide
Empirical Formula (Hill Notation):
C14H19BrO9
CAS Number:
Molecular Weight:
411.20
Beilstein/REAXYS Number:
96669
MDL number:
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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This Item
A7562A8292104477
Acetobromo-α-D-glucose ≥95% (TLC)

A1750

Acetobromo-α-D-glucose

Acetobromo-α-D-galactose ≥93% (TLC)

A7562

Acetobromo-α-D-galactose

1-Thio-β-D-glucose tetraacetate 97%

104477

1-Thio-β-D-glucose tetraacetate

assay

≥95% (TLC)

assay

≥93% (TLC)

assay

≥93% (GC)

assay

97%

Quality Level

300

Quality Level

200

Quality Level

200

Quality Level

-

form

powder

form

powder

form

powder

form

solid

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

color

white to off-white

color

white to off-white

color

white

color

-

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


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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)
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

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