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Merck
CN

A1750

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:
572-09-8
Molecular Weight:
411.20
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
24890582
MDL number:
MFCD00063254
Beilstein/REAXYS Number:
96669

Key Documents

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Product Name

Acetobromo-α-D-glucose, ≥95% (TLC)

InChI key

CYAYKKUWALRRPA-RGDJUOJXSA-N

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

biological source

synthetic (organic)

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

Quality Level

300

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Related Categories

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
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000453279
0000453279
0000440488
0000440488
0000433274

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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
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

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