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O9140

Sigma-Aldrich

Oligo-HA4

low endotoxin

Synonym(s):

Oligohyaluronan, Oligohyaluronic acid

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About This Item

Empirical Formula (Hill Notation):
C28H44N2O23
Molecular Weight:
776.65
UNSPSC Code:
12352201

form

powder

quality

low endotoxin

impurities

≤0.1 EU/mg endotoxin

storage temp.

−20°C

General description

The Oligo-HA products are small-molecular weight hyaluronic acid prepared with streptococcal or recombinant bacterial HA via testicular HAase digestion and purified by gel filtration. The hyaluronan disaccharide subunit is glucuronic acid-β-D-(1→3)-N-acetyl-D-glucosamine-β-D-(1→4) (GlcAβ3GlcNAcβ4), and each Oligo-HA is an defined oligomer of the subunit.

Application

Oligo-HA4 has been used in a study to assess microbial production and applications of chiral hydroxyalkanoates. It has also been used in a study to investigate in situ preparation and continuous fiber spinning of poly(p-phenylene benzobisoxazole) composites.

Other Notes

Oligo-HA4 is a monodisperse tetrasaccharide comprised of two hyaluronan disaccharide subunits (Nonreducing-GlcAβ3GlcNAcβ4GlcAβ3GlcNAcβ4-reducing end).
To gain a comprehensive understanding of our extensive range of Oligosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Analysis Note

May contain trace amounts of other oligomers. Sold on the basis of carbohydrate as determined by carbazole assay.

WGK

WGK 3

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’.

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In situ preparation and continuous fiber spinning of poly(p-phenylene benzobisoxazole) composites with oligo-hydroxyamide-functionalized multi-walled carbon nanotubes
Chengjun, Z., et al.
Polymer, 49, 2520-2530 (2008)
Guo-Qiang Chen et al.
Applied microbiology and biotechnology, 67(5), 592-599 (2005-02-09)
Polyhydroxyalkanoates (PHA) are a family of polyesters consisting of over 150 chiral hydroxyalkanoic acids (HA). This paper reviews the physiological functions of (R)-3-hydroxybutyric acid (3HB) and (R)-4-hydroxybutyric acid and summarizes the technologies developed to produce various HA [3HB, (R)-3-hydroxyoctanoic acid

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