O9140
Oligo-HA4
low endotoxin
Synonym(s):
Oligohyaluronan, Oligohyaluronic acid
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C28H44N2O23
Molecular Weight:
776.65
UNSPSC Code:
12352201
Recommended Products
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.
Storage Class Code
11 - Combustible Solids
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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)
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