Every marine polysaccharide can be taken apart, and what comes out of that process is where a lot of serious work happens. A monosaccharide is a fixed molecule with a defined formula and a CAS number; an oligosaccharide is a short chain whose behaviour depends on how many units long it is and how those units are linked. Between the two sits most of the material our customers order: reference monomers for analytical work, and oligosaccharide fractions made to a degree of polymerisation that their own experiments can rely on.
We supply both sides of that line. On one side, crystalline monomers — fucose, rhamnose, the uronic acids, the amino sugars — in analytical and bulk grades. On the other, oligosaccharide families prepared from alginate, fucoidan, agar, carrageenan, laminarin, chitin and ulvan, offered as broad fractions or as discrete DP series where the project calls for a single chain length. Each comes with the structural evidence behind it, not just a purity figure.
Marine sugars differ from the familiar plant sugars in small but decisive ways. Fucose carries a methyl group where other hexoses carry a hydroxyl, which makes it less hydrophilic and gives it a distinctive role on cell surfaces. The uronic acids — mannuronic, guluronic, glucuronic, iduronic — bring a carboxylate group, so they set charge density and metal binding in the polymer they came from. And 3,6-anhydro-L-galactose, the monomer that closes the agar chain, has no counterpart in land plants at all.
| Monomer |
Where it occurs in marine material |
CAS |
Typical purity |
Form supplied |
| L-Fucose |
Terminal unit of fucoidan and other sulfated fucans |
2438-80-4 |
≥ 98% (HPLC) |
White crystalline powder |
| L-Rhamnose |
Backbone sugar of ulvan from green algae |
3615-41-6 |
≥ 98% |
Crystalline powder |
| D-Mannuronic acid, sodium salt |
M-block of alginate from brown algae |
6814-36-4 |
≥ 98% |
Sodium salt, powder |
| L-Guluronic acid, sodium salt |
G-block of alginate from brown algae |
15769-56-9 |
≥ 98% |
Sodium salt, powder |
| D-Glucuronic acid |
Ulvan and various marine glycosaminoglycan-like structures |
6556-12-3 |
≥ 98% |
Crystalline powder |
| L-Iduronic acid |
Sulfated marine polysaccharides related to glycosaminoglycans |
On request |
≥ 95% |
Small-quantity standard |
| D-Galactose |
Backbone of agar and carrageenan fractions |
59-23-4 |
≥ 99% |
Crystalline powder |
| 3,6-Anhydro-L-galactose |
The unit that terminates the agarose chain |
On request |
≥ 95% |
Research standard |
| D-Xylose |
Side chains of ulvan and some red algal xylans |
58-86-6 |
≥ 99% |
Crystalline powder |
| N-Acetyl-D-glucosamine |
Chitin from shellfish and squid cartilage |
7512-17-6 |
≥ 98% |
Crystalline powder |
| D-Mannose |
Mannan fractions from red and green algae |
3458-28-4 |
≥ 99% |
Crystalline powder |
Figure 1 — Monomer standards, filled to order in milligram, gram or kilogram quantities.
What the purity figure covers
A purity percentage means very little on its own. For a monomer used as a calibration standard, the relevant questions are which method produced the number, what the impurity is, and whether water or counter-ion is included in the mass. For a monomer used as a process input, the questions shift to flowability, residual solvent and microbial count. We state all three, and we will tell you plainly which grade fits which use rather than steering every enquiry to the most expensive one.
| Grade |
Intended use |
Documentation supplied |
| Analytical standard |
Calibration, method development, reference comparison |
Chromatographic purity, identity by NMR or MS, weighing data |
| Research monomer |
Synthesis, enzyme assays, culture work |
Assay value, moisture, residual solvent, appearance |
| Bulk monomer |
Process input, scale-up, formulation trials |
Assay, ash, heavy metals, microbial limits, pack weight |
| Derivative forms |
Sodium salts, acetylated or methyl glycoside variants |
Structure confirmation and stability guidance |
| DP-series kits |
Chain-length resolved oligosaccharide sets (for example DP 1–5 or DP 1–10) |
Purity per member, MALDI-TOF or HPAEC trace, storage conditions |
Figure 2 — Crystal habit under magnification, one of the checks run before a monomer lot is released.
With oligosaccharides the critical number is not purity alone but degree of polymerisation — how many sugar units sit in the chain. A preparation of DP 2–5 behaves differently from one at DP 15–25, in solubility, in viscosity, in how it interacts with a receptor, and in how readily it crosses a barrier.
| Family |
Parent polymer and source |
Typical DP or molecular weight |
Structural feature that matters |
| Alginate oligosaccharide (AOS) |
Alginate from Laminaria and other brown algae |
DP 2–25; low-DP grades 400–1,000 Da; broader grades up to 10,000 Da |
M/G block pattern, and an unsaturated bond at the new chain end when made enzymatically |
| Manuronate and guluronate series |
M-block and G-block fractions of alginate |
Discrete members from DP 1 to DP 10, or kits spanning the range |
Single block type for binding and structure–activity work |
| Fucoidan oligosaccharide |
Sulfated fucan from brown algae |
Low-molecular-weight fractions, typically 500–5,000 Da |
Sulfate content and position, which set charge and binding |
| Chitooligosaccharide (COS) |
Chitin from shellfish processing and squid cartilage |
DP 2–10, sometimes higher |
Degree of deacetylation alongside DP |
| Agarooligosaccharide and neoagarooligosaccharide |
Agarose from red algae |
DP 4 upward; neoagaro-tetraose and -hexaose commonly isolated |
Alternating 3,6-anhydro-galactose and galactose repeat |
| Carrageenan oligosaccharide |
Kappa-, iota- and lambda-carrageenan from red algae |
DP 2–12 |
Sulfate position per carrageenan type |
| Laminarin oligosaccharide |
Beta-glucan storage polysaccharide of brown algae |
DP 2–10 |
Beta-1,3 backbone with 1,6 branches |
| Ulvan oligosaccharide |
Ulvan from Ulva and other green algae |
DP 2–12 |
Rhamnose and glucuronic acid content, with sulfate |
Figure 3 — Chromatographic separation, the step that resolves a crude hydrolysate into a DP window.
How chain length is set, and how we measure it
Two routes produce short chains from a long polymer: enzymatic cleavage with a specific lyase, and chemical hydrolysis. They do not give the same material. Enzymatic cleavage by alginate lyase leaves an unsaturated bond at the newly formed chain end, and that unsaturation is widely regarded as the source of much of the biological activity in alginate oligosaccharides; harsh chemical degradation reaches a similar molecular size but tends to destroy the feature. We run the enzymatic route unless a customer specifically asks for the chemical product.
| Question |
Method |
What the result tells you |
| How pure is it? |
HPAEC-PAD or HPLC with refractive index detection |
Chromatographic purity and the profile of minor components |
| How long are the chains? |
MALDI-TOF MS or ESI-MS |
Which DP members are present and in what proportion |
| What is the average size? |
High-performance size exclusion chromatography |
Molecular weight distribution, reported as Mn, Mw and dispersity |
| Is the structure right? |
NMR, supported by FT-IR |
Linkage pattern, anomeric configuration, sulfate position |
| How much sulfate is present? |
Elemental analysis or a colorimetric sulfate assay |
Degree of substitution as a percentage |
| Is the unsaturation intact? |
UV absorbance near 235 nm, plus MS confirmation |
Whether the enzymatic end group survived processing |
| What else is in the bottle? |
Residual protein, salt and solvent assays |
Ash figure, moisture, and any carry-over from purification |
Figure 4 — A freeze-dried oligosaccharide fraction: light, porous and quick to redissolve.
What appears on the specification
| Parameter |
Range or limit |
Note |
| Appearance |
White to off-white, or light yellow to tan for oligosaccharides |
Colour says a great deal about residual polyphenol and ash |
| Assay / purity |
≥ 90% for broad fractions; ≥ 98% for discrete DP members |
Method stated on the certificate |
| Degree of polymerisation |
Stated as a window, or as a single DP for isolated members |
The value most likely to change results between lots |
| Molecular weight |
Reported as Mn and Mw with dispersity |
Not interchangeable with a single 'average' figure |
| Sulfate content |
Typically 5–35% for sulfated families |
Reported as percentage sulfate by weight |
| Moisture |
≤ 8% for oligosaccharide fractions |
Gravimetric; matters for accurate weighing |
| Ash and residual salt |
Quoted per grade |
Reflects desalting and membrane steps |
| pH, 1% solution |
4.0–7.0 for alginate-derived material |
Relevant for formulation compatibility |
| Heavy metals |
Arsenic ≤ 1 ppm, lead ≤ 2 ppm on food-contact grades |
ICP-MS per lot |
| Microbiology |
Total plate count and yeast and mould within agreed limits |
Tested on hygroscopic powders before release |
| Solubility |
Freely soluble in water for most families |
Confirmed at the concentration the customer will use |
| Storage |
2–8 °C, dry and sealed; some fractions held frozen |
Stated per product rather than generically |
Figure 5 — Routine chromatographic checks run on released fractions and retained samples.
Where the material goes
The uses split fairly cleanly into two groups. Monomers and discrete oligosaccharide standards tend to go into analytical and mechanistic work, where the structure has to be known exactly. Broad oligosaccharide fractions go into formulation and process development, where cost per kilogram and consistency matter more than having a single chain length in the bottle.
| Field of work |
What the material is used for |
Scale typically ordered |
| Analytical standards |
Calibration curves, method validation, identification of unknowns |
Milligrams to grams |
| Glycobiology research |
Structure–activity work on defined chain lengths and sulfate patterns |
Milligrams to grams |
| Enzyme characterisation |
Substrates for lyase and glycosidase assays, kinetics and specificity |
Milligrams to grams |
| Microbiota and fermentation studies |
Defined carbohydrate substrates for culture and fermentation trials |
Grams to kilograms |
| Plant signalling research |
Elicitor and stress-tolerance trials in seedling and crop models |
Grams to kilograms |
| Cosmetic ingredient development |
Low-molecular-weight fractions for formulation stability and sensory trials |
Grams to kilograms |
| Feed and aquaculture trials |
Immunostimulant and gut-health studies in fish and shrimp models |
Kilograms |
| Biomaterials and hydrogels |
Building blocks for films, beads, and functionalised carriers |
Grams to kilograms |
| Bioprocess feedstocks |
Carbon sources and fermentation inputs derived from marine biomass |
Kilograms and above |
Figure 6 — Freeze drying, the step that turns a purified fraction into a stable powder.
Keeping a fraction reproducible
- The DP window is measured on every lot, because it is the property most likely to drift when a harvest or an enzyme batch changes.
- Retained samples are kept from each production run, so a repeat order can be matched against the material a customer already has on the bench.
- Where a project needs a single chain length rather than a window, we isolate the individual DP member and quote the purity of that member, not of the mixture.
- Sulfated fractions are reported with their sulfate percentage, since charge density shifts results as much as chain length does.
- Hygroscopic powders are packed under conditions that limit moisture uptake, and the certificate states the moisture at release rather than at manufacture.
Prepared to your specification
Custom work here usually starts with one of three requests: a chain length that is not in the catalogue, a parent polymer from a species we do not routinely run, or a quantity somewhere between a standard pack and a production batch. All three are workable, and the table shows how each is handled.
| What you specify |
What we do |
| A degree of polymerization |
Target the window during hydrolysis, then cut it by chromatography and confirm by MS |
| A single chain length |
Isolate the individual DP member and report purity for that member |
| A parent polymer or species |
Extract the polysaccharide from the named biomass, then depolymerise to your window |
| A sulfate level |
Select or desulfate the fraction to land inside the requested range |
| A labelled or derivatised form |
Supply salts, reduced ends, or tagged derivatives where chemistry allows |
| An analytical package |
Add NMR, MS, HPAEC or sulfate data to the standard certificate |
| A pack size |
From milligram standards in sealed vials to kilogram lots in foil-lined drums |
Send us the structure
Tell us the monomer or the chain length you need, the purity your method can tolerate, and the quantity the project actually requires. We will come back with what is available, what has to be prepared, and the data that will travel with the material.
For Research or Industrial Raw Materials, Not For Personal Medical Use!