Alginate is the hydrocolloid you switch on rather than cook. A sodium alginate solution can sit at room temperature as a clear, pourable liquid almost indefinitely; add calcium and the same liquid turns into a gel within seconds and will not melt again on reheating. No gelling agent behaves quite this way, which explains why the same polymer appears in a textile print paste, in the coating on a welding electrode, inside an immobilised-cell bead and in a 3D bioprinting bath — four rooms that otherwise share no chemistry.
We supply the material in three working forms. The first is the salts and esters that carry the everyday job of thickening, gelling and film forming. The second is oligosaccharide fractions, where the specification is chain length rather than molecular weight. The third is functionalised derivatives, with reactive groups already attached so that a hydrogel can be crosslinked on demand, conjugated to a protein or tracked under a microscope. All three descend from the same brown seaweed feedstock and all three are graded on the same two backbone variables: the ratio of guluronic to mannuronic acid, and the chain length of the polymer itself.
The three families we keep in stock
Each family answers a different question. If the job is rheology, the salt or ester form is what you need; if the job is a defined molecule with a repeating unit count, the oligosaccharide range is the answer; if the material has to react after it has been placed, the derivatives are where the conversation starts.
| Family |
Forms supplied |
What defines the grade |
Where it earns its place |
| Alginates salts & esters |
Sodium, potassium, ammonium and calcium salts; alginic acid; propylene glycol ester (PGA) |
M/G ratio, viscosity of a stated reference solution, mesh, calcium residue, ash |
Thickening and gelling, film and sheet casting, textile printing, paper sizing, binders, encapsulation |
| Alginate oligosaccharides |
Depolymerised mixtures and single chain-length fractions |
Degree of polymerisation, molecular weight distribution, terminal structure, purity |
Signalling and fermentation studies, enzyme assay substrates, formulation and stability work |
| Functionalized Alginate Derivatives |
Oxidised, methacrylated, thiolated, sulfated, peptide-conjugated and fluorescently labelled |
Degree of substitution, reactive group content, bioburden and endotoxin grade |
Photocrosslinked hydrogels, bioprinting, scaffold studies, controlled-release carriers |
Sodium alginate as it leaves the mill — a near-white, free-flowing powder that hydrates readily in cold water.
Two uronic acids set every rule
Alginate is a linear copolymer of two uronic acids: β-D-mannuronic acid (M) and α-L-guluronic acid (G). The two are not interchangeable. G residues carry the calcium-binding pockets that build rigid junction zones; M residues make the chain more flexible and easier to dissolve but form fewer crosslinks. Because the enzyme machinery of a given seaweed species arranges those residues in a characteristic pattern, the M/G ratio is effectively a fingerprint of the raw material — and the single most useful number on the specification sheet.
| Backbone segment |
Behaviour in solution |
Behaviour as a gel |
What it decides for you |
| G-blocks (guluronate-rich) |
Stiffer chain, higher viscosity per unit of weight |
Tight calcium junction zones; firm, rigid, more brittle gel |
Shape retention, mechanical firmness, bead hardness, salt tolerance |
| M-blocks (mannuronate-rich) |
More flexible chain, wider solubility window |
Softer, more elastic, cohesive gel with fewer junction points |
Flexibility, freeze-thaw tolerance, smoother flow, lower gelling tendency |
| Alternating MG / GM runs |
Interrupt ordered junction formation |
Reduce brittleness and control water release |
Blend design, syneresis control, intermediate grades |
Alginate salts and esters
The counterion decides where the polymer can be used before any other property is considered. Sodium, potassium and ammonium alginates dissolve in cold water and build viscosity; calcium alginate does not dissolve at all in plain water but swells and, in fibrous form, absorbs many times its own weight in fluid; alginic acid is insoluble below about pH 3.5, which is exactly why it precipitates in the stomach and floats. The propylene glycol ester sits apart from all of them, because esterification of the carboxyl groups makes it the one alginate that stays functional in acid and in high-salt systems.
| Form |
Appearance |
Reference viscosity |
Dissolution and stability |
Typical use |
| Sodium alginate, low viscosity |
White to pale yellow powder |
20–200 mPa·s (1 %, 20 °C) |
Cold-water soluble |
Spraying, dipping, low-viscosity carriers, beverage systems |
| Sodium alginate, medium viscosity |
White to pale yellow powder |
200–600 mPa·s (1 %, 20 °C) |
Cold-water soluble, high shear helps dispersion |
General thickening, restructured pieces, bakery and dairy work |
| Sodium alginate, high viscosity |
White to cream powder |
600–1500 mPa·s (1 %, 20 °C) |
Requires good dispersion to avoid lumps |
Print pastes, coating rheology, heavy thickening |
| Ultra-low viscosity sodium alginate |
Fine white powder |
20–600 mPa·s (10 %, 20 °C) |
Soluble at high solids loading |
High-concentration systems, spray and dip baths, low-viscosity gels |
| Potassium alginate |
White to cream powder |
100–600 mPa·s (1 %, 20 °C) |
Cold-water soluble |
Faster calcium setting and higher gel modulus than the sodium salt |
| Calcium alginate |
Off-white powder or fibre |
Not applicable — insoluble |
Swelling, not dissolving; exchanges to soluble form in sodium-rich media |
Fibre and non-woven work, immobilisation matrices, absorbent structures |
| Ammonium alginate |
White to yellowish powder |
Low to medium |
Cold-water soluble, ammonia odour |
Coatings, water treatment, ceramic bodies |
| Alginic acid |
White to pale yellow powder |
Not applicable — insoluble |
Insoluble below pH 3.5, swells and gels in acid |
pH-triggered precipitation work, floating-raft studies, hydride-free coatings |
| Propylene glycol alginate (PGA) |
Creamy white powder |
100–1000 mPa·s (1 %, 20 °C) |
Esterified 40–85 %, stable at pH 3–5 and in hard water |
Acid beverages, foam stabilisation, emulsion systems, acid dressings |
A 1 % alginate solution drawn on a glass rod. That persistent thread is the shear-thinning behaviour formulators buy the polymer for.
How to read a viscosity figure
A viscosity number means nothing without the solution it was measured in, so we always print the concentration, temperature and spindle conditions next to the value. The reason is practical: a 10 % solution of an ultra-low grade and a 1 % solution of a high grade can read the same, yet behave nothing alike once they are diluted, pumped or gelled. If you send us a target viscosity without the conditions, we will ask for them — or test at the concentration you intend to run.
| Band |
Reference solution |
Reported range |
Where it fits |
| Ultra-low |
10 % at 20 °C |
20–600 mPa·s |
High-solids formulations, gellable liquids that must still pour |
| Low |
1 % at 20 °C |
20–200 mPa·s |
Fine dispersion, films, spraying, suspension at low dose |
| Medium |
1 % at 20 °C |
200–600 mPa·s |
The general-purpose band for thickening, binding and restructured products |
| High |
1 % at 20 °C |
600–1500 mPa·s |
Print pastes and coatings where flow control under shear matters |
| Very high |
1 % at 20 °C |
1500–2500 mPa·s |
Maximum thickening power from the smallest addition |
Gelation is the property with no substitute
Drop a sodium alginate solution into a calcium bath and gelation happens on contact, at room temperature, without heat and without a pH shift. The calcium source you pair with it controls how fast and how evenly that happens — which is why we keep several on the shelf and will advise on the pairing rather than leave you to discover it in production.
| Calcium source |
Setting speed |
Gel character |
Where it fits |
| Calcium chloride |
Very fast, surface-driven |
Firm, brittle, prone to water release |
Beads, fibres and threads formed in a setting bath |
| Calcium lactate or gluconate |
Slow, gradual |
Elastic, even, low syneresis |
Casting films and sheets, restructured pieces, delicate shapes |
| Calcium sulfate |
Moderate |
Balanced firmness with workable open time |
Composite systems and gelling solutions that must be handled first |
| Calcium carbonate with D-glucono-δ-lactone |
Delayed, acid-triggered |
Internal setting, homogeneous throughout |
Thick-section shapes and printing baths where the whole volume must set together |
Calcium-crosslinked beads formed by dripping a sodium alginate solution into a setting bath.
Two extraction routes, and why they are not equivalent
Almost all commercial alginate is extracted from brown seaweed with alkali, but what happens next splits the market in two. The calcium route passes the polymer through an insoluble calcium alginate intermediate before converting it back to a soluble salt; the direct route neutralises the extract straight to sodium alginate. The direct route is cheaper. It also carries more of the seaweed's co-extracted colour, protein and polyphenol with it, which shows up as higher ash and a wider batch-to-batch spread — the difference that separates a research-grade line from a commodity thickener.
| Stage |
Calcium route (two-stage) |
Direct neutralisation route |
| Alkali extraction |
Identical — dried seaweed digested in alkali |
Identical — dried seaweed digested in alkali |
| Intermediate |
Insoluble calcium alginate, washed before conversion |
None — extract neutralised directly to sodium alginate |
| Purity |
Higher; most co-extracted material removed at the wash step |
Lower; colour bodies and protein fragments carried through |
| Calcium residue |
Controlled and typically low |
Depends entirely on the washing regime |
| Ash and water-insoluble matter |
Low, narrow band |
Higher and more variable |
| Best suited to |
Research and high-specification industrial grades |
General-purpose thickening and industrial duty |
Extraction and ion-exchange vessels, where the seaweed polymer is converted into a soluble salt.
Alginate oligosaccharides: chain length is the specification
Below roughly ten repeating units the polymer stops behaving like a thickener and starts behaving like a molecule. Viscosity becomes irrelevant; what matters is how many units are in the chain, how the chain ends, and how narrow the distribution is. Depending on the route used to shorten the polymer, the fragment can carry an unsaturated uronic acid at its non-reducing end — a detail that is either an analytical convenience or a complication, and worth telling us which.
| Fraction |
Starting polymer |
Chain length |
Terminal chemistry |
Typical use |
| Alginate oligosaccharide mixture |
Sodium alginate, enzymatically digested |
DP 2–10, average 3–6 |
Unsaturated Δ-uronic acid at the non-reducing end when lyase is used |
Signalling and fermentation studies, formulation screening |
| G-rich series |
High-G alginate |
DP 2–8, single-length fractions |
Saturated |
Structure and property work, reference comparisons |
| M-rich series |
High-M alginate |
DP 2–8, single-length fractions |
Saturated |
Chain-length series for binding and degradation studies |
| Unsaturated oligosaccharides |
Alginate lyase digestion |
DP 2–6 |
4,5-unsaturated uronic acid, measurable near 235 nm |
Enzyme assay substrates, chromophore-bearing probes |
| Low-molecular-weight alginate |
Controlled hydrolysis |
Mn 1–20 kDa |
Mixed |
Low-viscosity systems and starting material for further derivatisation |
Every fraction is released with the chain-length distribution it was actually measured to have. We report the numbers from size-exclusion chromatography and mass spectrometry rather than quoting a nominal range, and single-length fractions are separated rather than approximated by an average.
Functionalised derivatives for work that starts after placement
Where a plain alginate gel is set by diffusion, a functionalised one can be set by light, by a second reagent, or by the tissue it is in contact with. Introducing reactive groups onto the backbone leaves the calcium chemistry intact but adds a second, independent handle — usually the reason a research group moves away from the parent polymer.
| Derivative |
Group introduced |
Substitution |
Second crosslinking route |
Where it is used |
| Oxidised alginate |
Aldehyde, by periodate cleavage of the uronate ring |
Degrees of oxidation from around 5 % upward |
Schiff-base reaction with amines; gels in situ |
In-situ forming matrices, protein conjugation, crosslinkable blends |
| Methacrylated alginate (AlgMA / AIMA) |
Methacrylate |
Degree of substitution typically 15–25 % |
Photo-initiated radical polymerisation |
Photopatterning, bioprinting, scaffold formation |
| Thiolated alginate |
Thiol |
Set by the degree of thiolation requested |
Disulfide formation or Michael addition |
Hydrogels with mechanical properties tuned after casting |
| Sulfated alginate |
Sulfate ester |
Reported as sulfur or sulfate content |
With calcium |
Charged analogues for protein binding and interaction studies |
| Peptide-conjugated alginate |
Adhesion peptides |
Stated as peptide density per gram |
With calcium |
Matrix studies where surface interaction with cells matters |
| Fluorescently labelled alginate |
FITC or rhodamine |
Label density per gram |
With calcium |
Tracking distribution, diffusion and release inside a matrix |
A calcium-crosslinked lattice cast from functionalised alginate, photographed wet in its dish.
Where alginates are put to work
Textile printing remains the single largest outlet for technical alginate, for a reason worth stating plainly: the polymer does not react with reactive dyes, so the colour goes onto the fibre instead of onto the paste, and the paste washes out in cold water afterwards. The same logic — inert, washable, controllable — carries into paper sizing, electrode coatings, water treatment and an expanding list of biomedical and agricultural uses.
| Field |
Application |
Why alginate works there |
Typical dose |
| Textile printing |
Thickener for reactive-dye print paste |
No reaction with the dye, high fluidity at high viscosity, easy cold-water wash-off, low effluent load |
0.5–2 % of the paste |
| Paper and board |
Surface sizing and coating |
Controls coating rheology and builds an oil-resistant film |
0.2–1 % of the coating |
| Welding consumables |
Binder and plasticiser in electrode flux |
Thickens the water-glass flux mix so the coating adheres without cracking |
0.3–1.5 % of the flux |
| Water treatment |
Co-flocculant with metal salts |
Increases floc size and strength for faster settling |
Dose set by jar test |
| Paints, inks, coatings |
Thickener and anti-settling agent |
Shear-thinning flow with rapid viscosity recovery |
0.3–1.5 % |
| Ceramics and construction |
Suspending and plasticising aid |
Keeps high-solids slurries stable and workable |
0.2–1 % |
| Agriculture |
Seed coating, soil conditioning, carrier for actives |
Film formation and ion exchange in the root zone |
Coating dependent |
| Biological research |
Enzyme and cell immobilisation, entrapment beads |
Gels in place at room temperature with pores that can be tuned |
2 % solution typical |
| Biomaterials |
Bioinks, photocrosslinkable hydrogels, scaffolds |
Derivatised backbone sets on command with predictable mechanics |
Formulation dependent |
| Feed |
Pellet binder |
Binds without heat and reduces fines in water |
0.5–2 % |
A cast alginate film lifted from its plate — continuous, flexible and fully transparent.
Making one lot behave like the last
Alginates are natural polymers, so variation is a property of the raw material rather than a defect. What can be controlled is how tightly that variation is bounded and how openly it is reported.
- Viscosity is measured at the concentration, temperature and spindle conditions printed on the certificate — never quoted as a bare number.
- The M/G ratio is reported as a measured value per batch, obtained by NMR or by titration, so that a substitution decision can be checked rather than assumed.
- Gel strength is tested on a calcium-crosslinked gel under fixed conditions, which is the only way to compare firmness between grades.
- Calcium residue, ash and water-insoluble matter are controlled lot by lot, because a small excess of residual calcium is enough to leave a powder that will not dissolve cleanly.
- For biomaterials work, bioburden and endotoxin are reported separately, and low-endotoxin grades are handled under conditions that keep that figure valid.
- Retention samples are held from every batch, and blends are confined to a pre-agreed specification window rather than adjusted to hit an average.
Packaging, storage and handling
- Alginate is strongly hygroscopic. Standard supply is 25 kg in fibre drums or multi-wall bags with an inner liner; laboratory quantities come in sealed foil pouches.
- Keep containers closed between uses. Powder that has taken up moisture hydrates unevenly and will form lumps regardless of how much shear is applied.
- Store below about 30 °C away from direct light. Avoid long-term contact with bare metal in the case of alginates, which chelate divalent ions.
- Prepare solutions with high shear, then allow them to stand to release entrained air. Dispersing powder into rapidly stirred water, rather than dumping it in, is the difference between a smooth solution and a permanent lump.
- Solutions are best used within a day or two. Viscosity drifts downward with time, most quickly in high-M grades, so any specification should state the standing time it was measured at.
Grades built against your brief
Most enquiries are not for a catalogue item. They are for a viscosity at a stated concentration, a mesh that suits an existing feeder, a gel firmness that matches a mould, or a chain length that has to sit inside a narrow window. That is the part of the business we would rather do with you than for you — tell us the constraint and we will work back to the grade.
| What you need fixed |
What we adjust |
| Thickening or flow behaviour |
Viscosity band, tested at the concentration and conditions you actually run |
| Gel firmness and elasticity |
M/G ratio from high-G through intermediate to high-M |
| Solubility profile |
Counterion form — sodium, potassium, ammonium, calcium or the free acid |
| Performance in acid or brine |
Propylene glycol ester with a stated degree of esterification |
| Handling in your plant |
Mesh and particle size distribution, from coarse low-dust grades to fast-hydrating fine powders |
| Powder wetting and lumping |
Dissolution behaviour tuned for the mixer you have, not the one we assume |
| Downstream chemistry |
Reactive group and substitution level on oxidised, methacrylated, thiolated or labelled derivatives |
| Chain-length sensitive work |
Oligosaccharide DP window, single-length fractions and reported distribution |
| Documentation and grade of handling |
Bioburden and endotoxin reporting, retention samples, batch traceability |
| Pack size |
Laboratory quantities from 100 g through to 25 kg industrial units and full loads |
Send us the specification you are working to, or the problem you have not managed to solve with the grade you have, and we will come back with a concrete recommendation and a sample to test.
For Research or Industrial Raw Materials, Not For Personal Medical Use!