Formulation Science20 Oct 20267 min read

What is an emulsion? Oil-in-water vs water-in-oil, and why creams separate

How an emulsion holds oil and water together, how oil-in-water and water-in-oil types differ, the four ways creams separate, and the stability tests that catch each one.

By CSL Formulation science team, Cosmetic Science Lab · Reviewed by Dr. Premalatha, Ph.D., Life Science, Regulatory Consultant

Topic: emulsion stabilityCovers: O/W, W/O, failure modesFor: brands and formulators
A cream jar, serum bottles and petri dishes on a lab bench, representing cosmetic emulsion formulation

Quick answer

  • What is an emulsion? A mixture of two liquids that do not normally blend, usually oil and water, where one is broken into fine droplets and held inside the other by an emulsifier.
  • In an oil-in-water (O/W) emulsion, oil droplets sit in water: light lotions and most creams. In a water-in-oil (W/O) emulsion, water droplets sit in oil: rich, occlusive barrier creams.
  • Creams separate in four ways: creaming, flocculation, coalescence and Ostwald ripening [1], [2]. Only the first two can be reversed.
  • No emulsion is permanently stable. Good formulation slows separation until it falls outside the product's shelf life.

Take-home message for formulators

  • Match the emulsifier blend to the oil phase's required HLB first
  • Pick stability tests by the failure mode you need to rule out

Take-home message for brand owners

  • A cream that separates once is usually two or three variables failing together
  • Adding an acid active late can collapse a stable formula

01What is an emulsion?

Most creams, lotions and conditioners are emulsions. When one separates on the shelf, the brand pays in returns and reformulation. Every emulsion has two parts:

  • Dispersed phase: the liquid broken into droplets.
  • Continuous phase: the liquid that surrounds those droplets.

Oil and water resist mixing because of interfacial tension. Water molecules bond strongly to each other and push oil away, so the system always drifts back towards two separate layers. An emulsifier sits at the boundary between the phases, lowers that tension and wraps every droplet in a protective film. Flocculation and coalescence both begin at that film, which is why emulsifier choice matters so much [1].

02Oil-in-water vs water-in-oil emulsion

The two main types are named by which phase surrounds the other.

Side-by-side diagram: oil-in-water emulsion with yellow oil droplets in a blue continuous water phase, and water-in-oil emulsion with blue water droplets in a yellow continuous oil phase
Figure 1. Oil-in-water (left): oil droplets in a continuous water phase. Water-in-oil (right): water droplets in a continuous oil phase.
Table 1. Oil-in-water and water-in-oil emulsions compared
FeatureOil-in-water (O/W)Water-in-oil (W/O)
Continuous phaseWater (an aqueous solution)Oil
Dispersed phaseOil dropletsWater droplets
Skin feelLight, fast-absorbingRich, occlusive, water-resistant
Typical productsDaily moisturisers, body lotions, milky serumsBarrier creams, night creams, some sun care
Emulsifier HLBHigh, about 9–18 [4]Low, about 3–6 [4]
Quick testDilutes in water; conducts electricityDilutes in oil; does not conduct

The HLB (hydrophile-lipophile balance) scale, introduced by Griffin in 1949, shows which type an emulsifier favours [3]. High-HLB emulsifiers build an oil-in-water emulsion; low-HLB emulsifiers build a water-in-oil emulsion. Most skin care launches use oil-in-water because consumers prefer the lighter feel. Matching the emulsifier blend to the oil phase's required HLB is the first stability decision a formulator makes.

03Formulation variables that decide emulsion stability

Four variables decide whether a formula holds for its full shelf life. They interact, so changing one often shifts another:

  1. Use level

    Too little emulsifier leaves bare droplet surface and invites coalescence. Too much can thin the product or irritate skin. Totals of 2–5% of the formula are common.

  2. pH

    Many emulsifiers and thickeners only work within a set pH window. In one carbomer gel study, viscosity was far lower at pH 4.7 than at pH 6 [5]. Adding an acid active such as lactic acid late in development can do the same to a carbomer-thickened cream, collapsing viscosity and starting creaming within days.

  3. Compatibility

    Electrolytes, alcohol, botanical extracts and charged actives can strip the droplet film or break the thickener network.

  4. Process

    Phase temperatures, order of addition, shear rate, homogenisation time and cooling speed set the final droplet size. The same formula made two ways can give two different shelf lives.

04Why creams separate: four failure modes

An emulsion fails in four main ways [1], [2]. Some can be reversed by shaking; others mean the droplets have merged for good.

Four panels showing emulsion failure modes: creaming with droplets rising to the top, flocculation with droplets clumped together, coalescence with droplets merged into one large drop and an oil layer, and Ostwald ripening with small droplets shrinking as large ones grow
Figure 2. The four ways an emulsion breaks down: creaming, flocculation, coalescence and Ostwald ripening.
Table 2. Emulsion failure modes: what you see, the cause and the fix
Failure modeWhat you seeMain causeFix
CreamingA paler layer at the top that remixes on shakingDensity gap, large droplets, thin continuous phaseSmaller droplets; add a rheology modifier
FlocculationGrainy look, uneven textureDroplets clump but keep their film; weak charge barrier, high electrolyteRaise droplet charge; add polymeric stabilisers
CoalescenceOil pools, permanent splitInterfacial film ruptures and droplets mergeCorrect HLB; raise emulsifier level; add a co-emulsifier
Ostwald ripeningDroplets slowly grow over weeksSmall droplets dissolve and redeposit onto large onesAdd a highly insoluble oil; narrow the droplet size range

Creaming and flocculation are early warnings. Coalescence is the end point: once droplets merge, mixing cannot rescue the product [1]. Ostwald ripening is driven by the higher pressure inside small droplets, which makes their oil slightly more soluble. It is most common when the oil phase is partly water-soluble, as with light esters or fragrance oils [6].

Syneresis is a related failure in gelled or thickened products. The gel network contracts and squeezes liquid out, leaving a watery layer on the surface [7]. It usually points to an under-hydrated thickener, pH drift or freeze-thaw stress.

05Stokes' law: why viscosity and droplet size matter

Stokes' law gives the speed at which a droplet rises or sinks, and it explains most creaming problems in one line [1]:

Stokes' law equation: v equals 2 times the density difference between dispersed and continuous phase, times g, times r squared, divided by 9 eta
Figure 3. Stokes' law. v is creaming speed, ρd and ρc are the densities of the dispersed and continuous phase, g is gravity, r is droplet radius and η is continuous-phase viscosity.
  • Droplet size dominates. Speed scales with radius squared, so halving droplet size cuts creaming speed by 75%. That is why homogenisation is the biggest single lever against creaming.
  • Viscosity slows movement. Doubling continuous-phase viscosity halves creaming speed. That is the job of a rheology modifier such as a carbomer or xanthan gum.
  • The density gap sets direction. Oil is lighter than water, so oil droplets rise in an O/W cream.

06Which stability test catches which failure

Stability tests stress a product so problems show in weeks, not months. Choose them by the failure you need to rule out:

Table 3. Matching stability tests to emulsion failure modes
TestBest at exposing
CentrifugationCreaming, early coalescence
Elevated-temperature storageCoalescence, viscosity loss, colour and odour change
Freeze-thaw cyclingCoalescence, syneresis, crystallised butters
Droplet size over time (microscopy, particle sizing)Flocculation, Ostwald ripening
Accelerated tests estimate shelf life; they do not prove it

Heat can trigger failures that never happen at room temperature and miss slow ones that do. Confirm with real-time data in the final pack. See our stability testing service.

07How CSL diagnoses a separating emulsion

When a brand sends us a separating cream, we work from symptom to root cause instead of guessing at a fix. We confirm the emulsion type and whether the split is reversible, measure droplet size by microscopy and particle sizing, and profile viscosity and yield point. Then we audit HLB, use level, pH drift and incompatible actives, and compare batch temperatures and shear with the lab method. The fix is proven with accelerated, centrifuge and freeze-thaw testing.

Is your emulsion separating?

A separating product is rarely one problem. It is usually two or three variables pulling the same way, and a fix only holds when every one is addressed. Send us the formula, the process sheet and a photo of the failed sample. Ask for a root-cause review.

08Questions readers ask

Is lotion an emulsion?

Yes. Most lotions and creams are oil-in-water emulsions: oil droplets held in water by an emulsifier. Richer barrier creams are often water-in-oil.

Why does my cream separate after adding an active?

Usually because the active changed the pH or added electrolytes. Both can weaken the emulsifier film or the thickener network. Check pH before and after the addition, and test the final formula, not the base.

Need a cream that stays stable for its full shelf life?

We diagnose separating emulsions, rebuild the emulsifier system and prove the fix before you scale up.

Explore formulation servicesTalk to a formulator

09References

  1. Agno Pharmaceuticals. Emulsion stability and testing (technical brief). 2019. Agno Pharma
  2. McClements DJ. Critical review of techniques and methodologies for characterization of emulsion stability. Crit Rev Food Sci Nutr. 2007;47(7):611–649. DOI
  3. Griffin WC. Classification of surface-active agents by "HLB". J Soc Cosmet Chem. 1949;1(5):311. SCC library
  4. PCC Group. HLB: what is it? Hydrophilic-lipophilic balance. PCC Group
  5. Maslii Y, Ruban O, Kasparaviciene G, et al. The influence of pH values on the rheological, textural and release properties of carbomer Polacril® 40P-based dental gel formulation with plant-derived and synthetic active components. Molecules. 2020;25(21):5018. DOI
  6. Taylor P. Ostwald ripening in emulsions. Adv Colloid Interface Sci. 1998;75(2):107–163. DOI
  7. IUPAC. Syneresis. Compendium of Chemical Terminology (Gold Book), 5th ed. 2025. DOI
CSL
CSL Formulation science teamCosmetic Science Lab · Reviewed by Dr. Premalatha, Ph.D., Life Science, Regulatory Consultant · Last reviewed 20 Oct 2026Product formulation

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  • Published by Cosmetic Science Lab

This article is general technical information, not legal, regulatory or medical advice. Confirm requirements for your product and market before launch.

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