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Al222
Al222 (25118 pt) 2026-Jan-04 10:30

Povidone K30

Polyvinylpyrrolidone (PVP) K30 – (water-soluble polymer, K≈30 grade)

Synonyms: PVP K30, povidone K30, polyvinylpyrrolidone K30, poly(1-vinyl-2-pyrrolidone)
INCI / functions: film former, hair fixative, binder, suspension stabilizer, support for dispersibility and solubilization of actives/powders

Definition

Povidone K30 is a polyvinylpyrrolidone (PVP) grade characterized by a K-value around 30 (an index correlated with intrinsic viscosity and, in practical terms, with molecular weight). From a compositional standpoint, the ingredient consists mainly of PVP polymer chains (repeating units derived from N-vinyl-2-pyrrolidone), with possible trace levels of residual monomer (vinylpyrrolidone) and process-related impurities/auxiliaries (e.g., peroxides in traces) within the specification limits of the selected grade (cosmetic or pharmaceutical). In formulations it behaves as a film-forming and binding polymer, improves cohesion of solid or dispersed systems, and supports physical stability thanks to its strong affinity for water and its ability to interact with surfaces and particulates.

Calories (energy value)

MetricValue
Energy value (100 g)Not practically significant at typical use levels (technological use, not nutritional)
Technical noteHigh-molecular-weight polymer: in cosmetic use and as an excipient, the energy impact on the finished product is generally negligible


Identification data and specifications

ParameterValue
NamePovidone K30
INCIPVP (the “K30” designation is a supply/grade specification)
Chemical naturehydrophilic polymer, nonionic (strongly polar)
CAS number9003-39-8
EC number618-363-4
K-value (indicative, 1% in water)~27–33 (often 29–32 for many K30 grades)
Molecular weight (order of magnitude, indicative)~40,000 Da (method-dependent; the “K” remains the practical selection criterion)


PropertyIndicative (typical)
Appearancewhite to off-white powder
Odornone to slight
Solubilityvery soluble in water; variable compatibility in hydroalcoholic systems depending on the water/alcohol ratio and grade
Hygroscopicitymoderate–high (tends to absorb moisture)
pH (5% solution in water, indicative)~3.0–5.0 (depends on grade and specification)
Clarity (aqueous solutions)generally clear if properly hydrated and compatible with the system


Quality parameterControl limits / values (examples, typical pharma grade, indicative)
Water (KF)≤ 5.0%
Sulfated ash≤ 0.1%
Nitrogen (on anhydrous basis)~11.5–12.8%
Residual vinylpyrrolidone (HPLC)very low (order of ≤ 0.001% in some specifications)
Peroxides (as H₂O₂)very low (order of ≤ 0.04% in some specifications)


Functional role and clarification “film former / hair fixative / binder”

FunctionWhat it does in the formulationTypical use
Film formerforms a continuous, transparent film that improves uniformity and performancehair styling, make-up, film-forming treatments
Hair fixativeincreases hold and resistance to humidity (grade-dependent)sprays, gels, mousses
Binderincreases cohesion of powders/compacts and adhesion between particlescompacts, pressed powders; also tablets (pharma)
Suspension stabilizerhelps keep solids/pigments dispersed (in synergy with rheology)opaque cleansers, make-up, aqueous suspensions
Solubilization/dispersibility supportmay improve wetting and handling of particulates/activesdispersions and multi-solvent systems


Formulation compatibility

System / variableCompatibilityControl notes
Aqueous systemsgenerally excellentre-check viscosity after 24–48 h (full hydration)
Hydroalcoholic systemsoften goodalcohol can reduce hydration/viscosity; verify low-temperature clarity
Electrolytes/saltsto be assessedhigh salinity can reduce rheological performance and suspension stability
Surfactantsgenerally compatiblepotential effects on foam/sensory profile; run stability testing
Other film formersoften synergistictack risk if total polymer solids are high: optimize the blend


Use guidelines (indicative)

ApplicationTypical rangeTechnical note
Hair styling (gels, mousses, sprays)0.5–10%K30 is a practical balance between hold and sensoriality; assess tack/flaking
Make-up (mascara, primer, foundation)0.2–5%supports adhesion and uniform film; check compatibility with salts/pigments
Opaque cleansers / rinse-off0.1–2%suspension support and feel; verify interference with electrolytes
Pressed powders (binder)0.5–5%depends on compression and target pick-up/release
Pharmaceutical use (excipient)variableused as binder and stabilizer/dispersant; select a compliant grade


TopicGood practices
Dispersion in wateradd slowly under agitation to prevent lumps; allow hydration and re-check
Tack managementif sticky: reduce dose, introduce a co-film former/plasticizer, re-balance solvents
Stabilitystress tests (heat/cool cycles, centrifuge) for separation and rheology drift


Typical applications

  • Hair care: fixatives (gels, mousses, sprays) with a transparent film and good hold.

  • Make-up: supports adhesion, wear, and film uniformity (mascara/primers/bases).

  • Powder/pigment systems: helps dispersion and cohesion (with appropriate rheology).

  • Pharmaceutical: excipient as binder and stabilizer/dispersant in solid dosage forms and suspensions.

Quality, grades and specifications

TopicDetail
Differences between “K” gradesK-value drives viscosity, film strength, and sensoriality (higher K → “stronger” film, but higher tack/flaking risk if not balanced)
Cosmetic gradefocus on organoleptic profile, impurities, and film performance
Pharmaceutical gradetighter controls on impurities/residues (e.g., monomers, peroxides), moisture, ash, and compliance with applicable monographs
Typical CoA parametersK-value, solution viscosity, water, ash, nitrogen (anhydrous basis), specific residues


Safety, regulation and environment

TopicOperational guidance
Use safetygenerally low toxicity at use levels; dust may irritate eyes and respiratory tract
Allergenicitynot typically associated with sensitization; always assess the finished formula
EU cosmeticsusable under general rules and GMP; verify finished product compliance
Environmentwater-soluble polymer: manage effluents and residues according to good practice; avoid uncontrolled dust dispersion


Formulation troubleshooting

IssuePossible causeCorrective actions
Lumps / “fish eyes”incomplete wetting, rapid additionslow sprinkling addition, higher shear, hydration time
Sticky film (tack)high dose, humidity, unbalanced polymer blendreduce dose, add co-polymers/plasticizer, re-balance solvents
Flakingfilm too rigid or high polymer solidsincrease plasticization, reduce solids, re-balance film formers
Haze in hydroalcoholic systemssolvent incompatibility / water–alcohol ratiore-tune solvent ratio, introduce a compatible co-solvent
Viscosity drift over timeprogressive hydration or salt interferencestandardize maturation time, reduce electrolytes, optimize addition order


Conclusion

Povidone K30 is a widely used PVP grade valued for its film-forming and binding profile, offering a practical balance between performance and formulation manageability. Being mainly composed of polyvinylpyrrolidone polymer chains (with tightly controlled trace process residues), it is versatile in hair styling, make-up, and dispersed systems. Real-world performance depends primarily on hydration, solvent ratio (especially in hydroalcoholic systems), electrolyte load, and overall polymer blend balance.



References__________________________________________________________________________

Liu, Zhao-xia, Qi-lei CHENG, and Lan HE. Impact of the excipient povidone K30 on drug quality control of valsartan capsules. Chinese Journal of Pharmaceutical Analysis 34.6 (2014): 1091-1099.

Abstract. Objective: To confirm the origin and structure of the unknown substance,eluted at 0.14 fold of the relative retention time of valsartan peak (RRT=0.14),which was detected in related substances test of valsartan capsules;to explore the influence of the unknown material on the quality of valsartan capsules,and to provide basis for the revision of the quality standards. Methods: The analysis was carried out on an Inertsil ODS-4 column(250 mm×4.6 mm,5μm)with a mobile phase of acetonitrile-water-glacial acetic acid(500: 500: 1)at a flow rate of 1 mL·min-1.The detective wavelength was set at 225 nm.UPLC-MS,IR,1H-NMR and MALDI-TOF-MS techniques were applied to confirm the origin and structure of the unknown substance. Results: The unknown substance was confirmed to be the excipient povidone K30(PVP K30). Conclusion: The excipient PVP K30 peak is not to be counted as the related substance of valsartan capsules,and it should be specified to deduct the excipient peak in ChP 2010 to eliminate the influence on the result of determination.

Phadke C, Sharma J, Sharma K, Bansal AK. Effect of Variability of Physical Properties of Povidone K30 on Crystallization and Drug-Polymer Miscibility of Celecoxib-Povidone K30 Amorphous Solid Dispersions. Mol Pharm. 2019 Oct 7;16(10):4139-4148. doi: 10.1021/acs.molpharmaceut.9b00452.

Abstract. In the present study, we have investigated the variability in physical properties of povidone K30 (PVP K30) and its impact on crystallization and drug-polymer miscibility of celecoxib-PVP K30 (CLB-PVP K30) amorphous solid dispersions (ASDs). CLB-PVP K30 ASDs were prepared using nine batches of PVP K30, in situ on glass slides by quench-cooling using the hot and cold stage of a microscope. Crystallization of the ASDs stored at 40 ± 2 °C/75 ± 5% relative humidity was captured using polarized light microscopy for up to 24 h and quantified using mean pixel counts of images. The quantitative drug-polymer miscibility of nine CLB-PVP K30 systems was determined using melting point depression. Pearson's correlation analysis was used to find the correlation between (i) % crystallization with drug-polymer miscibility and physical properties and (ii) drug-polymer miscibility and physical properties, of PVP K30. The % crystallization was significantly variable (p < 0.05) among the nine CLB-PVP K30 ASDs. The nine PVP K30 batches exhibited significant variability (p < 0.05) from batch to batch and/or source to source in physical properties. The % crystallization showed correlation to particle size distribution (PSD) (weak positive), glass transition (Tg) (weak positive), drug-polymer miscibility (moderate negative), true density, and porosity (moderate positive) and hygroscopicity (strong positive). Miscibility showed correlation between Tg (weak positive), hygroscopicity (weak negative), PSD (moderate negative), and true density and porosity (strong negative). The study suggests PSD, hygroscopicity, true density, and porosity of PVP K30 as the functionality related characteristics for its intended functionality of physical stability when it is used as a stabilizer in ASDs.