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admin (19653 pt) 2026-Jan-09 15:13

Sodium lauryl phosphate: anionic phosphate surfactant (sodium salt), INCI functions, identifiers, and formulation guidance

Sodium lauryl phosphate
Sodium salt of lauryl phosphate – alkyl phosphate (C12) in neutralized form (sodium)

Synonyms: sodium dodecyl phosphate, sodium monolauryl phosphate, sodium monododecyl phosphate, dodecyl phosphate, sodium salt
INCI / functions: surfactant – cleansing, surfactant – foaming, surfactant – emulsifying (anionic surfactant)

Definition

Sodium lauryl phosphate is the sodium salt of a C12 phosphate ester (the alkyl phosphates family), obtained by phosphorylation of lauryl alcohol (1-dodecanol) followed by neutralization with a sodium base. From a compositional standpoint, commercial grades may be described as the salt of the “monoester” species (dodecyl phosphate) or as a controlled mixture of related species (mono/di phosphate esters and their salts), depending on the process and producer specification. The sodium form is typically selected to improve water solubility, facilitate use in cleansing products, and make pH control more predictable than the acid form.

Main uses 

  • Cosmetics: cleansers (face/body), shampoos, foaming systems, and some O/W systems as an anionic surfactant/co-emulsifier.

  • Medicine: not typical as a standard ingredient; any use is specialized.

  • Pharmaceutical: not common as a mainstream excipient; use depends on dossier/specification.

  • Industrial use: surfactant/emulsifier and wetting agent in technical formulations.

Identification data and specifications

IdentifierValue
INCI nameSodium Lauryl Phosphate
Chemical framingalkyl phosphate, sodium salt (C12)
Reference chemical species (common)sodium dodecyl phosphate (salt of dodecyl phosphate)
CAS number50957-96-5 (frequently reported for sodium dodecyl phosphate)
EC/EINECS number256-865-1 (linked in various SDS to the CAS above)
Note on CAS/ECsome commercial grades may show alternative identifiers (mixture/registration); always rely on the manufacturer’s SDS/CoA
Molecular Formula
C12H26NaO4P
Molecular Weight
288.30 g/mol


Key constituents

ClassTypical componentsTechnical note
Surfactant phosphate fractionsodium salt of the monoester and, in some grades, a fraction of related speciesaffects foam, cleansing, clarity, and viscosity
CounterionsNa⁺ (predominant)defines the “sodium salt” form
Controlled traces/impuritiesprocess residues and related speciesmanaged through specifications and QC


Functional role and practical mechanism of action

FunctionWhat it does in the formulaTechnical note
Anionic cleansing surfactantreduces surface tension; improves wetting and soil removalperformance depends on pH and the surfactant package
Foaming agentcontributes to foam volume and qualitysynergistic with amphoterics/nonionics
Emulsifier/co-emulsifiersupports O/W systems and solubilization of lipophilic fractionsuseful in targeted blends


Formulation compatibility 

As an anionic surfactant, Sodium lauryl phosphate is generally compatible with anionic and amphoteric cleansing packages (e.g., betaines), where it can contribute to foam and wetting. Compatibility with cationic components (quaternaries, polyquaterniums, cationic conditioners) must be handled carefully due to the risk of complexation (haze, precipitates, performance loss): in “2-in-1” or strongly cationic conditioner systems it is not usually a primary choice unless the formulation architecture is specifically designed for it.

In “clear” systems, clarity depends on active level, electrolyte profile, co-surfactants, and temperature. Because the sodium form is already neutralized, pH management is typically simpler than with the acid form; however, it remains important to verify pH/viscosity stability over time and across thermal cycles. In O/W emulsions it can act as a co-emulsifier, but performance depends strongly on the overall emulsifier system and ionic strength: stability testing (thermal stress, centrifugation) is recommended.

Use guidelines (indicative)

ApplicationTypical rangeTechnical note
Face/body cleansers (gels, foams, liquid syndets)0.5–5.0%adjust based on mildness and foam target
Shampoo0.5–5.0%synergistic with amphoterics; optimize viscosity and electrolytes
Co-emulsifier / O/W solubilizer0.2–2.0%verify stability and electrolyte compatibility

(Percentages depend on the commercial grade and the active concentration of the raw material.)

Typical applications

  • Foaming face/body cleansers with an anionic profile, often blended with amphoterics to optimize mildness.

  • Shampoos and hair cleansing products where added foam and wetting are desired.

  • Specific O/W systems where the phosphate headgroup supports emulsification/solubilization in combination with other emulsifiers.

Quality, grades and specifications

QC parameterWhat to control
IdentityINCI alignment and CAS/EC per SDS/CoA
Assay/activesactive level and profile (mono/di esters, if declared)
pH (solution)range and batch-to-batch repeatability
Electrolytes/impuritiesresidual salts, free sulfates/phosphates (if applicable)
Color/odorstability and impact on clear formulas
Microbiology (if in solution)limits and preservation status, where relevant


Safety, regulatory and environment (discursive section)
As an anionic surfactant, Sodium lauryl phosphate should be evaluated primarily with respect to potential eye irritation upon direct contact (a common theme for foaming cleansers). Proper management is based on dosage, final pH, selection of co-surfactants (amphoterics/nonionics) and mildness additives, plus the safety assessment of the finished product under EU Regulation (EC) 1223/2009 and the CPSR process. Environmentally, the recommended approach is typical for surfactants: minimize uncontrolled industrial releases and manage effluents according to local regulation and good process practices.

Formulation troubleshooting

IssueLikely causeRecommended action
Haze/precipitates with cationic conditionersanionic–cationic complexationreduce/avoid cationics, separate functional phases, reformulate surfactant system
Loss of clarity in cleansing gelelectrolytes, temperature, co-surfactant profileretune salts, adjust amphoterics/nonionics, optimize thickener
Perceived irritationdosage/pH/surfactant system not optimizedreduce actives, use milder co-surfactants, adjust pH and soothing additives
Low or unstable foamsurfactant balance not correctincrease amphoterics, optimize anionic/amphoteric ratio, check electrolytes

Conclusion

Sodium lauryl phosphate is an anionic alkyl phosphate in sodium salt form, useful in cleansing products for its contribution to wetting, foam, and potential co-emulsifying behavior. Key success factors are correct surfactant-package balancing, management of compatibility with cationic components, and control of clarity and stability against pH/electrolytes to ensure repeatable performance and sensorial quality.

Mini-glossary

  • Alkyl phosphates: phosphate esters with alkyl chains; often used as surfactants/emulsifiers.

  • Anionic: surfactant carrying a negative charge in solution.

  • Neutralization: conversion of the acid form into a salt (here Na⁺) to tune pH and solubility.

  • GMP: Good Manufacturing Practice.

  • HACCP: Hazard Analysis and Critical Control Points (relevant as a process-control concept in regulated settings).

References__________________________________________________________________________

Hidaka S, Abe K. The effects of sodium lauryl sulphate and its oxidative breakdown products on calcium phosphate precipitation and transformation. Arch Oral Biol. 1992 Mar;37(3):159-65. doi: 10.1016/0003-9969(92)90085-m. 

Abstract. Most commercial dentifrices contain sodium lauryl sulphate, which oxidizes upon storage. The effects of aged sodium lauryl sulphate and its oxidative breakdown products on the conversion of amorphous calcium phosphate to hydroxyapatite were studied in vitro by a pH drop method. Hydroxyapatite was identified from its X-ray diffraction pattern. With storage time, the concentration of dodecanol [CH3(CH2)11OH], a breakdown product of sodium lauryl sulphate, increased. The storage dodecanol-containing sodium lauryl sulphate accelerated the conversion of amorphous calcium phosphate to hydroxyapatite. Dodecanol mixed with sodium lauryl sulphate accelerated the conversion when added both before and after initial formation of amorphous calcium phosphate. A stored commercial dentifrice also accelerated the conversion of amorphous calcium phosphate to hydroxyapatite. It was found that the concentration of dodecanol increased 2-fold over a 2-month period.

Mizutani T, Mori R, Hirayama M, Sagawa Y, Shimizu K, Okano Y, Masaki H. Sodium Lauryl Sulfate Stimulates the Generation of Reactive Oxygen Species through Interactions with Cell Membranes. J Oleo Sci. 2016 Dec 1;65(12):993-1001. doi: 10.5650/jos.ess16074. 

Abstract. Sodium lauryl sulfate (SLS), a representative anionic surfactant, is well-known to induce rough skin following single or multiple topical applications. The mechanism by which SLS induces rough skin is thought to result from the disruption of skin moisture function consisting of NMF and epidermal lipids. However, a recent study demonstrated that topically applied SLS easily penetrates into the living cell layers of the epidermis, which suggests that physiological alterations of keratinocytes might cause the SLS-induced rough skin. This study was conducted to clarify the effects of SLS on keratinocytes to demonstrate the contribution of SLS to the induction of rough skin. In addition, the potentials of other widely used anionic surfactants to induce rough skin were evaluated. HaCaT keratinocytes treated with SLS had increased levels of intracellular ROS and IL-1α secretion. Application of SLS on the surface of a reconstructed epidermal equivalent also showed the increased generation of ROS. Further, SLS-treated cells showed an increase of intracellular calpain activity associated with the increase of intracellular Ca2+ concentration. The increase of intracellular ROS was abolished by the addition of BAPTA-AM, a specific chelator of Ca2+. In addition, IL-1α also stimulated ROS generation by HaCaT keratinocytes. An ESR spin-labeling study demonstrated that SLS increased the fluidity of membranes of liposomes and cells. Together, those results indicate that SLS initially interacts with cell membranes, which results in the elevation of intracellular Ca2+ influx. Ca2+ stimulates the secretion of IL-1α due to the activation of calpain, and also increases ROS generation. IL-1α also stimulates ROS generation by HaCaT keratinocytes. We conclude from these results that the elevation of intracellular ROS levels is one of the causes of SLS-induced rough skin. Finally, among the other anionic surfactants tested, sodium lauryl phosphate has less potential to induce rough skin because of its lower generation of ROS.

Piret J, Désormeaux A, Cormier H, Lamontagne J, Gourde P, Juhász J, Bergeron MG. Sodium lauryl sulfate increases the efficacy of a topical formulation of foscarnet against herpes simplex virus type 1 cutaneous lesions in mice. Antimicrob Agents Chemother. 2000 Sep;44(9):2263-70. doi: 10.1128/AAC.44.9.2263-2270.2000. 

Abstract. The influence of sodium lauryl sulfate (SLS) on the efficacies of topical gel formulations of foscarnet against herpes simplex virus type 1 (HSV-1) cutaneous infection has been evaluated in mice. A single application of the gel formulation containing 3% foscarnet given 24 h postinfection exerted only a modest effect on the development of herpetic skin lesions. Of prime interest, the addition of 5% SLS to this gel formulation markedly reduced the mean lesion score. The improved efficacy of the foscarnet formulation containing SLS could be attributed to an increased penetration of the antiviral agent into the epidermis. In vitro, SLS decreased in a concentration-dependent manner the infectivities of herpesviruses for Vero cells. SLS also inhibited the HSV-1 strain F-induced cytopathic effect. Combinations of foscarnet and SLS resulted in subsynergistic to subantagonistic effects, depending on the concentration used. Foscarnet in phosphate-buffered saline decreased in a dose-dependent manner the viability of cultured human skin fibroblasts. This toxic effect was markedly decreased when foscarnet was incorporated into the polymer matrix. The presence of SLS in the gel formulations did not alter the viabilities of these cells. The use of gel formulations containing foscarnet and SLS could represent an attractive approach to the treatment of herpetic mucocutaneous lesions, especially those caused by acyclovir-resistant strains.