| Description | Phenoxyethanol is an organic chemical compound, a glycol ether often used in dermatological products such as skin creams and sunscreen. It is a colorless oily liquid. It is a bactericide (usually used in conjunction with quaternary ammonium compounds). Phenoxyethanol is used in many applications such as cosmetics, vaccines and pharmaceuticals as a preservative. |
| Chemical Properties | Phenoxyethanol is a colorless, slightly viscous liquid with a faint
pleasant odor and burning taste. |
| Chemical Properties | clear colorless liquid |
| Characteristics | Phenoxyethanol is a tried-and-tested preservative, which is welltolerated by the skin and has a low allergy risk. It can be used over a wide pH range. This means that other preservatives can lose their effectiveness if the product is not within the right pH range. It does not smell unpleasant or change the color of the product, which can be the case when using natural antimicrobial substances. |
| Uses | Phenoxyethanol is a preservative used in consumer and health care products, including vaccines, pen inks, ear drops, shampoos, skin cleansers, moisturizers, sun care products, and topical medicaments. The preservative Euxyl-K 400 also contains 2-phenoxyethanol, in combination with methyldibromoglutaronitrile.
Phenoxyethanol is commonly used in cosmetics for its antibacterial and antifungal properties. It is increasingly being used in vaccines as a substitute for thiomersal and is also a component of pen inks and, more rarely, ear drops.Reactions to phenoxyethanol have rarely been reported. Three cases of CoU induced by phenoxyethanol in cosmetics have been reported.2-Phenoxyethanol is used as a single agent and in combination with other preservatives such as 1,2-dibromo-2,4-dicyanobutane (Euxyl K 400) and parabens, or in conjunction with quaternary ammonium compounds.The possibility of immunological IgE-mediated reaction could not be confirmed because specific IgE against 2-phenoxyethanol was negative. |
| Uses | Ethylene glycol phenyl ether at a
1.0% level acts as a preservative in personal care products. |
| Uses | phenoxyethanol is a broad-range preservative with fungicidal, bactericidal, insecticidal, and germicidal properties. It has a relatively low sensitizing factor in leave-on cosmetics. Phenoxyethanol can be used in concentrations of 0.5 to 2.0 percent, and in combination with other preservatives such as sorbic acid or parabens. In addition, it is used as a solvent for aftershaves, face and hair lotions, shampoos, and skin creams of all types. It can be obtained from phenol. |
| Uses | Antimicrobial preservative; also used topically in treatment of bacterial infections. |
| Production Methods | Phenoxyethanol is prepared by treating phenol with ethylene oxide
in an alkaline medium. |
| Definition | ChEBI: 2-phenoxyethanol is an aromatic ether that is phenol substituted on oxygen by a 2-hydroxyethyl group. It has a role as an antiinfective agent and a central nervous system depressant. It is a primary alcohol, a glycol ether and an aromatic ether. It is functionally related to a phenol. |
| Synthesis Reference(s) | The Journal of Organic Chemistry, 40, p. 1356, 1975 DOI: 10.1021/jo00897a043 |
| General Description | Colorless liquid with a pleasant odor. Density 1.02 g / cm3. An irritant. |
| Air & Water Reactions | Oxidizes in air to form unstable peroxides that may explode spontaneously [Bretherick, 1979 p.151-154, 164]. Water soluble. |
| Reactivity Profile | 2-Phenoxyethanol may react violently with strong oxidizing agents. May generate flammable and/or toxic gases with alkali metals, nitrides, and other strong reducing agents. May initiate the polymerization of isocyanates and epoxides. |
| Health Hazard | May cause moderate eye irritation and moderate corneal injury. Excessive exposure may cause skin irritation and hemolysis. |
| Fire Hazard | 2-Phenoxyethanol is combustible. |
| Flammability and Explosibility | Not classified |
| Pharmaceutical Applications | Phenoxyethanol is an antimicrobial preservative used in cosmetics
and topical pharmaceutical formulations at a concentration of
0.5–1.0%; it may also be used as a preservative and antimicrobial
agent for vaccines.Therapeutically, a 2.2% solution or 2.0%
cream has been used as a disinfectant for superficial wounds, burns,
and minor infections of the skin and mucous membranes.
Phenoxyethanol has a narrow spectrum of activity and is thus
frequently used in combination with other preservatives, |
| Industrial uses | 2-Phenoxyethanol is used as a preservative in cosmetic formulations at a maximum concentration of 1.0%.
2-Phenoxyethanol is a broad spectrum preservative which has excellent activity against a wide range of Gram negative and Gram positive bacteria, yeast and mould. It is also used as a solvent and, because of its properties as a solvent, it is used in many blends and mixtures with other preservatives.
2-Phenoxyethanol is not registered as a food additive in the EU.
Scognamiglio et al. (ref. 105) reported that 2-phenoxyethanol is a fragrance ingredient used in many fragrance mixtures (see discussion). An ester of 2-Phenoxyethanol, 2-Phenoxyethyl isobutyrate and 2-Phenoxyacetic acid, the main metabolite of 2-Phenoxyethanol, were mentioned in a WHO publication where 43 flavouring agents in food were evaluated (WHO 2003, AR4), however at intakes assessed to be very low in Europe (around 1 µg/kg bw/day). |
| Contact allergens | Phenoxyethanol is an aromatic ether-alcohol used
mainly as a preservative, mostly with methyldibromoglutaronitrile
(in Euxyl? K 400) or with parabens.
Sensitization to this molecule is very rare. |
| Safety Profile | Moderately toxic by ingestion and skin contact. A skin and severe eye irritant. Mutation data reported. Some glycol ethers have dangerous human reproductive effects. Combustible when exposed to heat or flame; can react vigorously with oxidizing materials. When heated to decomposition it emits acrid smoke and irritating fumes. To fight fEe, use CO2, dry chemical. Used as a solvent for ester-type resins. See also GLYCOL ETHERS. |
| Safety | Phenoxyethanol produces a local anesthetic effect on the lips, tongue, and other mucous membranes. The pure material is a moderate irritant to the skin and eyes. In animal studies, a 10% v/v solution was not irritant to rabbit skin and a 2% v/v solution was not irritant to the rabbit eye.Long-term exposure to phenoxyethanol may result in CNS toxic effects similar to other organic solvents.Safety issues related to preservatives used in vaccines, including 2-phenoxyethanol have been reviewed.Contact urticaria has been reported upon exposure to 2-phenoxyethanol-containing cosmetics.
The US FDA has recommended avoiding at least one topical product containing phenoxyethanol due to concerns over inadvertant exposure to nursing infants.
LD50 (rabbit, skin): 5 g/kg
LD50 (rat, oral): 1.26 g/kg |
| storage | Aqueous phenoxyethanol solutions are stable and may be sterilized
by autoclaving. The bulk material is also stable and should be stored
in a well-closed container in a cool, dry place. |
| Incompatibilities | The antimicrobial activity of phenoxyethanol may be reduced by
interaction with nonionic surfactants and possibly by absorption by
polyvinyl chloride.The antimicrobial activity of phenoxyethanol
against Pseudomonas aeruginosa may be reduced in the presence of
cellulose derivatives (methylcellulose, sodium carboxymethylcellulose,
and hypromellose (hydroxypropylmethylcellulose)). |
| Regulatory Status | Included in the FDA Inactive Ingredients Database (topical
preparations). Included in nonparenteral medicines licensed in the
UK. Included in the Canadian List of Acceptable Non-medicinal
Ingredients.
Under European regulations for cosmetics (76/768/EEC), the
maximum authorized concentration (MAC) of 2-phenoxyethanol is
1.0%. |