PHENOXYETHANOL

PHENOXY ETHANOL (FENOKS ETANOL)

CAS NUMBER: 122-99-6

synonyms:

2-Phenoxy ethanol;Emuclens;Erisept;ethylene glycol monophenyl ether;phenoxethol;Phenoxy ethanol;2-Phenoxy ethanol;122-99-6;Phenoxy ethanol;Ethylene glycol monophenyl ether;Phenyl cellosolve;Phenoxytol;Ethanol, 2-phenoxy-;Phenoxethol;Phenoxyethyl alcohol;Phenoxetol;Arosol;Rose ether;Ethylene glycol phenyl ether;Phenylmonoglycol ether;2-Phenoxyethan-1-Ol;1-Hydroxy-2-phenoxyethane;Dowanol EP;2-Phenoxyethyl alcohol;Glycol monophenyl ether;Fenyl-cellosolve;2-Fenoxyethanol;2-Hydroxyethyl phenyl ether;Dowanol EPH;beta-Hydroxyethyl phenyl ether;Emery 6705;Emeressence 1160;Fenylcelosolv;Phenylglycol;Marlophen P;Marlophen P 7;2-Phenoxy-ethanol;Spermicide 741;Tritonyl 45;Ethylan HB 4;EGMPE;Fenylcelosolv [Czech];Phenooxy alcohol;2-Fenoxyethanol [Czech];Fenyl-cellosolve [Czech];Plastiazan-41 [Russian];UNII-HIE492ZZ3T;NSC 1864;Polyoxyethylene phenol ether;Polyoxyethylene phenyl ether;beta-Phenoxy ethanol;Phenol-ethylene oxide adduct;Glycols, polyethylene, monophenyl ether;Phenoxy ethanol [NF];Polyethylene glycol phenyl ether;.beta.-Hydroxyethyl phenyl ether;HSDB 5595;Phenyl monoglycol ether;PHE-G;PHE-S;Rose ether Phenoxy ethanol;EINECS 204-589-7;FR 214;.beta.-Phenoxyethyl alcohol;alpha-Phenyl-omega-hydroxypoly(oxy-1,2-ethanediyl);BRN 1364011;AI3-00752()C;9004-78-8;CHEBI:64275;C8H10O2;QCDWFXQBSFUVSP-UHFFFAOYSA-N;Poly(oxy-1,2-ethanediyl), ?-phenyl-?-hydroxy-;MFCD00002857;Phenoxy ethanol (NF);Poly(oxy-1,2-ethanediyl), alpha-phenyl-omega-hydroxy-;NCGC00090731-01;NCGC00090731-05;DSSTox_CID_1976;DSSTox_RID_76437;DSSTox_GSID_21976;2-Phenoxy ethanol-1,1-d2;Erisept;Plastiazan-41;56257-90-0;AS-122-99-6;Phenol, ethoxylated;.beta.-Phenoxy ethanol;monophenylglycol;Phenoxy ethanolum;Phenoxytolarosol;CCRIS 9481;Phenoxyl ethanol;arosol[qr];2-phenyloxyethanol;2-phenoxy ethanol;2-(phenoxy)ethanol;Dowanol EP / EPH;beta-phenoxyethylalcohol;ACMC-1BVYG;(2-Hydroxyethoxy)benzene;2-Phenoxy ethanol, 99%;2-phenoxyethylalcohol[qr];beta-hydroxyethylphenylether;WLN: Q2OR;phenol, ethoxyliert (6eo);polyethyleneglycolphenylether;AC1L1L7D;AC1Q7D8M;HIE492ZZ3T;SCHEMBL15708;2-Phenoxy ethanol, >=99%;4-06-00-00571 (Beilstein Handbook Reference);KSC174Q0P;MLS002174254;ethyleneglycol monophenyl ether;Euxyl K 400 (Salt/Mix);beta-hydroxyethylphenylether[qr];phenol, ethoxyliert, eo 4 mol;Jsp001544;CHEMBL1229846;DTXSID9021976;CTK0H4807;phenol, ethoxyliert, eo 30 mol;Ethylene glycol mono phenyl ether;NSC1864;MolPort-001-768-719;BB_SC-2741;HMS2268A20;Poly(oxy-1,2-ethanediyl), .alpha.-phenyl-.omega.-hydroxy-;NSC-1864;STR04582;ZINC1577061;Tox21_111002;Tox21_113532;Tox21_202111;Tox21_300842;ANW-18088;BBL027410;LS-672;SBB060485;STK802556;ZINC01577061;2-Phenoxy ethanol, analytical standard;Fungal Terminator [veterinary] (TN);AKOS000118741;Tox21_111002_1;MCULE-1828011376;RP20453;RTR-003651;TRA0162661;NCGC00090731-02;NCGC00090731-03;NCGC00090731-04;NCGC00090731-06;NCGC00090731-07;NCGC00090731-08;NCGC00254745-01;NCGC00259660-01;AJ-27363;AK110792;AN-19469;AN-22895;BC208517;CJ-05434;CJ-24993;Ethylene glycol monophenyl ether, >=90%;KB-25856;LP119824;LS-72941;OR034465;OR190422;SC-47140;SMR000112131;ETHANOL,2-PHENOXY MFC8 H10 O2;ST2417151;TR-003651;FT-0613280;P0115;P1953;ST51046662;2-Phenoxy ethanol(ethyleneglycolmonophenylether);2-Phenoxy ethanol, tested according to Ph.Eur.;D08359;97692-EP2287158A1;97692-EP2305662A1;97692-EP2372017A1;A805003;SR-01000838345;I01-8824;J-510235;SR-01000838345-2;F1905-6997;Z426194440;Ethylene glycol monophenyl ether, SAJ first grade, >=95.0%;Phenoxy ethanol, European Pharmacopoeia (EP) Reference Standard;Phenoxy ethanol, United States Pharmacopeia (USP) Reference Standard;InChI=1/C8H10O2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H;2-Phenoxy ethanol, pharmaceutical secondary standard; traceable to USP and PhEur;1020398-73-5;134367-25-2;18249-17-7;200260-63-5;37220-49-8;37813-33-5;79586-53-1;FENOKSETHANOL;FENOKSIETHANOL;FENOKSI ETHANOL;FENOKS ETHANOL;PHENOXY ETHANOL;PHENOXY ETANOL;FENOKS ETANOL;FENOKSI ETANOL;fenoksi ethanol;fenoks ethanol;phenoxy ethanol;phenoxy etanol;fenoksiethanol;Phenoxy ethanol;phenoxyetanol;fenoksethanol;Fenoksi Ethanol;Phenoxy Ethanol;Fenoksi Etanol;Phenoxy Etanol;FenoksiEthanol;Phenoxy ethanol;Fenoksi etanol;PhenoxyEtanol;fenoksiethanol;2-Phenoxy ethanol;2-Phenoxyethyl alcohol;3-ETHYL-2-HEPTANOL;DOWANOL(TM) EPH;ETHYLENE GLYCOL MONOPHENYL ETHER;ETHYLENE GLYCOL PHENYL ETHER;MONOPHENYL GLYCOL;PHENOXETOL;Phenoxy ethanol;Phenoxy ethanolUM;PHENYL CELLOSOLVE;PHENYLGLYCOL;ROSE ETHER;1-Hydroxy-2-phenoxyethane;1-hydroxy-2-phenoxyethane[qr];2-Fenoxyethanol;2-fenoxyethanol(czech)[qr];2-Hydroxyethyl phenyl ether;2-Hydroxyethylphenylether;2-hydroxyethylphenylether[qr];fenoksiethanolveuygulamalanlar;fenoksiethanolvekozmetik;fenoksi ethanol ve uygulamalar;fenoksi ethanol ve kozmetik;phonexyethanolandapplication;Phenoxy ethanolandcosmetics;phenoxy ethanol and application;phenoxy ethanol and cosmetics;PHENOXY ETHANOL AND APPLICATION; PHENOXY ETHANOL AND COSMETICS; PHENOXY ETHANOL ; FENOKS ETANOL; 2-Fenoksi etanol; (2-hidroksi-etil)-fenil eter; Fenoksetol, etilen glikol fenil eter; Phenoxy ethanol; fenoksi etanol; Fenoksi etanol; Phenoxy ethanol; Phenoxy ethanol ; FENOKSETANOL; PHENOKSY ETHANOL ; FENOXY ETANOL; Le phénoxyéthanol ;phénoxyéthanol

PHENOXY ETHANOL

Phenoxy ethanol

Phenoxy ethanol[1][2][3]

2-Phenoxy ethanol-Line-Structure.svg

Phenoxy ethanol 3d structure.png

Names

IUPAC name

2-Phenoxy ethanol

Other names

Phenoxy ethanol

Ethylene glycol monophenyl ether

Phenoxytolarosol

Dowanol EP / EPH

Protectol PE

Emery 6705

Rose ether

1-Hydroxy-2-phenoxyethane

β-hydroxyethyl phenyl ether

Phenyl cellosolve

Identifiers of Phenoxy ethanol

CAS Number of Phenoxy ethanol

122-99-6 ☑

3D model (JSmol)

Interactive image

ChEBI

CHEBI:64275 ☒

ChEMBL

ChEMBL1229846 ☒

ChemSpider

13848467 ☑

ECHA InfoCard 100.004.173

PubChem CID

31236

Properties of Phenoxy ethanol

Chemical formula of Phenoxy ethanol

C8H10O2

Molar mass of Phenoxy ethanol 138.166 g·mol-1

Appearance of Phenoxy ethanol Colorless oily liquid

Odor of Phenoxy ethanol faint rose-like

Density of Phenoxy ethanol1.102 g/cm3

Melting point of Phenoxy ethanol -2 °C (28 °F; 271 K)

Boiling point of Phenoxy ethanol 247 °C (477 °F; 520 K)

Solubility of Phenoxy ethanol in water

26 g/kg

Solubility of Phenoxy ethanol Chloroform, Alkali, diethyl ether: soluble

Solubility of Phenoxy ethanol in peanut oil slightly

Solubility of Phenoxy ethanol in olive oil slightly

Solubility of Phenoxy ethanol in acetone miscible

Solubility of Phenoxy ethanol in ethanol miscible

Solubility of Phenoxy ethanol in glycerol miscible

Vapor pressure of Phenoxy ethanol 0.001 kPa

Thermal conductivity 0.169 W/(m⋅K)

Refractive index (nD)

1.534 (20 ℃)

Hazards

NFPA 704 (fire diamond)

NFPA 704 four-colored diamond

130

Flash point of Phenoxy ethanol 121 °C (250 °F; 394 K)

Related compounds

phenetole

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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Infobox references

Phenoxy ethanol is a germicidal and germistatic glycol ether, phenol ether, and aromatic alcohol often used together with quaternary ammonium compounds.

Use of Phenoxy ethanol

Phenoxy ethanol is used as a perfume fixative; an insect repellent; an antiseptic; a solvent for cellulose acetate, dyes, inks, and resins; a preservative for pharmaceuticals, cosmetics and lubricants; an anesthetic in fish aquaculture; and in organic synthesis.

Phenoxy ethanol is an alternative to formaldehyde-releasing preservatives.[4] In Japan and the EU, its concentration in cosmetics is restricted to 1%.[5]

Production of Phenoxy ethanol

Phenoxy ethanol is produced by the hydroxyethylation of phenol (Williamson synthesis), for example, in the presence of alkali-metal hydroxides or alkali-metal borohydrides.[1]

Efficacy of Phenoxy ethanol

Phenoxy ethanol is effective against gram-negative and gram-positive bacteria, and the yeast Candida albicans.[6]

Phenoxy ethanol by Lanxess is used as a crosslinking agent. Phenoxy ethanol is effective against gram positive and gram negative bacteria and fungi. Phenoxy ethanol complies with FDA 21 CFR 175.105 for indirect food contact use in adhesives.

What is phenoxy ethanol?

Phenoxy ethanol is a preservative used in many cosmetics and personal care products. You may have a cabinet full of products containing this ingredient in your home, whether you know it or not.

Chemically, phenoxy ethanol is known as a glycol ether, or in other words, a solvent. CosmeticsInfo.org describes Phenoxy ethanol as “an oily, slightly sticky liquid with a faint rose-like scent.”

You likely come into contact with this chemical on a regular basis. But is it safe? The evidence is mixed.

We’ll review the most relevant scientific research about this common cosmetics ingredient. You can decide whether you’d like to keep or banish it from your personal care products arsenal.

How’s Phenoxy ethanol used?

Many mainstream and boutique cosmetics products contain Phenoxy ethanol. Phenoxy ethanol’s often used as a preservative or stabilizer for other ingredients that might otherwise deteriorate, spoil, or become less effective too quickly.

Phenoxy ethanol is also used in other industries, including in vaccines and textiles. This article focuses on Phenoxy ethanol’s role in topical cosmetics.

How does Phenoxy ethanol appear on the label?

You might see this ingredient listed in a few ways:

phenoxy ethanol

ethylene glycol monophenyl ether

2-Phenoxy ethanol

PhE

dowanol

arosol

phenoxetol

rose ether

phenoxyethyl alcohol

beta-hydroxyethyl phenyl ether

euxyl K® 400, a mixture of Phenoxy ethanol and 1,2-dibromo-2,4-dicyanobutane

What cosmetics is Phenoxy ethanol found in?

You can find phenoxy ethanol as an ingredient in a wide variety of cosmetics and hygiene products, including:

perfume

foundation

blush

lipstick

soaps

hand sanitizer

ultrasound gel, and more

Perhaps most famously in the public consciousness, Phenoxy ethanol was used in Mommy Bliss brand nipple cream. In 2008, the U.S. Food and Drug Administration (FDA)Trusted Source recalled it as unsafe for breastfeeding infants, due to concerns about how it affects their central nervous system.

Why is it added to cosmetics?

In perfumes, fragrances, soaps, and cleansers, Phenoxy ethanol works as a stabilizer. In other cosmetics, Phenoxy ethanol’s used as an antibacterial and/or a preservative to prevent products from losing their potency or spoiling.

When combined with another chemical, some evidence indicates that it’s effective at reducing acne. One 2008 study on 30 human subjects with inflammatory acne showed that after six weeks of twice-daily applications, more than half of the subjects saw a 50 percent improvement in their number of pimples.

Manufacturers who want to avoid using parabens, which have recently lost favor among health-conscious consumers, might use Phenoxy ethanol in their products as a substitute.

But is Phenoxy ethanol safer than parabens for topical use in humans?

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Is phenoxy ethanol safe?

Deciding whether or not you want to use products with this chemical is a complicated decision. There’s conflicting data about its safety. Most of the concern stems from recorded incidents of bad skin reactions and nervous system interaction in infants.

The FDA currently allows the use of this ingredient in cosmetics, and as an indirect food additive.

An expert panel from The Cosmetic Ingredient Review (CIR) first reviewed all available data on this chemical in 1990. They deemed it safe when applied topically in concentrations of 1 percent or lower.

In 2007, the panel reviewed newly available data, then confirmed their former decision that it’s safe for adults to use topically in very low concentrations.

The European Commission on Health and Food Safety also gives this chemical a “safe” rating when used in cosmetics at a 1-percent or less concentration. However, this report notes that using several products all containing a low dose could result in overexposure.

Japan also restricts use in cosmetics to a 1-percent concentration.

Possible health concerns

Allergies and skin irritation

In humans

Phenoxy ethanol is known to cause allergic-type reactions on the skin in some people. Some argue that these bad reactions are the result of allergies in the test subjects. Others argue that it’s simply a skin irritant that affects different people at different levels.

Several studies have shown both humans and animals can experience:

skin irritation

rashes

eczema

hives

In one study on a human subject, this chemical caused hives and anaphylaxis (a potentially life-threatening allergic reaction) in a patient who used topical skin products with the ingredient. Though, anaphylaxis from this chemical is very rare.

In another case report, ultrasound gel that contained this chemical caused contact dermatitis in a human subject.

Both of these cases are just examples of many similar incidences of this chemical causing irritation and rashes in humans. But the frequency of these symptoms is very low when compared to how often people are exposed with no notable side effects. And they’re generally thought to be caused by allergies.

In infants

Phenoxy ethanol is thought to cause central nervous system damage in exposed infants. However, there’s no known significant risk to the mother, or other healthy adults without allergies.

In animals

The European Commission on Health and Food Safety cites multiple studies where rabbits and rats exposed to the chemical had skin irritation, even at low levels.

The bottom line

You should avoid this chemical if you’re:

allergic to Phenoxy ethanol

pregnant

breastfeeding

considering using on a child under 3-years old

The risks outweigh the possible benefits in those cases.

However, if you’re a healthy adult with no history of skin allergy, you likely don’t need to worry about exposure through cosmetics under a 1-percent concentration. You should, however, be aware of layering too many products containing Phenoxy ethanol at one time, since Phenoxy ethanol can accumulate.

EC NUMBER: 204-589-7

Molecular Formula of Phenoxy Ethanol

C8H10O2

C6H5OC2H4OH

Chemical and Physical Properties of Phenoxy Ethanol

Property Name

Molecular Weight: 138.166 g/mol

Hydrogen Bond Donor Count: 1

Hydrogen Bond Acceptor Count: 2

Rotatable Bond Count: 3

Complexity: 77.3

Topological Polar Surface Area: 29.5 A^2

Monoisotopic Mass: 138.068 g/mol

Exact Mass: 138.068 g/mol

XLogP3: 1.2

Compound Is Canonicalized: true

Formal Charge: 0

Heavy Atom Count: 10

Defined Atom Stereocenter Count: 0

Undefined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

Isotope Atom Count: 0

Covalently-Bonded Unit Count: 1

Experimental Properties of Phenoxy Ethanol

Physical Description of Phenoxy Ethanol

Ethylene glycol phenyl ether is a colorless liquid with a pleasant odor. Density 1.02 g / cm3. An irritant.

Color of Phenoxy Ethanol

Oily liquid

Odor of Phenoxy Ethanol

Faint aromatic odor

Taste of Phenoxy Ethanol

Burning taste

Boiling Point of Phenoxy Ethanol

473.4° F at 760 mm Hg

Melting Point of Phenoxy Ethanol

57° F

Density of Phenoxy Ethanol

1.104

GENERAL DESCRIPTION & APPLICATIONS of Phenoxy Ethanol

Glycol ethers, with the combination of ether, alcohol and hydrocarbon chain in one molecule, provide versatile solvency characteristics with both polar and non-polar properties. The chemical structure of long hydrocarbon chain resist to solubility in water, while ether or alcohol groups introduce the promoted hydrophilic solubility performance. This surfactant-like structure provides the compatibility between water and a number of organic solvents, and the ability to couple unlike phases. Glycol ethers are characterized by their wide range of hydrophilic/hydrophobic balances. glycol ethers are used as diluents and levelling agents in the manufacture of paints and baking finishes. Glycol ether series are used in the manufacture of nitrocellulose and combination lacquers. They are used as an additive in brake fluid. They are formulated for dying textiles and leathers and for insecticides and herbicides. They provides performance in cleaners products with oil-water dispersions. They are used in printing industries as they have a slow evaporation rate. They are used as a fixative for perfumes, germicides, bactericides, insect repellents and antiseptic. They are used as an additive for jet fuel to prevent ice buildup. Glymes, dimethyl ethers, have two terminal methyl groups which offer stability and high solvency. They are useful as solubilizers and phase transfer catalysts. Glymes offer the property required as an inert reaction medium chemical reaction due to their low chemical reactivity. They are suitable particularly for organometallic and polymerization reactions. Glycol ethers which contain hydroxyl group are also useful chemical intermediate. The hydroxyl group will undergo reaction with aldehydes (or ketones) to produce hemiacetals (or acetals), with epoxides to produce polyether alcohols, with halogenating agents to produce alkoxy alkyl halides, with carboxylic acid compounds or inorganic acids to produce a number of esters.

Phenoxy ethanol is one of the most widely used preservatives in personal care products including detergents, cosmetics, toiletries and pharmaceuticals. It provides a broad spectrum anti-microbial activity against either gram-negative or gram-positive bacteria, yeasts and moulds. It is soluble in many non-polar ingredients and contributes solvency activity. Its activity is effective in protein-based products also. In most countries, it is permitted to a maximum of 1% concentration.

FENOKS ETANOL

Formul: C8H10O2

Tanm: Hafif karakteristik kokulu berrak renksiz hafif viskos sv.

Ambalaj ekli: 5 Litre

CAS No: 122-99-6

EINECS No: 204-589-7

INCI Name:Fenoksi etanol.

Kimyasal ad: 2-Fenoksi etanol; (2-hidroksi-etil)-fenil eter; Fenoksetol, etilen glikol fenil eter,

etilen glikol monofenil eter.

Fenoksi etanol Özellikleri:

Fenoksi etanol Dünyada kiisel bakm ürünlerinde en yaygn olarak kullanlan koruyuculardan biridir. Fenoksi etanol Banyo köpükleri gibi deterjan bazl ürünlerden cilt bakm fondotenleri, saç ürünleri ve göz makyaj malzemelerine kadar geni bir kullanm aralna sahip çok yönlü bir koruyucudur.Fenoksi etanol Ayrca metal ileme svlar, bask mürekkepleri, yaptrclar gibi endüstriyel ürünlerde bir koruyucu olarak kullanlrlar.Fenoksi etanol , mükemmel çözücü özellikleri dolaysyla, genel bir koformülant olarak olmasyla birlikte, antibakteriyel ve antifungal özellikleriyle bilinir.

Fenoksi etanol Faydalar:

Gram negatif, gram pozitif bakteriler, maya ve küfleri içeren geni spektrumlu aktivite,

Özellikle pseudomonasspp ve dier problem oluturan gram negatif bakterisine etkili,

pH : 3-8,5 arasnda kararl ve etkili,

Normal kullanm konsantrasyonlarnda gözleri, cildi ve mukus (mukoza) zarn tahri etmez,

Fenoksi etanol Cilt hassasiyeti göstermez,

Proteinler ve noniyonik yüzey aktifler ve kiisel bakm ürünlerinin dier bilinen bileenlerinin bir çounun varlnda aktivitelerini korurlar,

Fenoksi etanol Oda scaklnda düük uçuculuk gösterir, uzun depolamalarda bile koruyucu kayb yoktur,

Sv ilenme kolayl,

Fenoksi etanol Suda dikkate deer olarak tipik kullanm konsantrasyonlarnn üzerinde, yaklak % 2,4 orannda çözünür,

Avrupa, Amerika, Japonya ve dier önemli kiisel bakm marketlerinde kullanmna izin verilmitir.

Çözünürlük, stabilite, uygunluk:

Fenoksi etanol glikollerin ve alkollerin (etanol, propanol ve propilen glikol gibi) geni bir aralyla tamamen karr ve suda lml bir ekilde çözünür (% 2,4). Fenoksi etanol Bu geni bir formülasyon çeitliliinin içerisine kolay bir ekilde dahil olmasna imkan verir.Fenoksi etanol mükemmel solvent özelliklerine sahiptir, bundan dolay zayf çözünürlük profiline sahip aktif madde ve ham maddeleri çözmek için kullanlabilir.

Asitler ve alkaliler varlnda ayrca yüksek scaklk artlar altnda ar kararllk gösterir. Bu nedenle scak üretim proseslerinde dayankldr ve geni bir geni bir pH aralnda etkili kontrol salar.

Fenoksi etanol Genel olarak kullanlan yüzey aktiflerin çouyla uyumludur. (anyonik, katyonik, noniyonik ve amfoterik) Fenoksi etanol Ayrca dier antimikrobiyallerle uyumludur.(örn; 2,4 diklorobenzil alkol, 1,2-dibromo-2-4 diizosiyanobutan:DBDCB ve iodopropinilbutilkarbamat: IPBC ve parabenler gibi).

Fenoksi etanol Uygulamalar:

Fenoksi etanol, ampuan ve banyo köpükleri gibi deterjan bazl ürünlerde % 0,5-1,0 aralnda kullanlr. Fenoksi etanol Proteinlerle aktifliini kaybetmez ve protein bazl ürünlerde % 0,5-1,0 aralnda kullanlabilir.

Fenoksi etanol’ün düük konsantrasyonlar mantar kart aktiviteyi artrmak için parabenler gibi dier koruyucularla kombinasyon içerisinde kullanlabilirler.

Fenoksi etanol Suyla karan ve suyla emülsifiye edilebilen metal ileme svlar konsantrelerinde % 10-15 orannda kullanlabilir. Bu, final kullanm seyrelmesinde yaklak bir % 0,5 konsantrasyonu elde etmek için dizayn edilir, böylelikle Fenoksi etanol kullanmnda svya iyi bir antimikrobiyal koruma salar.

Dier endüstriyel muameleler için tavsiye edilen kullanm düzeyleri, sistem artlarna ve dier biositlerin varlna bal olarak % 0,5-1 aralndadr.

Fenoksi etanol Kullanm:

Bir çok susuz maddede Fenoksi etanol kolaylkla çözünür ve deterjan bazl ürünlere stmakszn direkt olarak eklenebilir. Emülsiyonlarda, ya emülsifikasyondan önceki faza yada hemen sonra hzl bir kartrmayla eklenebilir. Fenoksi etanol, çözücülük ve aktivite çifte avantajlarnn yardmyla bir çok geni spektrumlu koruyucularn sv karmlarnda kullanlr.

Fenoksi etanol Uygulama Alanlar:

Tüketici ürünleri korunmasnda Fenoksi etanol kullam: laç, kozmetik, tuvalet malzemeleri, gündelik ev eyalar ve hammaddelerin korunmasnda,

Endüstriyel ürünlerin korunmasndaFenoksi etanol kullam: Metal ileme svlar, yaptrc ve endüstriyel katk maddeleri gibi teknik ürünlerin korunmasnda,

Yüzey ve enstrumanlardaFenoksi etanol kullam: enfeksiyon önleyici olarak:

Sert yüzey ve tbbi malzemelerde enfeksiyon önleyici olarak Fenoksi etanol kullam: kullanlan ürün formülasyonlarnda kullanlr.

Fenoksi etanol

Fenoksi etanol yaps

Fenoksi etanol, C8H10O2 formüllü bir fenol eteri ve aromatik alkoldür. 247 °C derecede kaynar. Formaldehit salan koruyuculara alternatif olarak kullanlr. Alarda ve kozmetik ürünlerinde bulunur. Potansiyel alerjendir.

Tüm dünya genelinde üretilen kozmetik ürün çeitlerinde en yaygn ekilde kullanlan koruyucu maddelerden biri de Fenoksi etanol (fenoksi etanol) adl maddedir. Fondöten, banyo köpüü, göz makyaj ürünleri, cilt bakm ürünleri ve deterjan çeitleri gibi çeitli maddelerin üretiminde kullanlan koruyucu madde antibakteriyel ve ayn zamanda antifungal özellie sahip olmasyla da biliniyor. Bask mürekkepleri, yaptrc malzemeler, metal ileme svlar ve baz endüstriyel maddelerin üretiminde de kullanlan Fenoksi etanol (Fenoksi etanol) çözücü özellikte bir madde olmasyla da ön plana çkyor. deal oranda kullanldnda cilde, gözlere ve mukozaya herhangi bir zarar vermiyor olmas ve cilt hassasiyeti yaatmamas çeitli sektörlerde yaygn ekilde bu koruyucu maddenin kullanmn beraberinde getiriyor.

Fenoksi etanol guvenli mi?

Fenoksi etanol Kozmetiklerde hos olmayan icerik maddeleri var. Ancak bazi maddeler hic gunahlari olmadigi halde kotu damgasi yiyebiliyor. Ne yazikki 5 dakika internet okuyum Net PhD si alan sevgili bazi yabanci bloggerlar Fenoksi etanolü kotu noktaya oturtmak icin ellerinden geleni yapiyorlar.

Fenoksi etanol

Dedigim gibi bazi hanim kizlarimiz Fenoksi etanol kotu oggkk! diyorlar 1 litre icersen tabiki kotu ama kozmetiklerde kullanildigi amac ve miktariyla DEGIL.

Fenoksi etanol un kotu olmadigini bilimsel kanitlara dayanarak sizde goreceksiniz.

Fenoksi etanol nedir?

Fenoksi etanol, parabene alternatif olarak en cok kullanilan sentetik bir koruyucu (ingilizcesi: preservative).

Fenoksi etanol Ana ozellikleri: Koruyucu! Adi ustunde, koruyucular kozmetik ve kisisel bakim urunlerini ve siz kullanicilari, urun icinde ureyebilecek zararli bakteri ve kuflerden ve onlarin neden olabilecegi enfeksiyonlardan koruyor.Fenoksi etanol Urunde bakteri uremesini ve bozulmasini engelliyor. Fenoksi etanol sadece iyi birsey degil, sagligimizi korumak icin oldukca gerekli de! Fenoksi etanol de bir koruyucu ve tum yukarida soylediklerimi yerine getirmek amaciyla kozmetiklere ekleniyor.

Eger “preservative free (koruyucusuz)” urun gorurseniz, kullanmadan once iki kere dusunun birle demiyorum, kosarak urunden uzaklasin diyorum. Neden mi? Koruyucu olmayan su bazli urunlerde neler urer: mikrop, hem de cesit cesit alasindan!

Fenoksi etanolun kaynagi: Sentetik veya dogal turevli. Fenoksi etanol formaldehit salmayan koruyuculardan. S

Fenoksi etanol ne yapar?

Bakteri, kuf, mantar ve diger miktoplari oldurur ve kozmetik urunlerin bozulmasini engeller.

Neden kozmetik urunun icinde Fenoksi etanol onemli?

Formulunde su olan kisisel bakim urunleri (sampuan, nemlendirici, krem, losyon mesela) veya kozmetikler (rimel, lip gloss, ruj, sivi farlar vs) sagliginizi kotu etkileyebilecek kotu bakteri, mantar ve kuflerin buyumesi icin muhtesem bir ortam. Urunun gorunusu ve kokusu iyi gibi gorunse de, bakteri veya mantar olabilir. Bu nedenle icerisinde iyi koruyucu sistemi olan urunleri secmek ve kullanma tarihi veya PAO’su gecmis urunleri ASLA kullanmamak gerekiyor.

Yandaki resimde uygun ortamda uremis mikroorganizmalari gorebilirsiniz. Birde bunlari zamani gecmis urunleriniz de dusunun, ve hemen gecmis urunleri cope atin lutfen!

Avrupa Tuketici Guvenligi Bilimsel Komitesi (SCCS) Fenoksi etanol hakkinda ne diyor? Kozmetiklerde kullanilmasi guvenli mi?

Avrupa Tuketici Guvenligi Bilimsel Komitesi [The Scientific Committee on Consumer Safety (SCCS)] yiyecek disi urunler ve kozmetikler uzerinde saglik ve guvenlik riskleri konusunda arastirma yaparak fikirlerini bildiren bir komite. Komitenin yapisinda bir cok bilim adami ve konusunda uzman insanlar var. Gecmislerini ve CV lerini surada gorebilirsiniz.

16 Mart 2016 tarihinde , SCCS Fenoksi etanolun koruyucu olarak 1% seviyesine kadar kozmetik formulasyonlarda kullanilmasinin guvenli oldugunu tespit etti. Avrupa Konseyi ve Japonya kozmetik regulasyonlari tarafindan Fenoksi etanolun 1%’e kadar kullanilmasini onayliyor ve izin veriyor. SCCS nin yayinladigi raporu surada okuyabilirsiniz .

Kozmetik formulatorler, formullerde hic bir zaman gereginden fazla madde kullanmak istemezler. Koruyucularin miktarini (ornegin: Fenoksi etanol) mumkun oldugu kadar dusuk tutarak ve ethylhexylglycerin gibi destekleyici maddeler ekleyerek formulun en isi sekilde korunmasina odaklanirlar. Boylece hem tuketicinin, hemde urunun en iyi sekilde korunmasini saglar ve SCCS tarafindan onaylanan Fenoksi etanol seviyesini dengelemeye calisirlar.

Sonuc: Avrupa Tuketici Guvenligi Bilimsel Komitesi (SCCS) Fenoksi etanol’ un koruyucu olarak kozmetiklerde 1%’ e kadar kullaniminin guvenli oldugunu soyluyor.

Fenoksi etanol ve Cocuklar

Avrupa Komisyonu, cocuklarda olasi potansiyel etkilerin incelenmesi icin Avrupa Tuketici Guvenligi Bilimsel Komitesine (SCCS) Fenoksi etanol’u incelemelerini istedi. SCCS bu yas gurubunda bu koruyucunun bir risk teskil etmedigini tesbit etti. Bu konudaki yayini incelemek isterseniz buraya tik tik.

Avrupa Tuketici Guvenligi Bilimsel Komitesinin sonucu (SCCS) :

Avrupa Tuketici Guvenligi Bilimsel Komitesi (SCCS) SCCS Fenoksi etanolun kozmetiklerde 1% e kadar kullanimin guvenli oldugunu konfirme ediyor mu?

Evet! Fenoksi etanol kullanimi (maksimum seviye 1%) tum yas gurubundaki tuketiciler icin guvenlidir.

Avrupa Tuketici Guvenligi Bilimsel Komitesi (SCCS) kozmetik urunlerde Fenoksi etanolun kullanimiyla ilgili baska bilimsel kaygilari var mi?

Hayir. SCCS Fenoksi etanol raporu (tiktik) kozmetik disinda baska yerlerden maruz kalmayi nazari itibare almamistir.

Neden Fenoksi etanol dogal kozmetik ve kisisel bakim urunlerinde kullaniliyor?

Tum amac urun bozulmasini ve urunlerde bakteri buyumesini engellemek! Cogu dogal korunmus veya dogal koruyucu kullanilmis urunlerin raf omru oldukca kisa. Acildiktan ve havaya maruz kaldiktan sonra, kullanim sureleri 3 ila 6 ay arasinda. Bu noktadan sonra, ureme veya kotu koku/goruntu gormeniz gayet mumkun! Hic birmiz sagligimizin kotu olmasini istemiyoruz. Parabenlerin gitmesiyle, kozmetik endustrisinde en az yan etkiye sahip ve en etkili koruyucu Fenoksi etanol. SCCS’in onayi, Avrupa ve Japon regulasyonlarinin izni, 1%’den daha az Fenoksi etanolun dogal urunlerde kullanimini, tuketicilerin sagligini korumak icin cok onemli bir noktaya koyuyor.

Cevre Koruma

Avrupa Birligi Ecolabel programi, Fenoksi etanolun biyocozunur oldugunu ve su ve toprakta ortama zarar vermeden cozunup gittigini gosterdi.

EWG (Environmental Working Group/ Cevre Calisma Grubu) say on Fenoksi etanol?

ABD’de onemli cevreci ve zararli maddeler konusunda tuketicileri bilinclendirmeye calisan EWG’nin Fenoksi etanol sayfasi surada (tik tik). Ozetle, Fenoksi etanol icin dedikleri sunlar:

Toplam risk: dusuk

Kansere katkisi yok

Gelisim ve ureme toksikligi katkisi yok

Allerji ve immuntoksisite konusunda dusuk risk

Agiz ici kullanimda zararli olabilir (ozetle yemeyin!)

Cevresel toksin degil

EWG Verified damgasi, yani EWG onayi alan urunler, 1%’den az Fenoksi etanol icermesinde sorun yok.

Bitkilerde dogal Fenoksi etanol var mi?

Evet, yesil cay ve hindiba bitkilerinde dogal olarak Fenoksi etanol bulunuyor. Ilginc degil mi?

Zamani gecmis, ve hatta kuvvetli koruyucu kullanilmamis koruyucularda neler urer?

Londra Metropolitan Universitesi bilim adamlari, kullanim zamanlari gecmis allik (blusher), fondoten (foundation), rimel (mascara), ruj (lip stick) ve lip gloss urunlerini test ettiler. Bu zamani gecmis urunlerde yuksek oranda ve potansiye olarak oldurucu bakterilerin uredigini tespit ettiler

Bir de urunde koruyucu olmadigini ve icinde bir sure sonra hangi kotu bakterilerin ureyebilecegini hayal etmeye calisin. Korkutucu degil mi?

Sonuc, iyi mi kotu mu?

Kozmetiklerde Fenoksi etanolun, SCCS ve Avrupa Konseyinin uygun gordugu seviyede kullanilmasi IYI! Bu koruyucu bizi ve urunu kotu mikroplara karsi koruyor.

Uluslararasi bilimsel komite, bilim adamlari ve arastirmayla kanitlanip yayinlandigina gore artik kulaktan dolma, korkutma amacli laflari sallamiyoruz.

Bir cok kimyasala karsi allerjik reaksiyonunuz varsa, cildiniz cok hassassa ve bu kadar bilimsel kanittan sonra hala Fenoksi etanolden uzak duracagim diyorsaniz, o zaman dogal korunmus urunlere bakin. Ancak aklinizdan bu urunlerin cok kisa kullanim zamani oldugunu ve cok cabuk bozulabilecegini, ureme olabilecegini cikarmayin ve ona gore kullanin.

EC SAYISI: 204-589-7

Fenoksi Etanolün Moleküler Formülü

C8H10O2

C6H5OC2H4OH

Fenoksi Etanolün Kimyasal ve Fiziksel Özellikleri

Özellik ad

Fenoksi etanol Moleküler Arlk: 138.166 g / mol

Fenoksi etanol Hidrojen Bam Balayc Says: 1

Fenoksi etanol Hidrojen Ba Alc Says: 2

Fenoksi etanol Dönebilen Bond Says: 3

Fenoksi etanol Karmaklk: 77.3

Fenoksi etanol Topolojik Polar Yüzey Alan: 29.5 A ^ 2

Fenoksi etanol Monoizotopic Kütle: 138.068 g / mol

Fenoksi etanol Tam Kütle: 138.068 g / mol

Fenoksi etanol XLogP3: 1.2

Fenoksi etanol Bileik Canonicalized: true

Fenoksi etanol Resmi arj: 0

Fenoksi etanol Ar Atom Says: 10

Fenoksi etanol Tanml Atom Stereocenter Says: 0

Fenoksi etanol Tanmsz Atom Stereocenter Says: 0

Fenoksi etanol Tanml Bono Stereocenter Says: 0

Fenoksi etanol Tanmlanmam Bond Stereocenter Says: 0

Fenoksi etanol zotop Atom Says: 0

Fenoksi etanol Kovalent Bal Birim Says: 1

Fenoksi Etanolün Deneysel Özellikleri

Fenoksi Etanolün Fiziksel Tanm

Fenoksi etanol ho bir kokuya sahip renksiz bir svdr. Fenoksi etanol Younluu 1.02 g / cm3.

Fenoksi etanol tahri edicidir.

Fenoksi Etanolun Rengi

Yal sv

Fenoksi Etanol Kokusu

Kötü aromatik koku

Fenoksi Etanol Tad

Yanan tad

Fenoksi Etanol Kaynama Noktas

760 mm Hg’de 473.4 ° F

Fenoksi Etanol Erime Noktas

57 ° F

Fenoksi Etanol Younluu

1,104

Fenoksi Etanolün Genel Tantm ve Uygulamalar

Fenoksi etanol, bir molekül içinde eter, alkol ve hidrokarbon zincirinin kombinasyonuyla hem kutupsal hem de polar olmayan özelliklere sahip çok yönlü ödeme gücü özellikleri salar. Uzun hidrokarbon zincirinin kimyasal yaps, suda çözünürlüe kar direnirken, eter veya alkol gruplar yükseltilmi hidrofil çözünürlük performansn getirir. Bu sürfaktan benzeri yap, su ve bir dizi organik çözücü arasnda uyumluluu ve farkl fazlar birletirmeyi salar. Fenoksi etanol geni hidrofilik / hidrofobik dengeleriyle karakterizedir. Fenoksi etanol, boya ve frn kaplamalar imalatnda seyrelticiler ve dengeleyici ajanlar olarak kullanlrlar. Fenoksi etanol, nitroselüloz ve kombinasyon vernikleri üretiminde kullanlr. Fren svsnda katk maddesi olarak kullanlrlar. Boyanan tekstil ve deri için, böcek öldürücü ve herbisitler için formüle edilmitir. Yal su dispersiyonlu temizleyici ürünlerinde performans salarlar. Yava buharlama oran nedeniyle bask endüstrilerinde kullanlrlar. Parfümler, mikrop öldürücü ilaçlar, bakterisitler, böcek kovucular ve antiseptik için bir fiksatif madde olarak kullanlrlar. Buz birikimini önlemek için jet yakt için katk maddesi olarak kullanlrlar. Glymes, dimetil eterler, kararllk ve yüksek ödeme gücü salayan iki terminal metil grubuna sahiptir. Çözündürücüler ve faz transfer katalizörleri olarak faydaldrlar. Glymes, düük kimyasal tepkimelerinden dolay inert bir reaksiyon orta kimyasal reaksiyon olarak gerekli mülkiyet sunar. Özellikle organometalik ve polimerizasyon reaksiyonlar için uygundurlar. Hidroksil grubu içeren glikol eterleri de yararl kimyasal ara ürünlerdir. Hidroksil grubu, polieter alkoller üretmek üzere epoksi ile hemiasetaller (veya asetaller) üretmek üzere aldehitler (veya ketonlar) ile reaksiyona girerek bir dizi ester üretmek üzere karboksilik asit bileikleri veya inorganik asitler ile alkoksi alkil halojenürler üretmek üzere halojenleme ajanlar ile reaksiyona girer.

Fenoksi etanol, deterjanlar, kozmetik ürünleri, tuvalet malzemeleri ve ilaçlar içeren kiisel bakm ürünlerinde en yaygn kullanlan koruyucu maddelerden biridir. Bu, gram negatif veya gram pozitif bakterilere, mayalara ve kalplara kar geni bir yelpazede anti-mikrobik etkinlik salar. Birçok kutupsuz terkip maddesinde çözünür ve ödeme gücü faaliyete katkda bulunur.Fenoksi etanol Etkinlii protein bazl ürünler için de etkilidir. Çou ülkede, maksimum% 1 Fenoksi etanol konsantrasyona izin verilir.

Le phénoxyéthanol

Le phénoxyéthanol est un éther de glycol aromatique de formule semi-développée C6H5O-CH2-CH2OH utilisé dans les produits dermatologiques tels que les crèmes pour la peau et les crèmes solaires pour ses propriétés d’agent de conservation et de solvant.

Utilisation

Le phénoxyéthanol est présent à l’état naturel dans le thé vert8 et la chicorée9. Mais il est la plupart du temps synthétisé et utilisé comme10 :

solvant pour peintures, vernis, laques, encres d’imprimerie, colorants ;

Intermédiaires de synthèses ;

biocide entrant dans la composition de produits d’entretien ménagers et industriels (agents de nettoyage, désinfectants…), de liquides pour systèmes de refroidissement, de produits pour l’industrie mécanique ou métallurgique (agent anti-corrosion, lubrifiants, fluides d’usinage des métaux…), l’industrie textile, agent de coalescence pour colles au latex ;

biocides, répulsif d’insectes ;

agents de conservation pour cosmétiques, de produits d’hygiène corporelle et de produits pharmaceutiques à usage humain ou vétérinaire, fixateur de parfum (par exemple dans le conservateur EUXYL K400 (qui s’est révélé être un puissant sensibilisant11,12,13 et allergène14,15,16 et où l’on trouve aussi 20 % de méthylglutaronitrile, qui y est le principal allergène17).

Ce conservateur sert aussi souvent de solvant pour d’autres conservateurs, en particulier pour les parabènes. En aquaculture, Le phénoxyéthanol est utilisé comme anesthésique pour certaines espèces de poissons18,19.

Utilisé en pharmacie comme conservateur, Le phénoxyéthanol est présent dans la plupart des vaccins, et listé comme ingrédient pour de nombreux vaccins par les Centres pour le contrôle et la prévention des maladies20.

Propriétés physico-chimiques

Le phénoxyéthanol est un liquide huileux incolore de faible odeur aromatique. Il est modérément soluble dans l’eau, très soluble dans l’alcool, l’éther, l’acétone, le glycérol, le propylène glycol, les solutions de soude, légèrement soluble dans les huiles minérales10. Le 2-phénoéthanol est un produit stable dans les conditions normales de température et de pression. Le phénoxyéthanol est également stable en présence d’acides et de bases. Le phénoxyéthanol peut réagir vivement avec les oxydants forts avec risque d’incendie et d’explosion. Le phénoxyéthanol est un produit combustible. Les produits de la combustion sont des oxydes de carbone10. Son noyau benzènique lui confère également des propriétés parfumantes. C’est un bactéricide (généralement utilisé avec des composés d’ammonium quaternaire), souvent utilisé à la place de l’azoture de sodium dans les tampons biologiques car moins toxique et ne réagissant pas avec le cuivre et le plomb.

Toxicologie

Le phénoxyéthanol est bien absorbé par voie orale ou cutanée. Il est métabolisé en acide 2-phénoxyacétique et est éliminé essentiellement dans l’urine10.

Toxicité sur l’homme

Le phénoxyéthanol existe peu de données concernant la toxicité du 2-phénoxyéthanol chez l’homme. Les effets décrits sont des allergies cutanées et des troubles neurologiques10. Concernant la toxicité aiguë, les concentrations jusqu’à 10 % (dans la vaseline) appliquées sur la peau de volontaires ne provoquent pas d’effets irritants. Par contre plusieurs cas de sensibilisation cutanée (eczéma ou urticaire) sont rapportés. La fréquence est faible et les cas sont le plus souvent en rapport avec une utilisation régulière dans des cosmétiques10. On ne dispose pas de données sur les risques cancérigènes ou les effets sur la reproduction liés au 2-phénoxyéthanol10. Toutefois Le phénoxyéthanol est déconseillé depuis le 26 novembre 2012 par l’ANSM (Agence nationale de sécurité du médicament et des produits de santé) dans les lingettes pour bébés car Le phénoxyéthanol est suspecté d’être toxique au niveau du développement et de la reproduction21.

Le Comité scientifique européen pour la sécurité des consommateurs (CSSC) a considéré, dans son avis final sur le phénoxyéthanol du 6 octobre 2016, que le phénoxyéthanol utilisé à 1 % en tant que conservateur dans les produits cosmétiques est sûr pour la santé, quel que soit le groupe d’âge.22

Toxicologie professionnelle

Des mesures de prévention10 sont définies pour le stockage et la manipulation du 2-phénoxyéthanol. À l’embauche, Le phénoxyéthanol conviendra de chercher des signes d’atteinte neurologique et cutanée chronique. Le suivi médical devra comporter un examen clinique visant à identifier une éventuelle atteinte neurologique ainsi que des irritations cutanées. Un dépistage des troubles neurologiques centraux régulier est recommandé.

Origine(s) : Synthétique

Autres langues : Fenossietanolo, Fenoxietanol

Nom INCI : Phenoxy ethanol

Nom chimique : 2-Phenoxy ethanol

N° EINECS/ELINCS : 204-589-7

Classification : Règlementé, Alcool, Conservateur

À SAVOIRLe Phenoxy ethanol est un conservateur synthétique connu sous l’acronyme de EGPhE, très utilisé en cosmétique et de plus en plus controversé. Depuis 2012, l’ANSM (Agence nationale de sécurité du médicament et des produits de santé) recommande que ce conservateur ne soit pas utilisé dans les produits cosmétiques destinés au siège des bébés et que sa teneur maximale soit fixée à 0,4% pour les autres produits destinés aux enfants de moins de 3 ans. Elle dénonce également sa toxicité hépatique, ses effets potentiellement néfastes sur la reproduction ainsi que bon nombre d’autres désagréments : les conclusions du rapport de l’ANSM de 2012 sont alarmants.

Dans son avis de mai 2018, le Comité scientifique spécialisé temporaire (CSST) chargé de la réévaluation du phénoxyéthanol au niveau de l’Europe, a quant à lui conclu : “La recommandation par l’Ansm de non-utilisation du phénoxyéthanol dans les produits cosmétiques destinés au siège doit être maintenue. Il est souhaitable de l’élargir aux lingettes qui sont très habituellement utilisées aussi pour nettoyer le siège des jeunes enfants. Dans tous les autres produits cosmétiques destinés aux enfants de 3 ans ou moins, la concentration maximale de phénoxyéthanol pourrait rester de 1 %.” Le CSST suivrait donc l’ANSM pour les lingettes mais pas pour la concentration. En tout cas, réglementairement, le Phenoxy ethanol est toujours autorisé dans les lingettes bébés !!!

Le Phenoxy ethanol est produit par éthoxylation (un procédé chimique très polluant) en faisant réagir du phénol et de l’oxyde d’éthylène à une température et une pression élevées. Notez toutefois que le Phenoxy ethanol est présent naturellement dans le thé vert, mais ce n’est pas cette version du composé qui est utilisé en cosmétique. En raison de son procédé de fabrication, le Phenoxy ethanol est interdit en Bio.

Restriction en Europe : V/29

La concentration maximale autorisée dans une préparation prête à l’emploi est de 1%.

CAS Number: 122-99-6; IUPAC name: 2-Phenoxyethanol; Phenoxyethanol; Ethylene glycol monophenyl ether; Phenoxytolarosol;Dowanol EP / EPH; Protectol PE; Emery 6705; Rose ether;1-Hydroxy-2-phenoxyethane

;β-hydroxyethyl phenyl ether; Phenyl cellosolve;Ethylene glycol phenyl ether;2-PHENOXYETHANOL; Cas No: 122-99-6; Phenoxyethanol; Ethylene glycol monophenyl ether; Ethanol, 2-phenoxy-; Phenyl cellosolve; Phenoxytol; Phenoxethol; Phenoxetol; Ethylene glycol phenyl ether; Phenoxyethyl alcohol

; 2-Phenoxyethan-1-Ol; 1-Hydroxy-2-phenoxyethane; Rose ether; Phenylmonoglycol ether; Arosol; Dowanol EP; 2-Phenoxyethyl alcohol; Glycol monophenyl ether; 2-Hydroxyethyl phenyl ether; Phenylglycol

;Fenyl-cellosolve; 2-Fenoxyethanol; Dowanol EPH; 2-Phenoxy-ethanol; Emery 6705; Emeressence 1160; Fenylcelosolv; Marlophen P; beta-Hydroxyethyl phenyl ether; 2-phenoxy ethanol;2-phenoxyethanol; Emuclens;Erisept; ethylene glycol monophenyl ether; phenoxethol; phenoxyethanol

2-Phenoxyethanol, also known as phenyl cellosolve or phenoxytol, belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. 2-Phenoxyethanol exists as a solid, soluble (in water), and an extremely weak acidic (essentially neutral) compound (based on its pKa). 2-Phenoxyethanol has been detected in multiple biofluids, such as feces and saliva. Within the cell, 2-phenoxyethanol is primarily located in the cytoplasm. 2-Phenoxyethanol exists in all eukaryotes, ranging from yeast to humans. 2-Phenoxyethanol can be biosynthesized from phenol. 2-Phenoxyethanol is a potentially toxic compound.

Phenoxyethanol is a germicidal and germistatic glycol ether, phenol ether, and aromatic alcohol often used together with quaternary ammonium compounds.

Use: Phenoxyethanol is used as a perfume fixative; an insect repellent; an antiseptic; a solvent for cellulose acetate, dyes, inks, and resins; a preservative for pharmaceuticals, cosmetics and lubricants; an anesthetic in fish aquaculture; and in organic synthesis.

Phenoxyethanol is an alternative to formaldehyde-releasing preservatives.In Japan and the European Union, its concentration in cosmetics is restricted to 1%.

Production: Phenoxyethanol is produced by the hydroxyethylation of phenol (Williamson synthesis), for example, in the presence of alkali-metal hydroxides or alkali-metal borohydrides.

Efficacy: Phenoxyethanol is effective against gram-negative and gram-positive bacteria, and the yeast Candida albicans

Safety: Phenoxyethanol is a vaccine preservative and potential allergen, which may result in a nodular reaction at the site of injection. It reversibly inhibits NMDAR-mediated ion currents.

Ingestion may cause central nervous system and respiratory depression, vomiting and diarrhea in infants, particularly when combined with chlorphenesin

Phenoxyethanol, is the most commonly used globally-approved preservative in personal care formulations. It is extremely easy to use in most types of formulations and is chemically very stable. Phenoxyethanol

has a broad spectrum antimicrobial activity against bacteria, yeasts, and mold. The typical use level in formulations is 0,5 – 0,8%, and it is often combined with other preservatives, like Ethylhexyl glycerin, Hexylene glycol, Benzyl alcohol, Benzoic acid, Potassium

sorbate, Dehydroacetic acid, Chlorphenesin or Capryl glycol. The European Economic Community (EEC). Cosmetics Derivative and the Cosmetics Regulation of the European Union approved Phenoxyethanol in concentrations up 1%.

APPLICATIONS: Skin care – Make up – Hair care – Deodorant- ToiletriesCleansers- Sun care – Body care – Fragrances – Wet wipes

FORMULATION AND RECOMMENDATIONS: Phenoxyethanol, is the most commonly used globally-approved preservative in personal care formulations. It is extremely easy to use in most types of formulations and is chemically very stable. Phenoxyethanol

has a broad spectrum antimicrobial activity against bacteria, yeasts, and mold. The typical use level in formulations is 0,5 – 0,8%, and it is often combined

with other preservatives, like Ethylhexyl glycerin, Hexylene glycol, Benzyl alcohol, Benzoic acid, Potassium sorbate, Dehydroacetic acid, Chlorphenesin or Capryl glycol. The European Economic Community (EEC)

Cosmetics Derivative and the Cosmetics Regulation of the European Union approved Phenoxyethanol in concentrations up 1%.

Chemical formula: C8H10O2

Molar mass: 138.166 g·mol−1

Appearance: Colorless oily liquid

Odor: faint rose-like

Density: 1.102 g/cm3

Melting point: −2 °C (28 °F; 271 K)

Boiling point: 247 °C (477 °F; 520 K)

Solubility in water: 26 g/kg

Solubility: Chloroform, Alkali, diethyl ether: soluble

Solubility in peanut oil: slightly

Solubility in olive oil: slightly

Solubility in acetone: miscible

Solubility in ethanol: miscible

Solubility in glycerol: miscible

Vapor pressure: 0.001 kPa (0.00015 psi)

Thermal conductivity: 0.169 W/(m⋅K)

Refractive index (nD): 1.534 (20 ℃)

Phenoxyethanol is used as a preservative in cosmetic products and also as a stabilizer in perfumes and soaps. Exposure to phenoxyethanol has been linked to reactions ranging from eczema

to severe, life-threatening allergic reactions. Infant oral exposure to phenoxyethanol can acutely affect nervous system function.

FOUND IN: Moisturizer, eye shadow, foundation, sunscreen, conditioner, mascara, eye liner, shampoo, lip gloss, concealer, body wash, hand cream, blush, hair color, hair spray, lip balm,

lotion, nail polish, baby wipes, baby lotions and soaps, soap (liquid and bar), shaving cream, deodorant, toothpaste, fragrance, hair removal waxes, hand sanitizer and ultrasound gel.

WHAT IS PHENOXYETHANOL? Phenoxyethanol is used as a preservative in cosmetic products to limit bacterial growth. A review of 43 cosmetic products demonstrated that only 25 percent of

the products had concentrations of phenoxyethanol greater than 0.6 percent and the mean concentration of phenoxyethanol was 0.46 percent.[5] Phenoxyethanol is also used as to stabilize

components found in perfumes and soaps.

What Is It?

Phenoxyethanol is an oily, slightly sticky liquid with a faint rose-like scent. It is used as a preservative in a wide variety of both leave-on and rinse-off cosmetics and personal care products, including skin care, eye makeup, fragrances, blushers, foundations, lipstick, bath soaps, and detergents, among others. Phenoxyethanol has been reviewed by experts worldwide who have concluded it is safe as used in these products.

Why is it used in cosmetics and personal care products?

Phenoxyethanol has been used safely since the 1950s as a preservative in cosmetics and personal care products. It is highly effective in preventing the growth of fungi, bacteria, and yeast that could cause products to spoil, just like food. The use of preservatives enhances products’ shelf life and safety.

Products that contain water are susceptible to mold, discoloration, or unpleasant odors caused by the bacteria and fungi naturally present in the environment. As cosmetics are used, they come in contact with the skin and applicators that contact the skin, thus potentially exposing the product to these harmful microorganisms.

Under certain conditions, an inadequately preserved product can become contaminated, which could cause health problems such as irritation or infection. Products contaminated by microorganisms may also negatively impact how the product performs, looks, feels, and smells. Preservatives like phenoxyethanol help prevent such problems.

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 hydroxyether, a primary alcohol and an aromatic ether. It derives from a phenol.

Ethylene glycol phenyl ether is a colorless liquid with a pleasant odor. Density 1.02 g / cm3. An irritant.

2-PHENOXYETHANOL; Cas No: 122-99-6; Phenoxyethanol; Ethylene glycol monophenyl ether; Ethanol, 2-phenoxy-; Phenyl cellosolve; Phenoxytol; Phenoxethol; Phenoxetol; Ethylene glycol phenyl ether; Phenoxyethyl alcohol

; 2-Phenoxyethan-1-Ol; 1-Hydroxy-2-phenoxyethane; Rose ether; Phenylmonoglycol ether; Arosol; Dowanol EP; 2-Phenoxyethyl alcohol; Glycol monophenyl ether; 2-Hydroxyethyl phenyl ether; Phenylglycol

;Fenyl-cellosolve; 2-Fenoxyethanol; Dowanol EPH; 2-Phenoxy-ethanol; Emery 6705; Emeressence 1160; Fenylcelosolv; Marlophen P; beta-Hydroxyethyl phenyl ether; 2-phenoxy ethanol

Marlophen P 7

Spermicide 741

Tritonyl 45

Ethylan HB 4

EGMPE

Fenylcelosolv [Czech]

2-Fenoxyethanol [Czech]

Fenyl-cellosolve [Czech]

Plastiazan-41 [Russian]

Polyoxyethylene phenol ether

Polyoxyethylene phenyl ether

Phenol-ethylene oxide adduct

MFCD00002857

Glycols, polyethylene, monophenyl ether

Phenoxyethanol [NF]

Polyethylene glycol phenyl ether

.beta.-Hydroxyethyl phenyl ether

HSDB 5595

PHE-G

PHE-S

2-Phenoxyethanol, 99%

EINECS 204-589-7

9004-78-8

.beta.-Phenoxyethyl alcohol

alpha-Phenyl-omega-hydroxypoly(oxy-1,2-ethanediyl)

ethyleneglycol monophenyl ether

Phenoxyethanol (NF)

Poly(oxy-1,2-ethanediyl), alpha-phenyl-omega-hydroxy-

Erisept

Plastiazan-41

CAS-122-99-6

Phenol, ethoxylated

PHG

.beta.-Phenoxyethanol

phenoxy-ethanol

phenylcellosolve

Phenoxyethanolum

CCRIS 9481

Ethylene glycol-monophenyl ether

Dalpad A

2-phenyloxyethanol

Newpol EFP

2-Phenoxyethanol.

2-(phenoxy)ethanol

beta-Hydroxyphenetole

2-phenoxy-1-ethanol

beta-phenoxyethylalcohol

ACMC-1BVYG

2-Phenoxyethanol, 9CI

WLN: Q2OR

EC 204-589-7

SCHEMBL15708

2-Phenoxyethanol, >=99%

4-06-00-00571 (Beilstein Handbook Reference)

Euxyl K 400 (Salt/Mix)

[O]CCOC1=CC=CC=C1

2-PHENOXYETHANOL 500ML

Ethylene glycol mono phenyl ether

C(O)[C]OC1=CC=CC=C1

2-Phenoxyethanol, analytical standard

Fungal Terminator [veterinary] (TN)

Ethylene glycol monophenyl ether, >=90%

ETHANOL,2-PHENOXY MFC8 H10 O2

2-Phenoxyethanol, tested according to Ph.Eur.

Ethylene glycol monophenyl ether, SAJ first grade, >=95.0%

Phenoxyethanol, European Pharmacopoeia (EP) Reference Standard

Phenoxyethanol, United States Pharmacopeia (USP) Reference Standard

2-Phenoxyethanol, Pharmaceutical Secondary Standard; Certified Reference Material

GLOBAL REGULATORY

EU: EINECS) 204-589-7,(Annex I Index No.) 3-098-00-9

USA: (TSCA)Existing chemical

Canada: (DSL)

China: IECSC) Existing chemica

Japan: Existing chemical:(9)-1277, (3)-558

ASEAN (Indonesia, Malaysia, Philippines, Singapore,

Vietnam, Burma, Cambodia, Thailand, Laos, Brunei): (PICSS)

Existing chemical

South Korea: KE-28257 　　

Australia (NICNAS – Cosmetics): No limitation

New Zealand: HSR003045

PHENOXYETHANOL

SPECIFICATION

Description: Phenoxyethanol is an oily, slightly sticky

liquid with a faint rose-like odour. It is used as a preservative

in a wide variety of cosmetic and personal care products.

Research shows that this ingredient is safe when used in

these products.

INCI: Phenoxyethanol

EFFICACY

Escherichia coli (bacteria gram negative) -.32%

Pseudomonas aeruginosa (bacteria gram negative) -.32%

Staphylococcus aureus (bacteria gram positive) -.64%

Aspergillus niger (mold) -.32%

Candida albicans (yeast) -.32%

Phenoxyethanol is a glycol ether used as a preservative in cosmetic products. It is used in many skin care, make-up, hair care products. Because of its anti-bacterial properties, it is also used in baby wipes and hand sanitizer.

PHENOXYETHANOL is classified as :

Preservative

CAS Number 122-99-6

EINECS/ELINCS No: 204-589-7

Restriction (applies to EU only): VI/29

COSING REF No: 36522

PHARMACEUTICAL EUROPEAN NAME: phenoxyethanolum

Chem/IUPAC Name: 2-Phenoxyethanol

Consumer products

Preservation of cosmetics, toiletry and household products and their raw materials. Phenoxyethanol is often used in combination with other preservatives and in some cases positive synergetic effects can be obtained. It is also used in acne treatment. Due to its low evaporation, Phenoxyethanol is used as a fixative in perfumes and fragrance.

Industrial products

It can be used in water mixable lubricants, in paints and varnishes as coalescing agent and as a modifier in melamine formaldehyde resins. It is used as a solvent in ball pen and printing inks. Phenoxyethanol is used as a striping agent and in the surface treatment of metals as degreaser. Its biostatic abilities is often used in combination with other actives to preserve metal working fluids, glues and industrial adhesives.

Safety

Eye contact may cause moderate irritation or moderate corneal injury. Repeated skin contact may result in absorption of harmful amounts. Swallowing small amounts is unlikely to result in injury. Swallowing large amounts may result in injury.

Phenoxyethanol is a high boiling liquid with a low vapor pressure, so exposure to vapors is unlikely at room temperature.

Phenoxyethanol is thermally stable at typical storage and use temperatures. It can oxidize at elevated temperatures. Phenoxyethanol is readily biodegradable and has a low potential for bioconcentration. It is practically nontoxic to aquatic organisms.

Handling and storage

Contact with eyes and skin should be avoided. Safety googles must be worn when handling the concentrated product. The product should be stored at seald packaging as supplied, in dry conditions, at temperatures not exceeding 30

Classification according to UN criteria: Not classified as hazardous under transport regulation

Packaging & Shelf Life:

Under proper storage conditions the shelf life is 24 month.

Health & Safety:

Detailed information on the product can be found in our Material Safety Data Sheet.

Phenoxyethanol

Other

Translated names

2-fenoksietanol (hr)

2-Fenoksietanoli (fi)

2-fenoksietanolis (lt)

2-Fenoksietanols (lv)

2-fenoksyetanol (no)

2-fenoksüetanool (et)

2-Fenossietanol (mt)

2-fenossietanolo (it)

2-Fenoxietanol (es)

2-fenoxyetanol (sk)

2-fenoxyethan-1-ol (cs)

2-Fenoxyethanol (nl)

2-phenoxyethanol (da)

2-phénoxyéthanol (fr)

2-φαινοξυ-αιθανόλη (el)

2-φαινοξυαιθανόλ (el)

2-феноксиетанол (bg)

eter monofenylowy glikolu etylenowego (pl)

fenil glicol (it)

fenylglykol (sv)

fenoksietanol(tr)

fenoksi etanol (tr)

fenoksiethanol (tr)

fenoksi ethanol (tr)

CAS names: Ethanol, 2-phenoxy-

Other IUPAC names:

1-HYDROXY-2-PHENOXYETHANE

2-(phenoxy)ethanol

2-(phenoxyethanol

2-Phenoxy-1-ethanol

2-phenoxyethan-1-ol

2-PhenoxyethanolRD_CLP_122-99-6_Ethanol, 2-phenoxy-_V1_20180112_TS

Ethylene glycol monophenyl ether

Ethylene glycol phenyl ether

Ethyleneglycol monophenyl ether

SHINING COLOR BLUE EU CONC

Trade names

(2-hydroxy-ethyl)-phenyl-ether (alternative chemical name)

.beta.-Hydroxyethyl phenyl ether

.beta.-Phenoxyethanol

.beta.-Phenoxyethyl alcohol

2-Hydroxyethyl phenyl ether

2-Phenoxyethyl alcohol

Arosol

Beta-phenoxyethylalcohol (alternative chemical name)

Dalpad A

DALPAD™ A Coalescing Agent

Dowanol EP

Dowanol EPh

Dowanol EPH Glycol Ether

DOWANOL™ EPH Glycol Ether

DOWANOL™ EPH GLYCOL ETHER, EXTRA LOW PHENOL GRADE

ENSOLINE

Ethanol, 2-phenoxy- (6CI, 7CI, 8CI, 9CI)

Ethylene glycol monophenyl ether (alternative chemical name)

H 4644

MARLOPHEN P 1 AB

MARLOPHEN P 1 ABn

Marlosol PHE

Monophenylglykol

Phenoxethol

Phenoxetol

Phenoxyethanol (INCI name and CTFA adopted name)

Phenoxyethyl alcohol

Phenyl cellosolve

Protectol EPE (trade name)

Protectol PE (trade name)

SHINING COLOR BLUE, BR BLUE, LT BLUE EU CONC

STERO PE

Phenoxyethanol [Wiki]

122-99-6 [RN]

1-Hydroxy-2-phenoxyethane

204-589-7 [EINECS]

2-phenoxyethan-1-ol

2-Phenoxyethanol [ACD/IUPAC Name]

2-Phenoxyethanol [German] [ACD/IUPAC Name]

2-Phenoxy-ethanol

2-Phénoxyéthanol [French] [ACD/IUPAC Name]

DOWANOL(R) EPh

Ethanol, 2-phenoxy- [ACD/Index Name]

Ethylene glycol monophenyl ether

HIE492ZZ3T

KM0350000

PhE [Formula]

PHE-G

Phenoxyethanolum

PHENOXYETHYL ALCOHOL

Phenyl cellosolve

Phenylglycol

PHE-S

PHG

Rose ether

(2-Hydroxyethoxy)benzene

??2-phenoxyethanol

[122-99-6]

1219804-65-5 [RN]

134367-25-2 [RN]

18249-17-7 [RN]

2-(phenoxy)ethanol

200260-63-5 [RN]

21273-38-1 [RN]

268

2-Fenoxyethanol

2-Fenoxyethanol [Czech]

2-Hydroxyethyl phenyl ether

2-PHENOXY ETHANOL

2-Phenoxyethan-1-ol|(2-Hydroxyethoxy)benzene

2-phenoxyethanol 99%

2-phenoxyethanol, ??? 98.5%

2-phenoxyethanol, 94%

2-phenoxyethanol, 99%

2-Phenoxyethanol, 9CI

2-PHENOXYETHANOL-1,1-D2

2-Phenoxyethyl alcohol

2-Phenoxyethyl-1,1,2,2-d4 Alcohol

2-PHENOXYETHYL-2,2-D2 ALCOHOL

2-Phenoxyethyl–d4 Alcohol

37220-49-8 [RN]

4-06-00-00571 (Beilstein Handbook Reference) [Beilstein]

438620-17-8 [RN]

56257-90-0 [RN]

79586-53-1 [RN]

AI3-00752()C

Arosol

BB_SC-2741

C8H10O2

Dalpad A

Diethylene glycol monophenyl ether

Dowanol EP

Dowanol EPH

EGMPE

EINECS 204-589-7

Emeressence 1160

ETHANOL,2-PHENOXY MFC8 H10 O2

Ethylan HB 4

Ethylene glycol mono phenyl ether

ethylene glycol monobenzyl ether

ethylene glycol monophenyl ether 98%

ETHYLENE GLYCOL PHENYL ETHER

Ethylene glycol-monophenyl ether

Ethyleneglycol monophenyl ether

Ethyleneglycol-monophenyl ether

ETYLENEGLYCOL MONOPHENYL ETHER

Euxyl K 400 (Salt/Mix)

Fenyl-cellosolve

Fenyl-cellosolve [Czech]

Fenylcelosolv

Fenylcelosolv [Czech]

Glycol monophenyl ether

Glycols, polyethylene, monophenyl ether

http://www.hmdb.ca/metabolites/HMDB0041607

https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:64275

InChI=1/C8H10O2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H

Jsp001544

Marlophen P

Marlophen P 7

NCGC00090731-02

NCGC00090731-03

Newpol EFP

Phenol, ethoxylated

Phenol-ethylene oxide adduct

Phenoxethol

Phenoxetol

Phenoxydiglycol

phenoxyethanol, reagent

Phenoxyethanol, USP-NF grade

Phenoxyl ethanol

Phenoxytol

Phenylcellosolve

Phenylmonoglycol ether

Plastiazan-41 [Russian]

Polyethylene glycol phenyl ether

Polyoxyethylene phenol ether

Polyoxyethylene phenyl ether

Spermicide 741

STR04582

Tritonyl 45

UNII:HIE492ZZ3T

UNII-HIE492ZZ3T

WLN: Q2OR

α-Phenyl-ω-hydroxypoly(oxy-1,2-ethanediyl)

β-Hydroxyethyl phenyl ether

β-Phenoxyethanol

β-Phenoxyethyl alcohol

苯氧乙醇 [Chinese]

Numéro CAS: 122-99-6; Nom IUPAC: 2-phénoxyéthanol; Phénoxyéthanol; Éther monophénylique d’éthylène glycol; Phénoxytolarosol, Dowanol EP / EPH; Protectol PE; Emery 6705; Rose éther, 1-hydroxy-2-phénoxyéthane, β-hydroxyéthylphényléther; Phényl cellosolve; éther phénylique d’éthylène glycol; 2-PHÉNOXYÉTHANOL; N ° CAS: 122-99-6; Phénoxyéthanol; Éther monophénylique d’éthylène glycol; Éthanol, 2-phénoxy-; Phenyl cellosolve; Phenoxytol; Phenoxethol; Phenoxetol; Éther phénylique d’éthylène glycol; Alcool phénoxyéthylique

; 2-phénoxyéthan-1-Ol; 1-hydroxy-2-phénoxyéthane; Rose éther; Éther de phénylmonoglycol; Arosol; Dowanol EP; Alcool 2-phénoxyéthylique; Éther monophénylique de glycol; 2-hydroxyéthylphényléther; Phénylglycol

; Fenyl-cellosolve; 2-fénoxyéthanol; Dowanol EPH; 2-phénoxy-éthanol; Emery 6705; Emeressence 1160; Fenylcelosolv; Marlophen P; l’éther bêta-hydroxyéthylphénylique; 2-phénoxy éthanol, 2-phénoxyéthanol; Emuclens, Erisept; l’éther monophénylique d’éthylène glycol; phénoxethol; phénoxyéthanol

Le 2-phénoxyéthanol, également connu sous le nom de phényl cellosolve ou phénoxytol, appartient à la classe des composés organiques appelés éthers phénoliques. Ce sont des composés aromatiques contenant un groupe éther substitué par un cycle benzénique. Le 2-phénoxyéthanol existe sous forme de composé solide, soluble (dans l’eau) et extrêmement faible acide (essentiellement neutre) (basé sur son pKa). Le 2-phénoxyéthanol a été détecté dans plusieurs biofluides, tels que les matières fécales et la salive. Dans la cellule, le 2-phénoxyéthanol est principalement situé dans le cytoplasme. Le 2-phénoxyéthanol existe dans tous les eucaryotes, allant de la levure à l’homme. Le 2-phénoxyéthanol peut être biosynthétisé à partir du phénol. Le 2-phénoxyéthanol est un composé potentiellement toxique.

Le phénoxyéthanol est un éther de glycol germicide et germistatique, un éther de phénol et un alcool aromatique souvent utilisés avec des composés d’ammonium quaternaire.

Utilisation: Le phénoxyéthanol est utilisé comme fixateur de parfum; un insectifuge; un antiseptique; un solvant pour l’acétate de cellulose, les colorants, les encres et les résines; un conservateur pour produits pharmaceutiques, cosmétiques et lubrifiants; un anesthésique en pisciculture; et en synthèse organique.

Le phénoxyéthanol est une alternative aux conservateurs libérant du formaldéhyde.Au Japon et dans l’Union européenne, sa concentration dans les cosmétiques est limitée à 1%.

Production: Le phénoxyéthanol est produit par l’hydroxyéthylation du phénol (synthèse de Williamson), par exemple, en présence d’hydroxydes de métaux alcalins ou de borohydrures de métaux alcalins.

Efficacité: le phénoxyéthanol est efficace contre les bactéries Gram négatif et Gram positif, et la levure Candida albicans

Innocuité: Le phénoxyéthanol est un agent de conservation du vaccin et un allergène potentiel, qui peut entraîner une réaction nodulaire au site d’injection. Il inhibe de manière réversible les courants ioniques médiés par NMDAR.

L’ingestion peut provoquer une dépression du système nerveux central et respiratoire, des vomissements et de la diarrhée chez les nourrissons, en particulier lorsqu’elle est associée à la chlorphénésine

Le phénoxyéthanol est le conservateur le plus couramment utilisé dans le monde dans les formulations de soins personnels. Il est extrêmement facile à utiliser dans la plupart des types de formulations et est chimiquement très stable. Le phénoxyéthanol a une activité antimicrobienne à large spectre contre les bactéries, les levures et les moisissures. Le niveau d’utilisation typique dans les formulations est de 0,5 à 0,8%, et il est souvent combiné avec d’autres conservateurs, comme l’éthylhexyl glycérine, l’hexylène glycol, l’alcool benzylique, l’acide benzoïque, le sorbate de potassium, l’acide déhydroacétique, la chlorphénésine ou le capryl glycol. La Communauté économique européenne (CEE). Le dérivé cosmétique et le règlement cosmétique de l’Union européenne ont approuvé le phénoxyéthanol à des concentrations en hausse de 1%.

APPLICATIONS: Soin de la peau – Maquillage – Soin des cheveux – Déodorant – Produits de toilette Nettoyants – Soin solaire – Soin du corps – Parfums – Lingettes humides

FORMULATION ET RECOMMANDATIONS: Le phénoxyéthanol est le conservateur le plus couramment utilisé dans le monde dans les formulations de soins personnels. Il est extrêmement facile à utiliser dans la plupart des types de formulations et est chimiquement très stable. Le phénoxyéthanol a une activité antimicrobienne à large spectre contre les bactéries, les levures et les moisissures. Le niveau d’utilisation typique dans les formulations est de 0,5 à 0,8%, et il est souvent combiné

avec d’autres conservateurs, comme l’éthylhexyl glycérine, l’hexylène glycol, l’alcool benzylique, l’acide benzoïque, le sorbate de potassium, l’acide déhydroacétique, la chlorphénésine ou le capryl glycol. Le dérivé cosmétique de la Communauté économique européenne (CEE) et le règlement cosmétique de l’Union européenne ont approuvé le phénoxyéthanol à des concentrations allant jusqu’à 1%.

Formule chimique: C8H10O2

Masse moléculaire: 138,166 g · mol − 1

Apparence: Liquide huileux incolore

Odeur: légèrement rose

Densité: 1,102 g / cm3

Point de fusion: -2 ° C (28 ° F; 271 K)

Point d’ébullition: 247 ° C (477 ° F; 520 K)

Solubilité dans l’eau: 26 g / kg

Solubilité: Chloroforme, alcali, éther diéthylique: soluble

Solubilité dans l’huile d’arachide: légèrement

Solubilité dans l’huile d’olive: légèrement

Solubilité dans l’acétone: miscible

Solubilité dans l’éthanol: miscible

Solubilité dans le glycérol: miscible

Pression de vapeur: 0,001 kPa (0,00015 psi)

Conductivité thermique: 0,169 W / (m⋅K)

Indice de réfraction (nD): 1,534 (20 ℃)

Le phénoxyéthanol est utilisé comme conservateur dans les produits cosmétiques et également comme stabilisant dans les parfums et les savons. L’exposition au phénoxyéthanol a été liée à des réactions allant de l’eczéma

à des réactions allergiques graves et potentiellement mortelles. L’exposition orale du nourrisson au phénoxyéthanol peut affecter gravement le fonctionnement du système nerveux.

TROUVÉ DANS: Hydratant, ombre à paupières, fond de teint, crème solaire, revitalisant, mascara, eye-liner, shampooing, brillant à lèvres, correcteur, gel douche, crème pour les mains, blush, couleur de cheveux, laque pour cheveux, baume à lèvres,

lotion, vernis à ongles, lingettes pour bébé, lotions et savons pour bébé, savon (liquide et pain), crème à raser, déodorant, dentifrice, parfum, cires d’épilation, désinfectant pour les mains et gel à ultrasons.

QU’EST-CE QUE LE PHÉNOXYÉTHANOL? Le phénoxyéthanol est utilisé comme conservateur dans les produits cosmétiques pour limiter la croissance bactérienne. Un examen de 43 produits cosmétiques a démontré que seulement 25% des

les produits avaient des concentrations de phénoxyéthanol supérieures à 0,6 pour cent et la concentration moyenne de phénoxyéthanol était de 0,46 pour cent. [5] Le phénoxyéthanol est également utilisé pour stabiliser

composants trouvés dans les parfums et les savons.

Qu’Est-ce que c’est?

Le phénoxyéthanol est un liquide huileux légèrement collant avec une légère odeur de rose. Il est utilisé comme conservateur dans une grande variété de cosmétiques et de produits de soins personnels sans rinçage et à rincer, notamment les soins de la peau, le maquillage des yeux, les parfums, les fards à joues, les fonds de teint, les rouges à lèvres, les savons de bain et les détergents, entre autres. Le phénoxyéthanol a été examiné par des experts du monde entier qui ont conclu qu’il est sans danger tel qu’il est utilisé dans ces produits.

Pourquoi est-il utilisé dans les cosmétiques et les produits de soins personnels?

Le phénoxyéthanol est utilisé en toute sécurité depuis les années 1950 comme conservateur dans les cosmétiques et les produits de soins personnels. Il est très efficace pour empêcher la croissance de champignons, de bactéries et de levures qui pourraient altérer les produits, tout comme les aliments. L’utilisation d’agents de conservation améliore la durée de conservation et la sécurité des produits.

Les produits contenant de l’eau sont sensibles aux moisissures, à la décoloration ou aux odeurs désagréables causées par les bactéries et les champignons naturellement présents dans l’environnement. Lors de l’utilisation de produits cosmétiques, ils entrent en contact avec la peau et les applicateurs qui entrent en contact avec la peau, exposant ainsi potentiellement le produit à ces micro-organismes nocifs.

Dans certaines conditions, un produit mal conservé peut devenir contaminé, ce qui pourrait entraîner des problèmes de santé tels qu’une irritation ou une infection. Les produits contaminés par des microorganismes peuvent également avoir un impact négatif sur les performances, l’apparence, la sensation et l’odeur du produit. Les conservateurs comme le phénoxyéthanol aident à prévenir de tels problèmes.

Le 2-phénoxyéthanol est un éther aromatique qui est un phénol substitué sur l’oxygène par un groupe 2-hydroxyéthyle. Il a un rôle d’agent anti-infectieux et de dépresseur du système nerveux central. C’est un hydroxyéther, un alcool primaire et un éther aromatique. Il dérive d’un phénol.

L’éther phénylique de l’éthylène glycol est un liquide incolore à l’odeur agréable. Densité 1,02 g / cm3. Un irritant