API

Home - Products - API

Pehg

  • Product Name: Pehg
  • CasNo: 122-99-6
  • Purity:
  • Appearance: colorless or light yellow liquid

Mobile/Wechat/WhatsApp: +447394406898

Email:wibson.aris@gmail.com

Inquiry

CasNo: 122-99-6

Molecular Formula: C8H10O2

Appearance: colorless or light yellow liquid

99% Pure Reputable Factory Supply Pehg 122-99-6 with Cheapest Price

  • Molecular Formula:C8H10O2
  • Molecular Weight:138.166
  • Appearance/Colour:colorless or light yellow liquid 
  • Vapor Pressure:0.01 mm Hg ( 20 °C) 
  • Melting Point:11-13 °C 
  • Refractive Index:1.5386 
  • Boiling Point:245.199 °C at 760 mmHg 
  • PKA:14.36±0.10(Predicted) 
  • Flash Point:105.275 °C 
  • PSA:29.46000 
  • Density:1.102 g/cm3 
  • LogP:1.05770 

2-Phenoxyethanol(Cas 122-99-6) Usage

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.

Production Methods

Phenoxyethanol is prepared by treating phenol with ethylene oxide in an alkaline medium.

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

Notclassified

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%.

Consumer Uses

This substance is used in the following products: lubricants and greases, polishes and waxes, adhesives and sealants, coating products, fillers, putties, plasters, modelling clay, anti-freeze products, washing & cleaning products and cosmetics and personal care products. Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

InChI:InChI=1/C8H10O2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2

122-99-6 Relevant articles

Zirconium complexes with pendant aryloxy groups attached to the metallocene moiety by ethyl or hexyl spacers

Cho, Won Seok,Kim, So Han,Kim, Da Jung,Mun, Sang-Deok,Kim, Ran,Go, Min Jeong,Park, Myung Hwan,Kim, Min,Lee, Junseong,Kim, Youngjo

, p. 205 - 212 (2014)

Four zirconium complexes with pendant ar...

-

Patat et al.

, p. 322,330, 331 (1952)

-

2-(1-naphthyloxy)ethylamines with enhanced affinity for human 5-HT(1Dβ) (h5-HT(1B)) serotonin receptors

Ismaiel,Dukat,Law,Kamboj,Fan,Lee,Mazzocco,Buekschkens,Teitler,Pierson,Glennon

, p. 4415 - 4419 (1997)

Although the β-adrenergic antagonist pro...

-

Bobleter

, p. 483,489 (1956)

-

Carbonates as reactants for the production of fine chemicals: The synthesis of 2-phenoxyethanol

Ziosi,Tabanelli,Fornasari,Cocchi,Cavani,Righi

, p. 4386 - 4395 (2014)

The solventless and heterogeneously cata...

-

Patat et al.

, (1954)

-

Preparation and structure investigation of novel Schiff bases using spectroscopic, thermal analyses and molecular orbital calculations and studying their biological activities

Zayed, Ehab M.,Zayed,El-Desawy

, p. 155 - 164 (2015)

Two novel Schiff's bases (EB1 and L1) as...

-

Smith

, p. 994 (1940)

-

Olefin oxidative cleavage and dioxetane formation using triethylsilyl hydrotrioxide: Applications to preparation of potent antimalarial 1,2,4-trioxanes

Posner,Oh,Milhous

, p. 4235 - 4238 (1991)

Oxidative cleavage of alkenyl esters and...

Diradicals Photogeneration from Chloroaryl-Substituted Carboxylic Acids

Di Terlizzi, Lorenzo,Protti, Stefano,Ravelli, Davide,Fagnoni, Maurizio

, (2022/04/09)

With the aim of generating new, thermall...

Novel Bis[N-alkyl-N-(2-diphenylphosphinylethyl)]diglycolamides: Synthesis and NMR Spectroscopy Studies

Bondarenko,Tcarkova,Belus’,Artyushin,Peregudov

, p. 181 - 189 (2021/03/20)

Abstract: Pentadentate bis[N-alkyl-N-(2-...

Ligand-Free Copper-Catalyzed Ullmann-Type C?O Bond Formation in Non-Innocent Deep Eutectic Solvents under Aerobic Conditions

Capriati, Vito,García-álvarez, Joaquín,Marinò, Manuela,Perna, Filippo M.,Quivelli, Andrea Francesca,Vitale, Paola

, (2021/12/09)

An efficient and novel protocol was deve...

Electrophotocatalytic C?H Heterofunctionalization of Arenes

Huang, He,Lambert, Tristan H.

supporting information, p. 11163 - 11167 (2021/04/19)

The electrophotocatalytic heterofunction...

122-99-6 Process route

oxirane
75-21-8,99932-75-9

oxirane

phenol
108-95-2,27073-41-2

phenol

2-Phenoxyethanol
122-99-6,56257-90-0,9004-78-8

2-Phenoxyethanol

2-(2-phenoxyethoxy)ethanol
104-68-7,9004-78-8

2-(2-phenoxyethoxy)ethanol

2-(2-(2-phenoxyethoxy)ethoxy)ethan-1-ol
7204-16-2,9004-78-8

2-(2-(2-phenoxyethoxy)ethoxy)ethan-1-ol

2-<2-<2-(2-phenoxyethoxy)ethoxy>ethoxy>ethanol
36366-93-5,9004-78-8

2-<2-<2-(2-phenoxyethoxy)ethoxy>ethoxy>ethanol

Conditions
Conditions Yield
trifluoroacetic acid; at 160 ℃; for 5.00333 - 5.01167h; Product distribution / selectivity;
 
at 140 ℃; for 5.00333 - 5.01167h; Product distribution / selectivity;
 
propylene glycol
57-55-6,63625-56-9

propylene glycol

ethylene glycol
107-21-1

ethylene glycol

phenol
108-95-2,27073-41-2

phenol

2-Phenoxyethanol
122-99-6,56257-90-0,9004-78-8

2-Phenoxyethanol

1-phenoxy-2-propanol
770-35-4,130879-97-9

1-phenoxy-2-propanol

2-phenoxy-1-propanol
4169-04-4

2-phenoxy-1-propanol

Conditions
Conditions Yield
With sodium carbonate; urea; zinc(II) oxide; at 175 ℃;
 

122-99-6 Upstream products

  • 75-21-8
    75-21-8

    oxirane

  • 139-02-6
    139-02-6

    sodium phenoxide

  • 108-95-2
    108-95-2

    phenol

  • 100-67-4
    100-67-4

    potassium phenolate

122-99-6 Downstream products

  • 16529-54-7
    16529-54-7

    oxydi-acetic acid bis-(2-phenoxy-ethyl ester)

  • 100118-46-5
    100118-46-5

    4-[4-(2-hydroxy-ethoxy)-phenyl]-4-oxo-butyric acid

  • 22855-36-3
    22855-36-3

    bis(2-phenoxyethyl)carbonate

  • 34743-87-8
    34743-87-8

    1-chlorocarbonyloxy-2-phenoxy-ethane

Leave Your Message

Relevant Products