免费v片在线观看视频网站软件亮点,亚洲最大AV资源网在线观看,亚洲精品ⅴ在线观看,2021真实偷拍各种走光福利

  • <sup id="33bym"></sup>
    1. <strike id="33bym"></strike>
      <ol id="33bym"></ol>
    2. Cosmetic Raw Materials

      Home - Products List - Cosmetic Raw Materials

      Phenoxyethanol (2-Phenoxyethanol)

      • Product Name: Phenoxyethanol (2-Phenoxyethanol)
      • CAS: 122-99-6
      • Purity:
      • Appearance: colorless or light yellow liquid

      Contact Us: +86-15508631887(WhatsApp/WeChat)

      Email:sales@finerchem.com

      Inquiry

      Factory sells Phenoxyethanol (2-Phenoxyethanol) 122-99-6 with sufficient production capacity

      • 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%.

      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...

      Electrophotocatalytic C?H Heterofunctionalization of Arenes

      Huang, He,Lambert, Tristan H.

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

      The electrophotocatalytic heterofunction...

      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...

      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-...

      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