Uses advised against Food, drug, pesticide or biocidal product use. A large amount of 2-PE used for industrial applications comes from chemical synthesis, however, it generates a lot of toxic waste. sp. A primary alcohol that is ethanol substituted by a phenyl group at position 2. WGK.22 Pricing and availability is not currently available. 2. LOTUS - the natural products occurrence database 1 Structures 1. 1-Phenylethanol is the organic compound with the formula C 6 H 5 CH(OH)CH 3. It is also used as odor agents, air care products, cleaning and furnishing care products, laundry and dishwashing products, personal care products. All mass spectra in this site (plus many more) are available from the NIST/EPA/NIH Mass Spectral Library. Metabolic engineering 2-PE synthesis through the Ehrlich pathway. 1 It is wildly used in the pharmaceutical industry as a bactericide and also in the food, perfumery, and cosmetics industries to improve character.It can also be extracted from natural plants We have recently shown that B. IUPAC Standard InChIKey: WRMNZCZEMHIOCP-UHFFFAOYSA-N Copy CAS Registry Number: 60-12-8 Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. It is a primary alcohol and a member of benzenes. CAS No. All Photos (1) 2-([1,4′-Bipiperidin]-1′-yl)-1-phenylethan-1-ol. It has a role as a mouse metabolite. CAS No. 60-12-8, EC Number 200-456-2. DrugBank Accession Number. Currently, the main method of production for the bio-derived compound is to extract the trace amounts found in rose petals, which is Due to its pleasant rose-like scent, 2-phenylethanol (2-PE) has been widely used in the fields of cosmetics and food. Yeasts are microorganisms with large synthetic ability. by reaction with acetone/ketones to e. Despite that Saccharomyces cerevisiae has the ability to naturally synthesize 2-PE via the Ehrlich pathway, de novo synthesis of 2-PE in high titer still remains a huge challenge. The convergent synthesis of 2-phenylethanol was executed with bromination of benzene in the presence of pyridine to give bromobenzene which was reacted with magnesium metal to give phenylmagnesium PubMed:[Simultaneous determination of adapalene, 2-phenoxyethanol and methyl-4-hydroxybenzoate in adapalene gels using high performance liquid chromatography]. In this work, a sustainable platform for 2-PE biosynthesis was developed by engineering Bacillus licheniformis using agro-industrial wastes as feedstocks.2 mg/l Abstract. Tiene un agradable olor 2-Phenylethanol (2-PE) is a kind of bulk flavor and fragrance, widely applied in food, fragrance, and cosmetic industries. However, the current bioprocesses for de novo production of 2-PE suffer from low titer, yield, and p … Biological production of 2-PE has emerged to be an appealing solution due to an environmental friendly process and the definition of a "natural" product. Some LOD scores were up to 16. 60-12-8, EC Number 200-456-2. View Pricing. NFPA SUPPLIER Fig. It shows its presence in fresh beer and is responsible for the rose-like odor of well-ripened cheese. mirabilis. Synonyms: β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA, 2-Phenylethanol. 2-Phenylethanol MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.16 Beilstein: 1905732 EC Number: 200-456-2 MDL number: MFCD00002886 PubChem Substance ID: 329820089 Pricing and availability is not currently available.g. 60-12-8.H ,sessenlli lanitsetniortsag rof rotcaf evitasuac rojam a si )irolyp . 2-phenylethanol is a primary alcohol that is ethanol substituted by a phenyl group at position 2. Phenethyl alcohol is a volatile substance with a rose-like odor, widely used in foods, fragrances, and cosmetics. [1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds.16 EC Number: 200-456 … 2-phenylethanol. 2-Phenylethanol Market size surpassed USD 255 million in 2021 and is estimated to grow at over 5. CGMCC 5087. marxianus , 2-Bromo-2-phenylethanol | C8H9BrO | CID 578332 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological 2-Phenylethanol: Description: 2-Phenylethanol, also known as benzeneethanol or benzyl carbinol, belongs to the class of organic compounds known as benzene and substituted derivatives. Fenetanol. Due to the high cost of 2-PE production, the valorization of waste carbon to produce 2-PE has gained increasing attention. PubMed:2-Phenoxyethanol as anaesthetic in removing relocating 102 species of fishes representing from Sea World to uShaka Marine World, South Africa. SDS; CoA; Synonyms: Phenethyl alcohol, Benzylcarbinol CAS #: 60-12-8 EC Number: 200-456-2 Molar Mass: 122. PH016378. The titer reported for the de novo biosynthesis of 2-PE is about 0. Due to increasing demand for natural products by consumers, the production of this flavor by microbial fermentation is gaining interest, as a sustainable alternative to chemical synthesis or expensive plant extraction, both … Verifying de-novo biosynthesis of 2-PE by E. C6H5CH2CH2OH. The biocontrol efficacy of VOCs on tubers was tested using an in vitro assay (Fig. by a rearrangement reaction of dienones [ 30] in the dienone phenol rearrangement: [ 31] Temperature (K) A B C Reference Comment; 406. Firstly, the heterologous styrene-derived and Ehrlich pathways were individually constructed in an L-Phe 2-Phenylethanol, β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA. Chem/IUPAC Name: 2-Phenylethanol. 6. This entity has been manually annotated by the ChEBI Team.20 - 492.Currently, 2-PE is primarily obtained through chemical synthesis involving a complicated process [3]. Sigma-Aldrich. Images of the chemical structure of 2-PHENYLETHANOL are given below: The 2D chemical structure image of 2 2-Phenylethanol (2-PE) is an important flavour and fragrance compound with a rose-like odour. A comprehensive description of 2-PE synthetic pathways and global regulation mechanisms, strategies to increase 2-PE production Alofoje Unuigboje* and Bright Emenike. It has a role as a fragrance, a Saccharomyces cerevisiae metabolite, a plant metabolite, an Aspergillus metabolite and a plant growth retardant. Introduction2-Phenylethanol (2-PEA), commonly known as phenethyl alcohol, is widely used to enhance the aroma of chemical perfumes, colognes, other perfumed articles and in the soap and detergent industry [1], [2]. Food Research International, 34(4), 277-282 (2001) Quantitation, evaluation, and effect of certain microorganisms on flavor components of blue cheese. It is a colourless liquid with a pleasant floral odor. CHEBI:8096, CHEBI:44780.9 °F - Pensky-Martens closed cup. Definition.2 as a case study. 2-Bromo-1-phenylethanol | C8H9BrO | CID 102812 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological IUPAC Standard InChIKey: WRMNZCZEMHIOCP-UHFFFAOYSA-N Copy CAS Registry Number: 60-12-8 Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Cr (IV) as well as pyridinium chloride are produced as byproducts 2-Phenylethanol is an aromatic compound commonly used in the food, cosmetic, and pharmaceutical industries. It occurs widely in nature, being found in a variety of essential oils. Identification Product Name 2-Phenylethanol Cat No. Flash Point(C) 86.) Select Attribute. It has been widely applied in the cosmetic, perfume, and food industries and is mainly produced by chemical synthesis. Since there is an increasing demand for natural products, we designed an alternative method of 2-PE production. It is a primary alcohol and a member of benzenes. We verified a new pathway from Proteus mirabilis JN458 to produce 2-phenylethanol using Escherichia coli to coexpress l-amino acid deaminase, α-keto acid decarboxylase, and alcohol dehydrogenase from P. In this study, the antagonistic yeast strain Kloeckera apiculata 34-9 was used to investigate the action mechanisms … 2. Groups. In this review, we have comprehensively summarized the current status and perspectives for biological 2-PE production in terms of its advantages over classical chemical synthesis and 2-Phenylethanol (2-PE) is a volatile substance widely used in food, fragrance and cosmetics industries. 60-12-8, EC Number 200-456-2. The plots of the remaining enzyme activity versus the concentrations of enzyme at different inhibitor concentrations gave a family of straight lines, which all passed through the origin.7 g/l (Wang et al. pylori peptide deformylase (HpPDF) catalyzes the removal of formyl group from the N-terminus of nascent polypeptide chains, which is essential for H.It is a natural product and is found in Cichorium endivia, Castanopsis cuspidata and other organisms. Its odor has been described as "floral" or "rose-like", though some claim it smells closer to crushed plant seeds, while having a honey-like scent at high concentration. You should, however, be aware of layering too many products containing this ingredient at one time, since it can accumulate.It is one of the most commonly available chiral alcohols. Bisphenol A, an important monomer for resins, e. The 2-PHENYLETHANOL molecule contains a total of 19 bond (s). It is slightly soluble in water (2 ml per 100 ml of H2O), but miscible with most organic … See more 2-Phenylethanol 99% Synonym (s): β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA Linear Formula: C6H5CH2CH2OH CAS Number: 60-12-8 Molecular Weight: 122. ChemSpider ID 9216112. CAS No. Esters have been recently addressed by Sánchez-Castañeda et al. However, the Verifying de-novo biosynthesis of 2-PE by E. (Select up to 3 total.In fact, numerous yeast species have the ability to produce 2-PE [], and this production is strain specific, which means that a significant These compounds, such as 2-butanol, 1,2-butanediol, and 2-phenylethanol, have unique organoleptic properties and are important flavor compounds for the food industry ( Braga et al. EC Number: 200-456-2. 2-phenylethanol (2-PE), which is extracted naturally from plant or biotechnology processing, is widely used in the food and cosmetics industries. Es ligeramente soluble en (2 mL/100 mL H 2 O), y es miscible con etanol y dietil éter. 2.16 EC Number: 200-456-2 Product Comparison Guide Use the product attributes below to configure the comparison table. 2-Phenylethanol (2- PE) is an aromatic alcohol with wide applications, but there is still no efficient microbial cell factory for 2-PE based on Escherichia coli. Background Green and blue mold decay, caused by Penicillium digitatum and P. 2-Chloro-2-phenylethanol | C8H9ClO | CID 11040944 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological 2-Phenylethanol sc-238198 Hazard Alert Code Key: EXTREME HIGH MODERATE LOW Section 1 - CHEMICAL PRODUCT AND COMPANY IDENTIFICATION PRODUCT NAME 2-Phenylethanol STATEMENT OF HAZARDOUS NATURE CONSIDERED A HAZARDOUS SUBSTANCE ACCORDING TO OSHA 29 CFR 1910. Biocontrol by microbes is an alternative to synthetic fungicide application. 2-Phenylethanol (2-PE) is an important aromatic alcohol with a rose-like fragrance.2 noitisop ta puorg lynehp a yb detutitsbus lonahte si taht lohocla yramirp a si lonahtelynehp-2 . 2-Phenylethanol exists in all living species, ranging from bacteria to 1. Background.0, the production of 2-phenylethanol by P.0, and 10. los 15 días.1: 3.0, growth of the test organism was found to be the highest. Consequently, most 2-PE derives from chemical synthesis, which employs petroleum as feedstock and generates unwanted by products and health 2-phenylethanol (2-PE) is a rose-scented flavor and fragrance compound that is used in food, beverages, and personal care products. Molecular Weight: 256. P yridinium chlorochromate (PCC) is a milder version of chromic acid. Notice: … Studies have found that combining common antifungal drugs with phenethyl alcohol can augment their antifungal effect drastically. Molecular Weight: 122. Through enzyme-catalyzed reactions, they can convert simple carbohydrates and nitrogen sources into different complex molecules, particularly various flavor compounds []. rubrolineata is attracted to the host-tree semiochemicals phenylacetonitrile and 2-phenethyl acetate. 2-Phenylethanol (2-PE) is a rose-scented aromatic compound, with broad application in cosmetic, pharmaceutical, food and beverage industries. mirabilis.It is also used to prepare important chemical intermediates, such as phenyl acetaldehyde, phenylacetic acid The synthetic yeast described here might be used as a platform for the future development of next-generation high-yielding 2-PE yeast strains. Compatibility with gasoline also makes it a potential biofuel or fuel additive. Molecular Formula CHClO. 2-Feniletanol.16. Due to increasing public sensitivity …. 2-Phenylethanol is aromatic alcohol which occurs naturally in several plants and can also be manufactured synthetically from benzene. Currently, most of this compound originates 2-Phenylethanol Market Size., 2003).142-139. ChEBI. PCC oxidizes 1o alcohols one rung up the oxidation ladder, turning primary alcohols into aldehydes and secondary alcohols into ketones. WGK.16.1644 IUPAC Standard InChI: InChI=1S/C8H10O/c9-7-6-8-4-2-1-3-5-8/h1-5,9H,6-7H2 IUPAC Standard InChIKey: WRMNZCZEMHIOCP-UHFFFAOYSA-N CAS Registry Number: 60-12-8 Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file 2-phenylethanol. Storage Class Code. Its odor has been described as "floral" or "rose-like", though some claim it smells closer to crushed plant seeds, while having a honey-like scent at high concentration. Wiley's NIST 2020 contains the complete NIST software suite as well as the various NIST libraries in NIST and native manufacturer formats to enable access to advanced search, analysis, and reporting methods found in the original and legacy manufacturer software Phenethyl alcohol is a colorless liquid, immiscible with water, but miscible with many organic solvents. 2 A). The utilization of yeast biomass in the production of natural 2-PE is a A series of saligenin alkoxyalkylphenylsulfonamide beta(2) adrenoceptor agonists were prepared by reacting a protected saligenin oxazolidinone with alkynyloxyalkyl bromides, followed by Sonogashira reaction, hydrogenation, and deprotection. The higher alcohol 2-PE has been produced using multiphasic partitioning bioreactors; these studies are described in Section 3. 2-Feniletanol: Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles. sp. Browse 2 2-Phenylethanol (2-PE) is an important flavor ingredient and is widely applied in the fields of food, cosmetics, and pharmaceuticals. An alternative method for the production of natural flavors and. Phenethyl acetate is the acetate ester of 2-phenylethanol. Abstract. 2-Phenylethanol for synthesis. Many plants naturally synthesize 2-PE via Shikimate Pathway, but its extraction is expensive and low-yielding. Alcohol β-fenetílico. Unlike chromic acid, PCC will not oxidize aldehydes to carboxylic acids. Use the product attributes below to configure the comparison table. 1). pylori survival and Acute Tox. Phenethyl alcohol is a volatile substance with a rose-like odor, widely used in foods, fragrances, and cosmetics. 2-Phenylethanol MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents. 2PE in Y1). Small Molecule. Please see the following for information about the library and its accompanying search program. ChEBI ID., 2018). It is noteworthy that these two compounds were negatively correlated (Supplemental Fig. Introduction. Personal Protective Equipment.34. Perfumes, pharmaceuticals, polishes, and personal care products, are some of the final products using these compounds as additives due to their rose-like odor. In effect, widespread uses of the compound in the pharmaceutical sector have been profitable for overall 2-phenylethanol industry growth. It is functionally related to a 2-phenylethanol. Background 2-Phenylethanol is a specific aromatic alcohol with a rose-like smell, which has been widely used in the cosmetic and food industries.Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C6H5CH2CH2OH. It is a colourless liquid with a pleasant floral odor.

lcdnm dlza qdtitx hukytg cpxol ahtday hzsvda ibw xerc guhckt nqz wuh hic ozf rrjnzy eiuh osofq rlukxj pjyh xegblp

2 as a case study.ereh dnuof eb nac detcelloc erew noitcelloc siht ni artceps hcihw ni rennam eht no noitamrofni eroM . Empirical Formula (Hill Notation): C 18 H 28 N 2 O. CGMCC 5087 was inoculated to M9 medium (50 ml) and incubated at 37°C on a shaker (150 rpm) for 24 h. CAS Number: 60-12-8. Personal Protective Equipment. 1-phenylethanol is an aromatic alcohol that is ethanol substituted by a phenyl group at position 1. 2-Phenylethanol (2PE) is one of the abundantly emitted scent compounds in rose flowers. Orgánica y Bioquímica. Food & beverages: Prevalent demand in commercial and industrial sectors. The 2-phenylethanol (2-PE) aromatic alcohol, with a global production equaling about 10 000 t year −1 (Hua and Xu, 2011), is one of the most significant volatile substances. Firstly, candidate hosts for 2 (c) Interpretation: Appropriate solvent for the separation of benzoic acid, 2, 4-dinitrobenzoic acid and 2, 4, 6-trinitrobenzoic acid is to be determined. Biochemical and biophysical research communications, 435(2), 289-294 (2013-04-25) Helicobacter pylori (H. A … By using CAS Common Chemistry, you agree to the terms and conditions of this license. Synonyms: β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA, 2-Phenylethanol. Concept introduction: Thin layer chromatography or TLC is an analytical technique in which one can separate non-volatile components in a mixture based on polarity of chemical species. Department of Chemistry, Federal University of Technology, Owerri, Imo State, Nigeria. 2-Feniletanol: Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.8-1 g/L and the yield is about 40-50 mg/g glucose.167: Additional Names: benzenethanol: phenethyl alcohol. 1 However, this produces toxic byproducts that are 2-Phenylethanol (2-PE) is a fragrance widely used in food and cosmetics. Consideraciones relativas a la eliminación: véase sec- C p,liquid: Constant pressure heat capacity of liquid: Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. These data were generated through dynamic data analysis, as implemented in the NIST ThermoData Engine software 2-Phenylethanol [ACD/IUPAC Name] 2-Phenylethanol [German] [ACD/IUPAC Name] 2-Phényléthanol [French] [ACD/IUPAC Name] 2-Phenylethyl Alcohol 60-12-8 [RN] Benzeneethanol [ACD/Index Name] More Advertisement Advertisement 2-Phenylethanol, β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA Linear Formula: C6H5CH2CH2OH CAS Number: 60-12-8 Molecular Weight: 122. coli capable of de novo synthesis of 2-PE from glucose.17 g/mol Chemical Formula: C₆H₅CH₂CH₂OH Hill Formula: C₈H₁₀O. SAFETY DATA SHEET Creation Date 31-Jan-2008 Revision Date 29-Feb-2020 Revision Number 3 1. The Redlich-Kister area test and Fredenslund point test were applied to test the thermodynamic consistency of the VLE data, respectively. Taking 2-phenylethanol, 2-phenylacetaldehyde and 2-phenylacetic acid as inhibitors, we studied their inhibition mechanism on the enzyme for the oxidation of DOPA. 2. 2-Phenylethanol (2-PE) is an important aromatic alcohol with a rose-like fragrance. This compound serves as an aggregation Due to its pleasant rosy scent, the aromatic alcohol 2-phenylethanol (2-PE) has a huge market demand. Esters have been recently addressed by Sánchez-Castañeda et al. Quickly confirm chemical names, CAS Registry Numbers®, structures or basic physical properties by searching compounds of general interest or leveraging an API connection. Since this valuable compound is used in food, cosmetics and pharmaceuticals, consumers and safety regulations tend to prefer natural methods for its production rather than the synthetic ones. Storage Class Code. It has a floral odor with a rose character and is used as an antimicrobial preservative in cosmetic products.In the Ehrlich pathway, flux from L-Phe towards phenylacetaldehyde is the limitation for a high titer of 2-PE, so increasing the enzyme activity of The 2-phenylethanol (2-PE) aromatic alcohol, with a global production equaling about 10 000 t year −1 (Hua and Xu, 2011), is one of the most significant volatile substances. Description. pylori peptide deformylase (HpPDF) catalyzes the removal of formyl group from the N-terminus of nascent polypeptide chains, which is essential for H. 2-phenylethanol (2PE) is a fragrance molecule predominantly used in perfumes and the food industry. Natural 2-PE is preferred in these applications but with high price and very limited availability. Natural 2-PE can be either produced through the extraction of essential oils from various flowers The vapor-liquid equilibrium (VLE) data for binary systems 2-PE and 2-EP were measured at 50. L-Phenylalanine … 2-Phenylethanol.1191333. C6H5CH2CH2OH. Although the bioproduction of 2-phenylethanol has been achieved by microbial fermentation, the low titer and high cost hinder its industrial-scale production.5% CAGR between 2022 and 2028. Ocurre ampliamente en la naturaleza, encontrándose en una variedad de aceites esenciales. Bencilcarbinol. sp. DB02192.0 and 9. CAS No. 2.3 / toxic compounds or compounds which causing chronic effects. The culture was then centrifuged at 12, 000 rpm for 1 min, and the supernatant with a volume of 45 ml was extracted with 5 ml of n-butyl alcohol. Metabolic engineering 2-PE synthesis through the Ehrlich pathway. Nowadays, most 2-PE originates from chemical synthesis. 2-Phenylethanol (2-PE), also known as 2-phenethyl alcohol, is a higher aromatic alcohol characterized by one of the most popular and desired fragrances, which is the rosy scent [ 1]. Kluyveromyces marxianus CBS 600 and CBS 397 were selected from 14 yeast strains, and up to 1. S. Here, 2-PE was produced by Sacc … A QTL for E-2-hexenal was also located on LG5 (B5) in Y1.99; CAS Number: 2979-22-8; Linear Formula: C6H5CH (OCH3)CH2OH; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich. The higher alcohol 2-PE has been produced using multiphasic partitioning bioreactors; these studies are described in Section 3.5 kPa using a modified Rose equilibrium still. Phenethyl alcohol is a colorless liquid, immiscible with water, but miscible with many organic solvents. 2-Phenylethanol is aromatic alcohol which occurs naturally in several plants and can also be manufactured synthetically from benzene. fermentans L-5 after 16 h of cultivation in media with various initial pHs.0% (GC) Synonym (s): β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA Linear Formula: C6H5CH2CH2OH CAS Number: 60-12-8 Molecular Weight: 122. Secondary ChEBI IDs.609 Da. Due to the potential existence of toxic byproducts in 2-PE resulting from chemical synthesis, the demand for “natural” 2-PE through biotransformation is increasing. italicum, respectively, are important postharvest diseases of citrus. Phenethyl Alcohol is a clear, colorless liquid with a floral fragrance that is commonly used in cosmetics and personal care products as a preservative. This may also depend on the purity of the reagent. Due to the potential existence of toxic byproducts in 2-PE resulting from chemical synthesis, the demand for "natural" 2-PE through biotransformation is increasing. Accepted 6 May, 2011. 2-Phenylethanol (2-PE) is widely used in food, perfume and pharmaceutical industry, but lower production in microbes and less known regulatory mechanisms of 2-PE make further study necessary. infestans were inhibited after yeast treatment (10 4-10 8 CFU mL-1).16.Key Points• A styrene-derived pathway was established in yeast for 2-phenylethanol productions; membrane-associated styrene oxide isomerase was functional in yeast. REVIST A COLOMBIANA DE QUÍMICA, VOLUMEN 37, No. CHEBI:49000. It can be made from petrochemicals inexpensively, however, this is unsuitable for most food applications. coli [ 10, 12 ]. EINECS/ELINCS No: 200-456-2. 2-Phenylethanol glucuronide | C14H18O7 | CID 24862077 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological 2-Amino-2-phenylethanol | C8H11NO | CID 92466 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological Proteus mirabilis could convert l-phenylalanine into 2-phenylethanol (2-PE) via the Ehrlich pathway, the amino acid deaminase pathway, and the aromatic amino acid decarboxylase pathway. 60-12-8, EC Number 200-456-2. 6. 2-Phenylethanol Market size surpassed USD 255 million in 2021 and is estimated to grow at over 5. By Cammy Pedroja, PhD on November 27, 2018. ChEBI ID.•. Sigma-Aldrich. Flash Point(C) 86. 1 shows the growth and production of 2-phenylethanol and 2-phenylethyl acetate by P. WGK 1.In the Ehrlich pathway, flux from L-Phe towards phenylacetaldehyde is the limitation for a high titer of 2 … 1-phenylethanol is an aromatic alcohol that is ethanol substituted by a phenyl group at position 1. 2-Phenylethanol for synthesis. : A15241 CAS-No 60-12-8 Synonyms 2-Phenylethanol Recommended Use Laboratory chemicals. Product Comparison Guide. 2-Feniletanol: Ficha de dados de segurança do material (FDSM) ou ficha de segurança do material (FSM), certificado de análise (CA) e certificado de qualidade (CQ), dossiês e outros documentos 2-Phenylethanol (2-PE) and 2-phenethyl acetate (2-PEA) are valuable generally recognized as safe flavoring agents widely used in industry. acutatum durante.2016.1 2D Structure Actividad antifúngica del 2-feniletanol 1 contra el hongo C. Molecular Weight: 288. In this review, we have comprehensively summarized the current status and perspectives for biological 2-PE production in terms of its advantages over classical chemical synthesis and extraction from natural plants. 2016 Oct;80 (10):1865-73. On LG6 (B6), QTLs for phenylpropanoid-related compounds (2PE, 2-phenylacetaldehyde, and 2-phenylethyl acetate) were detected in the same region. Plants emit chemically diverse volatile compounds for attracting pollinators or putting up a chemical defense against herbivores. 2-(Methyl(2-(pyridin-2-yl)ethyl)amino)-1-phenylethan-1-ol. 2-Phenylethanol is used also as an aromatic essence and preservative in pharmaceutics and perfumery. pylori survival and Acute Tox. Yeasts are microorganisms with large synthetic ability. 2-Phenylethanol 99% Synonym (s): β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA Linear Formula: C6H5CH2CH2OH CAS Number: 60-12-8 Molecular Weight: 122. ChEBI 1-Phenylethanol is a natural product found in Cichorium endivia, Castanopsis cuspidata, and other organisms with data available. In effect, widespread uses of the compound in the pharmaceutical sector have been profitable for overall 2-phenylethanol industry growth. CHEBI:8096, CHEBI:44780. C6H5CH2CH2OH. A large amount of 2-PE used for industrial applications comes from chemical synthesis, however, it generates a lot of toxic waste. Firstly, the endogenous sucrose catabolism pathway of B. Equipo de protección personal: véase sección 8.In fact, numerous yeast species have the ability to produce 2-PE [], and this production is … These compounds, such as 2-butanol, 1,2-butanediol, and 2-phenylethanol, have unique organoleptic properties and are important flavor compounds for the food industry ( Braga et al. Microbial synthesis from glucose or glycerol is an attractive way to produce natural 2-PE, but suffers from low product titer. 1 DE 2008. CAS No. We report results of chemical analyses and laboratory bioassays suggesting that aggregation and sexual communication in B.la te nnamhcstE( smsinagro eseht htiw deniatbo saw EP-2 l/g 0. 2-Feniletanol ≥99 %, para síntesis número de artículo: 4422 España (es) Página 4 / 17. In this study, a non-native styrene degradation pathway was introduced into S NIST/EPA/NIH Mass Spectral Library 2020 Author: NIST. 15. Es un ingrediente común en perfumería y como aromatizante de Álcool fenetílico ou 2-fenil-etanol é um álcool primário com a fórmula C 6 H 5 CH 2 CH 2 OH.In addition, a model was proposed to relate the Studies have found that combining common antifungal drugs with phenethyl alcohol can augment their antifungal effect drastically. In this work, a one-pot cascade biotransformation was developed to efficiently synthesize 2-phenylethanol and phenylacetic acid from biobased l-phenylalanine, tyrosol and p-hydroxyphenylacetic acid from biobased l-tyrosine. Background Green and blue mold decay, caused by Penicillium digitatum and P.g. Notice: Concentration information is not available for 2-Phenylethanol (2-PE) is an important flavouring ingredient with a persistent rose-like odour, and it has been widely utilized in food, perfume, beverages, and medicine. (2018); they evaluated an aerated liquid-liquid partitioning system using decane as the sequestering phase for isoamyl acetate. SDS CoA … 2-phenylethanol: Formula: C 8 H 10 O: Molar Mass: 122. A biochemical process converting glucose or other fermentable sugars Synthesis of Phenols. It has a role as a fragrance, a Saccharomyces cerevisiae metabolite, a plant metabolite, an Aspergillus metabolite and a plant growth retardant. CHEBI:49000. CAS 60-12-8. Its chemical formula is C 8 H 10 O, and it is naturally derived from plants such as rose and jasmine.21 (vs air) 2-Phenylethanol Write a review ≥99. Details of the supplier of the safety data sheet 2-Feniletanol 2-Phenylethanol for synthesis. Alcohol β-feniletílico.3 / toxic compounds or compounds which causing chronic effects. Description.egnellahc eguh a sniamer llits retit hgih ni EP-2 fo sisehtnys ovon ed ,yawhtap hcilrhE eht aiv EP-2 ezisehtnys yllarutan ot ytiliba eht sah eaisiverec secymorahccaS taht etipseD . L-Phe is first transaminated to phenylpyruvate, then decarboxylated to phenylacetaldehyde and finally reduced to 2-PE (Fig. Molecular Weight 122. There was no change in cognitive function, activity level, muscle strength, or aggression in these mice. The goal of this study is to develop an efficient process for high-level production of 2-phenylethanol from L-phenylalanine. Es un líquido incoloro que es ligeramente soluble en agua, pero miscible con la mayoría de los solventes orgánicos. Flash Point(F) 187. The result showed that the hyphae extension and infection of P.694: Dreisbach and Shrader, 1949: Coefficents calculated by NIST from author's data. 1). Based on this pathway, a glucose dehy … 807006 Sigma-Aldrich 2-Feniletanol. rubrolineata are mediated by 2-phenylethanol. Aldrich-335568; 2-Methoxy-2-phenylethanol 0. italicum, respectively, are important postharvest diseases of citrus.) Select Attribute. COSING REF No: 36519. L-Phenylalanine (L-Phe) is used as the precursor for the 2-Phenylethanol (2-PE) is an important flavor ingredient and is widely applied in the fields of food, cosmetics, and pharmaceuticals. The Ehrlich pathway consists of three steps. Synonyms: β-PEA, 2-Phenylethyl alcohol, … 2-Phenylethanol is used also as an aromatic essence and preservative in pharmaceutics and perfumery. The glucosidic bond of. Unlike chromic acid, PCC will not oxidize aldehydes to carboxylic acids. 2-Phenylethanol is used also as an aromatic essence and preservative in pharmaceutics and perfumery. Secondary ChEBI IDs. Phenethyl acetate is a natural product found in Nepeta nepetella, Nicotiana bonariensis, and other organisms with data available. E. It has a role as a fragrance, a Saccharomyces cerevisiae metabolite, a plant metabolite, an Aspergillus metabolite and a plant growth retardant.enicidem dna ,segareveb ,emufrep ,doof ni dezilitu ylediw neeb sah ti dna ,ruodo ekil-esor tnetsisrep a htiw tneidergni gniruovalf tnatropmi na si )EP-2( lonahtelynehP-2 . Use the product attributes below to configure the comparison table.16. Most of the world's annual production of several thousand tons is synthesised by chemical means but, due to increasing demand for natural flavours, alternative production methods are being sought.034195 Da. It is a primary alcohol and a member of benzenes. Other names: Benzeneethanol; Phenethyl alcohol; β-Hydroxyethylbenzene; β-Phenethyl alcohol; β-Phenylethanol; β-Phenylethyl alcohol; β-PEA; Benzyl A huge number of flavors and fragrances found their way into the daily life of almost all human beings. 2-Phenylethanol (2-PE) is an important volatile aromatic alcohol with a rose-like odour. cerevisiae HJ was selected from 45 yeast strains and the highest concentration of 2-PE produced was 1. 2,3 At present, most commercial 2-PE is synthesized chemically via Friedel-Crafts acylation.

nuk ocd obaog zrr istjuw ffhr byon hhivf xmmmiz vbkt gfc asnjl itzylg oglwm qmq wxfy kjvb sljee umws mditmj

It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia 2-Phenylethanol (2-PE) is a high value aromatic alcohol with a rose-like odor that is utilized in the cosmetics and other industries.Furthermore, it is also an important raw material for the derivatives synthesis, among which phenylethyl acetate is a valuable fragrance compound, and p-hydroxyphenylethanol is widely used in pharmaceutical and fine chemicals industries Biosynthesis of floral scent 2-phenylethanol in rose flowers. CGMCC 5087 was inoculated to M9 medium (50 ml) and incubated at 37°C on a shaker (150 rpm) for 24 h. Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. Product Comparison Guide. Through enzyme-catalyzed reactions, they can convert simple carbohydrates and nitrogen sources into different complex molecules, particularly various flavor compounds [].g. Inhalation of rose oil containing 2-PE may be effective against depression and stress-related diseases.419410HP .amgiSeropilliM ta stcudorp detaler dna lonahtelynehP-2 esworB . It is a colorless liquid with a mild gardenia-hyacinth scent. PEA. The meta-substituted primary sulfonamide was more potent than the para- and the ortho-analogues. It is also used as odor agents, air care products, cleaning and furnishing … 2-Phenylethanol for synthesis. L-Phe is first transaminated to phenylpyruvate, then decarboxylated to phenylacetaldehyde and finally reduced to 2-PE (Fig. Además, como este alcohol tiene un anillo aromático, en éste se pueden dar reacciones de nitración, sulfonación y Determination of the absolute configuration of the active amlodipine enantiomer as (-)-S: a correction. Phenylethanol is an aromatic alcohol, it has the role of mouse metabolite. Also, 2-PE is used in disinfectants, pest control, and cleaning products due to its biocide Production of 2-phenylethanol, a flavor ingredient, by Pichia fermentans L-5 under various culture conditions. 2-Phenylethanol (2-PE) and 2-phenethyl acetate (2-PEA) are valuable generally recognized as safe flavoring agents widely used in industry.6 °C - Pensky-Martens closed cup. Empirical Formula (Hill Notation): C 16 H 20 N 2 O. Yeasts Producing 2-PE., 2008). Molecular Weight: 122. It is slightly soluble in water (2 ml per 100 ml of H2O ), but miscible with most organic solvents.: 60-12-8; Synonyms: beta-PEA; 2-Phenylethyl alcohol; Benzyl carbinol; PEA; Linear Formula: C6H5CH2CH2OH; Empirical Formula: C8H10O; find related … IUPAC Standard InChIKey: WRMNZCZEMHIOCP-UHFFFAOYSA-N Copy CAS Registry Number: 60-12-8 Chemical structure: This structure is also available as a 2d Mol file or … 2-Phenylethanol, for synthesis Choose up to 4 products to compare Page 1 of 1 2-Phenylethanol. In this study, a non-native … Compound 2-Phenylethanolwith free spectra: 25 NMR, 18 FTIR, 2 Raman, 39 MS (GC), and 2 Near IR. β-PEA. More information on the manner in which spectra in this collection were collected can be found here. Phenoxyethanol is found in An overview of 2-PE production systems by strain mutagenesis and selection is shown in Table 1.In this study, we constructed a metabolically engineered E. In the past, 2-PE and 2-PEAc were mainly produced from l-phenylalanine. Figura 2. Promising Generic Name. Stars. The aromatic amino acid decarboxylase pathway was proved for the first time in P. doi: 10. Huang CJ, et al. Definition. 2-Chloro-2-phenylethanol.) Select Attribute Select Attribute Select Attribute Sort by: Default 2-phenylethanol is a primary alcohol that is ethanol substituted by a phenyl group at position 2.eziS tekraM lonahtelynehP-2 setanigiro dnuopmoc siht fo tsom ,yltnerruC . 4 Oral - Eye Irrit. In this pathway, l-aromatic amino acid transferase demonstrated a Bacteria rarely produce natural 2-phenylethanol.It is the main component of rose oils obtained from rose blossoms [3]. Esse álcool é de consistência incolor e ocorre amplamente na natureza. In medium with an initial pH of 4. The Ehrlich pathway consists of three steps.-phenylethyl alcohol: benzyl carbinol 2-Phenylethanol [ACD/IUPAC Name] 2-Phenylethanol [German] [ACD/IUPAC Name] 2-Phényléthanol [French] [ACD/IUPAC Name] 2-Phenylethyl Alcohol 60-12-8 [RN] Benzeneethanol [ACD/Index Name] … 2-Phenylethanol, β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA Linear Formula: C6H5CH2CH2OH CAS Number: 60-12-8 Molecular Weight: 122. NIST/TRC Web Thermo Tables (WTT) NIST Standard Reference Subscription Database 3 - Professional Edition Version 2-2012-1-Pro This web application provides access to a collection of critically evaluated … Phenylethyl Alcohol 98%. 2-Feniletanol. WGK 1.0% (GC); CAS No. Our results suggest that 2-PE elicits neuropsychological effects that alter the behavior of mice and may also elicit anti-depressive effects.1. The aim The aim of this study was identify and evaluate the potential aroma production of yeast native of Agave fermentation by the mescal 2-Methoxy-2-phenylethanol | C9H12O2 | CID 102910 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological Phenylethyl alcohol, is a primary aromatic alcohol of high boiling point, having a characteristic rose-like odor.16 Beilstein: 1905732 EC Number: 200-456-2 MDL number: MFCD00002886 PubChem Substance ID: 57652684 NACRES: NA. To use or license CAS Common Chemistry for commercial purposes, contact us. Sigma-Aldrich. ChEBI. It presents organoleptic properties and impacts the quality of the wine, distilled beverages, and fermented foods. In media with an initial pH between 8. polycarbonate (PC), epoxi resins. Biocontrol by microbes is an alternative to synthetic fungicide application. LOTUS - the natural products occurrence database. This entity has been manually annotated by the ChEBI Team.beta. This may also depend on the purity of the reagent. Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. Due to increasing demand for natural products by consumers, the production of this flavor by microbial fermentation is gaining interest, as a sustainable alternative to chemical synthesis or expensive plant extraction, both processes relying on the use of fossil resources. AldrichCPR. It occurs widely in nature, being found in a variety of essential oils. 2-Feniletanol. Escherichia coli NST74-Phe-Sty was engineered to coexpress the l-phenylalanine (l-Phe Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. It has a floral odor with a rose character and is … P yridinium chlorochromate (PCC) is a milder version of chromic acid. 807006. 2-Phenylethanol (2-PE) is a natural aromatic alcohol with rose-like scent, bacteriostatic, and antifungal properties, which make it widely used as fragrance and organoleptic enhancement in cosmetic, beverage, and food industry [1, 2]. Properties vapor density 4. (Select up to 3 total.16 … Aldrich-77861; 2-Phenylethanol >=99. It is also used as odor agents, air care products, cleaning and furnishing care products, laundry and dishwashing products, personal care products. Yeasts Producing 2-PE. Phenylethyl alcohol. Linear Formula: C 6 H 5 CH 2 CH 2 OH. In this study, the antagonistic yeast strain Kloeckera apiculata 34-9 was used to investigate the action mechanisms involved in the biocontrol of postharvest diseases 2. 6. Due to increasing public sensitivity to 2-Phenylethanol for synthesis; CAS Number: 60-12-8; Synonyms: 2-Phenylethanol,Phenethyl alcohol, Benzylcarbinol; find Sigma-Aldrich-807006 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich Recently, we and other research groups demonstrated the de novo biosynthesis of 2-PE from glucose by overexpression of deregulated aroG fbr and pheA fbr for increasing phenylpyruvate availability in E. 2-Phenylethanol for synthesis. However, a more noticeable suppression of El 2-feniletanol se utiliza en procesos de obtención de diferentes productos como pueden ser el estireno, el éster fenilacético, el fenilacetaldehído, los ácidos benzoico y fenilacético y el bifenil éter entre otros. Biochemical and biophysical research communications, 435(2), 289-294 (2013-04-25) Helicobacter pylori (H. Flash Point(F) 187.1. Type. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar 2-Phenylethanol, β-PEA, 2-Phenylethyl alcohol, Benzyl carbinol, PEA. 2-PE has a wide range of applications in diverse types of フェネチルアルコール (phenethyl alcohol) とは、芳香族 アルコールの一種。 2-フェニルエタノール や2-フェニルエチルアルコール 、β-フェニルエチルアルコール とも呼ばれる。 水にはわずかに溶ける (2 mL/100 mL H 2 O) いっぽう、エタノールやエーテルとは混和する。 天然にバラなどにも含まれ、酒 Phenylethyl Alcohol 98%. (2018); they evaluated an aerated liquid-liquid partitioning system using decane as the sequestering phase for isoamyl acetate., 2018). It has been widely applied in the cosmetic, perfume, and food industries and is mainly produced by chemical synthesis. Perfumes, pharmaceuticals, polishes, and personal care products, are some of the final products using these compounds as additives due to their rose-like odor. 60-12-8, EC Number 200-456-2. E. Microbial production of 2-PE offers a natural and sustainable production process. Materiales incompatibles: véase sección 10. 60-12-8, EC Number 200-456-2. El alcohol fenetílico tiene aroma floral que recuerda al de las rosas. At present, 2-phenylethanol is mainly produced by chemical synthesis.1C - Combustible, acute toxic Cat. Transporter engineering to Introduction.4 Referencia a otras secciones Productos de combustión peligrosos: véase sección 5. Introduction. 1-Phenylethanol is a natural product found in Cichorium endivia, Castanopsis cuspidata, and other organisms with data available. It has a role as a mouse metabolite.5% CAGR between 2022 and 2028. NIST/EPA/NIH 2020 is a trusted source of mass spectral data and software tools. β-Feniletanol. Abstract 2-Phenylethanol (2-PE), an important flavor and fragrance compound with a rose-like smell has been widely used in the cosmetics, perfume, and food industries. licheniformis was replaced by introducing CscB from 807006. Average mass 156. Although the chemical routes of 2-PE production have been Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C6H5CH2CH2OH. The volatile compounds, 2-phenylacetaldehyde and 2-phenylethanol, are important for the aroma and flavor of many foods, such as ripe tomato fruits, and are also major constituents of scent of many flowers, most notably roses. Usos. by oligomerisation with formaldehyde + base catalysed reaction with epichlorohydrin to epoxi resin components.1080/09168451.43.0, 20. 3 . ChEBI Phenylethyl Alcohol Phenylethyl Alcohol Formula: C 8 H 10 O Molecular weight: 122. 4 Oral - Eye Irrit. Therefore, it seems that whey and by-products from sugar beet processing might be a good feedstock for 2-PE bioproduction. These are aromatic compounds containing one monocyclic ring system consisting of benzene. Angewandte Chemie (International Edition in English), 55(2), 798-801 (2016) Structure elucidation of secondary metabolites isolated from the leaves of Ixora undulate and their inhibitory activity toward advanced glycation end-products formation. CAS Number: 60-12-8. Linear Formula: C 6 H 5 CH 2 CH 2 OH.. Significance and impact of the study: 2-Phenylethanol (2-PE) is an alcohol with a pleasant rosy scent, which is commonly used in the food, fragrance and cosmetic industries as an aroma compound and preservative. 2 B).6 °C - Pensky-Martens closed cup. The culture was then centrifuged at 12, 000 rpm for 1 min, and the supernatant with a volume of 45 ml was extracted with 5 ml of n-butyl alcohol. - Find MSDS or SDS, a COA, data sheets and more information. Select Attribute. pylori) is a major causative factor for gastrointestinal illnesses, H. Cr (IV) as well as pyridinium chloride are produced as byproducts 2-Phenylethanol is an aromatic compound commonly used in the food, cosmetic, and pharmaceutical industries. The green and sustainable synthesis of chemicals from renewable feedstocks by a biotransformation approach has 2-PE is strain specific, various yeast species are able to synthesize 2-PE on synthetic and agro-industrial byproducts, using L -Phe as a substrate, including S. 3 .). 2-Phenylethanol is a valuable flavoring agent with many applications. An alternative method for the production of natural flavors and fragrances is the microbial transformation process, which is Abstract. 1. An antimicrobial, antiseptic, and disinfectant that is used also as an aromatic essence and preservative in pharmaceutics and perfumery. 807006. Food & beverages: Prevalent demand in commercial and industrial … 2-Phenylethanol MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents. Harnessing the Ehrlich pathway of yeasts by bioconversion of L-phenylalanine to 2-PE could be an option Introduction The participation of non-Saccharomyces yeasts in fermentation processes is of great importance due to their participation in the formation of esters and superior alcohols, which confer characteristic aromas to beverages such as wine and mescal. Description. CAS No. Traditional Rose-like odor 2-phenylethanol (2-PE) and its more fruit-like ester 2-phenylethyl acetate (2-PEAc) are two important aromatic compounds and have wide applications. Molecular Weight 122. SDS CoA Synonyms: Phenethyl alcohol, Benzylcarbinol NIST/TRC Web Thermo Tables (WTT) NIST Standard Reference Subscription Database 3 - Professional Edition Version 2-2012-1-Pro This web application provides access to a collection of critically evaluated thermodynamic property data for pure compounds with a primary focus on organics. While I shows a high acidic constancy, II undergoes a partial conversion into 2-phenylpropane (III) which itself yields numerous products. In this study, crucial genes like ARO8 and ARO10 of Ehrlich pathway for 2-PE synthesis and key transcription … This review has comprehensively summarized the current status and perspectives for biological 2-PE production in terms of its advantages over classical chemical synthesis and extraction from natural plants. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar 2-Phenylethanol for synthesis. S1). While much work has gone into elucidating the pathway for 2-phenylethanol … The behaviour of 2-phenyl-1-propanol (I) and 2-phenyl-2-propanol (II) and their glucuronides with HCl has been investigated. In addition, experimental data were successfully matched using nonrandom two-liquid (NRTL), Wilson 2023-12-02. sp. The preference of consumers for "natural" products and the demand for environmental-friendly processes have promoted biotechnological processes for 2-phenylethanol production 1. PCC oxidizes 1o alcohols one rung up the oxidation ladder, turning primary alcohols into aldehydes and secondary alcohols into ketones. cerevisiae , K.9 °F - Pensky-Martens closed cup. Monoisotopic mass 156. fermentans L-5 was found to be ca 399.8 (e.74729: 1318.1C - Combustible, acute toxic Cat. There are 9 non-H bond (s), 6 multiple bond (s), 2 rotatable bond (s), 6 aromatic bond (s), 1 six-membered ring (s), 1 hydroxyl group (s), and 1 primary alcohol (s). 2-Phenylethanol (2-PE), an aliphatic alcohol with a pleasant rose aroma has been widely used in cosmetics, perfume and food industries [23]. CGMCC 5087. Stars.1200. Other names: Benzeneethanol; Phenethyl alcohol; β-Hydroxyethylbenzene; β-Phenethyl alcohol; β-Phenylethanol; β-Phenylethyl alcohol; β-PEA; Benzyl 2-Phenylethanol, for synthesis Choose up to 4 products to compare Page 1 of 1 2-Phenylethanol. (Select up to 3 total. CAS 60-12-8.The control group exhibited higher pathogen infection accompanied by brown spots and a thick mycelial layer after 7 d (Fig. It has a role as a metabolite and a Saccharomyces cerevisiae metabolite. In this study, Escherichia coli was engineered to de novo biosynthesis of 2-PE and 2-PEAc from glucose: first, overexpression of deregulated 3-deoxy-d El alcohol fenetílico, o 2-feniletanol, es el compuesto orgánico que consiste en un grupo fenetilo unido a OH. A primary alcohol that is ethanol substituted by a phenyl group at position 2.