W209902

Alcool d'anisyle

≥98%, FCC, FG

• Synonyme(s) : Alcool 4-méthoxybenzylique, Alcool de p-anisyle, Alcool anisique, Alcool d'anis
• Formule linéaire : CH₃OC₆H₄CH₂OH
• Numéro CAS: 105-13-5
• Poids moléculaire : 138.16
• Numéro FEMA: 2099
• Numéro Beilstein : 636654
• Numéro CE : 203-273-6
• Conseil de l'Europe Nº : 66
• Numéro MDL: MFCD00004653
• Code UNSPSC : 12164502
• ID de substance PubChem : 24900859
• Numéro Flavis : 2.128
• Nomenclature NACRES : NA.21

Propriétés

• Source biologique: synthetic
• Niveau de qualité: 400
• Qualité: FG; Halal; Kosher
• Agence: meets purity specifications of JECFA
• Conformité réglementaire: EU Regulation 1334/2008 & 178/2002; FCC; FDA 21 CFR 117; FDA 21 CFR 172.515
• Pureté: ≥98%
• Indice de réfraction: n20/D 1.544 (lit.)
• Point d'ébullition: 259 °C (lit.)
• Pf: 22-25 °C (lit.)
• Densité: 1.113 g/mL at 25 °C (lit.)
• Application(s): flavors and fragrances
• Documentation: see Safety & Documentation for available documents
• Allergène alimentaire: no known allergens
• Propriétés organoleptiques: floral; sweet; vanilla
• Chaîne SMILES: COc1ccc(CO)cc1
• InChI: 1S/C8H10O2/c1-10-8-4-2-7(6-9)3-5-8/h2-5,9H,6H2,1H3
• Clé InChI: MSHFRERJPWKJFX-UHFFFAOYSA-N

Description

Description générale

L'alcool d'anisyle est un composé aromatique volatil principalement présent dans les extraits de vanille et l'huile d'anis. Il est utilisé comme agent aromatisant et comme ingrédient de parfums.

Application

• De Novo Biosynthesis of Anisyl Alcohol and Anisyl Acetate in Engineered Escherichia coli.: This study explores the biosynthesis of anisyl alcohol and anisyl acetate in genetically modified E. coli, highlighting the potential for sustainable production of these compounds. The engineered bacteria demonstrated efficient conversion of substrates, opening new avenues for biotechnological applications in flavor and fragrance industries (Pan et al., 2023).


• Aryl-alcohol Oxidase Involved in Lignin Degradation: A Mechanistic Study Based on Steady and Pre-steady State Kinetics and Primary and Solvent Isotope Effects with Two Alcohol Substrates.: This research investigates the role of aryl-alcohol oxidase in lignin degradation, focusing on the enzyme′s kinetics and its interaction with anisyl alcohol. The findings provide insights into lignin biodegradation, which is crucial for biofuel production (Ferreira et al., 2009).


• First Evidence of Catalytic Mediation by Phenolic Compounds in the Laccase-induced Oxidation of Lignin Models.: This paper presents the first evidence of phenolic compounds mediating the laccase-catalyzed oxidation of lignin models, including anisyl alcohol. The study advances the understanding of lignin valorization, which is important for developing sustainable biorefineries (d′Acunzo and Galli, 2003).

Informations sur la sécurité

• Pictogrammes: GHS07
• Mention d'avertissement: Warning
• Mentions de danger: H315 - H317 - H319
• Conseils de prudence: P261 - P264 - P272 - P280 - P302 + P352 - P305 + P351 + P338
• Classification des risques: Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1B
• Code de la classe de stockage: 10 - Combustible liquids
• Classe de danger pour l'eau (WGK): WGK 1
• Point d'éclair (°F): 235.4 °F - closed cup
• Point d'éclair (°C): 113 °C - closed cup
• Équipement de protection individuelle: Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter