W209910

Alcool 4-méthoxybenzylique

natural, ≥98%, FG

• Synonyme(s) : 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 : 24900860
• Numéro Flavis : 2.128
• Nomenclature NACRES : NA.21

Propriétés

• Qualité: FG; Fragrance grade; Halal; Kosher; natural
• Niveau de qualité: 400
• Agence: follows IFRA guidelines; meets purity specifications of JECFA
• Conformité réglementaire: EU Regulation 1223/2009; EU Regulation 1334/2008 & 178/2002; FDA 21 CFR 117; FDA 21 CFR 172.515
• Pureté: ≥98%
• Composition: Contains Anise alcohol
• 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
• Allergène de parfum: anise alcohol
• Propriétés organoleptiques: anise; honey; 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

Natural occurrence: Anise, honey, bourbon, vanilla.

Application

• De Novo Biosynthesis of Anisyl Alcohol and Anisyl Acetate in Engineered Escherichia coli.: This study discusses the biosynthesis of anisyl alcohol and its acetate derivatives in engineered E. coli strains. It highlights the potential applications of these compounds in the food and flavor industries due to their aromatic properties. The research demonstrates the feasibility of microbial production of anisyl alcohol as a sustainable alternative to traditional chemical synthesis (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 paper investigates the role of aryl-alcohol oxidase in the degradation of lignin, focusing on the enzyme′s kinetics and mechanisms. Anisyl alcohol is used as a substrate to study these processes, providing insights into the enzyme′s function and its potential applications in biotechnological lignin valorization (Ferreira et al., 2009).


• Biotransformations of propenylbenzenes by an Arthrobacter sp. and its t-anethole blocked mutants.: This research explores the biotransformation of propenylbenzenes, including anisyl alcohol, using an Arthrobacter species and its mutants. The study highlights the microbial conversion pathways and the potential for producing valuable aromatic compounds through biocatalysis (Shimoni et al., 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