W266825

L-Menthyl acetate

natural, ≥98%, FCC, FG

• Synonyme(s) : (1R)-(−)-Menthyl acetate
• Formule empirique (notation de Hill): C₁₂H₂₂O₂
• Numéro CAS: 2623-23-6
• Poids moléculaire : 198.30
• Numéro FEMA: 2668
• Numéro Beilstein : 2208505
• Numéro CE : 220-076-0
• Numéro MDL: MFCD00001482
• Code UNSPSC : 12164502
• ID de substance PubChem : 24901233
• Numéro Flavis : 9.016
• Nomenclature NACRES : NA.21

Propriétés

• Qualité: FG; Fragrance grade; Halal; Kosher; natural
• Niveau de qualité: 400
• Agence: follows IFRA guidelines
• Conformité réglementaire: EU Regulation 1223/2009; EU Regulation 1334/2008 & 178/2002; FCC; FDA 21 CFR 117; FDA 21 CFR 182.20
• Pureté: ≥98%
• Activité optique: [α]20/D −73°, neat
• Indice de réfraction: n20/D 1.447 (lit.)
• Point d'ébullition: 229-230 °C (lit.)
• Densité: 0.92 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: no known allergens
• Propriétés organoleptiques: herbaceous; minty
• Chaîne SMILES: CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(C)=O
• InChI: 1S/C12H22O2/c1-8(2)11-6-5-9(3)7-12(11)14-10(4)13/h8-9,11-12H,5-7H2,1-4H3/t9-,11+,12-/m1/s1
• Clé InChI: XHXUANMFYXWVNG-ADEWGFFLSA-N

Description

Application

• Inclusion complexes of β-cyclodextrin with isomeric ester aroma compounds: Preparation, characterization, mechanism study, and controlled release.: This study examines the formation of inclusion complexes between β-cyclodextrin and isomeric esters like l-Menthyl acetate, emphasizing their controlled release properties which could have significant implications in food flavoring and pharmaceuticals (Xiao et al., 2024).


• Enhancing the Enantioselectivity and Catalytic Efficiency of Esterase from Bacillus subtilis for Kinetic Resolution of l-Menthol through Semirational Design.: Research focuses on optimizing esterase enzymes for the kinetic resolution of l-Menthol using l-Menthyl acetate, highlighting advances in biocatalysis that enhance selectivity and efficiency in synthetic chemistry (Zhou et al., 2024).


• Engineering a Bacillus subtilis esterase for selective hydrolysis of d, l-menthyl acetate in an organic solvent-free system.: This publication details the engineering of an esterase for efficient hydrolysis of l-Menthyl acetate, demonstrating the potential for more sustainable and efficient biochemical processes in industry (Qiao et al., 2023).


• Conversion and Hydrothermal Decomposition of Major Components of Mint Essential Oil by Small-Scale Subcritical Water Treatment.: Investigates the decomposition of l-Menthyl acetate within mint essential oil under subcritical water conditions, providing insights into the stability and transformation of flavor compounds under industrial processing conditions (Chiou et al., 2020).


• Enhancement in skin permeation of 5-aminolevulinic acid using l-menthol and its derivatives.: This study explores the use of l-Menthyl acetate to enhance the skin permeation of 5-aminolevulinic acid, suggesting its potential application in transdermal drug delivery systems (Tokuoka et al., 2008).

Actions biochimiques/physiologiques

Taste at 25 ppm

Autres remarques

Natural occurrence: Mentha arvensis, peppermint, scotch spearmint, raspberry, mango, buchu oil, lemon balm, ginger and orange juice eucalyptus oil.

Informations sur la sécurité

• Pictogrammes: GHS09
• Mentions de danger: H411
• Conseils de prudence: P273 - P391 - P501
• Classification des risques: Aquatic Chronic 2
• Code de la classe de stockage: 10 - Combustible liquids
• Classe de danger pour l'eau (WGK): WGK 2
• Point d'éclair (°F): 170.6 °F - closed cup
• Point d'éclair (°C): 77 °C - closed cup
• Équipement de protection individuelle: Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)