W266825

L-Menthyl acetate

natural, ≥98%, FCC, FG

• Sinónimos: (1R)-(−)-Menthyl acetate
• Fórmula empírica (notación de Hill): C₁₂H₂₂O₂
• Número de CAS: 2623-23-6
• Peso molecular: 198.30
• Número de FEMA: 2668
• Beilstein: 2208505
• Número CE: 220-076-0
• Número MDL: MFCD00001482
• Código UNSPSC: 12164502
• ID de la sustancia en PubChem: 24901233
• Número Flavis: 9.016
• NACRES: NA.21

Propiedades

• grado: FG; Fragrance grade; Halal; Kosher; natural
• Nivel de calidad: 400
• Agency: follows IFRA guidelines
• cumplimiento norm.: EU Regulation 1223/2009; EU Regulation 1334/2008 & 178/2002; FCC; FDA 21 CFR 117; FDA 21 CFR 182.20
• Análisis: ≥98%
• actividad óptica: [α]20/D −73°, neat
• índice de refracción: n20/D 1.447 (lit.)
• bp: 229-230 °C (lit.)
• densidad: 0.92 g/mL at 25 °C (lit.)
• aplicaciones: flavors and fragrances
• Documentación: see Safety & Documentation for available documents
• alérgeno alimentario: no known allergens
• alérgeno de la fragancia: no known allergens
• Organoléptico: herbaceous; minty
• cadena 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
• Clave InChI: XHXUANMFYXWVNG-ADEWGFFLSA-N

Descripción

Aplicación

• 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).

Acciones bioquímicas o fisiológicas

Taste at 25 ppm

Otras notas

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

Información de seguridad

• Pictogramas: GHS09
• Frases de peligro: H411
• Consejos de prudencia: P273 - P391 - P501
• Clasificaciones de peligro: Aquatic Chronic 2
• Código de clase de almacenamiento: 10 - Combustible liquids
• Clase de riesgo para el agua (WGK): WGK 2
• Punto de inflamabilidad (°F): 170.6 °F - closed cup
• Punto de inflamabilidad (°C): 77 °C - closed cup
• Equipo de protección personal: Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)