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关于此项目
经验公式(希尔记法):
C12H22O2
化学文摘社编号:
分子量:
198.30
Flavis number:
9.016
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
2668
NACRES:
NA.21
EC Number:
220-076-0
MDL number:
Beilstein/REAXYS Number:
2208505
eCl@ss:
32040100
Organoleptic:
herbaceous; minty
Grade:
FG, Fragrance grade, Halal, Kosher, natural
Agency:
follows IFRA guidelines
Food allergen:
no known allergens
grade
FG, Fragrance grade, Halal, Kosher, natural
agency
follows IFRA guidelines
reg. compliance
EU Regulation 1223/2009, EU Regulation 1334/2008 & 178/2002, FCC, FDA 21 CFR 117, FDA 21 CFR 182.20
assay
≥98%
optical activity
[α]20/D −73°, neat
sustainability
Sustainability features
refractive index
n
bp
229-230 °C (lit.)
density
0.92 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
fragrance allergen
no known allergens
organoleptic
herbaceous; minty
SMILES string
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
InChI key
XHXUANMFYXWVNG-ADEWGFFLSA-N
General description
We are committed to bringing you greener alternative products, which adhere to one or more of the 12 Principles of Green Chemistry. This product is Biobased and thus aligns with "Less Hazardous Chemical Syntheses" and "Use of Renewable Feedstocks".
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).
Biochem/physiol Actions
25ppm 时的味道
Other Notes
天然存在:Mentha arvensis、胡椒薄荷、苏格兰薄荷、悬钩子、芒果、布枯油、柠檬香蜂草、姜汁和橙汁、桉树油。
危险代码
预防性声明
Hazard Classifications
Aquatic Chronic 2
存储类别
10 - Combustible liquids
WGK
WGK 2
闪点 (F)
170.6 °F - closed cup
闪点 (°C)
77 °C - closed cup
PPE(个人防护设备)
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
