W268003
2-甲基苯甲醚
≥99%, FG
别名:
o-Methylanisole
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关于此项目
线性分子式:
CH3C6H4OCH3
化学文摘社编号:
分子量:
122.16
FEMA Number:
2680
Council of Europe no.:
187
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
4.014
EC Number:
209-426-3
NACRES:
NA.21
MDL number:
Organoleptic:
floral; earthy; walnut
Grade:
FG
Halal
Kosher
Halal
Kosher
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens
产品名称
2-甲基苯甲醚, ≥99%, FG
SMILES string
COc1ccccc1C
InChI
1S/C8H10O/c1-7-5-3-4-6-8(7)9-2/h3-6H,1-2H3
InChI key
DTFKRVXLBCAIOZ-UHFFFAOYSA-N
biological source
synthetic
grade
FG
Halal
Kosher
agency
meets purity specifications of JECFA
reg. compliance
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515
assay
≥99%
refractive index
n20/D 1.516 (lit.)
bp
170-172 °C (lit.)
density
0.985 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
floral; earthy; walnut
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General description
2-Methylanisole is found in mastic oils, virgin olive oils and frankincense.
Application of solid-phase microextraction to the analysis of volatile compounds in virgin olive oils from five new cultivars
Baccouri B, et al.
Food Chemistry, 102(3), 850-856 (2007)
Frankincense and myrrh resources of Ethiopia: II. Medicinal and industrial uses.
Lemenith M & Teketay D.
SINET: Ethiopian Journal of Science, 26(2), 161-172 (2003)
Quality profile determination of Chios mastic gum essential oil and detection of adulteration in mastic oil products with the application of chiral and non-chiral GC?MS analysis.
Paraschos S, et al.
Fitoterapia, 114, 12-17 (2016)
Graziela G Bianco et al.
The Journal of organic chemistry, 74(6), 2561-2566 (2009-02-24)
The first synthesis of the natural product (+)-mutisianthol was accomplished in 11 steps and in 21% overall yield from 2-methylanisole. The synthesis of its enantiomer was also performed in a similar overall yield. The absolute configuration of the sesquiterpene (+)-mutisianthol
Elodie Guyonnet Bilé et al.
ChemSusChem, 5(1), 91-101 (2012-01-18)
Optically active amphiphilic compounds derived from N-methylephedrine, N-methylprolinol, or cinchona derivatives possessing bromide or chiral lactate counterions were efficiently used as protective agents for rhodium(0) nanoparticles. The full characterization of these surfactants and the obtained nanocatalysts was performed by means
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