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Merck
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Key Documents

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W268003

Sigma-Aldrich

2-Methylanisole

≥99%, FG

Sinónimos:

o-Methylanisole

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About This Item

Fórmula lineal:
CH3C6H4OCH3
Número de CAS:
578-58-5
Peso molecular:
122.16
FEMA Number:
2680
EC Number:
209-426-3
Council of Europe no.:
187
MDL number:
MFCD00008373
UNSPSC Code:
12164502
PubChem Substance ID:
24901245
Flavis number:
4.014
NACRES:
NA.21

biological source

synthetic

Quality Level

400

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

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

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General description

2-Methylanisole is found in mastic oils, virgin olive oils and frankincense.

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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)
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)
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)
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
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
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