Identification | More | [Name]
2-Methoxy-4-methylphenol | [CAS]
93-51-6 | [Synonyms]
1-HYDROXY-2-METHOXY-4-METHYLBENZENE 2-HYDROXY-5-METHYLANISOLE 2-METHOXY-4-CRESOL 2-METHOXY-4-METHYLPHENOL 2-METHOXY-P-CRESOL 4-hydroxy-3-methoxy-1-methyl-benzene 4-HYDROXY-3-METHOXYTOLUENE 4-METHYLCATECHOL 2-METHYL ETHER 4-METHYLGUAIACOL 4-METHYLGUAJACOL CREOSOL FEMA 2671 homocatechol monomethyl ether METHYL GUAIACOL TIMTEC-BB SBB008258 VALSPICE 2-methoxy-4-methyl-pheno 2-Methoxy-4-methylphenol (4-methylguaiacol) 2-methoxy-4-methylphenol (creosol) 2-methoxy-p-creso | [EINECS(EC#)]
202-252-9 | [Molecular Formula]
C8H10O2 | [MDL Number]
MFCD00002378 | [Molecular Weight]
138.16 | [MOL File]
93-51-6.mol |
Chemical Properties | Back Directory | [Appearance]
Clear colorless to slightly yellow liquid | [Melting point ]
5 °C (lit.) | [Boiling point ]
221-222 °C (lit.) | [density ]
1.092 g/mL at 25 °C(lit.)
| [FEMA ]
2671 | [refractive index ]
n20/D 1.537(lit.)
| [Fp ]
211 °F
| [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
Chloroform (Sparingly), Methanol (Slightly) | [form ]
Liquid | [pka]
10.27±0.18(Predicted) | [color ]
colorless to light yellow | [Specific Gravity]
1.091.092 | [Odor]
at 10.00 % in dipropylene glycol. spicy clove vanilla phenolic medicinal leathery woody smoky burnt | [Odor Type]
spicy | [Water Solubility ]
Slightly soluble in water. | [JECFA Number]
715 | [Merck ]
14,2571 | [BRN ]
1862340 | [Dielectric constant]
11.0 | [LogP]
1.65 | [CAS DataBase Reference]
93-51-6(CAS DataBase Reference) | [NIST Chemistry Reference]
Phenol, 2-methoxy-4-methyl-(93-51-6) | [EPA Substance Registry System]
93-51-6(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . S24/25:Avoid contact with skin and eyes . | [RIDADR ]
2810 | [WGK Germany ]
3
| [RTECS ]
GP1755000
| [F ]
10 | [TSCA ]
Yes | [HazardClass ]
6.1(a) | [PackingGroup ]
II | [HS Code ]
29095090 |
Hazard Information | Back Directory | [Description]
2-Methoxy-4-methylphenol has a characteristic aromatic odor
(sweet, spicy, slightly vanilla-like) and a somewhat bitter taste
(vanilla-like). May be prepared by methylation of homopyrocatechin using dimethyl sulfate and alkali; also by hydrogenation of
vanillin. | [Chemical Properties]
2-Methoxy-4-methylphenol has a characteristic aromatic odor (sweet, spicy, slightly vanilla-like) and a somewhat bitter
taste (vanilla-like). | [Chemical Properties]
Clear colorless to slightly yellow liquid | [Occurrence]
Occurs in beechwood tar; also identified in the essential oils of ylang-ylang, jasmine and anise seeds; it is
one of the active constituents of creosote. Reported found in Gruyere cheese, smoked fish, cured pork, beer, rum, bourbon whiskey,
malt and Scotch whiskey, sherry, white and red wine, cocoa, coffee, tea, mushrooms, mango, pear brandy, malt, wort, dried bonito,
Bourbon vanilla, cuttlefish and green maté. | [Uses]
2-Methoxy-4-methylphenol is used for blending baking and smoked food flavors.
| [Uses]
2-Methoxy-4-methylphenol is used in preparation of renewable bis(cyanate) esters. | [Definition]
ChEBI: 2-Methoxy-4-methylphenol is a member of phenols and a member of methoxybenzenes. | [Preparation]
By methylation of homopyrocatechin using dimethyl sulfate and alkali; also by hydrogenation of vanillin. | [Aroma threshold values]
Detection: 90 ppb. Aroma characteristics at 1.0%: smoky, sweet, phenolic, vanilla, spicy clove with a floral
carnation nuance. | [Taste threshold values]
Taste characteristics at 1.0 to 1.25 ppm: sweet phenolic, spice, vanilla, medicinal, clove-like, smoky, guaia col-like with a woody, phenolic nuance. | [General Description]
2-Methoxy-4-methylphenol is the major component of black-ripe table olive aroma. It is the major anti-inflammatory compound in bamboo vinegar. Kinetics of reaction of 2-methoxy-4-methylphenol with chlorine atoms was studied. | [Biochem/physiol Actions]
Odor at 1.0% |
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