4-methyl-2,6-dimethoxyphenol

2,6-dimethoxy-p-cresol

CAS: 6638-05-7 C9 H12 O3 MW: 168.19224000 phenolic phenolic

Identification

Name4-methyl-2,6-dimethoxyphenol
CAS Number6638-05-7
EINECS229-641-6
FDA UNIIFJJ5MYE75W
Molecular FormulaC9 H12 O3
Molecular Weight168.19224000
MDL NumberMFCD00017289
Nikkaji NumberJ27.322H

Regulatory

JECFA Food Flavoring722 4-methyl-2,6-dimethoxyphenol
DG SANTE Food Flavourings04.053 4-methyl-2,6-dimethoxyphenol
FEMA Number3704
FDANo longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF)6638-05-7 ; 4-METHYL-2,6-DIMETHOXYPHENOL

Physical Properties

Appearance yellow to orange solid (est)
Assay 97.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 37.00 to 42.00 °C. @ 760.00 mm Hg
Boiling Point 145.00 to 146.00 °C. @ 14.00 mm Hg
Vapor Pressure 0.005000 mmHg @ 25.00 °C. (est)
Flash Point > 230.00 °F. TCC ( > 110.00 °C. )
logP (o/w) 1.859 (est)
Soluble in alcohol
Insoluble in water

Organoleptic Properties

Odor Description
at 10.00 % in dipropylene glycol.
Phenolic, smokey, medicinal, woody, spicy, eugenol-like and rooty with a caramellic nuance
Taste Description at 10.00 ppm.

Safety Information

Preferred SDSView
European informationMost important hazard(s):
Oral/Parenteral Toxicityoral-rat LD50 [sex: M,F] 1700 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
Recommendation for 4-methyl-2,6-dimethoxyphenol usage levels up to0.1000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU)0.054 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA)0.04 (μg/capita/day)
Structure ClassI
baked goods-
beverages(nonalcoholic)-
beverages(alcoholic)-
breakfast cereal-
cheese-
chewing gum-
condiments / relishes-
confectionery froastings-
egg products-
fats / oils-
fish products-
frozen dairy-
fruit ices-
gelatins / puddings-
granulated sugar-
gravies-
hard candy-
imitation dairy-
instant coffee / tea-
jams / jellies-
meat products-
milk products-
nut products-
other grains-
poultry-
processed fruits-
processed vegetables-
reconstituted vegetables-
seasonings / flavors-
snack foods-
soft candy-
soups-
sugar substitutes-
sweet sauces-

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Potential Uses

FL bacon FL horseradish FL salmon smoked salmon FL smoke FR spice FR vanilla FR woody

Natural Occurrence

apple fruit PMC celery cheese gruyere cheese PMC cheese swiss chesse PMC cider PMC cocoa elderberry fruit juice fish lean fish PMC grape juice PMC honey PMC katsuobushi PMC orange fruit juice plum fruit pork PMC scallop PMC soybean strawberry wild strawberry fruit wine

Synonyms

p- cresol, 2,6-dimethoxy- 3,5- dimethoxy-4-hydroxytoluene 2,6- dimethoxy-4-methyl phenol 2,6- dimethoxy-4-methylphenol 2,6- dimethoxy-p-cresol 2,6- dimethoxy-para-cresol 4- hydroxy-3,5-dimethoxytoluene 4- methyl syringol 1- methyl-3,5-dimethoxy-4-hydroxybenzene 4- methylsyringol phenol, 2,6-dimethoxy-4-methyl- PubMed: Determination of the importance of in-mouth release of volatile phenol glycoconjugates to the flavor of smoke-tainted wines. PubMed: Characterisation of volatile compounds in a smoke flavouring from rice husk. PubMed: Ultraviolet spectroscopy of fundamental lignin subunits: guaiacol, 4-methylguaiacol, syringol, and 4-methylsyringol. PubMed: Determination of Eucalyptus spp lignin S/G ratio: a comparison between methods. PubMed: Measurement of urinary methoxyphenols and their use for biological monitoring of wood smoke exposure.