methyl isoferulate

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2-propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, methyl ester, (2E)-

CAS: 16980-82-8 C11 H12 O4 MW: 208.21344000
All Ingredients Aromatic Ingredients CAS Numbers Found in Nature M.W Index

Identification

Namemethyl isoferulate
IUPACmethyl (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate
CAS Number16980-82-8
FDA UNIISearch
Molecular FormulaC11 H12 O4
Molecular Weight208.21344000
Nikkaji NumberJ1.677.512F
XlogP31.80 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 369.00 to 370.00 °C. @ 760.00 mm Hg (est)
Flash Point 293.00 °F. TCC ( 145.10 °C. ) (est)
logP (o/w) 2.034 (est)
Soluble in water, 1398 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
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

Categorynatural substances and extractives
Recommendation for methyl isoferulate usage levels up tonot for fragrance use.
Recommendation for methyl isoferulate flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

cinnamic acid, 3-hydroxy-4-methoxy-, methyl ester (E)-3-(3- hydroxy-4-methoxy-phenyl)-acrylic acid methyl ester 3- hydroxy-4-methoxycinnamic acid methyl ester methyl (2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate methyl (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate methyl 3-(3-hydroxy-4-methoxyphenyl)acrylate 2- propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, methyl ester, (2E)- PubMed: Potent inhibitor design against H1N1 swine influenza: structure-based and molecular dynamics analysis for M2 inhibitors from traditional Chinese medicine database. PubMed: Propolis allergy (IV). Studies with further sensitizers from propolis and constituents common to propolis, poplar buds and balsam of Peru. PubMed: Methyl cinnamate derivatives enhance UV-induced mutagenesis due to the inhibition of DNA excision repair in Escherichia coli B/r.