diisoeugenol

1H-inden-5-ol, 1-ethyl-2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2-methyl-

CAS: 522-09-8 C20 H24 O4 MW: 328.40808000

Identification

Namediisoeugenol
IUPAC1-ethyl-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2-methyl-2,3-dihydro-1H-inden-5-ol
CAS Number522-09-8
FDA UNIISearch
Molecular FormulaC20 H24 O4
Molecular Weight328.40808000
Nikkaji NumberJ443.998H

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 476.56 °C. @ 760.00 mm Hg (est)
Flash Point 468.00 °F. TCC ( 242.00 °C. ) (est)
logP (o/w) 4.456 (est)
Soluble in water, 0.9835 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

Categoryinformation only not used for fragrances or flavors
Recommendation for diisoeugenol usage levels up tonot for fragrance use.
Recommendation for diisoeugenol flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

1- ethyl-2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2-methyl-1H-inden-5-ol 1H- inden-5-ol, 1-ethyl-2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2-methyl- PubMed: Scavenger Activity Evaluation of the Clove Bud Essential Oil (Eugenia caryophyllus) and Eugenol Derivatives Employing ABTS Decolorization. PubMed: Induction of early apoptosis and ROS-generation activity in human gingival fibroblasts (HGF) and human submandibular gland carcinoma (HSG) cells treated with curcumin. PubMed: Induction of cytotoxicity and apoptosis and inhibition of cyclooxygenase-2 gene expression, by curcumin and its analog, alpha-diisoeugenol. PubMed: Dehydrodiisoeugenol, an isoeugenol dimer, inhibits lipopolysaccharide-stimulated nuclear factor kappa B activation and cyclooxygenase-2 expression in macrophages. PubMed: Antioxidant properties of demethyldiisoeugenol. PubMed: Inhibition of platelet thromboxane formation and phosphoinositides breakdown by diisoeugenol. PubMed: The constituents of natural phenolic resins; the structure of diisoeugenol.