36115-41-0

Basic information

• Product Name: 4-epoxyisoeugenol
• Synonyms: 4-epoxyisoeugenol;Oxirane, [[2-methoxy-4-(1-propenyl)phenoxy]methyl]-
• CAS NO: 36115-41-0
• Molecular Formula: C₁₃H₁₆O₃
• Molecular Weight: 220.26
• Mol File: 36115-41-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 59-60 °C(Solv: ethyl acetate (141-78-6); ligroine (8032-32-4))
• Boiling Point: 346.0±22.0 °C(Predicted)
• Appearance: /
• Density: 1.108±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-epoxyisoeugenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-epoxyisoeugenol(36115-41-0)
• EPA Substance Registry System: 4-epoxyisoeugenol(36115-41-0)

Safety Data

• Hazardous Substances Data: 36115-41-0(Hazardous Substances Data)

Usage

Description

4-epoxyisoeugenol is a naturally occurring chemical compound found in various plants, such as Myristica fragrans and Eugenia caryophyllata. It is a derivative of isoeugenol and is known for its aromatic and spicy scent.
Used in Food Industry:
4-epoxyisoeugenol is used as a flavoring agent for its aromatic and spicy scent, enhancing the taste and aroma of various food products.
Used in Cosmetic Industry:
4-epoxyisoeugenol is used as a fragrance ingredient in perfumes, soaps, and other personal care products, providing a pleasant and spicy scent.
Used in Pharmaceutical Industry:
4-epoxyisoeugenol is used as a potential medicinal compound for its antioxidant and anti-inflammatory effects, offering therapeutic benefits in various health applications.

Upstream product

• 97-54-1 2-methoxy-4-propenylphenol 
• 106-89-8 epichlorohydrin 

Downstream Products

• 815578-89-3 1-((4-chlorphenyl-1-1piperazinyl)-2-propanol-3-oxy)-(2-methoxy-4-propylenyl)-benzene 
• 36227-46-0 1-[(4-prop-1-enyl-2-methoxy)phenoxy]-3-(isopropylamino)propan-2-ol 

Relevant articles and documents

Diglycidylether of iso-eugenol: A suitable lignin-derived synthon for epoxy thermoset applications

A novel lignin-based synthon, diglycidylether of iso-eugenol (DGE-isoEu) is used as a prepolymer for the preparation of thermosetting resins. DGE-isoEu is synthesized in a two-step procedure with a satisfactory yield from bio-based iso-eugenol (isoEu, 2-m

A new aspect of view in synthesizing new type β-adrenoceptor blockers with ancillary antioxidant activities

A series of vanilloid-type β-adrenoceptor blockers derived from traditional Chinese herbal medicines were synthesized and tested for their antioxidant and adrenoceptor antagonistic activities. They all possessed significant β-adrenoceptor blocking activities under in vitro experiments and radioligand binding assays. In addition, some compounds were further examined in in vito tests and produced antagonist effects matching that of propranolol and labetalol by measurements of antagonism toward (-)isoproterenol-induced tachycardia and (-)phenylephrine-induced pressor responses in anesthetized rats. Furthermore, all of the compounds had antioxidant effects inherited from their original structures. In conclusion, compound 11 had the most potent β-adrenoceptors blocking activity, 12 and 13 possessed high cardioselectivity, whereas 14, 15 and 16 possessed additional α-adrenoceptor blocking activity and 15 is the most effective antioxidant of all. the antioxidant activity may be due to their @α and β unsaturated side chain at position 1 and ortho-substituted methoxy moiety on 4-phenoxyethylamine. Copyright