2-methoxy-4-vinylphenol is a member of the class of phenols that is guaiacol in which the hydrogen para- to the hydroxy group is replaced by a vinyl group.
Definition
2-methoxy-4-vinylphenol is a member of the class of phenols that is guaiacol in which the hydrogen para- to the hydroxy group is replaced by a vinyl group. It has a role as a pheromone, a flavouring agent and a plant metabolite.
Source: PubChem
US FDA substance register · UNII DA069CTH0O · registered name 2-METHOXY-4-VINYLPHENOL · single chemical substance
Cosmetic roles
More data — names, identifiers, properties, test records, literature
Names & identifiers
- CAS No.chemical registry number
- 7786-61-0
- EC No.EU chemical inventory number
- 232-101-2
- DTXSIDUS EPA chemical ID
- DTXSID7052529
- DTXCIDUS EPA compound ID
- DTXCID8031102
- IUPAC
- 4-Ethenyl-2-methoxyphenol
- Molecular formula
- C9H10O2
- Molecular weight
- 150.177 g/mol
What products actually use it for
What the 5 products reported to the US EPA with this ingredient use it for. Products outside cosmetics are included, so the top few rows are its main uses.
- Fragrance3
- Flavouring and nutrient2
Source: US EPA CompTox dashboard
Irritation and sensitisation studies
1 skin studies and 0 eye studies are on record.
The study conclusions largely agree (100%). These tests are on the raw material itself; irritation at the amount in a finished product is a different question.
See all 1 studies
- SkinIrr2
Skin Irritation · QSAR Predicted
Source: US EPA CompTox dashboard
Related literature
- High cell‐density cultivation of phenolic acid decarboxylase‐expressing Escherichia coli and 4‐vinylguaiacol bioproduction from ferulic acid by whole‐cell catalysis · 2018
- Direct Affinity-Immobilized Phenolic Acid Decarboxylase by a Linker Peptide on Zeolite for Efficient Bioconversion of Ferulic Acid into 4-Vinylguaiacol · 2020
- Bioproduction of High-Concentration 4-Vinylguaiacol Using Whole-Cell Catalysis Harboring an Organic Solvent-Tolerant Phenolic Acid Decarboxylase From Bacillus atrophaeus · 2019
Linked databases 14
- Australian Industrial Chemicals Inventory (AICIS)
- ChEBI
- ChEMBL
- EU CosIng ingredient list 2
- NIST Chemistry WebBook
- PubChem
- Tlooto literature search 2 3
- UniChem cross-reference IDs
- US EPA CompTox dashboard 2
- US EPA DSSTox chemical database
- US FDA substance registration (GSRS)
- US FDA Unique Ingredient Identifier (UNII)
- Wikidata
- Wikipedia · English · Japanese