| Record Information |
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| Version | 1.0 |
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| Creation date | 2018-04-10 11:13:09 UTC |
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| Update date | 2018-04-27 10:29:22 UTC |
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| FoodComEx ID | PC001061 |
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| FoodDB Record | FDB015496 |
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| Chemical Information |
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| Name | Coniferyl alcohol |
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| Description | Coniferyl alcohol is an intermediate in biosynthesis of eugenol and of stilbene and coumarin. This colourless crystalline solid is a phytochemical, one of the monolignols. When copolymerized with related aromatic compounds, coniferyl alcohol forms lignin or lignans. |
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| CAS Number | 458-35-5 |
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| Structure | |
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| Synonyms | | Synonym | Source |
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| (e) 3-(4-Hydroxy-3-methoxyphenyl)-2-propen-1-ol | HMDB | | 3-(4-Hydroxy-3-methoxyphenyl)-2-propen-1-ol | db_source | | 3-(4-Hydroxy-3-methoxyphenyl)allyl alcohol | biospider | | 4-((1e)-3-Hydroxy-1-propenyl)-2-methoxyphenol | HMDB | | 4-(3-Hydroxy-1-propenyl)-2-methoxy-phenol | HMDB | | 4-(3-Hydroxy-1-propenyl)-2-methoxyphenol | ChEBI | | 4-(3-Hydroxy-1-propenyl)-2-methoxyphenol, 9CI | db_source | | 4-[(1E)-3-Hydroxy-1-propenyl]-2-methoxyphenol | biospider | | 4-[(1e)-3-Hydroxyprop-1-en-1-yl]-2-methoxyphenol | HMDB | | 4-Hydroxy-3-methoxycinnamic alcohol | biospider | | 4-Hydroxy-3-methoxycinnamyl alcohol | HMDB | | Coniferol | biospider | | Coniferyl alcohol | db_source | | Coniferyl-alcohol | HMDB | | Coniferylic alcohol | biospider | | e-Coniferyl alcohol | HMDB | | epsilon-Coniferyl alcohol | HMDB | | gamma-Hydroxyisoeugenol | HMDB | | Lubanol | db_source | | p-hydroxy-m-methoxycinnamyl alcohol | biospider | | trans-Coniferyl alcohol | biospider |
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| Chemical Formula | C10H12O3 |
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| IUPAC name | 4-[(1Z)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenol |
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| InChI Identifier | InChI=1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2- |
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| InChI Key | JMFRWRFFLBVWSI-IHWYPQMZSA-N |
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| Isomeric SMILES | [H]\C(CO)=C(/[H])C1=CC(OC)=C(O)C=C1 |
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| Average Molecular Weight | 180.2005 |
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| Monoisotopic Molecular Weight | 180.07864425 |
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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. |
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| Kingdom | Organic compounds |
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| Super Class | Benzenoids |
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| Class | Phenols |
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| Sub Class | Methoxyphenols |
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| Direct Parent | Methoxyphenols |
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| Alternative Parents | |
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| Substituents | - Cinnamyl alcohol
- Methoxyphenol
- Phenoxy compound
- Anisole
- Methoxybenzene
- Styrene
- Phenol ether
- 1-hydroxy-2-unsubstituted benzenoid
- Alkyl aryl ether
- Monocyclic benzene moiety
- Ether
- Primary alcohol
- Alcohol
- Hydrocarbon derivative
- Organic oxygen compound
- Organooxygen compound
- Aromatic homomonocyclic compound
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| Molecular Framework | Aromatic homomonocyclic compounds |
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| External Descriptors | |
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| Physico-Chemical Properties - Experimental |
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| Property | Value | Reference |
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| Experimental logP | Not Available | |
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| Experimental Water Solubility | Not Available | |
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| Melting Point | Mp 78° (74-75°) | DFC |
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| Foods of Origin |
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| Food | Content Range | Average | Reference |
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| Food | | | Reference |
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| Production Data |
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| Production Method | commercial |
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| Production Method Reference | Not Available |
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| Production Method Reference File | Not Available |
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| Quantity Available | 1 to 5 mg |
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| Delivery Time | 2 weeks |
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| Storage Form | powder |
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| Storage Conditions | 4°C |
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| Stability | Not Available |
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| Purity | >95% |
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| Spectra |
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| Spectral Data Upon Request | Not Available |
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| Provider Information |
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| Contact Name | Contact Institution | Contact Email |
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| Claudine Manach | INRAE, Human Nutrition, Research Center Clermont-Auvergne-Rhône-Alpes, Clermont-Ferrand, FR, F-63122 | claudine.manach@inra.fr |
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| Commercial Vendors |
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| AKSci | 6307AB |
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