Category: natural substances and extractives
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | colorless to pale yellow clear liquid (est) |
Assay: | 95.00 to 100.00 %
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Food Chemicals Codex Listed: | No |
Specific Gravity: | 1.02100 to 1.02400 @ 20.00 °C.
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Pounds per Gallon - (est).: | 8.506 to 8.531
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Refractive Index: | 1.54300 to 1.54700 @ 20.00 °C.
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Melting Point: | -7.00 to -5.00 °C. @ 760.00 mm Hg
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Boiling Point: | 219.00 to 221.00 °C. @ 760.00 mm Hg
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Vapor Pressure: | 0.078000 mmHg @ 25.00 °C. (est) |
Flash Point: | 190.00 °F. TCC ( 87.78 °C. )
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logP (o/w): | 2.441 (est) |
Soluble in: |
| alcohol | | water, 1110 mg/L @ 25 °C (est) |
Insoluble in: |
| water |
Similar Items: note |
4-allyl phenol |
Organoleptic Properties:
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Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
Safety Information:
Preferred SDS: View |
European information : |
Most important hazard(s): | C - Corrosive. |
R 21/22 - Harmful in contact with skin and if swallowed. R 34 - Causes burns. S 01/02 - Keep locked up and out of the reach of children. S 20/21 - When using do not eat, drink or smoke. S 24/25 - Avoid contact with skin and eyes. S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S 36/37/39 - Wear suitable clothing, gloves and eye/face protection. S 45 - In case of accident or if you feel unwell seek medical advice immediately.
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Hazards identification |
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Classification of the substance or mixture |
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
None found. |
GHS Label elements, including precautionary statements |
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Pictogram | |
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Hazard statement(s) |
None found. |
Precautionary statement(s) |
None found. |
Oral/Parenteral Toxicity: |
Not determined
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Dermal Toxicity: |
Not determined
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Inhalation Toxicity: |
Not determined
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Safety in Use Information:
Category: | natural substances and extractives |
IFRA Purity Specification: | < 0.1% free allyl alcohol |
Recommendation for 2-allyl phenol usage levels up to: | | not for fragrance use.
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Recommendation for 2-allyl phenol flavor usage levels up to: |
| not for flavor use.
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Safety References:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
o- | allyl phenol | ortho- | allyl phenol | 2- | allyl-phenol | 2- | allylphenol | o- | allylphenol | ortho- | allylphenol | | phenol, (2-propenyl)- | | phenol, 2- (2-propenyl)- | | phenol, 2-(2-propen-1-yl)- | | phenol, 2-(2-propenyl)- | | phenol, 2-allyl- | | phenol, o-allyl- | 2-( | prop-2-en-1-yl)phenol | 2- | prop-2-en-1-ylphenol | 2- | prop-2-enyl phenol | 2- | prop-2-enylphenol | 2- | propenyl-2-phenol | 2-(2- | propenyl) phenol | (2- | propenyl)phenol | 2-(2- | propenyl)phenol |
Articles:
PubMed: | 2-Allylphenol Reduces IL-1? and TNF-à, Promoting Antinociception through Adenosinergic, Anti-Inflammatory, and Antioxidant Mechanisms |
PubMed: | Metabolism of fungicide 2-allylphenol in Rhizoctonia cerealis |
PubMed: | Synthesis and antifungal activity of 2-allylphenol derivatives against fungal plant pathogens |
PubMed: | Synthesis and In Vitro Growth Inhibition of 2-Allylphenol Derivatives Against Phythopthora cinnamomi Rands |
PubMed: | Inhibitory effect of bionic fungicide 2-allylphenol on Botrytis cinerea (Pers. ex Fr.) in vitro |
PubMed: | Laboratory Evaluation of Natural and Synthetic Aromatic Compounds as Potential Attractants for Male Mediterranean fruit Fly, Ceratitis capitata |
PubMed: | Residue analysis and dissipation of a new fungicide 2-allylphenol in tomato |
PubMed: | Synthesis of 2,3-Dihydrobenzofurans via the Palladium Catalyzed Carboalkoxylation of 2-Allylphenols |
PubMed: | Spectroscopic and theoretical studies on intramolecular OH-pi hydrogen bonding in 4-substituted 2-allylphenols |
PubMed: | Coumaric acid analogues inhibit growth and melanin biosynthesis in Cryptococcus neoformans and potentialize amphotericin B antifungal activity |
PubMed: | Isolation of an unusual metabolite 2-allyloxyphenol from a marine actinobacterium, its biological activities and applications |
PubMed: | Pd-Catalyzed regioselective hydroesterification of 2-allylphenols to seven-membered lactones without external CO gas |
PubMed: | Fabrication of a Novel, Cost-Effective Double-Sided Indium Tin Oxide-Based Nanoribbon Electrode and Its Application of Acute Toxicity Detection in Water |
PubMed: | Inhibition of rat, mouse, and human glutathione S-transferase by eugenol and its oxidation products |
PubMed: | Whole ceramic-like microreactors from inorganic polymers for high temperature or/and high pressure chemical syntheses |
PubMed: | Acid-promoted direct electrophilic trifluoromethylthiolation of phenols |
PubMed: | Chloroperoxidase, a janus enzyme |
PubMed: | Reactions of Allyl Phenyl Ether in High-Temperature Water with Conventional and Microwave Heating |
PubMed: | Antioxidant Activity of Magnolol and Honokiol: Kinetic and Mechanistic Investigations of Their Reaction with Peroxyl Radicals |
PubMed: | Intramolecular hydroalkoxylation of non-activated C=C bonds catalysed by zeolites: an experimental and theoretical study |
PubMed: | Proton, electron and energy transfer processes in excited phenol-olefin dyads |
PubMed: | Picoamperometric detection of glucose at ultrasmall platinum-based biosensors: preparation and characterization |
PubMed: | Male sex pheromonal components derived from methyl eugenol in the hemolymph of the fruit fly Bactrocera papayae |
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