2-allyl phenol
2-(2-propenyl)phenol
 
Notes:
None found
  • BOC Sciences
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      Product(s):
      1745-81-9 2-Allylphenol 95%
       
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    • TCI AMERICA
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      Product(s):
      A0233 2-Allylphenol >97.0%(GC)
       
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CAS Number: 1745-81-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 217-119-0
FDA UNII: O04F145ZJZ
Nikkaji Web: J34.550D
Beilstein Number: 0742121
MDL: MFCD00002250
XlogP3: 2.70 (est)
Molecular Weight: 134.17790000
Formula: C9 H10 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.02100 to 1.02400 @  20.00 °C.
Pounds per Gallon - (est).: 8.506 to  8.531
Refractive Index: 1.54300 to 1.54700 @  20.00 °C.
Melting Point: -7.00 to  -5.00 °C. @ 760.00 mm Hg
Boiling Point: 219.00 to  221.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.078000 mmHg @ 25.00 °C. (est)
Flash Point: 190.00 °F. TCC ( 87.78 °C. )
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
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
2-Allylphenol 95%
EMD Millipore
For experimental / research use only.
2-Allylphenol
Santa Cruz Biotechnology
For experimental / research use only.
2-Allylphenol
Sigma-Aldrich: Aldrich
For experimental / research use only.
2-Allylphenol 98%
TCI AMERICA
For experimental / research use only.
2-Allylphenol >97.0%(GC)
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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.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
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.
 
Recommendation for 2-allyl phenol flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA GENetic TOXicology: Search
EPA Substance Registry Services (TSCA): 1745-81-9
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 15624
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 2923
WGK Germany: 1
 2-prop-2-enylphenol
Chemidplus: 0001745819
RTECS: SJ3850000 for cas# 1745-81-9
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References:
 2-prop-2-enylphenol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 1745-81-9
Pubchem (cid): 15624
Pubchem (sid): 134980535
Pherobase: View
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2907.19.5000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 guava fruit oil reunion @ 0.10%
Data  GC  Search Trop  Picture
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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
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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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