EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

homovanillyl alcohol
benzeneethanol, 4-hydroxy-3-methoxy-

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Name: 4-(2-hydroxyethyl)-2-methoxyphenol
CAS Number: 2380-78-1Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:219-175-1
FDA UNII: 9A7EE8MS6A
Nikkaji Web:J172D
MDL:MFCD00002903
XlogP3:0.50 (est)
Molecular Weight:168.19224000
Formula:C9 H12 O3
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
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Perfumer and Flavorist:Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 98.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 40.00 to 42.00 °C. @ 760.00 mm Hg
Boiling Point: 316.00 to 317.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.000169 mmHg @ 25.00 °C. (est)
Flash Point:> 230.00 °F. TCC ( > 113.00 °C. )
logP (o/w): 0.470
Soluble in:
 alcohol
 water, 8.053e+004 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Homovanillyl alcohol >95%
Odor: characteristic
Use: Homovanillyl alcohol is a natural phenolic compound found in strawberries, grapes and olive oil. Homovanillyl alcohol shows high scavenging activities and can inhibit homocysteine-induced endothelial cell adhesion.
Santa Cruz Biotechnology
For experimental / research use only.
homoVanillyl Alcohol 99%
Sigma-Aldrich: Aldrich
For experimental / research use only.
homoVanillyl alcohol 99%
sds
 
Safety Information:
Preferred SDS: View
 
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
 
Safety in Use Information:
Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :16928
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
4-(2-hydroxyethyl)-2-methoxyphenol
Chemidplus:0002380781
 
References:
  4-(2-hydroxyethyl)-2-methoxyphenol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):16928
Pubchem (sid):134981594
 
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
HMDB (The Human Metabolome Database):HMDB38925
FooDB:FDB018391
YMDB (Yeast Metabolome Database):YMDB01712
Export Tariff Code:2909.50.4500
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 apis mellifera capensis
Search Trop Picture
 
Synonyms:
 benzeneethanol, 4-hydroxy-3-methoxy-
4-hydroxy-3-methoxyphenethanol
4-hydroxy-3-methoxyphenethyl alcohol
2-(4-hydroxy-3-methoxyphenyl)ethanol
4-hydroxy-3-methoxyphenylethyl alcohol
4-(2-hydroxyethyl) guaiacol
4-(2-hydroxyethyl)-2-methoxyphenol
4-(2-hydroxyethyl)-2-methoxyphenol
4-(2-hydroxyethyl)guaiacol
3-methoxy-4-hydroxyphenylethanol
homovanillin alcohol
homovanillylalcohol
 

Articles:

PubMed:Enzymatic surface erosion of high tensile strength polycarbonates based on natural phenols.
PubMed:Simultaneous determination of phenylethanoid glycosides and aglycones by capillary zone electrophoresis with running buffer modifier.
PubMed:Dose-dependent metabolic disposition of hydroxytyrosol and formation of mercapturates in rats.
PubMed:Protective activity of hydroxytyrosol metabolites on erythrocyte oxidative-induced hemolysis.
PubMed:Picea mariana bark: a new source of trans-resveratrol and other bioactive polyphenols.
PubMed:Phenylpropanoid glycoside analogues: enzymatic synthesis, antioxidant activity and theoretical study of their free radical scavenger mechanism.
PubMed:Antioxidant activities of hydroxytyrosol main metabolites do not contribute to beneficial health effects after olive oil ingestion.
PubMed:Simultaneous quantification of oleuropein and its metabolites in rat plasma by liquid chromatography electrospray ionization tandem mass spectrometry.
PubMed:Dopamine receptor activation by honey bee queen pheromone.
PubMed:Olive oil phenolic compounds inhibit homocysteine-induced endothelial cell adhesion regardless of their different antioxidant activity.
PubMed:Detection and quantification of phenolic compounds in olive oil by high resolution 1H nuclear magnetic resonance spectroscopy.
PubMed:Convenient synthesis of hydroxytyrosol and its lipophilic derivatives from tyrosol or homovanillyl alcohol.
PubMed:Inhibition of platelet aggregation by olive oil phenols via cAMP-phosphodiesterase.
PubMed:Queen pheromone modulates brain dopamine function in worker honey bees.
PubMed:Minor components of olive oil modulate proatherogenic adhesion molecules involved in endothelial activation.
PubMed:Daily consumption of a high-phenol extra-virgin olive oil reduces oxidative DNA damage in postmenopausal women.
PubMed:Hydroxytyrosol excretion differs between rats and humans and depends on the vehicle of administration.
PubMed:Olive oils rich in natural catecholic phenols decrease isoprostane excretion in humans.
PubMed:The effect of low-level deoxynivalenol on neurotransmitter levels measured in pig cerebral spinal fluid.
PubMed:Preparation of an optimum mobile phase for the simultaneous determination of neurochemicals in mouse brain tissues by high-performance liquid chromatography with electrochemical detection.
PubMed:Human class I alcohol dehydrogenases catalyze the interconversion of alcohols and aldehydes in the metabolism of dopamine.
PubMed:[Assay of urinary homovanillic acid by gas phase chromatography with a capillary tube].
 
Notes:
metabolite of serotonin and norepinephrine. Isol. from various plant spp. Constit. of mandibular secretion of honeybees [CCD]
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