homovanillyl alcohol

benzeneethanol, 4-hydroxy-3-methoxy-

CAS: 2380-78-1 C9 H12 O3 MW: 168.19224000

Identification

Namehomovanillyl alcohol
IUPAC4-(2-hydroxyethyl)-2-methoxyphenol
CAS Number2380-78-1
EINECS219-175-1
FDA UNII9A7EE8MS6A
Molecular FormulaC9 H12 O3
Molecular Weight168.19224000
MDL NumberMFCD00002903
Nikkaji NumberJ172D
XlogP30.50 (est)

Regulatory

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

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch

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Potential Uses

None Found

Natural Occurrence

apis mellifera capensis

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 homo vanillin alcohol homo vanillylalcohol 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].