oakmoss phenol
orcinyl (Givaudan)
 
Notes:
None found
  • BOC Sciences
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      Product(s):
      3209-13-0 3-Methoxy-5-methylphenol 95%
       
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      Product(s):
      08-64900 3-HYDROXY-5-METHOXYTOLUENE
       
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      Product(s):
      M0895 3-Methoxy-5-methylphenol >98.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 3209-13-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 221-716-1
FDA UNII: UYA9W3L847
Nikkaji Web: J208.735I
MDL: MFCD00059261
XlogP3-AA: 1.90 (est)
Molecular Weight: 138.16610000
Formula: C8 H10 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: fragrance agents
 
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
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: white to tan powder (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 254.00 to  255.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.010000 mmHg @ 25.00 °C. (est)
Flash Point: 275.00 °F. TCC ( 135.00 °C. )
logP (o/w): 2.385 (est)
Soluble in:
 alcohol
 water, 4810 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: mossy
 
Odor Strength: medium ,
recommend smelling in a 10.00 % solution or less
 
Substantivity: 400 hour(s) at 20.00 %
 
 oakmoss  fruity  marine  woody  hay  
Odor Description:
at 10.00 % in dipropylene glycol. 
oakmoss fruity iodine woody hay
Luebke, William tgsc, (1985)
 
Odor and/or flavor descriptions from others (if found).
 
Givaudan
Orcinyl 3
Odor Description: Oakmoss, Sweet, Phenolic
Due to its typical oakmoss note, Orcinyl 3 reinforces the character of this absolute in all compounds. It can be substituted for oakmoss when used together with Evernyl. It blends very well with chypre, leather,woody and tobacco accords.
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
BOC Sciences
For experimental / research use only.
3-Methoxy-5-methylphenol 95%
Frinton Laboratories
For experimental / research use only.
3-Methoxy-5-methylphenol
Givaudan
Orcinyl 3
Odor: Oakmoss, Sweet, Phenolic
Use: Due to its typical oakmoss note, Orcinyl 3 reinforces the character of this absolute in all compounds. It can be substituted for oakmoss when used together with Evernyl. It blends very well with chypre, leather,woody and tobacco accords.
Penta International
3-HYDROXY-5-METHOXYTOLUENE
Santa Cruz Biotechnology
For experimental / research use only.
3-Methoxy-5-methylphenol
Sigma-Aldrich: Aldrich
For experimental / research use only.
3-Methoxy-5-methylphenol 97%
TCI AMERICA
For experimental / research use only.
3-Methoxy-5-methylphenol >98.0%(GC)
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
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 37/39 - Wear suitable gloves and eye/face protection.
 
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:
oral-rat LD50  1500 mg/kg
Due to its typical oakmoss note, Orcinyl 3 reinforces the character of this absolute in all compounds. It can be substituted for oakmoss when used together with Evernyl. It blends very well with chypre, leather,woody and tobacco accords.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for oakmoss phenol usage levels up to:
  1.0000 % in the fragrance concentrate.
 
Recommendation for oakmoss 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 Substance Registry Services (TSCA): 3209-13-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 76674
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 3-methoxy-5-methylphenol
Chemidplus: 0003209130
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References:
 3-methoxy-5-methylphenol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 3209-13-0
Pubchem (cid): 76674
Pubchem (sid): 135035388
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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
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2909.49.1500
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
aldehydic
 citrus carbaldehydeFR
2-methyl undecanal (aldehyde C-12 mna)FL/FR
animal
isobutyl quinolineFR
citrus
 dimyrcetol (IFF)FR
 marine decadienalFR
 marine nitrileFR
 orange nitrileFR
 tetrahydromyrcenyl acetateFR
floral
 boronia butenalFR
 cassis specialtyFR
 genet concreteFR
 muguet carboxaldehydeFR
fruity
 rhubarb pyranFR
green
(E)-2-hexen-1-yl phenyl acetateFL/FR
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
hay
 hay absoluteFR
 tobacco leaf absoluteFL/FR
herbal
 acorn acetateFR
 apium graveolens seed oilFL/FR
 apium graveolens seed oil indiaFL/FR
 celery seed oil CO2 extractFL/FR
 celery seed oil replacerFR
 celery specialtyFR
 floral nitrileFR
curled parsley leaf oilFL/FR
 saffron indenoneFL/FR
 yerba mate absoluteFL/FR
leathery
4-tert-butyl phenolCS
marine
green algae absoluteFL/FR
 marine hexaneFR
 ocean carboxaldehydeFR
mossy
 longiborneol 
 oakmoss absoluteFL/FR
 oakmoss concreteFR
 sea resorcylateFR
 veramoss (IFF)FR
nutty
3-acetyl pyridineFL/FR
smoky
 pyroligneous acidsFL/FR
spicy
 allspice berry oilFL/FR
 allspice leaf oilFL/FR
beta-caryophyllene alcoholFL/FR
 caryophyllene alcoholFL/FR
 clove bud absoluteFL/FR
 clove bud oil CO2 extractFL/FR
4-ethyl guaiacolFL/FR
 eugenolFL/FR
 levisticum officinale root oilFL/FR
terpenic
D-(+)-beta-pineneFL/FR
tobacco
3-ethyl pyridineFL/FR
waxy
 decanal diethyl acetalFL/FR
woody
delta-methyl iononeFL/FR
beta-thujaplicinFR
 
For Flavor
 
No flavor group found for these
green algae absoluteFL/FR
beta-caryophyllene alcoholFL/FR
 caryophyllene alcoholFL/FR
(E)-2-hexen-1-yl phenyl acetateFL/FR
 longiborneol 
delta-methyl iononeFL/FR
D-(+)-beta-pineneFL/FR
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
caramellic
3-ethyl pyridineFL/FR
grassy
 tobacco leaf absoluteFL/FR
green
 oakmoss absoluteFL/FR
herbal
 apium graveolens seed oilFL/FR
 apium graveolens seed oil indiaFL/FR
 celery seed oil CO2 extractFL/FR
curled parsley leaf oilFL/FR
 saffron indenoneFL/FR
 yerba mate absoluteFL/FR
nutty
3-acetyl pyridineFL/FR
smoky
 pyroligneous acidsFL/FR
spicy
 allspice berry oilFL/FR
 allspice leaf oilFL/FR
 clove bud absoluteFL/FR
 clove bud oil CO2 extractFL/FR
 eugenolFL/FR
 levisticum officinale root oilFL/FR
waxy
 decanal diethyl acetalFL/FR
2-methyl undecanal (aldehyde C-12 mna)FL/FR
woody
4-ethyl guaiacolFL/FR
 
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Potential Uses:
 amberFR
 hay new mown hayFR
 mossFR
 ocean seaFR
 orientalFR
 topnotes 
 woodyFR
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
3-hydroxy-5-methoxytoluene
5-methoxy-3-methylphenol
3-methoxy-5-methyl phenol
3-methoxy-5-methylphenol
5-methoxy-m-cresol
5-methoxy-meta-cresol
 oak moss phenol
 oakmoss phenol
 orcinol monomethyl ether
 orcinyl (Givaudan)
 orcinyl 3 (Givaudan)
 orcinyl-3 (Givaudan)
 phenol, 3-methoxy-5-methyl-
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Articles:
PubMed: Effects of oakmoss and its components on biofilm formation of Legionella pneumophila.
PubMed: Chemometric profile of root extracts of Rhodiola imbricata Edgew. with hyphenated gas chromatography mass spectrometric technique.
PubMed: The antibacterial activity of compounds isolated from oakmoss against Legionella pneumophila and other Legionella spp.
PubMed: The antibacterial activity of fragrance ingredients against Legionella pneumophila.
PubMed: Identification of atranorin and related potential allergens in oakmoss absolute by high-performance liquid chromatography-tandem mass spectrometry using negative ion atmospheric pressure chemical ionization.
PubMed: Nematocidal principles in "oakmoss absolute" and nematocidal activity of 2,4-dihydroxybenzoates.
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