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

walrycin A
4-methoxy-1-naphthol

Supplier Sponsors

Name:4-methoxynaphthalen-1-ol
CAS Number: 84-85-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:201-566-3
FDA UNII: Search
Nikkaji Web:J40.492F
Beilstein Number:1818465
MDL:MFCD00003976
XlogP3:3.30 (est)
Molecular Weight:174.19910000
Formula:C11 H10 O2
NMR Predictor:Predict (works with chrome, Edge 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
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 962.8 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.
4-Methoxy-1-naphthol
Santa Cruz Biotechnology
For experimental / research use only.
4-Methoxy-1-naphthol ≥98%
Sigma-Aldrich: Aldrich
For experimental / research use only.
4-Methoxy-1-naphthol ≥97%
sds
TCI AMERICA
For experimental / research use only.
4-Methoxy-1-naphthol >98.0%(GC)
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:
natural substances and extractives
Recommendation for walrycin A usage levels up to:
 not for fragrance use.
 
Recommendation for walrycin A flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):84-85-5
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :66542
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
4-methoxynaphthalen-1-ol
Chemidplus:0000084855
 
References:
 4-methoxynaphthalen-1-ol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):66542
Pubchem (cas):84-85-5
 
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):HMDB32727
FooDB:FDB010688
Export Tariff Code:2909.50.5000
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 asperula odorata root
Search Trop Picture
 
Synonyms:
1-hydroxy-4-methoxynaphthalene
4-methoxy-1-naphthol
4-methoxy-alpha.naphthol
4-methoxynaphthalen-1-ol
1-naphthalenol, 4-methoxy-
 

Articles:

PubMed:The first structural and spectroscopic characterisation of a ring-opened form of a 2H-naphtho[1,2-b]pyran: a novel photomerocyanine.
PubMed:[Identification and secondary metabolites of endophytic fungal strain PR35 from Paeonia delavayi].
PubMed:The novel antibacterial compound walrycin A induces human PXR transcriptional activity.
PubMed:Aromatic C-H bond hydroxylation by P450 peroxygenases: a facile colorimetric assay for monooxygenation activities of enzymes based on Russig's blue formation.
PubMed:Novel antibacterial compounds specifically targeting the essential WalR response regulator.
PubMed:4-Methoxy-1-naphthol: chains formed by O-H...O hydrogen bonds and pi-pi stacking interactions.
PubMed:Synthesis and identification of 3-(4-hydroxy-1-naphthoxy)lactic acid as a metabolite of propranolol in the rat, in man, and in the rat liver 9000 g supernatant fraction.
PubMed:Serum alpha-fetoprotein subfractions in pregnant women identified by the modified method of lectin affinity crossed-line immunoelectrophoresis.
 
Notes:
Constit. of the roots of Asperula odorata (sweet woodruff)
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