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1,8-dimethyl naphthalene
naphthalene, 1,8-dimethyl-

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Name:1,8-dimethylnaphthalene
CAS Number: 569-41-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:209-314-4
FDA UNII: 22P9FW1L76
Nikkaji Web:J116.788J
Beilstein Number:2039841
MDL:MFCD00004040
XlogP3:4.30 (est)
Molecular Weight:156.22764000
Formula:C12 H12
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
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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
Melting Point: 65.00 °C. @ 760.00 mm Hg
Boiling Point: 270.00 °C. @ 760.00 mm Hg
logP (o/w): 4.260
Soluble in:
 water, 12.94 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.
1,8-Dimethylnaphthalene
Santa Cruz Biotechnology
For experimental / research use only.
1,8-Dimethylnaphthalene
Sigma-Aldrich: Aldrich
For experimental / research use only.
1,8-Dimethylnaphthalene 95%
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 1,8-dimethyl naphthalene usage levels up to:
 not for fragrance use.
 
Recommendation for 1,8-dimethyl naphthalene flavor usage levels up to:
 not for flavor use.
 
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 :11287
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
1,8-dimethylnaphthalene
Chemidplus:0000569415
 
References:
 1,8-dimethylnaphthalene
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):11287
Pubchem (sid):134975955
 
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
KEGG (GenomeNet):C14703
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2902.90.9000
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
 wheat flour heated
Search Trop Picture
 
Synonyms:
1,8-dimethylnaphthalene
 naphthalene, 1,8-dimethyl-
 

Articles:

PubMed:Influence of the macroring size on the self-association thermodynamics of cyclodextrins with a double-linked naphthalene at the secondary face.
PubMed:A novel bisphosphonate inhibitor of squalene synthase combined with a statin or a nitrogenous bisphosphonate in vitro.
PubMed:Interaction of native alpha-cyclodextrin, beta-cyclodextrin and gamma-cyclodextrin and their hydroxypropyl derivatives with selected organic low molecular mass compounds at elevated and subambient temperature under RP-HPLC conditions.
PubMed:1,8-Dimethylnaphthalene-bridged diphosphine ligands: synthesis and structural comparison of their palladium complexes.
PubMed:Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys.
PubMed:[6,8-Dimethyl-2-piperidinomethyl-2,3-dihydrothiazolo[2,3-f]xanthine: a new inductor of the monooxygenase system inhibits experimental intrahepatic cholestasis in rats].
PubMed:Hamigerin A and a hamigerin D decomposition product.
PubMed:Volatile components of green walnut husks.
PubMed:NO(2)(+) nitration mechanism of aromatic compounds: electrophilic vs charge-transfer process
PubMed:Antimutagenic effects and possible mechanisms of action of vitamins and related compounds against genotoxic heterocyclic amines from cooked food.
PubMed:Arohynapenes A and B, new anticoccidial agents produced by Penicillium sp. Taxonomy, fermentation, and structure elucidation.
PubMed:Isoprenoid quinones of Campylobacter cryaerophila, C. cinaedi, C. fennelliae, C. hyointestinalis, C. pylori, and "C. upsaliensis".
PubMed:Isoprenoid quinone content and cellular fatty acid composition of Campylobacter species.
PubMed:Detection of menaquinone-6 and a novel methyl-substituted menaquinone-6 in Campylobacter jejuni and Campylobacter fetus subsp. fetus.
PubMed:[Spasm-activity caused by interaction of benzo- and naphtho-1.3-dioxole-carboxylic acids of mice (author's transl)].
PubMed:[Study of the initial reaction of enzymatic oxidation of 1,8-dimethylnaphthalene].
PubMed:Microbial hydrocarbon co-oxidation. I. Oxidation of mono- and dicyclic hydrocarbons by soil isolates of the genus Nocardia.
 
Notes:
None found
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