1,8-dimethyl naphthalene
naphthalene, 1,8-dimethyl-
Identification
| Name | 1,8-dimethyl naphthalene |
| IUPAC | 1,8-dimethylnaphthalene |
| CAS Number | 569-41-5 |
| EINECS | 209-314-4 |
| FDA UNII | 22P9FW1L76 |
| Molecular Formula | C12 H12 |
| Molecular Weight | 156.22764000 |
| MDL Number | MFCD00004040 |
| Nikkaji Number | J116.788J |
| Beilstein | 2039841 |
| XlogP3 | 4.30 (est) |
Regulatory
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) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| 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. |
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Potential Uses
Natural Occurrence
Synonyms
1,8-
dimethylnaphthalene
naphthalene, 1,8-dimethyl-
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.
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Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys.
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[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].
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Hamigerin A and a hamigerin D decomposition product.
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Volatile components of green walnut husks.
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NO(2)(+) nitration mechanism of aromatic compounds: electrophilic vs charge-transfer process
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Antimutagenic effects and possible mechanisms of action of vitamins and related compounds against genotoxic heterocyclic amines from cooked food.
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Arohynapenes A and B, new anticoccidial agents produced by Penicillium sp. Taxonomy, fermentation, and structure elucidation.
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Isoprenoid quinones of Campylobacter cryaerophila, C. cinaedi, C. fennelliae, C. hyointestinalis, C. pylori, and "C. upsaliensis".
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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.