(Z+E)-decahydronaphthalene
(Z+E)-decahydronaphthalene
Identification
| Name | (Z+E)-decahydronaphthalene |
| CAS Number | 91-17-8 |
| EINECS | 202-046-9 |
| FDA UNII | 88451Q4XYF |
| Molecular Formula | C10 H18 |
| Molecular Weight | 138.25346000 |
| MDL Number | MFCD00004130 |
| Nikkaji Number | J4.335D |
| Beilstein | 0878165 |
Regulatory
| FDA Mainterm (IAUFC) | 91-17-8 ; DECAHYDRONAPHTHALENE |
Physical Properties
| Appearance | colorless to pale yellow clear liquid (est) |
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Specific Gravity | 0.89600 @ 25.00 °C. |
| Melting Point | -43.00 °C. @ 760.00 mm Hg |
| Boiling Point | 155.50 °C. @ 760.00 mm Hg |
| Vapor Pressure | 0.735000 mmHg @ 25.00 °C. (est) |
| Vapor Density | 4.76 ( Air = 1 ) |
| Flash Point | 135.00 °F. TCC ( 57.22 °C. ) |
| logP (o/w) | 4.815 (est) |
| Soluble in | water, 0.889 mg/L @ 25 °C (exp) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | oral-rat LD50 4170 mg/kg |
| Dermal Toxicity | skin-rabbit LD50 5900 uL/kg |
| Inhalation Toxicity | inhalation-guinea pig LCLo 319 ppm/8H |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | pharmaceuticals / chemical synthisis |
| Recommendation for (Z+E)-decahydronaphthalene usage levels up to | not for fragrance use. |
| Recommendation for (Z+E)-decahydronaphthalene flavor usage levels up to | not for flavor use. |
Penta International Corporation
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Potential Uses
Natural Occurrence
Synonyms
de-kalin
decahydro-naphthalene
1,2,3,4,4a,5,6,7,8,8a-
decahydronaphthalene
decalin
dekalin
per
hydronaphthalene
naphthalene, decahydro-
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Superparamagnetic-oil-filled nanocapsules of a ternary graft copolymer.
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Investigation of the interactions involved in the formation of nanotubes from organogelators.
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The infinite possible growth ambients that support single-wall carbon nanotube forest growth.
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Highly stable glasses of cis-decalin and cis/trans-decalin mixtures.
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Carbonaceous sorbents for high-temperature interactive liquid chromatography of polyolefins.
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Far infrared (terahertz) spectroscopy of a series of polycyclic aromatic hydrocarbons and application to structure interpretation of asphaltenes and related compounds.
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Sonochemical effect on size reduction of CaCO3 nanoparticles derived from waste eggshells.
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Synthesis of monodisperse, highly cross-linked, fluorescent PMMA particles by dispersion polymerization.
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Electrophoresis of concentrated colloidal dispersions in low-polar solvents.
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Determination of absolute photoionization cross-sections of alkanes and cyclo-alkanes.
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trans-Decahydronaphthalene (decalin) from powder diffraction data.
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Aerobic biotransformation of decalin (decahydronaphthalene) by Rhodococcus spp.
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Enzymatic cyclizations of squalene analogs with threo- and erythro-diols at the 6,7- or 10,11-positions by recombinant squalene cyclase. Trapping of carbocation intermediates and mechanistic insights into the product and substrate specificities.
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Alpha 2u-globulin nephropathy and carcinogenicity following exposure to decalin (decahydronaphthalene) in F344/N rats.
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Single administration toxicokinetic studies of decalin (decahydronaphthalene) in rats and mice.
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How hard is a colloidal "hard-sphere" interaction?
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Chemical influences on adsorption-mediated self-propelled drop movement.
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Ultrasound-induced cracking and pyrolysis of some aromatic and naphthenic hydrocarbons.
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Hydroxylated decahydroquinolines as ligands for the vesicular acetylcholine transporter: synthesis and biological evaluation.
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Configurational relaxation of "Van Der Waals complexes" in solution.
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(1 beta, 5 alpha, 6 beta)-10,10- (1,2-ethylenedioxy)-1,5-dimethylbicyclo[4.4.0]decan-4-one.
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A decalin-consuming bacterial community.
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The effects of levamisole on urinary enzyme measurements and proximal tubule cell inclusions in male rats.
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Molecular weight distribution of a bulk ultra-high molecular weight polyethylene product--impax 5M + UHMW-NAT.
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Correlation of cocarcinogenic activity among n-alkanes with their physical effects on phospholipid micelles.
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[Effect of industrial solvents tetrahydronaphthalene (tetraline), decahydronaphthalene (decaline) and solvent naphtha I on the skin].
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The synthesis of some stereoisomeric derivatives of decahydronaphthalene.
PubMed:
On the mechanism of oxidation of trans-decahydronaphthalene at 100 degrees C.