294772
Decahydronaphthalene, mixture of cis + trans
anhydrous, ≥99%
Sinónimos:
Decalin™
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Fórmula empírica (notación de Hill):
C10H18
Número CAS:
Peso molecular:
138.25
UNSPSC Code:
12190000
NACRES:
NA.21
PubChem Substance ID:
EC Number:
202-046-9
Beilstein/REAXYS Number:
878165
MDL number:
Assay:
≥99%
Grade:
anhydrous
Bp:
189-191 °C (lit.)
Vapor pressure:
42 mmHg ( 92 °C), 741 mmHg ( 188 °C)
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anhydrous
Quality Level
vapor density
4.76 (vs air)
vapor pressure
42 mmHg ( 92 °C), 741 mmHg ( 188 °C)
assay
≥99%
form
liquid
autoignition temp.
482 °F
expl. lim.
0.7-4.9 %, 100 °F
impurities
<0.002% water, <0.005% water (100 mL pkg)
refractive index
n20/D 1.474 (lit.)
bp
189-191 °C (lit.)
mp
−125 °C (lit.)
density
0.896 g/mL at 25 °C (lit.)
SMILES string
C1CCC2CCCCC2C1
InChI
1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2
InChI key
NNBZCPXTIHJBJL-UHFFFAOYSA-N
Application
Decahydronaphthalene, mixture of cis + trans has been used as a liquid phase to study the reaction rate of hydrogenation of cyclohexene in the presence of a Pd–Al/biomorphic carbon catalyst.
Legal Information
Decalin is a trademark of Sigma-Aldrich Co. LLC
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1C
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 3
flash_point_f
134.6 °F - closed cup
flash_point_c
57 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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The Densities and Surface Tensions of cis-and trans-Decahydronaphthalene between-30 and 180?1.
Seyer WF and Davenport CH.
Journal of the American Chemical Society, 63(9), 2425-2427 (1941)
Conformational isomerization of cis-decahydronaphthalene over zeolite catalysts.
Lai WC and Song C.
Catalysis Today, 31(1), 171-181 (1996)
Manuel F Wagenhofer et al.
Science advances, 6(19), eaax5331-eaax5331 (2020-05-20)
Unsupported Ni-Mo sulfides have been hydrothermally synthesized and purified by HCl leaching to remove Ni sulfides. Unblocking of active sites by leaching significantly increases the catalytic activity for dibenzothiophene hydrodesulfurization. The site-specific rates of both direct (hydrogenolytic) and hydrogenative desulfurization