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Product Name: | Indan | Synonyms: | 1,2-Hydrindene;1H-Indene, 2,3-dihydro-;INDANE OEKANAL, 250 MG;Indane,95%;1,2-dihydroindene;Indan Odor Standard;Hydrinden;Bicyclo[4.3.0]nona-1,3,5-triene | CAS: | 496-11-7 | MF: | C9H10 | MW: | 118.18 | EINECS: | 207-814-7 | Product Categories: | | Mol File: | 496-11-7.mol | |
| Indan Chemical Properties |
Melting point | -51 °C (lit.) | Boiling point | 176 °C (lit.) | density | 0.965 g/mL at 25 °C (lit.) | vapor pressure | 1.5 at 25 °C (extrapolated, Ambrose and Sprake, 1975) | refractive index | n20/D 1.537(lit.) | Fp | 50 °C | storage temp. | Sealed in dry,Room Temperature | solubility | Soluble in alcohol, ether (Weast, 1986), and many aliphatic hydrocarbons (hexane, pentane), and
aromatic hydrocarbons (benzene) | pka | >14 (Schwarzenbach et al., 1993) | form | Liquid | color | Clear colorless to yellow | Odor Threshold | 0.0037ppm | Water Solubility | Soluble in ethanol, diethyl ether, chloroform (slightly), and ether. Insoluble in water. | Merck | 14,4931 | BRN | 1904376 | Henry's Law Constant | (x 10-3 atm?m3/mol):
2.14 at 25 °C (approximate - calculated from water solubility and vapor pressure) | Stability: | Stable. Flammable. Incompatible with strong oxidizing agents. | InChIKey | PQNFLJBBNBOBRQ-UHFFFAOYSA-N | CAS DataBase Reference | 496-11-7(CAS DataBase Reference) | EPA Substance Registry System | Indan (496-11-7) |
Hazard Codes | Xn,F | Risk Statements | 10-65 | Safety Statements | 23-24/25-62 | RIDADR | UN 3295 3/PG 3 | WGK Germany | 3 | RTECS | NK3750000 | Hazard Note | Flammable | TSCA | Yes | HazardClass | 3 | PackingGroup | III | HS Code | 29029090 |
| Indan Usage And Synthesis |
Chemical Properties | Indane is a colourless to faintly yellow liquid. Insoluble in water, soluble in alcohol, ether and other organic solvents in any proportion. | Uses | Indane, is used as a catalytic agent, Petrochemical additive, used in organic synthesis. It is also used as pharmaceutical and chemical intermediate. | Application | Indane is used as anti-vibration agent for aviation fuel and anti-vibration agent for rubber industry. Its derivatives can be used in pharmaceuticals and solvents. Indane can be cracked to produce benzene compounds. | Preparation | Taking heavy benzene with a Indan content of 35% as a raw material, rectifying it through an emulsification tower, and cutting the 182°C fraction from the top of the tower, that is, Indan with a content of more than 90%.? | Definition | ChEBI: Indane is an ortho-fused bicyclic hydrocarbon consisting of a benzene ring fused to a cyclopentane ring; a high-boiling (176°C) colourless liquid. It is a member of indanes and an ortho-fused bicyclic hydrocarbon. | Synthesis Reference(s) | Journal of the American Chemical Society, 111, p. 314, 1989 DOI: 10.1021/ja00183a048 The Journal of Organic Chemistry, 41, p. 1184, 1976 DOI: 10.1021/jo00869a022 | Hazard | Irritant to skin and eyes. | Synthesis | 3-phenyl-1-propene is isomerized to give indane in the presence of AlCl3:
| Source | Detected in distilled water-soluble fractions of 87 octane gasoline (0.40 mg/L), 94 octane
gasoline (0.23 mg/L), Gasohol (0.50 mg/L), No. 2 fuel oil (0.05 mg/L), jet fuel A (0.15 mg/L), and
diesel fuel (0.06 mg/L) (Potter, 1996). Based on laboratory analysis of 7 coal tar samples, indan
concentrations ranged from ND to 3,800 ppm (EPRI, 1970). | Environmental fate | Photolytic. Gas-phase reaction rate constants for OH radicals, NO3 radicals, and ozone at 24 °C
were 1.9 x 10-11, 6.6 x 10-15, and <3 x 10-19 cm3/molecule?sec, respectively (Kwok et al., 1997). | Purification Methods | Shake indane with conc H2SO4, then water, dry and fractionally distil it. [Beilstein 5 H 486, 5 I 234, 5 II 376, 5 III 1200, 5 IV 1371.] |
| Indan Preparation Products And Raw materials |
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