- 1-Phenyloctane
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- $30.00 / 5mg
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2026-01-05
- CAS:2189-60-8
- Min. Order:
- Purity: 96.08%
- Supply Ability: 10g
- 1-Phenyloctane
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- $0.00 / 25kg
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2025-12-01
- CAS:2189-60-8
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1000kg
- N-OCTYLBENZENE
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- $101.00 / 1KG
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2025-09-25
- CAS:2189-60-8
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | N-OCTYLBENZENE Basic information |
| | N-OCTYLBENZENE Chemical Properties |
| Melting point | -36 °C (lit.) | | Boiling point | 261-263 °C (lit.) | | density | 0.858 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.484(lit.) | | Fp | 226 °F | | storage temp. | Sealed in dry,Room Temperature | | form | Liquid | | color | Clear colorless | | Water Solubility | Immiscible with water. | | BRN | 1906253 | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. | | InChI | 1S/C14H22/c1-2-3-4-5-6-8-11-14-12-9-7-10-13-14/h7,9-10,12-13H,2-6,8,11H2,1H3 | | InChIKey | CDKDZKXSXLNROY-UHFFFAOYSA-N | | SMILES | CCCCCCCCc1ccccc1 | | CAS DataBase Reference | 2189-60-8(CAS DataBase Reference) | | NIST Chemistry Reference | n-Octylbenzene(2189-60-8) | | EPA Substance Registry System | Benzene, octyl- (2189-60-8) |
| Safety Statements | 23-24/25 | | WGK Germany | 3 | | TSCA | TSCA listed | | HS Code | 29029090 | | Storage Class | 10 - Combustible liquids |
| | N-OCTYLBENZENE Usage And Synthesis |
| Chemical Properties | colourless liquid | | Uses | n-octylbenzene is used as a solvent to study the self-assembly of derivatives of tetrathiafulvalene (TTF) on graphite and their visualization by scanning tunnelling microscopy (STM). It is also involved in the study the effects and substitution of these compounds. It is also used to prepare charge-transfer complexes with fluoranil and 1,3,5-trinitrobenzene. | | Uses | 1-Phenyloctane is used as a solvent to study the self-assembly of derivatives of tetrathiafulvalene (TTF) on graphite and their visualization by scanning tunnelling microscopy (STM). It is also used to study the effects of the substitution of these compounds on the interactions between them. | | Synthesis Reference(s) | Journal of the American Chemical Society, 111, p. 314, 1989 DOI: 10.1021/ja00183a048
Tetrahedron Letters, 27, p. 6369, 1986 DOI: 10.1016/S0040-4039(00)87811-9 | | General Description | Octylbenzene (1-Phenyloctane) forms charge-transfer complexes with fluoranil and 1,3,5-trinitrobenzene. | | Synthesis | A 100 ml four-necked flask equipped with a mechanical stirrer, thermometer, nitrogen inlet and septum was charged with CuCl2 (40 mg, 0.3 nmol, 3 mol%), octyl bromide (1.93 g, 10 nmol, 1 equiv.), benzonitrile (103 mg, 1 nmol, 10 mol%) and THF (9 mL). The reaction mixture was cooled to -5 ??C. A t-BuMgCl solution was added to THF (10 mL, 1.2 M, 12 nmol, 1.2 eq.) using a syringe pump for 15 min (40 mL/h). The reaction mixture was heated to 10??C. stirred for 2 hr. The solution was quenched with 1naq hydrochloric acid solution (20 ml). The aqueous phase was extracted with Et2O (3 x 20 mL). The combined organic layer was dried with MgSO4, filtered and concentrated under reduced pressure (0.13 bar) at ambient temperature. The crude residue was purified by silica gel (PE) flash column chromatography to afford 1-phenyloctane with purity >98%. |
| | N-OCTYLBENZENE Preparation Products And Raw materials |
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