Identification | More | [Name]
N-TRIACONTANE | [CAS]
638-68-6 | [Synonyms]
ALKANE C30 N-TRIACONTANE TRIACONTANE TRIACONTANE, STANDARD FOR GC N-TRIACONTANE, 500MG, NEAT n-Triacontane,99+% melissane | [EINECS(EC#)]
211-349-5 | [Molecular Formula]
C30H62 | [MDL Number]
MFCD00009410 | [Molecular Weight]
422.81 | [MOL File]
638-68-6.mol |
Chemical Properties | Back Directory | [Appearance]
white waxy solid | [Melting point ]
64-67 °C(lit.) | [Boiling point ]
258-259 °C3 mm Hg(lit.) | [density ]
0.7750 g/cm3 (78 ºC) | [refractive index ]
1.4352 (589.3 nm 70℃) | [Fp ]
238 °C
| [storage temp. ]
room temp | [solubility ]
chloroform: 10 mg/mL, clear
| [form ]
Shiny Flakes | [color ]
White | [Stability:]
Stable. Combustible. Incompatible with strong oxidizing agents. | [Water Solubility ]
Soluble in benzene, chloroform and toluene. Insoluble in water. | [BRN ]
1777281 | [LogP]
15.992 (est) | [CAS DataBase Reference]
638-68-6(CAS DataBase Reference) | [EPA Substance Registry System]
Triacontane (638-68-6) |
Hazard Information | Back Directory | [General Description]
Aliphatic hydrocarbon waxy solid. | [Reactivity Profile]
Saturated aliphatic hydrocarbons, such as N-TRIACONTANE(638-68-6), may be incompatible with strong oxidizing agents like nitric acid. Charring of the hydrocarbon may occur followed by ignition of unreacted hydrocarbon and other nearby combustibles. In other settings, aliphatic saturated hydrocarbons are mostly unreactive. They are not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents. When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, they burn exothermically to produce carbon dioxide and water. | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
Flash point data on this compound is not available, but N-TRIACONTANE is probably combustible. | [Chemical Properties]
white waxy solid | [Uses]
n-Triacontane is used to improve the threshold voltage and mobility for electrons of ambipolar organic light emitting field effect transistors with modified asymmetric electrodes. | [Definition]
ChEBI: A straight-chain alkane with 30 carbon atoms. |
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