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Hexane (/ ˈ h ɛ k s eɪ n /) or n-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C 6 H 14. [ 7 ] Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately 69 °C (156 °F).
log 10 of Hexane vapor pressure. Uses formula: log e P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ( 760 101.325 ) − 13.99935 log e ( T + 273.15 ) − 7284.572 T + 273.15 + 105.9605 + 1.410325 × 10 − 5 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-13.99935\log _{e}(T+273.15 ...
Aliphatic diisocyanates are used in specialty applications, such as enamel coatings which are resistant to abrasion and degradation by ultraviolet light.
This colorless liquid is one of the isomeric amines of hexane. At standard temperature and pressure, it has the ammonia/bleach odor common to amines and is soluble in almost all organic solvents. Applications
Inhalation overexposure causes primarily central nervous system (CNS) effects (headaches, dizziness, nausea, fatigue, and incoordination). In general, the toxicity is more pronounced with petroleum ethers containing higher concentrations of aromatic compounds. n-Hexane is known to cause axonal damage in peripheral nerves. [3]
Perfluorohexane (C 6 F 14), or tetradecafluorohexane, is a fluorocarbon.It is a derivative of hexane in which all the hydrogen atoms are replaced by fluorine atoms. It is used in one formulation of the electronic cooling liquid/insulator Fluorinert for low-temperature applications due to its low boiling point of 56 °C and freezing point of −90 °C.
Hexamethylenediamine or hexane-1,6-diamine, is the organic compound with the formula H 2 N(CH 2) 6 NH 2. The molecule is a diamine , consisting of a hexamethylene hydrocarbon chain terminated with amine functional groups .
Hexadecyl is an alkyl radical of carbon and hydrogen derived from hexadecane, with formula C 16 H 33 and with mass 225.433, [11] occurring especially in cetyl alcohol. [12] It confers strong hydrophobicity on molecules containing it. [13]