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Isoborneol is a bicyclic organic compound and a terpene derivative. The hydroxyl group in this compound is placed in an exo position. The endo diastereomer is called borneol .
Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: ... K f [2] K b [1] Water: 100.00 0.512 0.00 ... Boiling-point elevation; References
Boiling point: 213 °C (415 °F; 486 K) Solubility in water. ... Isobornyl is the univalent radical C 10 H 17 that is derived from isoborneol. [20]
Boiling point: 209 °C (408 °F; 482 K) Solubility in water. 1.2 g·dm −3: ... Hydrolysis of this ester gives isoborneol which can be oxidized to give racemic camphor.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
For the equivalent in degrees Fahrenheit °F, see: Boiling points of the elements (data page) Some values are predictions Primordial From decay Synthetic Border shows natural occurrence of the element
Water boiling at 99.3 °C (210.8 °F) at 215 m (705 ft) elevation. The boiling point of a substance is the temperature at which the vapor pressure of a liquid equals the pressure surrounding the liquid [1] [2] and the liquid changes into a vapor. The boiling point of a liquid varies depending upon the surrounding environmental pressure.
Isobornyl acetate is an organic compound consisting of the acetate ester or the terpenoid isoborneol. It is a colorless liquid with a pleasant pine-like scent, and it is produced on a multi-ton scale for this purpose. The compound is prepared by reaction of camphene with acetic acid in the presence of a strongly acidic catalyst such as sulfuric ...