Solvent Chemicals-19

Polysulfone, any of a class of resinous organic chemical compounds belonging to the family of polymers in which the main structural chain most commonly consists of benzene rings linked together by sulfonyl (―SO2―), ether (―O―), and isopropylidene (―C(CH3)2―) groups.

Octanol appears as a clear colorless liquid with a penetrating aromatic odor. Insoluble in water and floats on water. Vapors heavier than air. Vapors may irritate the eyes, nose, and respiratory system.

Is the ester of cinnamic acid and ethanol. It is present in the essential oil of cinnamon. Pure ethyl cinnamate has a "fruity and balsamic odor, reminiscent of cinnamon with an amber note"

Is a colorless to white crystalline (sand-like) solid. It is used in explosives, flares, rocket propellants, photography, as a medication, and as an agent in automobile safety air bags.

A naturally occurring alcohol found in fruits and vegetables and used as an osmotic diuretic. Mannitol is freely filtered by the glomerulus and poorly reabsorbed from the renal tubule, thereby causing an increase in osmolarity of the glomerular filtrate.

It is white, crystalline powder or white, granular crystals, slightly deliquescent in moist air, freely soluble in water, practically insoluble in alcohol.

A chemical compound that is used to make one of the building blocks of DNA and RNA. It is also a part of many substances in the body that give energy to cells.

Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH3CH2SH. is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH3CH2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in

Is a an organic compound with the chemical formula O(C6H5)2. Like other phenyl rings, diphenyl oxide is subject to various reactions like hydroxylation, halogenation, nitration, Friedel Crafts alkylation and sulfonation.

The compound is usually sold as a mixture of the E- and Z-isomers, which differ with respect to the relative position of the methyl and formyl groups. The E-isomer is more common