About 10 results for P-Toluenesulfonic acid
en.wikipedia.org › P-Toluenesulfonic_acid

P-Toluenesulfonic acid

para-Toluenesulfonic acid (PTSA, pTSA, or pTsOH) or tosylic acid (TsOH) is an organic compound with the formula CH3C6H4SO3H. It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. The...

Updated: October 13, 2026
en.wikipedia.org › Tosyl_group

Tosyl group

In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos) is a univalent functional group with the chemical formula −SO2−C6H4−CH3. It consists of a tolyl group, −C6H4−CH3, joined to a sulfonyl group, −SO2−, with the open...

Updated: June 14, 2026
en.wikipedia.org › Pyridinium_p-toluenesulfonate

Pyridinium p-toluenesulfonate

Pyridinium p-toluenesulfonate (PPTS) is a colourless solid salt of pyridine and p-toluenesulfonic acid.

Updated: April 23, 2026
en.wikipedia.org › Sulfanilic_acid

Sulfanilic acid

Sulfanilic acid (4-aminobenzenesulfonic acid) is an organic compound with the formula H3NC6H4SO3. It is an off-white solid. It is a zwitterion, which explains its high melting point compared to the related compounds aniline and benzenesulfonic acid.

Updated: October 13, 2026
en.wikipedia.org › Collidinium_p-toluenesulfonate

Collidinium p-toluenesulfonate

Collidinium p-toluenesulfonate or CPTS is a salt between p-toluenesulfonic acid and collidine (2,4,6-trimethylpyridine). It is used as a mild glycosylation catalyst in chemistry.

Updated: January 6, 2025
en.wikipedia.org › Sulfonic_acid

Sulfonic acid

In organic chemistry, sulfonic acid (or sulphonic acid) refers to a member of the class of organosulfur compounds with the general formula R−S(=O)2−OH, where R is an organic alkyl or aryl group and the S(=O)2(OH) group a sulfonyl hydroxide. A...

Updated: October 9, 2026
en.wikipedia.org › Di-n-propyl_ether

Di-n-propyl ether

Dipropyl ether is the symmetrical ether of two n-propyl groups. It is a colorless, flammable liquid with a sweet odor typical of ethers.

Updated: July 31, 2025
en.wikipedia.org › Fischer_indole_synthesis

Fischer indole synthesis

The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde or ketone under acidic conditions. The reaction was discovered in 1883 by Emil Fischer....

Updated: October 31, 2026
en.wikipedia.org › Acid_dissociation_constant

Acid dissociation constant

In chemistry, an acid dissociation constant (also known as acidity constant, or acid-ionization constant; denoted ⁠ K a {\displaystyle K_{a}} ⁠) is a...

Updated: October 11, 2026
en.wikipedia.org › Acid_strength

Acid strength

Acid strength is the tendency of an acid, symbolised by the chemical formula HA, to dissociate into a proton, H+, and an anion, A−. The dissociation or ionization of a strong acid in solution is effectively complete, except in its most concentrated...

Updated: October 9, 2026