Phenol sulfonic acids

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Phenol sulfonic acids
Surname 2-phenolsulfonic acid 3-phenolsulfonic acid 4-phenolsulfonic acid
other names o -Phenolsulfonic acid
2-Hydroxybenzenesulfonic acid Sozenic acid
m -phenolsulfonic acid
3-hydroxybenzenesulfonic acid
 
p -phenolsulphonic acid
4-hydroxybenzenesulphonic acid
 
Structural formula Structure of 2-phenolsulfonic acid Structure of 3-phenolsulfonic acid Structure of 4-phenolsulfonic acid
CAS number 609-46-1 585-38-6 98-67-9
PubChem 11867 11451 4765
ECHA InfoCard 100.009.266 100,008,688 100.002.447
Molecular formula C 6 H 6 O 4 S
Molar mass 174.18 g mol −1
Physical state firmly firmly
Brief description yellowish solid colorless crystal needles
Melting point 145 ° C (decomposition) 50 ° C (decomposition)
boiling point
solubility soluble in water
GHS
labeling
no classification available
no classification available
05 - Corrosive
danger
H and P phrases no H-phrases no H-phrases 314-290
see above see above no EUH phrases
see above see above 280-305 + 351 + 338-310

The phenol sulfonic acids (or hydroxybenzenesulfonic acids) form a group of substances in chemistry that is derived from both phenol and benzenesulfonic acid. The structure consists of a benzene ring with attached hydroxyl  (–OH) and sulfonic acid groups  (–SO 2 OH) as substituents . Their different arrangement results in three constitutional isomers with the empirical formula C 6 H 6 O 4 S. 2-Phenolsulfonic acid is rarely referred to by its common name as socolic acid.

properties

The phenolsulfonic acids are colorless to yellowish solids or liquids.

presentation

2-phenol and 4-phenolsulfonic acid can be prepared by sulfonation of phenol with concentrated sulfuric acid are recovered, wherein a mixture of the two compounds occurs. Another, more vigorous sulfonation of the phenol leads to phenol-2,4-disulfonic acid .

Individual evidence

  1. David R. Lide, George WA Milne, Handbook of Data on Common Organic Compounds, ISBN 0-8493-0404-0 .
  2. Entry on hydroxybenzenesulfonic acids. In: Römpp Online . Georg Thieme Verlag, accessed on April 28, 2019.
  3. a b Entry for CAS no. 98-67-9 in the GESTIS substance database of the IFA , accessed on December 27, 2019(JavaScript required) .
  4. ^ Beyer / Walter : Textbook of Organic Chemistry , 19th edition, S. Hirzel Verlag, Stuttgart 1981, ISBN 3-7776-0356-2 , p. 467.