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2-Sulfobenzoic anhydride

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2-Sulfobenzoic anhydride Basic information

Product Name:
2-Sulfobenzoic anhydride
Synonyms:
  • 2-SULFOBENZOIC ANHYDRIDE
  • 2-SULPHOBENZOIC ANHYDRIDE
  • 2-SULFOBENZOIC ACID ANHYDRIDE
  • 2-SULFOBENZOIC ACID CYCLIC ANHYDRIDE
  • 2,1-BENZOXATHIOL-3-ONE-1,1-DIOXIDE
  • 1,3-DIHYDRO-2,1LAMBDA6-BENZOXATHIOLE-1,1,3-TRIONE
  • 3-Oxo-3H-2,1-benzoxathiole 1,1-dioxide
  • 3H-Benzo[c][1,2]oxathiol-3-one 1,1-dioxide
CAS:
81-08-3
MF:
C7H4O4S
MW:
184.17
EINECS:
201-322-6
Product Categories:
  • pharmacetical
Mol File:
81-08-3.mol
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2-Sulfobenzoic anhydride Chemical Properties

Melting point:
116-124 °C
Boiling point:
184-186 °C18 mm Hg(lit.)
Density 
1.6114 (rough estimate)
refractive index 
1.6290 (estimate)
Flash point:
184-186°C/18mm
storage temp. 
Store below +30°C.
solubility 
soluble in Toluene
form 
Crystals or Crystalline Powder
color 
White to beige
Sensitive 
Moisture Sensitive
BRN 
139893
CAS DataBase Reference
81-08-3(CAS DataBase Reference)
NIST Chemistry Reference
2-Sulfobenzoic acid cyclic anhydride(81-08-3)
EPA Substance Registry System
3H-2,1-Benzoxathiol-3-one, 1,1-dioxide (81-08-3)
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Safety Information

Hazard Codes 
C
Risk Statements 
34-20/21/22
Safety Statements 
22-24/25-45-36/37/39-26
RIDADR 
2923
WGK Germany 
3
21
TSCA 
Yes
HS Code 
29163900

MSDS

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2-Sulfobenzoic anhydride Usage And Synthesis

Chemical Properties

White to beige crystals or crystalline powder

Uses

Polymerization inhibitor.

Purification Methods

The anhydride is purified by distillation in a vacuum and readily solidifies to a crystalline mass on cooling. [Heitman J Am Chem Soc 34 1594 1912.] Alternatively purify it by dissolving it in the minimum volume of toluene and refluxing for 2hours using a Dean-Stark trap. Evaporate under reduced pressure and distil the anhydride at 18mm. It is then recrystallised three times from its own weight of dry *C6H6. It is sensitive to moisture and should be stored in the dark in a dry atmosphere. The O-methyloxime has m 110-112o [Levy Tetrahedron Lett 3289 1972]. If the sample has hydrolysed extensively (presence of OH band in the IR) then treat with an equal bulk of SOCl2, reflux it for 3hours (CaCl2 tube), evaporate and distil the residue in a vacuum, then recrystallise it from *C6H6, Et2O/*C6H6 or CHCl3 (EtOH free by passing through Al2O3, or standing over CaCl2). [Clarke & Dreger Org Synth Coll Vol I 495 1941.] It is used for modifying -amino functions of lysyl residues in proteins [Bagree et al. FEBS Lett 120 275 1980]. [Beilstein 19 I 659, 19 II 137, 19 III/IV 1641, 19/4 V 215.]

2-Sulfobenzoic anhydride Preparation Products And Raw materials

Preparation Products

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