4-Chloromercuribenzoic acid

Summary

4-Chloromercuribenzoic acid (p-chloromercuribenzoic acid, PCMB) is an organomercury compound that is used as a protease inhibitor, especially in molecular biology applications.

4-Chloromercuribenzoic acid[1]
Names
IUPAC name
(4-Carboxyphenyl)chloromercury
Other names
p-Chloromercurybenzoic acid; p-Chloromercuribenzoate; 4-Chloromercuribenzoate
Identifiers
  • 59-85-8 checkY
3D model (JSmol)
  • Interactive image
Abbreviations PCMB
3662892
ChEBI
  • CHEBI:28420 checkY
ChEMBL
  • ChEMBL575867 checkY
ChemSpider
  • 1667 checkY
ECHA InfoCard 100.000.402 Edit this at Wikidata
EC Number
  • 200-442-6
261316
KEGG
  • C03444
  • 1730
UNII
  • E1LE0WZ4BO checkY
  • DTXSID8040725 Edit this at Wikidata
  • InChI=1S/C7H5O2.ClH.Hg/c8-7(9)6-4-2-1-3-5-6;;/h2-5H,(H,8,9);1H;/q;;+1/p-1 checkY
    Key: YFZOUMNUDGGHIW-UHFFFAOYSA-M checkY
  • InChI=1/C7H5O2.ClH.Hg/c8-7(9)6-4-2-1-3-5-6;;/h2-5H,(H,8,9);1H;/q;;+1/p-1/rC7H5ClHgO2/c8-9-6-3-1-5(2-4-6)7(10)11/h1-4H,(H,10,11)
    Key: YFZOUMNUDGGHIW-PSWPUYSSAS
  • O=C(O)c1ccc([Hg]Cl)cc1
Properties
C7H5ClHgO2
Molar mass 357.16 g·mol−1
Melting point 287 °C (549 °F; 560 K) (dec.)
Hazards
GHS labelling:
GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
Danger
H300, H310, H330, H373, H410
P260, P262, P264, P270, P271, P273, P280, P284, P301+P310, P302+P350, P304+P340, P310, P314, P320, P321, P322, P330, P361, P363, P391, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

PCMB reacts with thiol groups in proteins and is therefore an inhibitor of enzymes that are dependent on thiol reactivity, including cysteine proteases such as papain and acetylcholinesterase. Because of this reactivity with thiols, PCMB is also used in titrimetric quantification of thiol groups in proteins.

See also edit

References edit

  1. ^ 4-Chloromercuribenzoic acid at Sigma-Aldrich