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2-Iodosobenzoic acid

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2-Iodosobenzoic acid manufacturers

2-Iodosobenzoic acid Basic information
Product Name:2-Iodosobenzoic acid
Synonyms:2-iodosyl-benzoicaci;2-iodosylbenzoicacid;o-iodoso-benzoicaci;o-iodosylbenzoicacid;2-IODOSOBENZOIC ACID;2-Iodosobenzoic acid 97%;2-iodosobenzoic acid moistened with water (H2O ~10%);Iodosobenzoicacid
CAS:304-91-6
MF:C7H5IO3
MW:264.02
EINECS:206-159-4
Product Categories:Hypervalent Iodine Compounds;Oxidation;Synthetic Organic Chemistry;Reagents for Chemical Cleavage of Proteins;Enzymatic and Chemical Protein Cleavage;Mass Spectrometry;proteinmod
Mol File:304-91-6.mol
2-Iodosobenzoic acid Structure
2-Iodosobenzoic acid Chemical Properties
Melting point 230 °C (dec.)(lit.)
storage temp. −20°C
form Powder
pka2.84±0.36(Predicted)
color White to off-white
Water Solubility Insoluble in water.
Sensitive Light Sensitive
BRN 1939973
InChI1S/C7H5IO3/c9-7(10)5-3-1-2-4-6(5)8-11/h1-4H,(H,9,10)
InChIKeyIFPHDUVGLXEIOQ-UHFFFAOYSA-N
SMILESOC(=O)c1ccccc1[I]=O
CAS DataBase Reference304-91-6(CAS DataBase Reference)
EPA Substance Registry System2-Iodosylbenzoic acid (304-91-6)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS DH3056550
F 8-23
Hazard Note Irritant
HS Code 29163990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2-Iodosobenzoic acid Usage And Synthesis
Chemical PropertiesWhite powder
Uses1-Organosulfonyloxy-1, 2-benziodoxol-3-(1H)-ones (3, 4, 5) can be prepared in one step from 2-iodosobenzoic acid and the corresponding sulfonic acids. 2-carboxydiphenyliodonium salts was prepared by the acid-catalyzed condensation of 2-iodosobenzoic acid with benzene, mesitylene, and cyclohexylbenzene.
DefinitionChEBI: A benzoic acid compound having an iodosyl substituent at the ortho-position.
Biological Activity2-Iodosobenzoic acid (IBA) may be used to study enzyme structure and activity. IBA is used as an oxidant which oxidizes vicinal sulfhydryls to disulfides (cysteine residues) within enzymes leading to their inactivation or conformational changes. IBA is also used to cleave tryptophanyl peptide bonds.
Purification MethodsCrystallise the acid from EtOH and dry it in vacuo.[Beilstein 9 H 363.]
2-Iodosobenzoic acid Preparation Products And Raw materials
Tag:2-Iodosobenzoic acid(304-91-6) Related Product Information
Ferrous sulfate Citric acid 2-Acetylbenzoic acid 2-Iodobenzoic acid Methyl 2-iodobenzoate 2-Iodoxybenzoic acid Sodium lauroylglutamate Ascoric Acid 1-Hydroxy-1,3-dioxo-1,3-dihydro-1L5-benzo[d][1,2]iodoxole-4-carboxylic acid 2-Iodosobenzoic acid o-Iodosobenzoic acid, sodium salt Benzoic acid, 2-iodyl, 1-methylethyl ester 4-Propyl-2-iodosobenzoic acid 4-Pentyl-2-iodosobenzoic acid 4-Methyl-2-iodosobenzoic acid 4-Octyl-2-iodosobenzoic acid 4-Iodosobenzoic acid 4-Ethyl-2-iodosobenzoic acid