Chemodex

1-Hydroxy-1,2-benziodoxol-3-one

Product Code:
 
CDX-H0103
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
Short term: +4°C. Long term: -20°C
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Chemical Structure
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Chemical Structure

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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
IBA; o-Iodosobenzoic acid; NSC 364374; BR-43089
Appearance:
White to off-white powder.
CAS:
131-62-4
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C7H5IO3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4,10H
InChiKey:
AZJIXRYFAZOEMC-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 131-62-4. Formula: C7H5IO3. MW: 264.1. Synthetic. Heterocyclic iodane with catalytic activity in the hydrolytic cleavage of reactive phosphates, phosphonates and carboxylates. Used as catalyst for the micellar cleavage of activated esters and phosphates and shown to be powerful reagent for the cleavage of phosphates in an aqueous cetyltrimethylammonium chloride (CTAC) micellar medium.
MDL:
MFCD01658875
Molecular Formula:
C7H5IO3
Molecular Weight:
264.1
Package Type:
Vial
Product Description:
Heterocyclic iodane with catalytic activity in the hydrolytic cleavage of reactive phosphates, phosphonates and carboxylates. Used as catalyst for the micellar cleavage of activated esters and phosphates and shown to be powerful reagent for the cleavage of phosphates in an aqueous cetyltrimethylammonium chloride (CTAC) micellar medium.
Purity:
>98% (HPLC)
SMILES:
O[I]1OC(=O)C2=CC=CC=C12
Solubility Chemicals:
Soluble in toluene.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) E. Shefter & W. Wolf; J. Pharm. Sci. 54, 104 (1965) | (2) W. Wolf, et al.; J. Pharm. Sci. 54, 329 (1965) | (3) R.A. Moss, et al.; J. Am. Chem. Soc. 105, 681 (1983) | (4) M. Xin & Z. Chen; Synth. Commun. 30, 63 (2000) | (5) V.V. Zhdankin; e-EROS Encycl. Reag. Org. Synth. (2006)