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D124001

Sigma-Aldrich

3,5-Diiodosalicylic acid

99%

Synonym(s):

2-Hydroxy-3,5-diiodobenzoic acid, 3,5-Diiodo-2-hydroxybenzoic acid

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About This Item

Linear Formula:
I2C6H2(OH)CO2H
CAS Number:
133-91-5
Molecular Weight:
389.91
Beilstein:
2615358
EC Number:
205-124-0
MDL number:
MFCD00002444
UNSPSC Code:
12352100
PubChem Substance ID:
24893385
NACRES:
NA.22

Assay

99%

form

powder

mp

220-230 °C (dec.) (lit.)

SMILES string

OC(=O)c1cc(I)cc(I)c1O

InChI

1S/C7H4I2O3/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2,10H,(H,11,12)

InChI key

DHZVWQPHNWDCFS-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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D Restrepo et al.
The Journal of general physiology, 100(5), 825-846 (1992-11-01)
We have developed a new test to differentiate between ping-pong and simultaneous mechanisms for tightly coupled anion exchange. This test requires the use of a dead-end reversible noncompetitive inhibitor. As an example, we have applied the test to the anion
P Belgrader et al.
Journal of cell science, 98 ( Pt 3), 281-291 (1991-03-01)
Different agents have been employed to extract the histones and other soluble components from isolated HeLa S3 nuclei during nuclear matrix isolation. We report that 0.2M (NH4)2SO4 is a milder extracting agent than NaCl and LIS (lithium 3,5-diiodosalicylate), on the
L Simchowitz et al.
The American journal of physiology, 261(5 Pt 1), C906-C915 (1991-11-01)
Organotin derivatives represent a class of artificial ionophores that mediate Cl(-)-OH- exchange and thereby facilitate the chemical equilibrium distribution of Cl- and H+ across biological membranes. Imposing different pH and Cl- gradients by varying extracellular pH (pHo) and extracellular [Cl-]
Nuclear frameworks: concepts and operational definitions.
N Stuurman et al.
Cell biology international reports, 16(8), 837-852 (1992-08-01)
Z Avramova et al.
Plant molecular biology, 22(6), 1135-1143 (1993-09-01)
Nuclear matrices were isolated from maize leaves by the two conventional methods usually employed for the preparation of the corresponding structures of animal origin. It is demonstrated that functionally competent matrices, recognizing and specifically binding the MAR-containing DNA of the
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