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Merck
CN

D124001

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:
Molecular Weight:
389.91
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-124-0
Beilstein/REAXYS Number:
2615358
MDL number:
Assay:
99%
Form:
powder
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Quality Level

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



pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves



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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
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
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-]



Global Trade Item Number

SKUGTIN
D124001-25G04061831813470