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Merck

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:
133-91-5
Molecular Weight:
389.91
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893385
EC Number:
205-124-0
Beilstein/REAXYS Number:
2615358
MDL number:
MFCD00002444

Key Documents

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Product Name

3,5-Diiodosalicylic acid, 99%

InChI key

DHZVWQPHNWDCFS-UHFFFAOYSA-N

InChI

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

SMILES string

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

assay

99%

form

powder

mp

220-230 °C (dec.) (lit.)

Quality Level

100

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GHS07

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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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Certificates of Analysis (COA)

Lot/Batch Number
WXBF7006V
WXBF0540V
WXBF2080V
STBK1317
STBJ0625

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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)
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
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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