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
Beilstein:
2615358
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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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
Nuclear frameworks: concepts and operational definitions.
N Stuurman et al.
Cell biology international reports, 16(8), 837-852 (1992-08-01)
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-]
G J Agostino et al.
Research communications in chemical pathology and pharmacology, 49(3), 401-414 (1985-09-01)
Group A, type 12 streptococcal cell membranes were extracted by aqueous lithium diiodosalicylate (LIS) and the extract treated with trifluorotrichloroethane (Genetron). An initial component was isolated (GLCM) which was soluble in aqueous buffer, but was heavily contaminated with LIS. Dialysis
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