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About This Item
Linear Formula:
KI
CAS Number:
Molecular Weight:
166.00
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
Recommended Products
grade
JIS special grade
vapor pressure
1 mmHg ( 745 °C)
Assay
≥99.5%
form
solid
availability
available only in Japan
pH
~6.9 (20 °C, 50 g/L)
mp
681 °C (lit.)
SMILES string
[K+].[I-]
InChI
1S/HI.K/h1H;/q;+1/p-1
InChI key
NLKNQRATVPKPDG-UHFFFAOYSA-M
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Application
- A cost-effective and facile technique for realizing fabric-based microfluidic channels using beeswax and PVC stencils: This research explores the application of potassium iodide in developing affordable microfluidic channels for biomedical applications, providing a significant advancement in material science and engineering (P L et al., 2024).
- Evaluating the Effect of Silver Diamine Fluoride, with or without Glutathione and Potassium Iodide, on Fluoride Release, Dentin Microhardness and Surface Properties of Dentin: The study investigates potassium iodide′s role in dental treatments, specifically its effects on dentin′s properties when used with silver diamine fluoride, a critical insight for dental material sciences (Samani M et al., 2024).
- Supramolecular Gels Based on C(3)-Symmetric Amides: Application in Anion-Sensing and Removal of Dyes from Water: This paper highlights potassium iodide′s utility in environmental testing, particularly in water purification and dye removal, making it vital for environmental science research (Kuppadakkath G et al., 2024).
- Machine learning-aided evaluation of oxidative strength of cold atmospheric plasma-treated water: This innovative study utilizes potassium iodide to assess water treatment processes, enhancing both environmental safety and technological applications in water quality management (Irmak SE et al., 2024).
- Supramolecular Structure of the β-Cyclodextrin Metal-Organic Framework Optimizes Iodine Stability and Its Co-delivery with l-Menthol for Antibacterial Applications: Research on potassium iodide within a metal-organic framework presents new possibilities in drug delivery and antibacterial treatments, providing significant contributions to pharmaceutical sciences (Zhao X et al., 2024).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
STOT RE 1 Oral
Target Organs
Thyroid
Storage Class Code
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Pietro Santulli et al.
Human reproduction (Oxford, England), 30(1), 49-60 (2014-11-08)
Are protein oxidative stress markers [thiols, advanced oxidation protein products (AOPP), protein carbonyls and nitrates/nitrites] in perioperative peritoneal fluid higher in women with histologically proven endometriosis when compared with endometriosis-free controls? Protein oxidative stress markers are significantly increased in peritoneal
Zhi-Qi Lao et al.
Organic & biomolecular chemistry, 10(39), 7869-7871 (2012-09-06)
We have developed a new KI-catalyzed method for the imidation of an sp(3) C-H bond adjacent to an amide nitrogen atom by using TBHP (tert-butyl hydroperoxide, 70% aqueous solution) as the oxidant. This novel procedure tolerated air and moisture and
S C Clement et al.
Pediatric blood & cancer, 60(11), 1833-1838 (2013-07-09)
Thyroid dysfunction has been reported in up to 52% of patients 1.4 years after treatment with (131) I-Metaiodobenzylguanidine (MIBG) in children with neuroblastoma (NBL), despite the use of potassium-iodide (KI). Our aim was to investigate if the incidence and severity
J B Sterling et al.
Journal of the American Academy of Dermatology, 43(4), 691-697 (2000-09-27)
Potassium iodide (KI) is a useful drug in the dermatologic armamentarium. It is successfully used for inflammatory dermatoses, most notably erythema nodosum, subacute nodular migratory panniculitis, nodular vasculitis, erythema multiforme, and Sweet's syndrome. KI is also successfully used for cutaneous
Kirsti Parikka et al.
Biomacromolecules, 13(8), 2418-2428 (2012-06-26)
Carboxylated, anionic polysaccharides were selectively prepared using a combination of enzymatic and chemical reactions. The galactose-containing polysaccharides studied were spruce galactoglucomannan, guar galactomannan, and tamarind galactoxyloglucan. The galactosyl units of the polysaccharides were first oxidized with galactose oxidase (EC 1.1.3.9)
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