409278
Zinc iodide
anhydrous, beads, −10 mesh, 99.999% trace metals basis
Synonym(s):
Diiodozinc, Zinc diiodide
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About This Item
Linear Formula:
ZnI2
CAS Number:
Molecular Weight:
319.20
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
233-396-0
MDL number:
grade
anhydrous
Quality Level
assay
99.999% trace metals basis
form
beads
reaction suitability
reagent type: catalyst
core: zinc
particle size
−10 mesh
mp
445 °C (lit.)
density
4.74 g/mL at 25 °C (lit.)
SMILES string
I[Zn]I
InChI
1S/2HI.Zn/h2*1H;/q;;+2/p-2
InChI key
UAYWVJHJZHQCIE-UHFFFAOYSA-L
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT RE 2 Oral
target_organs
Thyroid
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
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Yuko Nakamura et al.
Journal of endodontics, 31(10), 755-758 (2005-09-28)
The purpose of this study was to investigate the cytotoxicity of iontophoresis treatment using direct current (DC) with or without antibacterial agents. The following antibacterial agents were used: diamine silver fluoride (AgF); sodium fluoride (NaF); and iodine zinc iodide (JJZ).
Y P Chau et al.
Histology and histopathology, 9(4), 649-656 (1994-10-01)
Cytochemical relationship between Golgi complex and dense-cored granules (DCGs) of small granule-containing (SGC) cells in rat superior cervical ganglia was examined in electron microscopy by zinc-iodide-osmium tetroxide (ZIO) method and by enzyme cytochemistry for thiamine pyrophosphatase (TPPase) and acid phosphatase
Mohammad Saquib et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(24), 6041-6049 (2009-05-07)
Simple and efficient syntheses, catalysed by a mixed Lewis acid system (ZrCl(4)/ZnI(2)), of enantiomerically pure 2- and 2,3-disubstituted furan derivatives--including important synthons such as 3-iodofuran and 3-(hydroxymethyl)furan derivatives--from commercially available 3,4,6-tri-O-acetyl-D-glucal are described. The transformation is achieved through a synergistic