S4007
Sodium iodate
≥99%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
NaIO3
CAS Number:
Molecular Weight:
197.89
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-672-5
MDL number:
Assay:
≥99%
Product Name
Sodium iodate, ≥99%
InChI key
WTCBONOLBHEDIL-UHFFFAOYSA-M
InChI
1S/HIO3.Na/c2-1(3)4;/h(H,2,3,4);/q;+1/p-1
SMILES string
[Na+].[O-]I(=O)=O
assay
≥99%
density
4.28 g/mL at 25 °C (lit.)
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
Sodium iodate (NaIO3) can be used as an oxidant in the following processes:
- NaIO3/neutral Al2O3 catalytic system is used to synthesize a variety of aromatic, aliphatic, and alicyclic disulfides via oxidation of the corresponding thiols.
- NaIO3/Na2SO3/HCl is used in the preparation of 2-amino-1-iodonaphthalene by iodination of 2-naphthylamine.
- NaIO3/acetic anhydride or glacial acetic acid is used in aromatic oxidative iodination reactions.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Ox. Sol. 2 - Skin Sens. 1
Storage Class
5.1B - Oxidizing hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Simple Oxidation of Thiols with Sodium Iodate under Solid-Solution Biphasic Conditions
Hirano M, et al.
Journal of chemical research. Synopses, (12), 816-817 (1998)
Iodination of both deactivated and activated arenes with sodium periodate or sodium iodate as the oxidants
Lulinski P and Skulski L
Bulletin of the Chemical Society of Japan, 73(4), 951-956 (2000)
Jie Huang et al.
Molecular vision, 26, 494-504 (2020-07-09)
To observe the effects of tetramethylpyrazine (TMP) on mice retinas injured by sodium iodate (NaIO3). Male mice (n = 45) were randomly divided into three groups: the control group (Group C), the NaIO3-degenerated group (Group I), and the TMP-treated group
Reaction of 2-Naphthylamine with Sodium Iodate/Sodium Sulfite: Synthesis of 2-Amino-1-iodonaphthalene
Taldone T, et al.
Synthetic Communications, 42(5), 635-638 (2012)
Anna Machalińska et al.
Experimental eye research, 112, 68-78 (2013-04-30)
The retinal pigment epithelium (RPE) has been reported to demonstrate feasible self-regenerative potential under specific conditions. However, the precise underlying mechanisms involved in this process are still elusive. Here, we performed a sequential morphological, molecular, and functional analysis of retinal
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service