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71702

Sigma-Aldrich

Sodium iodate

puriss. p.a., ≥99.5% (RT)

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About This Item

Linear Formula:
NaIO3
CAS Number:
7681-55-2
Molecular Weight:
197.89
EC Number:
231-672-5
MDL number:
MFCD00003533
UNSPSC Code:
12352302
PubChem Substance ID:
329763447
NACRES:
NA.21

grade

puriss. p.a.

Quality Level

200

Assay

≥99.5% (RT)

form

powder or crystals

impurities

≤0.005% total nitrogen (N)

pH

5.0-8.0 (25 °C, 50 mg/mL in H2O)

solubility

water: soluble(lit.)

density

4.28 g/mL at 25 °C (lit.)

anion traces

bromide, bromate, chloride, chlorate (as Cl-): ≤200 mg/kg
iodide (I-): ≤20 mg/kg
sulfate (SO42-): ≤50 mg/kg

cation traces

Ca: ≤100 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤10 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

SMILES string

[Na+].[O-]I(=O)=O

InChI

1S/HIO3.Na/c2-1(3)4;/h(H,2,3,4);/q;+1/p-1

InChI key

WTCBONOLBHEDIL-UHFFFAOYSA-M

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General description

Sodium iodate (NaIO3) is colorless sodium salt having rhombic crystals. It exhibits oxidizing properties. In nature, it is found in Chile saltpeter.

Application

Sodium iodate may be employed as a starting reagent in the preparation of iodine and its derivatives. It may be employed as a catalyst in the synthesis of bis-indol.

Pictograms

Flame over circleExclamation mark
GHS03,GHS07

Signal Word

Danger

Hazard Statements

H272,H302,H317

Hazard Classifications

Acute Tox. 4 Oral - Ox. Sol. 2 - Skin Sens. 1

Storage Class Code

5.1B - Oxidizing hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Bis (indolyl) methanes Synthesis Through Sodium Iodate and Sodium Hydrogen Sulfite in Water.
Mohammed Khan K, et al.
J. Chem. Soc. Pak., 36(6) (2014)
Alyson Wolk et al.
Redox biology, 37, 101681-101681 (2020-08-24)
Sorsby Fundus Dystrophy (SFD) is a rare inherited autosomal dominant macular degeneration caused by specific mutations in TIMP3. Patients with SFD present with pathophysiology similar to the more common Age-related Macular Degeneration (AMD) and loss of vision due to both
Lihua Gong et al.
Clinical & experimental ophthalmology, 36(7), 666-671 (2008-11-06)
The differentiation of rat bone marrow mesenchymal stem cells (MSCs) was investigated in a retinal pigment epithelium (RPE) damage model induced by the administration of sodium iodate. Cultured rat MSCs were transfected with enhanced green fluorescent protein and transplanted into
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
Anna Machalińska et al.
Investigative ophthalmology & visual science, 54(13), 8292-8305 (2013-11-23)
Retinal degenerative diseases targeting the RPE and adjacent photoreceptors affect millions of people worldwide. The field of stem cell- and gene-based therapy holds great potential for the treatment of such diseases. The present study sought to graft genetically engineered mesenchymal
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