Sodium periodate

Reagent grade, 99.5%

Reagent Code: #78801
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Alias sodium periodate; sodium metaperiodate, sodium periodate
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CAS Number 7790-28-5

science Other reagents with same CAS 7790-28-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.89 g/mol
Formula NaIO₄
badge Registry Numbers
EC Number 232-197-6
MDL Number MFCD00003534
thermostat Physical Properties
Melting Point 270 °C
Boiling Point 300°C
inventory_2 Storage & Handling
Density 3.865g/mL
Storage Room temperature, dry, sealed

description Product Description

Used extensively in organic synthesis, particularly for the oxidative cleavage of vicinal diols to produce aldehydes or ketones. This reaction is crucial in carbohydrate chemistry for analyzing and modifying sugar structures.

In biochemistry, it is employed to oxidize glycoproteins and glycolipids, aiding in the study of complex biomolecules. It also plays a role in labeling and detecting specific biomolecules in research.

Additionally, it is utilized in the preparation of diagnostic reagents and in the modification of surfaces for biosensor applications. Its strong oxidizing properties make it valuable in various industrial processes, including the production of specialty chemicals and materials.

format_list_bulleted Product Specification

Test Parameter Specification
Potassium (K) 0-0.01%
Manganese (Mn) 0-0.0002
Basis 99.5-100.5
Appearance White to light yellow powder
Clarity PASS
Solubility Clear or very slightly hazy (50 mg/mL, water)
X-ray Diffraction Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿1,680.00
inventory 2.5kg
10-20 days ฿29,500.00
inventory 500g
10-20 days ฿6,780.00
inventory 25g
10-20 days ฿490.00

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Sodium periodate
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Used extensively in organic synthesis, particularly for the oxidative cleavage of vicinal diols to produce aldehydes or ketones. This reaction is crucial in carbohydrate chemistry for analyzing and modifying sugar structures.

In biochemistry, it is employed to oxidize glycoproteins and glycolipids, aiding in the study of complex biomolecules. It also plays a role in labeling and detecting specific biomolecules in research.

Additionally, it is utilized in the preparation of diagnostic reagents

Used extensively in organic synthesis, particularly for the oxidative cleavage of vicinal diols to produce aldehydes or ketones. This reaction is crucial in carbohydrate chemistry for analyzing and modifying sugar structures.

In biochemistry, it is employed to oxidize glycoproteins and glycolipids, aiding in the study of complex biomolecules. It also plays a role in labeling and detecting specific biomolecules in research.

Additionally, it is utilized in the preparation of diagnostic reagents and in the modification of surfaces for biosensor applications. Its strong oxidizing properties make it valuable in various industrial processes, including the production of specialty chemicals and materials.

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