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Sodium isopropoxide / 5g

Synonym: Sodium propan-2-olate
Molecular Formula: C3H7NaO
Molecular Weight: 82.08
SKU: MND-127921
CAS Number: 683-60-3
MDL number: MFCD00061566
EC Number: 211-673-7
Form: Crystalline
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 5g  
43.26 EUR



Safety Information


Hazard Statements

H314
H228
H251

Precautionary Statements

P210
P280
P271
P240
P264b
P304 + P340
P305 + P351 + P338
P362 + P364
P403 + P233
P501c
P301 + P330 + P331
P303 + P361 + P353
P235 + P410

Pictograms



Properties

Melting Point70-75°

 Product Description

Sodium isopropoxide is an alkoxide, specifically a sodium alkoxide, derived from isopropanol. It is a white solid that dissolves readily in water and ethanol, making it useful in various chemical reactions and processes. Sodium isopropoxide is primarily used as a catalyst in the production of polymers and plastics, where it promotes the polymerization of olefins and other monomers. Its reactivity and solubility characteristics make it an essential component in the chemical industry.

 

Application:

In the chemical industry, sodium isopropoxide is employed as a catalyst in the polymerization of olefins, leading to the production of polypropylene and other polyolefin-based materials. Its role in initiating and accelerating the polymerization process allows for the control of polymer properties such as molecular weight and branching, which are critical for the performance of final products. Additionally, its use extends to the synthesis of other organic compounds and materials.

 

 

Articles:

- Nonequilibrium Anionic Ring-opening Polymerization of Tetraphenyltetramethylcyclotetrasiloxane (D4Me,Ph) Initiated by Sodium Isopropoxide

Publication Date: 26 Aug 2014

Xiyin Gao, Qian Wang, Hongjie Sun, Yongxia Tan, Zhijie Zhang & Zemin Xie

https://doi.org/10.1080/10426507.2013.860534

 

- The Reaction of 2,4,6-Trinitrotoluene and 2,4,6-Trinitrotoluene-d3 with Sodium Isopropoxide in Isopropyl Alcohol

Publication Date: May 1974

E. Buncel, A. R. Norris, K. E. Russell, P. Sheridan and H. Wilson

https://doi.org/10.1139/v74-252

 

- Azirines. III. The Preparation of Azirine Derivatives by the Base-Catalyzed Rearrangement of Quaternary Hydrazones

Publication Date: 27 March 2006

Shimao Sato

https://doi.org/10.1246/bcsj.41.1440