Neodymium(III) Trifluoromethanesulfonate CAS 34622-08-7 Purity >98.0% (Chelometric Titration) Nd 23.7~25.0%

Name: Neodymium(III) Trifluoromethanesulfonate

Synonyms: Neodymium(III) Triflate 

CAS: 34622-08-7

Purity: >98.0% (Chelometric Titration) 

Nd: 23.7~25.0% (Complexiometric EDTA)

White to Pink to Purple Powder or Crystals 

E-Mail: alvin@ruifuchem.com

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Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moistureShanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Neodymium(III) Trifluoromethanesulfonate (CAS: 34622-08-7) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com
Item Specifications
Appearance White to Pink to Purple Powder or Crystals
Purity / Analysis Method >98.0% (Chelometric Titration) (calcd.on anh.substance) 
Nd 23.7~25.0% (Complexiometric EDTA)
Water by Karl Fischer <20.0%
Infrared Spectrum Conforms to Structure
Test Standard Enterprise Standard

Description:

Specifications:

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Chemical Name Neodymium(III) Trifluoromethanesulfonate
Synonyms Neodymium(III) Triflate; Neodymium Trifluoromethanesulfonate; Trifluoromethanesulfonic Acid Neodymium(III) Salt; Neodymium Perfluoromethanesulfonate
CAS Number 34622-08-7
CAT Number RF-PI2105
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula Nd(CF3SO3)3
Molecular Weight 591.45
Density 1.7
Sensitivity Air Sensitive
Solubility Soluble in Water
Stability Hygroscopic
Storage Temp Argon Charged
Brand Ruifu Chemical

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Application:

Neodymium(III) Trifluoromethanesulfonate (CAS: 34622-08-7), Stable Lewis Acids in Aqueous Media. Neodymium(III) Trifluoromethanesulfonate is used in the Aldol reaction of silyl enol ethers with aldehydes and as a catalyst for dehydration of fructose, Diels-Alder reactions of cyclopentadiene and alkyl acrylates, α-amination reactions of pyrazolones, polymerization reactions of cyclosiloxanes, direct polycondensation of dicarboxylic acids and diols, regioselective reductive ring opening of benzylidene acetals, Paal-Knorr cyclocondensation and nitration of benzene. 

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