Bismuth(III) Trifluoromethanesulfonate CAS 88189-03-1 Purity >98.0% Bi 31.0~32.6%

Short Description:

Name: Bismuth(III) Trifluoromethanesulfonate

CAS: 88189-03-1

Purity: >98.0%

Bi (Complexiometric EDTA): 31.0~32.6%

Appearance: White to Off-White Powder

E-Mail: alvin@ruifuchem.com

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Product Detail

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Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Bismuth(III) Trifluoromethanesulfonate (CAS: 88189-03-1) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Properties:

Chemical Name	Bismuth(III) Trifluoromethanesulfonate
Synonyms	Bi(OTf)3; Bismuth Tris(trifluoromethanesulfonate); Bismuth(III) Triflate; Bismuth Triflate; Trifluoromethanesulfonic Acid Bismuth Salt
CAS Number	88189-03-1
CAT Number	RF-PI2098
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	C3BiF9O9S3
Molecular Weight	656.18
Melting Point	300℃
Sensitivity	Hygroscopic
Solubility	Soluble in Organics Acetonitrile, Dioxane, Dimethyl Formamide and Dimethyl Sulfoxide
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	White to Off-White Powder
Purity	>98.0%
Bi (Complexiometric EDTA)	31.0~32.6%
Fluorine NMR Spectrum	Conforms to Structure
Proton NMR Spectrum	Conforms to Structure
Infrared Spectrum	Conforms to Structure
Test Standard	Enterprise Standard

Package & Storage:

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 moisture

Advantages:

FAQ:

Application:

Bismuth(III) Trifluoromethanesulfonate (CAS: 88189-03-1) is powerful Lewis acid useful in a number of catalytic reactions. Catalyst for organic syntheses. Bismuth(III) Trifluoromethanesulfonate acts as a catalyst in Friedel-Crafts acylation and cycloisomerization of allene-enol ethers. It behaves as a direct substitution catalyst and involved in the substitution of allylic, propargylic, and benzylic alcohols with sulfonamides, carboxamides and carbamates. Further, it is also used in Mukaiyama aldol reactions. Bismuth(III) trifluoromethanesulfonate may be used as a catalyst in the following processes: deprotection of acetals; cleavage of 2-tert-butoxy derivatives of thiophenes and furans; allylation of acetals to form homoallyl ethers.