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CAS No 429-41-4 , tetrabutylazanium

  • Name: tetrabutylazanium
  • Synonyms: 22206-57-1;fluoride; 429-41-4; tetrabutylazanium fluoride; TBAF; TBAF solution; tetrabutylamine;Tetrabutylammonium fluoride; fluoride; CHEBI:51990;tetrabutylazanium;
  • CAS Registry Number:
  • Transport: UN 3261
  • Melting Point: 62-63 ºC
  • Flash Point: -17 ºC
  • Boiling Point: °Cat760mmHg
  • Density: 0.887
  • Refractive index: n20/D 1.456
  • Safety Statements: R11;R19;R34
  • Hazard Symbols: C: Corrosive;F: Flammable;
  • Flash Point: -17 ºC
  • EINECS: 207-057-2
  • Molecular Weight: 261.462143
  • InchiKey: FPGGTKZVZWFYPV-UHFFFAOYSA-M
  • InChI: InChI=1S/C16H36N.FH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,
    1-4H3;1H/q+1;/p-1
  • Risk Statements: S16;S26;S29;S33;S36/37/39;S45
  • Molecular Formula: C16H36FN
  • Molecular Structure:CAS No:429-41-4 tetrabutylazanium
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429-41-4 Tetrabutylammonium fluoride

  • Chemreagents is dedicated to bring high quality and cost effective chemical reagents and advanced intermediates to our global customers. Chemreagents has more than 30000 products in stock at our warehouse. In addition to the catalog products, Chemrea...
  • Min. Order: 1000
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  • United States Pure Chemistry Scientific Inc. [Manufacturer, Distributor/Wholesaler]
  • Tel: 1-857-9282050
  • Address: 108 Water Street, Room 4D Watertown,MAUnited States
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429-41-4 Tetrabutylammonium fluoride

  • used as a source of fluoride ion in organic solvents.
  • Min. Order: 1000
  • FOB Price: USD10 - 30 /
  • China Hunan Huateng Pharmaceutical Co. Ltd. [Manufacturer]
  • Tel: 86-0731-82251112
  • Address: Lugu Business Plaza E1, Yuelu District Changsha,HunanChina
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429-41-4 TETRA-N-BUTYLAMMONIUM FLUORIDE; 1M SOLUTION IN THF

  • Germany ABCR GmbH & Co KG [Manufacturer]
  • Tel: +49 721 95061-0
  • Fax: +49 721 95061-80
  • Address: Im Schlehert 10
    76187 Karlsruhe
    Germany null,nullGermany
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429-41-4 TETRA-N-BUTYLAMMONIUM FLUORIDE

  • Germany CHEMOS GmbH [Manufacturer]
  • Tel: 0049 9402/9336 0
  • Fax: 0049 9402/9336 13
  • Address: CHEMOS GmbH
    Werner-von-Siemensstr. 3
    93128 Regenstauf
    Germany null,nullGermany
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429-41-4 Tetrabutylammonium fluoride

  • China Watson International Ltd. null
  • Tel: +86-(512)-55117610
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  • Address: Room 1209, Asia Pacific Plaza, Huaqiao International Business Park, Kunshan, Jiangsu 215332, null,nullChina
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429-41-4 Tetrabutylammonium fluoride

  • United States HBCChem, Inc. [Manufacturers]
  • Tel: +1-510-219-6317
  • Fax: +1-510-675-0318
  • Address: null Union City,CaliforniaUnited States
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429-41-4 TETRABUTYLAMMONIUM FLUORIDE

  • United States Bromorganics Corporation [Manufacturer]
  • Tel: 847-238-9588
  • Fax: 847-238-9688
  • Address: Bromorganics Corporation
    P. O. Box 722
    Elk Grove Village, Illinois 60009 null,nullUnited States
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429-41-4 Tetrabutylammonium fluoride

  • China Shanghai Hanhong Chemical Co., Ltd. [Manufacturer, Trading Company, Agent]
  • Tel: +86-(21)-64762736, 64531573
  • Fax: +86-(21)-54291107
  • Address: 206-209, NO.1 Building , NO.245,Jiachuan Road, Xuhui District, Shanghai, Xuhui District,ShanghaiChina
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429-41-4 Tetrabutylammonium fluoride

  • China ORCHID CHEMICAL SUPPLIES LTD (OCS) [Importer/Exporter]
  • Tel: +86-571-85395792
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  • Address: 607, North Zhongshan Road, Hangzhou 310000 China null,ZhejiangChina
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429-41-4 Tetrabutyl Ammonium Fluoride

  • China Goly Chemical Co., Ltd. [Manufacturers]
  • Tel: +86-(632)-6163187
  • Fax: +86-(632)-5100028
  • Address: Room No.6.Building21 LongXingBeiLi,ShiZhong, ZaoZhua, ShanDong 277102, ZaoZhuang,ShanDongChina
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References of tetrabutylazanium
Title: Tetrabutylammonium Fluoride
CAS Registry Number: 429-41-4
CAS Name: N,N,N-Tributyl-1-butanaminium fluoride
Synonyms: TBAF
Molecular Formula: C16H36FN
Molecular Weight: 261.46
Percent Composition: C 73.50%, H 13.88%, F 7.27%, N 5.36%
Literature References: Catalytic reagent which is both a potent base and a source of nucleophilic fluoride. Prepn as hydrated form: D. L. Fowler et al., J. Am. Chem. Soc. 62, 1140 (1940). Instability of anhydrous form: R. K. Sharma, J. L. Fry, J. Org. Chem. 48, 2112 (1983). Use as fluoride source: D. P. Cox et al., ibid. 49, 3216 (1984); T. Kobayashi et al., ibid. 67, 3156 (2002). Synthesis and/or use as catalyst in cyclization reactions: J. Pless, ibid. 39, 2644 (1974); A. R. Gangloff et al., Tetrahedron Lett. 42, 1441 (2001); in addition reactions: P. Molina et al., Synlett 2003, 714. Deprotecting agent: M. Namikoshi et al., J. Org. Chem. 56, 5464 (1991); J. J. Parlow et al., Bioorg. Med. Chem. Lett. 8, 2391 (1998). Brief review in cleavage of silyl protecting groups: M. B. Kumar, Synlett 2002, 2125-2126.
Properties: Colorless oil which crystallizes on exposure to humidity.
Use: Reagent in organic syntheses in addition, condensation, base-catalyzed cyclization reactions, fluorination and desulfonylation reactions and as a deprotecting agent. Typically dried prior to use.