Substance

ID:335988

Tetrabutylammonium fluoride solution

Names and Identifiers
IUPAC name
tetrabutylazanium fluoride
Synonyms
TBAF 溶液TBAF solution四丁基氟化铵 溶液Tetrabutylammonium fluoride solution
IUPAC Traditional name
tetrabutylammonium fluoride
Registration numbers
MDL Number
CAS Number
Beilstein Number
PubChem SID
Properties
Physical Property
Flash Point
1.4 °F
-17 °C
Density
0.903 g/mL at 25 °C
Safety Information
Risk Statements
11-19-34-37
Storage Temperature
2-8°C
GHS Hazard statements
H225-H314-H335
GHS Precautionary statements
P210-P261-P280-P305+P351+P338-P310
German water hazard class
3
Packing Group
2
GHS Signal Word
Danger
Supplemental Hazard Statements
May form explosive peroxides.
European Hazard Symbols
Flammable Flammable (F)
Corrosive Corrosive (C)
GHS Pictograms
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
GHS05
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
UN Number
2924
MSDS Link
RID/ADR
UN 2924 3/PG 2
Safety Statements
16-26-36/37/39-45
Hazard Class
3
Product Information
Impurities
~5 wt. % water
Concentration
1.0 M in THF
Linear Formula
[CH3(CH2)3]4NF
Molecule Details
Frequently Asked Questions
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Packaging
1 L in Sure/Seal™
5 mL in glass bottle
2, 2.5 L in glass bottle
50, 100, 500 mL in Sure/Seal™
Application
Reactant for preparation of:
• Triple monoamine reuptake inhibitors as a new generation of antidepressants1
• Alcohols via hydrolysis of alkyl silyl ethers neutral pH in mixed organic-aqueous buffered solutions2
• Oligoribonucleotides with phosphonate-modified linkages3
• Aryl alkyl alcohols via Nozaki-Hiyama allylation catalyzed by chiral bipyridyldiol ligands and chromium trichloride4
• Conjugated dienoic acid esters using Suzuki coupling reactions5
• Macrocyclic o-aminobenzamide Hsp90 inhibitorwith antitumor activity6
• Phospshoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) dual inhibitors7
• Anti-diabetic polyacetylenic glucosides8
Molecular Spectra
No Data Available
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References
No Data Available
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