Tetrabutylammonium hydrogen difluoride solution(TBABF) - technical grade, ~50% in methylene chloride (T) , CAS No.23868-34-0

CAS: 23868-34-0 Cat. No.: T432356 Peso molecular: 281.48 Número EC: 629-504-4 PubChem CID: 10891295
Disponible para pedir
GRADE & PURITY Technical grade ? Technical grade — industrial-quality purity with no tight impurity guarantees. Use for large-scale or non-critical processes where cost matters most. ~50% in methylene chloride (T)
Synonyms
ZHBDKVWQJKYIFF-UHFFFAOYSA-M | tetrabutylazanium;fluoride;hydrofluoride | FT-0713578 | tetra-n-butylammonium bifluoride | D75244 | SCHEMBL1847525 | tetrabutylammonium fluoride hydrofluoride | Tetrabutylammonium bifluoride | MFCD00077877 | DTXSID10447386 |
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100ml
T432356-100ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

2.075,90US$

2.422,90US$
Guardar 347,00 US$ (14.32%)
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Why this grade

technical grade, ~50% in methylene chloride (T) Technical grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Application

Used as an etchant for silica films Reactant for: Nucleophilic fluorination Ring-opening fluorination reaction Substitution reactions Tetrabutylammonium hydrogen difluoride (TBABF) can be used as a reagent: For the conversion of aromatic boronic acids and esters into corresponding tetrabutylammonium trifluoroborate salts. These salts are utilized as surrogates of boronic acids in Suzuki-Miyaura cross-coupling reactions. In the nucleophilic fluorination of organic halides, tosylates, and triflates. For the regioselective synthesis of fluorohydrins by ring-opening of terminal epoxides.

Specifications

Sinónimos
ZHBDKVWQJKYIFF-UHFFFAOYSA-M | tetrabutylazanium;fluoride;hydrofluoride | FT-0713578 | tetra-n-butylammonium bifluoride | D75244 | SCHEMBL1847525 | tetrabutylammonium fluoride hydrofluoride | Tetrabutylammonium bifluoride | MFCD00077877 | DTXSID10447386 |
Especificaciones y pureza
technical grade, ~50% in methylene chloride (T)
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Technical grade
Nombres e identificadores
Sonrisas canónicasCCCC[N+](CCCC)(CCCC)CCCC.F.[F-]
IUPAC Nametetrabutylazanium;fluoride;hydrofluoride
InChIKeyZHBDKVWQJKYIFF-UHFFFAOYSA-M
INCHI1S/C16H36N.2FH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;;/h5-16H2,1-4H3;2*1H/q+1;;/p-1
Isómeros SMILES CCCC[N+](CCCC)(CCCC)CCCC.F.[F-]
PubChem CID 10891295
Peso molecular 281.48
Reaxy-Rn 4729304

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClaseOrganonitrogen compounds
SubclassQuaternary ammonium salts
Intermediate Tree Nodes Not available
Direct ParentTetraalkylammonium salts
Alternative Parents Organic salts  Hydrocarbon derivatives  Amines  Organic cations  
Molecular FrameworkAliphatic acyclic compounds
Substituents Tetraalkylammonium salt - Hydrocarbon derivative - Organic salt - Amine - Organic cation - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Peso molecular281.470 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count12
Exact Mass281.289 Da
Monoisotopic Mass281.289 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity116.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Calculadoras de soluciones
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