1-Cyano-4-(dimethylamino)pyridinium tetrafluoroborate

Base Information

• Chemical Name: 1-Cyano-4-(dimethylamino)pyridinium tetrafluoroborate
• CAS No.: 59016-56-7
• Molecular Formula: C8H10BF4N3
• Molecular Weight: 234.99
• Hs Code.: 29333990
• European Community (EC) Number: 626-423-6
• UNII: P4W72066JT
• DSSTox Substance ID: DTXSID90432275
• Wikidata: Q27286180
• Mol file: 59016-56-7.mol

Synonyms:59016-56-7;1-Cyano-4-(dimethylamino)pyridinium tetrafluoroborate;CDAP;1-CYANO-4-(DIMETHYLAMINO)PYRIDIN-1-IUM TETRAFLUOROBORATE;1-cyano-4-dimethylamino-pyridinium tetrafluoroborate;4-(dimethylamino)pyridin-1-ium-1-carbonitrile;tetrafluoroborate;P4W72066JT;MFCD00011998;J1.615.455E;1- Cyano-4-(dimethylamino)pyridinium tetrafluoroborate;Pyridinium, 1-cyano-4-(dimethylamino)-, tetrafluoroborate(1-) (1:1);SCHEMBL161677;UNII-P4W72066JT;1-Cyano-4-dimethylaminopyridinium tetra-fluoroborate;C8H10BF4N3;DTXSID90432275;MBLVMDCQDCVKNE-UHFFFAOYSA-N;AMY37395;AKOS015832910;CS-W012900;DS-10052;SY058029;C2348;FT-0760795;H10633;A851414;Q27286180;Not available;1-Cyano-4-(dimethylamino)pyridin-1-ium tetrafluoroborate

Chemical Property of 1-Cyano-4-(dimethylamino)pyridinium tetrafluoroborate

Chemical Property:

• Appearance/Colour: White to yellow powder
• Melting Point: 196-200 °C
• PSA: 30.91000
• LogP: 1.66928
• Storage Temp.: 2-8°C
• Water Solubility.: Soluble in water, and acetonitrile.
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 1
• Exact Mass: 235.0903901
• Heavy Atom Count: 16
• Complexity: 179

Purity/Quality:

98% ^*data from raw suppliers

1-Cyano-4-dimethylaminopyridinium tetrafluoroborate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi,Xn
• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36-60-36/37-9

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: [B-](F)(F)(F)F.CN(C)C1=CC=[N+](C=C1)C#N
• Uses: 1-Cyano-4-(dimethylamino)pyridinium tetrafluoroborate is a cyanylation reagent for protein sulfhydryl groups and used to prepare protein-polysaccharide conjugates. It is employed as an activating agent for polysaccharide resins and conjugation of lipopolysaccharides while retaining endotoxic activity.