Tetrabutylammoniumiodide

Product Information

Molecular Formula:
(CH3CH2CH2CH2)4NIC16H36IN
Molecular Weight:
369.38
Description
Tetrabutylammonium Iodide is one of numerous perovskite precursor materials
Synonyms
TBAI, Tetrabutyl ammonium iodide, Tetra-n-butylammonium iodide, Tetrabutylazanium iodide, N,N,N-Tributyl-1-butanaminium iodide
IUPAC Name
tetrabutylazaniumiodide
Canonical SMILES
CCCC[N+](CCCC)(CCCC)CCCC.[I-]
InChI
InChI=1S/C16H36N.HI/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
InChI Key
DPKBAXPHAYBPRL-UHFFFAOYSA-M
Melting Point
141-150ºC
Purity
95%
Density
1.2
Solubility
soluble in Alcohol,Ether
Appearance
white crystallization or white powder
Storage
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Safety Information

Hazards
H302 H315 H319
Precautionary Statement
P501 P270 P264 P280 P302 + P352 P337 + P313 P305 + P351 + P338 P362+P364 P332 + P313 P301 + P312 + P330
Signal Word
Warning

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
12
Exact Mass
369.18925 g/mol
Monoisotopic Mass
369.18925 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
18
Formal Charge
0
Complexity
116
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114163362-A Preparation method of N-benzenesulfonyl-4-halo-2-nitroaniline 2021-12-31
CN-114085192-A Method for refining gadoteridol intermediate 2021-12-30
CN-114133349-A Preparation method of 3, 4-disubstituted pyrrole derivative 2021-12-30
CN-114163399-A Synthesis method of 2H-benzothiazole C2 benzylated derivative 2021-12-14
CN-114163629-A Method for alkylating carbon-hydrogen bonds of polyether, polyethylene glycol and polyether polyol chains under iron catalysis 2021-12-14
CN-114177175-A Application of hydrophilic tetra-cation cyclic constructed based on TPE (thermoplastic elastomer) 2021-12-10
CN-114182270-A Method for preparing cyclic carbamate through continuous flow electric micro-reactor device 2021-12-10
CN-114016069-A Preparation method and application of gallium oxide-based liquid metal catalyst 2021-12-08
CN-114016058-A Method for electrochemically synthesizing alkyl sulfone compound 2021-12-07
CN-114085162-A Metal beta-lactamase inhibitor or pharmaceutically acceptable salt thereof, and preparation method and application thereof 2021-12-07

Literatures

PMID Publication Date Title Journal
22327513 2012-10-01 Novel nanostructure amino acid-based poly(amide-imide)s enclosing benzimidazole pendant group in green medium: fabrication and characterization Amino acids
22829307 2012-10-01 A series of amino acid functionalized tripodal hexaamide anion receptors: ion-pair-assisted capped-cleft formation by a pentafluorophenyl-functionalized amide Chemistry, an Asian journal
22875054 2012-09-25 Rhodium acetate/base-catalyzed N-silylation of indole derivatives with hydrosilanes Chemical communications (Cambridge, England)
22635072 2012-09-07 Thermal-induced dynamic self-assembly of adenine-grafted polyoxometalate complexes Dalton transactions (Cambridge, England : 2003)
22956458 2012-09-01 Convenient and efficient approach to the permanent or reversible conjugation of RNA and DNA sequences with functional groups Current protocols in nucleic acid chemistry
22790486 2012-08-28 A highly negatively charged γ-Keggin germanodecatungstate efficient for Knoevenagel condensation Chemical communications (Cambridge, England)
22838847 2012-08-23 Molecular and system parameters governing mass and charge transport in polar liquids and electrolytes The journal of physical chemistry. B
22733347 2012-08-07 Development of a new and environment friendly hollow fiber-supported liquid phase microextraction using vesicular aggregate-based supramolecular solvent The Analyst
22727328 2012-07-27 Extraction and stability of pesticide multiresidues from natural water on a mixed-mode admicellar sorbent Journal of chromatography. A
22832875 2012-07-25 Synthesis of 9,9'-[1,2-ethanediylbis(oxymethylene)]bis-2-amino-1,9-dihydro-6H-purin-6-one, an impurity of acyclovir Molecules (Basel, Switzerland)
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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