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86903

Supelco

Tetrabutylammonium iodide

suitable for ion pair chromatography, LiChropur™, ≥99.0%

Sinônimo(s):

TBAI

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About This Item

Fórmula linear:
(CH3CH2CH2CH2)4N(I)
Número CAS:
311-28-4
Peso molecular:
369.37
Beilstein:
3916152
Número CE:
206-220-5
Número MDL:
MFCD00011636
Código UNSPSC:
12000000
ID de substância PubChem:
329769349
NACRES:
NB.21

descrição

cationic

Nível de qualidade

100

Ensaio

≥99.0% (AT)
≥99.0%

forma

crystals

qualidade

LiChropur™

técnica(s)

ion pair chromatography: suitable

pf

141-143 °C (lit.)
144-148 °C

λ

10 % in acetonitrile

Absorção UV

λ: 290 nm Amax: 0.1
λ: 300 nm Amax: 0.05
λ: 320 nm Amax: 0.02
λ: 500 nm Amax: 0.02

adequação

corresponds to standard for filter test

cadeia de caracteres SMILES

[I-].CCCC[N+](CCCC)(CCCC)CCCC

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

chave InChI

DPKBAXPHAYBPRL-UHFFFAOYSA-M

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Descrição geral

Tetrabutylammonium iodide is an ion-pair chromatography (IPC) reagent suitable for anionic separation sorted by carbon chain length.

Aplicação

Tetrabutylammonium iodide may be used as a mobile phase additive in ion-pair high-performance liquid chromatography (IP-HPLC) assay of 4-aminopyridine in serum. Tetrabutylammonium iodide may also be used as a mobile phase additive in the analysis of tetracycline by reversed-phase IPC. The addition of tetrabutylammonium iodide regulates the retention of tetracyclines.

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Informações legais

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302,H315,H319

Classificações de perigo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
BCCK1244
BCCC3651
BCCB7747
1097190V
1097190

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Ion-pair high-performance liquid chromatographic assay of 4-aminopyridine in serum
Shinohara Y, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 230(2), 363-372 (1982)
Reversed-phase ion-pair liquid chromatography of tetracyclines
Eksborg S and Ekqvist B
Journal of Chromatography A, 209(2), 161-173 (1981)
Fabio Galeotti et al.
Journal of chromatography. A, 1284, 141-147 (2013-03-05)
In this study, by using tetrabutylammonium bisulfate as ion-pairing reagent, we were able to separate all the main heparin/heparan sulfate disaccharides generated by the action of heparinases along with the main Hep tetrasaccharide possessing a 3-O-sulfate group on the sulfoglucosamine
Erbo Shi et al.
Organic letters, 14(13), 3384-3387 (2012-06-27)
A metal-free C-H oxidation for the construction of allylic esters has been developed. The use of a commercially available and inexpensive catalyst and oxidant, and readily available starting materials, coupled with the operational simplicity of the reaction, renders the methodology
R Bryan Sears et al.
Journal of inorganic biochemistry, 121, 77-87 (2013-01-29)
The complex cis-[Ru(phpy)(phen)(CH3CN)2](+) (phpy=2-phenylpyridine, phen=1,10-phenanthroline) was investigated as a potential photodynamic therapy (PDT) agent. This complex presents desirable photochemical characteristics including a low energy absorption tail extending into the PDT window (600-850nm) and photoinduced exchange of the CH3CN ligands, generating
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